WO2015012803A1 - Packaging materials and methods for their preparation and use - Google Patents

Packaging materials and methods for their preparation and use Download PDF

Info

Publication number
WO2015012803A1
WO2015012803A1 PCT/US2013/051594 US2013051594W WO2015012803A1 WO 2015012803 A1 WO2015012803 A1 WO 2015012803A1 US 2013051594 W US2013051594 W US 2013051594W WO 2015012803 A1 WO2015012803 A1 WO 2015012803A1
Authority
WO
WIPO (PCT)
Prior art keywords
oil
shape
agent
memory polymer
shape memory
Prior art date
Application number
PCT/US2013/051594
Other languages
French (fr)
Inventor
Angele Sjong
William Brenden Carlson
Michael Keoni MANION
Original Assignee
Empire Technology Development Llc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Empire Technology Development Llc filed Critical Empire Technology Development Llc
Priority to CN201380078825.9A priority Critical patent/CN105555504A/en
Priority to PCT/US2013/051594 priority patent/WO2015012803A1/en
Priority to US14/907,285 priority patent/US20160159551A1/en
Publication of WO2015012803A1 publication Critical patent/WO2015012803A1/en

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B65CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
    • B65DCONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
    • B65D81/00Containers, packaging elements, or packages, for contents presenting particular transport or storage problems, or adapted to be used for non-packaging purposes after removal of contents
    • B65D81/24Adaptations for preventing deterioration or decay of contents; Applications to the container or packaging material of food preservatives, fungicides, pesticides or animal repellants
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C61/00Shaping by liberation of internal stresses; Making preforms having internal stresses; Apparatus therefor
    • B29C61/06Making preforms having internal stresses, e.g. plastic memory
    • B29C61/0608Making preforms having internal stresses, e.g. plastic memory characterised by the configuration or structure of the preforms
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B65CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
    • B65DCONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
    • B65D2203/00Decoration means, markings, information elements, contents indicators
    • B65D2203/12Audible, olfactory or visual signalling means

Definitions

  • Temperature control systems for packaging can help to maintain food quality. Refrigerated or cooled food items with non-ideal packaging that are transported between cold storage locations or not refrigerated by customers in a timely fashion would benefit from better insulation for storage, transport and post-purchase handling. Likewise, a self-heating packaging may allow a consumer to conveniently enjoy food that is meant to be heated. As such, there is a need for food packaging solutions that improve the quality of food as compared with standard packaging.
  • Embodiments disclosed in this document are directed to packaging having at least one agent disposed within a shape memory polymer which is adapted to release the agent in response to a stimulus.
  • Such packaging may be configured, for example, to hold food or beverages.
  • Such packaging may be used, for example, to detect environmental conditions during transport or storage, maintain a temperature of the food to preserve food quality, or provide a pleasant sensory experience to a consumer.
  • Some embodiments are directed to a method of making packaging including disposing at least one agent within a shape memory polymer, wherein the shape memory polymer is adapted to release the agent in response to a stimulus.
  • Some embodiments are directed to a method of using packaging including providing a packaging having at least one agent disposed within a shape memory polymer; and providing a stimulus to deform the shape memory polymer, whereby the agent is released from the shape memory polymer.
  • Figure 1 illustrates a schematic of exemplary packaging having a shape memory polymer in the shape of a cylindrical rod that opens up when exposed to a stimulus forming a decorative shape.
  • Figure 2 illustrates a schematic of exemplary packaging having a shape memory polymer having flat sheet walls shown on the left that contract, curling upward, when exposed to a stimulus, to form a decorative flower garnish as shown on the right and cause a burst release (shown by a starburst) of an agent when the encapsulant encasing the shape memory polymer ruptures in response to the contraction.
  • Figures 3A-3E illustrate shape memory polymer made to be garnishes of various shapes according to embodiments herein.
  • Figure 3A illustrates an example of a garnish shaped as a leaf that may be made using the methods of embodiments herein.
  • Figure 3B illustrates an example of a garnish shaped as a leaf that may be made using the methods of embodiments herein.
  • Figure 3C illustrates an example of a leaf garnish shaped as a bowl to hold food that may be made using the methods of embodiments herein.
  • Figure 3D illustrates an example of a leaf garnish packaging of embodiments herein as part of the packaging for sushi.
  • Figure 3E illustrates an example of a garnish shaped as a flower that may be made using the methods of embodiments herein.
  • Figures 4A-4D depict stages of transformation of exemplary shape memory polymers exposed to a stimulus according to embodiments herein.
  • Figure 4A depicts a shape memory polymer in a corkscrew spiral shape that slowly unravels as shown in Figure 4B when exposed to a stimulus.
  • Figure 4C a bent tubular shape, depicts further stages of transformation of the shape memory polymer that unravels as shown in Figure 4D to form a straight, fixed tubular shape.
  • Figures 5A-5C depict stages of transformation of shape memory polymers exposed to a stimulus according to embodiments herein.
  • Figure 5A illustrates a shape memory polymer at its original tubular shape which when exposed to stimulus, starts to curl inward as seen in Figure 5B, yielding a final corkscrew shape as seen in Figure 5C.
  • Figure 6 illustrates the shape change properties of a shape memory polymer of an embodiment described herein in response to changes in temperature.
  • the x- axis is time, and the y-axis is temperature.
  • Figures 7A-7D illustrate a molecular mechanism of light-induced SME of a grafted polymer network: the photosensitive groups (open triangles) of Figure 7A are covalently linked to the permanent polymer network (filled circles, permanent crosslinks) after stretching and photofixing forming photoreversible crosslinks (filled diamonds) as shown in Figure 7B; fixation shown in Figure 7C and recovery shown in Figure 7D of the temporary shape are realized by UV light irradiation of suitable wavelengths.
  • Figures 8A-8C illustrate a schematic of the shape-memory recovery process, in which Figure 8A illustrates the original shape where the switching segments are relaxed; Figure 8B illustrates a transition shape where the switching segments are fixed in transition due to an decrease in temperature; and Figure 8C illustrates a reversal back to the original shape where the switching segments are relaxed once again.
  • Figures 9A-9E illustrate a magnetically-induced shape-memory effect of a thermoplastic shape-memory composite from nanoparticles consisting of iron (II) oxide particles in a silica matrix and a polyetherurethane over 22 seconds.
  • Embodiments described herein are directed to packaging having at least one agent disposed within a shape memory polymer which is adapted to release the agent in response to a stimulus.
  • Such packaging may be configured, for example, to hold food or beverages.
  • the agent may be released from the shape memory polymer in a burst release fashion.
  • the agent may be released from the shape memory polymer in a slow release fashion.
  • the agent may include a cooling agent, a fragrance, a heating agent, a visual indicator or aid, an antibiotic, a drug, a medicinal agent, a noise-making agent, or a combination thereof.
  • the agent may include a salt capable of producing an exothermic reaction when dissolved in water, a salt capable of producing an endothermic reaction when dissolved in water, an essential oil, pressurized carbon dioxide, or a combination thereof.
  • the agent is disposed on the surface of a shape memory polymer.
  • the agent 102 may be stored in a core 101 of a shape memory polymer 100.
  • the shape memory polymer 100 may be shaped as a bulk polymer rod and the agent 102 released upon exposure to a stimulus by actuation into a hydrophilic matrix.
  • the bulk polymer rod can open upon exposure to the stimulus and release the agent 102, such as a cooling agent, a fragrance, a heating agent, a visual indicator or aid, an antibiotic, a drug, a medicinal agent, a noise-making agent, or a combination thereof, in order to create a sensory experience.
  • the agent 201 may be stored in a material encapsulant and coated on a sheet surface 203 of a shape memory polymer 200.
  • the agent 201 may be released by rupturing a capsule 204 that encapsulates the shape memory polymer 200 when the shape memory polymer contracts 202, going from a flat shape to a spiral shape upon exposure to a stimulus, such as a change in temperature.
  • the shape memory polymer may be shaped as a food garnish 300, such as food garnishes in the shape of a leaf ( Figure 3 A to 3D) or a flower (Figure 3E), and the shape change may be engineered such that it provides a decorative "origami" effect when the shape memory polymer transitions from one shape to another shape.
  • the agent may be a salt capable of producing an endo thermic reaction when dissolved in water.
  • the agent may be selected from ammonium nitrate, lithium chloride, potassium chloride, ammonium nitrite, potassium thiocyanate, ammonium thiocyanate, potassium iodide, ammonium chloride, sodium nitrite, sodium nitrate, sodium acetate, sodium carbonate, sodium chloride, sodium sulfate, sodium thiosulfate, sodium phosphate, urea, xylitol, sorbitol, glycerol, maltitol, sucrose, glucose, salivary amylase, lipase, mannose, a sugar, a carbohydrate, and a combination thereof.
  • the agent may be a salt capable of producing an exothermic reaction when dissolved in water.
  • the agent may be selected from lithium chloride, magnesium chloride, potassium carbonate, magnesium sulfate, calcium sulfate, calcium chloride, calcium oxide, aluminum chloride, aluminum sulfate, potassium aluminum sulfate, and a combination thereof.
  • the agent may be an essential oil selected from agar oil, ajwain oil, angelica root oil, anise oil, asafetida, balsam oil, basil oil, bay oil, bergamot oil, black pepper essential oil, buchu oil, birch oil, camphor, cannabis flower essential oil, caraway oil, cardamom seed oil, carrot seed oil, cedarwood oil, chamomile oil, calamus root, cinnamon oil, cistus oil, citronella oil, clary sage oil, clove oil, coriander oil, coffee, coriander, costmary oil, costus root, cranberry seed oil, cubeb, cumin oil, cypress, cypriol, curry leaf, davana oil, dill oil, elecampane, eucalyptus oil, fennel seed oil, fenugreek oil, fir, frankincense oil, galangal, galbanum, geran
  • shape memory polymers are polymers that have the ability to "memorize" a macroscopic (permanent) shape, be manipulated and fixed to a temporary and dormant shape under certain temperature and stress conditions, and relax to the macroscopic shape upon exposure to a stimulus.
  • shape memory alloys for example, metal alloys such as Ni-Ti
  • the shape memory polymers described herein may advantageously possess high elastic deformation (elastic deformity up to more than 200% for most of the materials), low density, biodegradability and biocompatibility, and may be low cost.
  • Such polymers may also be tailored for different applications and may be easily processed. The high elastic deformation of such shape memory polymers allows for large contractions when stimulated.
  • a prerequisite for stabilizing a temporary shape is the temporary fixation of the chain segments' conformation in the deformed shape.
  • the temporary, reversible crosslinks may be covalent bonds or physical crosslinks.
  • the physical crosslinks may be crystallites that reform to a viscous state.
  • the deformation causes the shape memory polymer to be fixed in a second, temporary shape.
  • This temporary shape may be retained until the shaped body is exposed to an appropriate stimulus, which induces the recovery of the original shape.
  • the temporary shape may recover its original shape as soon as a stimulus is terminated. The movement that occurs during recovery may be predefined as it reverses the mechanical deformation which led to the temporary shape.
  • Shape memory polymers of embodiments herein have the advantages of being lightweight and permitting high elongations.
  • the varying structural parameters of the molecular architecture may enable tailoring shape memory polymers to demands for specific food and beverage packaging applications, such as adjusting a transition temperature (T tra n s ) to initiate shape change allowing the shape memory polymer to burst release a cooling agent enclosed within.
  • T tra n s transition temperature
  • T t r a n s is the thermal transition temperature of the switching phase.
  • Figures 8A-8C illustrate the molecular architecture of a thermally induced shape memory polymer in which the switching segments are initially relaxed ( Figure 8A) and become elongated and fixed when the polymer is cooled ( Figure 8B).
  • switching segments are the functional groups or stimuli-sensitive domains that facilitate shape change. When heated, the shape memory polymer reverts back to its original shape ( Figure 8C), and the switching segments become relaxed once more.
  • a shape memory polymer may be adapted to undergo a shape change to release the agent in response to the stimulus.
  • the shape memory polymer may undergo a shape change from a flat shape to a coiled shape, from a coiled shape to a flat shape, from a tubular shape to a spiral shape, from a spiral shape to a tubular shape or a combination thereof.
  • the shape memory polymer may change from a closed configuration to an open configuration in response to the stimulus.
  • shape memory polymer may contract.
  • at least a portion of the shape memory polymer may rupture.
  • the shape change may cause a capsule comprising the agent to rupture where the capsule is formed from the shape memory polymer.
  • the shape change may be reversible or irreversible.
  • the shape change may be temporary or permanent.
  • the shape memory polymer may include cinnamic acid, starch, a polyetherurethane matrix, triphenylmethane leuco derivatives, azobenzene, biopolymers, poly(2-methyl-2-oxazoline), poly(silsesquioxane), high impact polystyrene, cross-linked polyethylene and polyethylene/nylon 6 graft copolymer, trans-polyisoprene, cross-linked ethylene-vinyl acetate copolymer, styrene-based polymers, acrylate -based polymers, polynorbornene, cross-linked polycyclooctene, epoxy-based polymers, thio-ene- based polymers, segmented polyurethane, segmented polyurethane ionomers, poly(3- hydroxyalkanoate), copolymers comprising dodecanedioic acid or sebacic acid monomers and bile acid-based
  • the shape memory polymer includes an edible polymer.
  • Edible polymers may include starch, oligo epsilon-caprolactone-co-glycolide- dimethacrylates, or other biopolymers.
  • a shape recovery ratio quantifies the ability of the shape memory polymer to memorize its permanent shape.
  • the shape memory polymer may have a shape recovery ratio of about 80% to about 1000%.
  • the shape recovery ratio may be about 80% to about 900%, about 80% to about 800%, about 80% to about 700%, about 80% to about 600%, about 80% to about 500%, about 80% to about 400%, about 80% to about 300%, about 80% to about 250%, about 80% to about 200%, about 80% to about 150%, about 80% to about 100%, about 100% to about 900%, about 100% to about 800%, about 100% to about 700%, about 100% to about 600%, about 100% to about 500%, about 100% to about 400%, about 100% to about 300%, about 100% to about 250%, about 100% to about 200%, about 100% to about 150%, about 150% to about 1000%, about 200% to about 1000%, about 250% to about 1000%, about 300% to about
  • the shape recovery ratio may be about 100%, about 150%, about 200%, about 250%, about 300%, about 400%, about 500%, about 600%, about 700%, about 800%, about 900%, about 1000%, or a range between any of these values.
  • thermomechanical experiment S p is the recovered strain in a cyclic, thermomechanical experiment, N is the number of cycles, and R r is the shape recovery ratio.
  • the strain that occurs during the programming step in the N* cycle S m - S p (N -1) is related to the change in strain that occurs during the present shape memory effect ("SME”) S m - S p (N).
  • the strain of the samples in two successively passed cycles in the stress-free state before application of yield stress is represented by S p (N -1) and S p (N).
  • S p (N -1) The strain of the samples in two successively passed cycles in the stress-free state before application of yield stress is represented by S p (N -1) and S p (N).
  • T low the temperature of the N th cycle E 1 (N)
  • the shape recovery ratio R r quantifies the ability of the material to memorize its permanent shape.
  • the change in strain that occurs during the programming step in the N th cycle S x (N)- £ p (N) is compared to the change in strain, which occurs as a result of the SME E 1 (N)- £ p (N -1).
  • a shape fixity ratio may be used to quantify the ability of the shape memory polymer to fix a deformation (such as, an elongation) resulting in a temporary shape.
  • the shape memory polymer may have a shape fixity ratio of about 100% to about 1000%.
  • the shape fixity ratio may be about 100% to about 900%, about 100% to about 800%, about 100% to about 700%, about 100% to about 600%, about 100% to about 500%, about 100% to about 400%, about 100% to about 300%, about 100% to about 250%, about 100% to about 200%, about 100% to about 150%, about 150% to about 1000%, about 200% to about 1000%, about 250% to about 1000%, about 300% to about 1000%, about 400% to about 1000%, or a combination thereof.
  • the shape fixity ratio may be about 100%, about 150%, about 200%, about 250%, about 300%, about 400%, about 500%, about 600%, about 700%, about 800%, about 900%, about 1000%, or a range between any of these values.
  • Rf is given by the ratio of the strain in the stress-free state after the withdrawal of the tensile stress in the N th cycle E u (N) and the maximum strain £ m .
  • the stimulus may include an increase in temperature, a decrease in temperature, ultraviolet (UV) light exposure, infrared (IR) light exposure, altering a magnetic field, pH change, change in ionic concentration, change in water concentration, change in electric field, or a combination thereof.
  • UV ultraviolet
  • IR infrared
  • shape memory polymers may undergo a photoreversible reaction to create reversible chemical crosslinks effectuating a shape change to fix the temporary shape.
  • the photoreversible stimulus may be light of suitable wavelengths, such as ultraviolet (UV) light or infrared (IR) light.
  • Light-sensitive groups may include triphenylmethane leuco- derivatives, azobenzene, or a combination thereof.
  • a triphenylmethane leuco-derivative may be stimulated by UV light having a wavelength of at least about 270 nm.
  • An azobenzene group may be stimulated by UV light having a wavelength of about 330 nm to about 380 nm for a trans-cis transition or at least about 420 nm for a cis-trans transition.
  • Figure 7 illustrates the molecular mechanism of light- induced SME of a grafted polymer network (Behl et al., Shape Memory Polymers and Shape-Changing Polymers, Advances in Polymer Science, Vol. 226, 2010, pp.1-40).
  • the photosensitive groups (open triangles) are covalently linked to the permanent polymer network (filled circles, permanent crosslinks) shown in Figure 7 A, forming photoreversible crosslinks (filled diamonds) shown in Figure 7B.
  • Fixation shown in Figure 7C and recovery shown in Figure 7D of the temporary shape are realized by UV light irradiation of suitable wavelengths.
  • Incorporation of light-sensitive groups such as molecular switches in the polymer networks may enable the development of light-induced SMPs. In this way, SME could be induced independently from any temperature effect. Instead of increasing the sample's temperature, light of different wavelength ranges can be used for the fixation of the temporary and the recovery of the permanent shape.
  • CA or cinnamyliden acetic acid (CAA) may be used as photosensitive molecular switches on the molecular level as they are able to form covalent crosslinks with each other in a [2+2] cycloaddition reaction when irradiated with light of suitable wavelengths.
  • the programming cycle may include deforming the samples to the maximum strain £ m and irradiating with UV-light of ⁇ >260 ⁇ afterwards so that the strained polymer chain segments can be fixed in their uncoiled conformation by the new covalent bonds created.
  • the permanent shape could be recovered when the sample was irradiated with light having wavelengths ⁇ 260 ⁇ and the newly formed covalent bonds were cleaved.
  • the shape change may be induced by a magnetic field.
  • magnetic nanoparticles may be added to a polymer.
  • the polymer may be a polyetherurethane matrix.
  • the stimulus may be an alternating magnetic field.
  • the alternating magnetic field may have a frequency of about 150 kHz to about 400 kHz, In some embodiments, the alternating magnetic field may have a magnetic field strength (H) of about 7 kAm "1 to about 30 kAm “1 , about 10 kAm “1 to about 30 kAm “1 , about 15 kAm “1 to about 30 kAm “1 , about 20 kAm “1 to about 30 kAm “1 , about 25 kAm "1 to about 30 kAm “1 , or a combination thereof.
  • H magnetic field strength
  • the alternating magnetic field may have a magnetic field strength (H) of about 7 kAm “1 , about 10 kAm “1 , about 15 kAm “1 , about 20 kAm “1 , about 25 kAm “1 , about 30 kAm “1 , or a range between any two of these values.
  • H magnetic field strength
  • Magnetic fields of different strength and/or frequencies may also be used within the scope of this disclosure.
  • the shape memory polymer may be coated with an encapsulant.
  • the encapsulant may break when the shape memory polymer undergoes a shape change.
  • the agent may be encapsulated.
  • the encapsulant may be selected from starch, poly (urea-formaldehyde), amino resin, polyamide, polyurethane, gelatin, cellulose, polyvinyl acetate, urea-resourcinol formaldehyde, or a combination thereof.
  • the shape memory polymer may be disposed within a hydrophilic matrix.
  • the agent may be released into the hydrophilic matrix.
  • the agent may react with the hydrophilic matrix upon release from the shape memory polymer.
  • the agent may react with the hydrophilic matrix in an exothermic process. In alternate embodiments, the agent may react with the hydrophilic matrix in an endothermic process.
  • the hydrophilic matrix may include a polymer with bound water. In some embodiments, release of the agent into the hydrophilic polymer matrix triggers an endothermic or exothermic reaction.
  • the polymer may be polyvinyl alcohol.
  • the hydrophilic matrix may form a portion of the packaging. For example, the hydrophilic matrix may form one layer of a 'leaf or flower petal in an exemplary package shaped like a flower.
  • the hydrophilic matrix may include hydroxypropyl methylcellulose (HPMC), hydroxypropylcellulose (HPC), polyethylene oxide (PEO), polyvinyl alcohol, or a combination thereof.
  • Some embodiments are directed to a method of making packaging including disposing at least one agent within a shape memory polymer, wherein the shape memory polymer is adapted to release the agent in response to a stimulus.
  • the agent as described above, may be released from the shape memory polymer in a burst release fashion or a slow release fashion.
  • the method further includes shaping the shape memory polymer around the at least one agent.
  • the shape memory polymer may be shaped around the at least one agent to form a capsule.
  • the method further includes coating the shape memory polymer with an encapsulant.
  • the encapsulant may be adapted to break when the shape memory polymer undergoes a shape change.
  • the method further includes encapsulating the agent.
  • the agent may be encapsulated before disposing the agent in the shape memory polymer.
  • the method further includes disposing the shape memory polymer encasing the agent within a hydrophilic matrix, such that the agent reacts with the hydrophilic matrix upon release from the shape memory polymer as described above.
  • Some embodiments are directed to a method of using packaging including providing packaging having at least one agent disposed within a shape memory polymer; and providing a stimulus to deform the shape memory polymer. Upon application of the stimulus, the agent may be released from the shape memory polymer. The method may further include providing a hydrophilic matrix, whereby the agent reacts with the hydrophilic matrix upon release from the shape memory polymer.
  • providing a stimulus may include increasing a temperature, decreasing a temperature, exposing the packaging to ultraviolet (UV) light, exposing the packaging to infrared (IR) light, altering a magnetic field, changing pH, changing an ion concentration, changing water concentration, changing an electric field, or a combination thereof.
  • providing a stimulus to deform the shape memory polymer may result in a shape change.
  • Example 1 Cooling Decorative Food Packaging.
  • Food packaging having potassium chloride disposed within a flower bud shaped polyesterurethane matrix is prepared.
  • the flower bud Upon exposure to a target temperature of 20°C, the flower bud bursts open to release the potassium chloride into a hydrophilic gel matrix having hydroxypropylcellulose.
  • the endothermic reaction between the potassium chloride and the hydroxypropylcellulose is expected to cool the food.
  • the burst release may occur subsequent to purchase and removal from a refrigerator.
  • a pasta dish is disposed in a dual layered plastic tray having a shape memory polymer composed of cross-linked polyethylene and polyethylene/nylon- 6 graft copolymer disposed between the two plastic layers.
  • a hydrophilic matrix composed of hydroxypropylcellulose is disposed on the layer above the shape memory polymer and calcium sulfate, lemongrass fragrance, and pressurized carbon dioxide capsules disposed beneath the shape memory polymer.
  • the shape memory polymer undergoes a shape change to a temporary shape and the calcium sulfate is released into the hydrophilic matrix.
  • the exothermic reaction of the calcium sulfate and hydroxycellulose is expected to maintain a warm temperature for the food.
  • the burst release also releases a lemongrass fragrance, and popping (crackling) noises due to the release of the pressurized carbon dioxide capsules in order to contribute a pleasant sensory experience for the consumer.
  • Example 3 Heat-Detecting Packaging.
  • Packaging having ammonium nitrate disposed in high impact polystyrene is used for storage and transport of a food substance.
  • a target temperature of 40°C when a target temperature of 40°C is reached, endothermic agents are released into a hydrophilic matrix having hydroxypropyl methylcellulose, thereby cooling the contents of the packaging.
  • the shape change of the high impact polystyrene may also notify the recipient that excessive storage temperatures were encountered.
  • Food packaging having magnesium sulfate disposed in a shape memory polymer is prepared.
  • the shape memory polymer includes azobenzene.
  • Magnesium sulfate will be released by directing a laser scanner (infrared light), such as during purchase of the food product, towards the packaging. The infrared light will cause the burst release of the magnesium sulfate into a hydrophilic gel matrix having polyethylene oxide, and the exothermic reaction of the magnesim sulfate and polyethylene oxide is expected to heat the food.
  • Example 5 Color changing bowl.
  • a bowl includes a spiral coiled polyesterurethane having a colorant to indicate when hot foods have cooled sufficiently to eat safely. After heating a hot food, such as soup, the soup is placed in the bowl and the polyesterurethane unravels releasing a colorant into the surrounding gel matrix within the bowl causing the bowl to change color, indicating when the soup is cooled enough to drink safely.
  • the unravelling of the spiral coiled polyesterurethane to release the colorant can be illustrated in Example 4.
  • Figures 4A-4D illustrate a thermally-induced transition of polyesterurethane (poly(e- caprlolactone)dimethacrylate) from a spiral structure to a temporary substantially straight structure in response to an increase in temperature (Behl et al., Shape Memory Polymers and Shape-Changing Polymers, Advances in Polymer Science, Vol. 226, 2010, pp.1-40).
  • Figure 4A depicts a shape memory polymer in a corkscrew spiral shape that slowly unravels as shown in Figure 4B when exposed to a stimulus.
  • Figure 4C a bent tubular shape, depicts further stages of transformation of the shape memory polymer that unravels as shown in Figure 4D to form a straight, fixed tubular shape.
  • the temporary fixation of the polyester switching segments may cause the shape change; while the urethane provides hard segments.
  • the oligo(e-caprolactone) segment is the switching segment.
  • the transition temperature is the melting temperature, T m> of the oligo(e- caprolactone) segments.
  • Elasticity is provided by the soft, amorphous poly(dimethacrylate) domains.
  • a second temporary shape is applied to a polymer by an external stress causing deformation of the polymer. The temporary shape is retained until the shaped body is exposed to an appropriate stimulus, which induces the recovery of the original shape.
  • Example 6 Heat-detection packagaing.
  • Figures 5A-5C illustrate a thermally-induced transition of a shape memory polymer from a temporary bar shape to a permanent cork-screw-like spiral (Behl et al., Shape Memory Polymers and Shape-Changing Polymers, Advances in Polymer Science, Vol. 226, 2010, pp.1-40).
  • Figure 5 A illustrates a shape memory polymer at its temporary bar shape which when exposed to a rise in temperature, starts to curl inward as seen in Figure 5B, yielding a permanent corkscrew shape as seen in Figure 5C. The recovery process took 35 seconds at 60°C.
  • f 258 kHz
  • thermoplastic material consisted either of a biodegradable multiblock copolymer (PDC), with poly(p-dioxanone) as the hard segment and poly(e-caprolactone) as the switching segment, or an aliphatic polyetherurethane (TFX) from methylene bis(p-cyclohexyl isocyanate), butanediol and polytetrahydrofuran.
  • PDC biodegradable multiblock copolymer
  • TFX aliphatic polyetherurethane
  • Magnetic nanoparticles of iron(III)oxide cores in a silica matrix were incorporated in both polymers. While TFX has an amorphous switching phase, PDC has a crystallizable switching segment.
  • the shape memory effect could be triggered in both samples by exposure to an alternating magnetic field.
  • the R r values of indirectly heated samples were comparable to samples where the environmental temperature has been increased. As the composite uncoils, an exothermic agent is released into a hydrophilic matrix
  • Example 8 Soup packaging with enhanced aroma.
  • a soup container includes extruded potato starch coated on the inside of the container. As the soup is heated the extruded potato starch curls and peels from the walls of the container, revealing and releasing essential oils underneath the starch coating that enhance the aroma of the soup.
  • Figure 6 illustrates the shape changing properties of extruded potato starch from spiral to flat shape (Sjong, Chaunier, L., Lourdin, S., The shape memory of starch, Starch/Starke 61 (2009) 116-118).
  • the edible polymer begins with a spiral shape at an initial temperature, and was subjected to a cycle of a decrease in temperature followed by an increase in temperature back to its initial temperature. The changes in the temperature resulted in the edible polymer switching from the spiral shape to the flat shape after the cycle completes. When subjected to another cycle of temperature changes, the edible polymer switches from the flat shape back to the spiral shape.
  • a range includes each individual member.
  • a group having 1-3 bonds refers to groups having 1, 2, or 3 bonds.
  • a group having 1-5 bonds refers to groups having 1, 2, 3, 4, or 5 bonds, and so forth.

Abstract

Food packaging and methods of making and using such packaging are disclosed. Food packaging having at least one agent may be disposed within a shape memory polymer which is adapted to release the agent in response to a stimulus. Such packaging may be used, for example, to detect environmental conditions during transport or storage, maintain a temperature of the food to preserve food quality, or provide a pleasant sensory experience to a consumer.

Description

PACKAGING MATERIALS AND METHODS FOR
THEIR PREPARATION AND USE
BACKGROUND
[0001] Temperature control systems for packaging can help to maintain food quality. Refrigerated or cooled food items with non-ideal packaging that are transported between cold storage locations or not refrigerated by customers in a timely fashion would benefit from better insulation for storage, transport and post-purchase handling. Likewise, a self-heating packaging may allow a consumer to conveniently enjoy food that is meant to be heated. As such, there is a need for food packaging solutions that improve the quality of food as compared with standard packaging.
SUMMARY
[0002] Embodiments disclosed in this document are directed to packaging having at least one agent disposed within a shape memory polymer which is adapted to release the agent in response to a stimulus. Such packaging may be configured, for example, to hold food or beverages. Such packaging may be used, for example, to detect environmental conditions during transport or storage, maintain a temperature of the food to preserve food quality, or provide a pleasant sensory experience to a consumer.
[0003] Some embodiments are directed to a method of making packaging including disposing at least one agent within a shape memory polymer, wherein the shape memory polymer is adapted to release the agent in response to a stimulus.
[0004] Some embodiments are directed to a method of using packaging including providing a packaging having at least one agent disposed within a shape memory polymer; and providing a stimulus to deform the shape memory polymer, whereby the agent is released from the shape memory polymer. [0005] The foregoing summary is illustrative only and is not intended to be in any way limiting. In addition to the illustrative aspects, embodiments, and features described above, further aspects, embodiments, and features will become apparent by reference to the drawings and the following detailed description.
BRIEF DESCRIPTION OF THE FIGURES
[0006] Figure 1 illustrates a schematic of exemplary packaging having a shape memory polymer in the shape of a cylindrical rod that opens up when exposed to a stimulus forming a decorative shape.
[0007] Figure 2 illustrates a schematic of exemplary packaging having a shape memory polymer having flat sheet walls shown on the left that contract, curling upward, when exposed to a stimulus, to form a decorative flower garnish as shown on the right and cause a burst release (shown by a starburst) of an agent when the encapsulant encasing the shape memory polymer ruptures in response to the contraction.
[0008] Figures 3A-3E illustrate shape memory polymer made to be garnishes of various shapes according to embodiments herein. Figure 3A illustrates an example of a garnish shaped as a leaf that may be made using the methods of embodiments herein. Figure 3B illustrates an example of a garnish shaped as a leaf that may be made using the methods of embodiments herein. Figure 3C illustrates an example of a leaf garnish shaped as a bowl to hold food that may be made using the methods of embodiments herein. Figure 3D illustrates an example of a leaf garnish packaging of embodiments herein as part of the packaging for sushi. Figure 3E illustrates an example of a garnish shaped as a flower that may be made using the methods of embodiments herein.
[0009] Figures 4A-4D depict stages of transformation of exemplary shape memory polymers exposed to a stimulus according to embodiments herein. Figure 4A depicts a shape memory polymer in a corkscrew spiral shape that slowly unravels as shown in Figure 4B when exposed to a stimulus. Figure 4C, a bent tubular shape, depicts further stages of transformation of the shape memory polymer that unravels as shown in Figure 4D to form a straight, fixed tubular shape.
[0010] Figures 5A-5C depict stages of transformation of shape memory polymers exposed to a stimulus according to embodiments herein. Figure 5A illustrates a shape memory polymer at its original tubular shape which when exposed to stimulus, starts to curl inward as seen in Figure 5B, yielding a final corkscrew shape as seen in Figure 5C.
[0011] Figure 6 illustrates the shape change properties of a shape memory polymer of an embodiment described herein in response to changes in temperature. The x- axis is time, and the y-axis is temperature.
[0012] Figures 7A-7D illustrate a molecular mechanism of light-induced SME of a grafted polymer network: the photosensitive groups (open triangles) of Figure 7A are covalently linked to the permanent polymer network (filled circles, permanent crosslinks) after stretching and photofixing forming photoreversible crosslinks (filled diamonds) as shown in Figure 7B; fixation shown in Figure 7C and recovery shown in Figure 7D of the temporary shape are realized by UV light irradiation of suitable wavelengths.
[0013] Figures 8A-8C illustrate a schematic of the shape-memory recovery process, in which Figure 8A illustrates the original shape where the switching segments are relaxed; Figure 8B illustrates a transition shape where the switching segments are fixed in transition due to an decrease in temperature; and Figure 8C illustrates a reversal back to the original shape where the switching segments are relaxed once again.
[0014] Figures 9A-9E illustrate a magnetically-induced shape-memory effect of a thermoplastic shape-memory composite from nanoparticles consisting of iron (II) oxide particles in a silica matrix and a polyetherurethane over 22 seconds. DETAILED DESCRIPTION
[0015] In the following detailed description, reference is made to the accompanying drawings, which form a part of this document. In the drawings, similar symbols typically identify similar components, unless the context dictates otherwise. The illustrative embodiments described in the detailed description, drawings, and claims are not meant to be limiting. Other embodiments may be used, and other changes may be made, without departing from the spirit or scope of the subject matter presented in this document. It will be readily understood that the aspects of the present disclosure, as generally described in this document, and illustrated in the Figures, can be arranged, substituted, combined, separated, and designed in a wide variety of different configurations, all of which are explicitly contemplated to be within the scope of this disclosure.
[0016] Embodiments described herein are directed to packaging having at least one agent disposed within a shape memory polymer which is adapted to release the agent in response to a stimulus. Such packaging may be configured, for example, to hold food or beverages. In some embodiments, the agent may be released from the shape memory polymer in a burst release fashion. In some embodiments, the agent may be released from the shape memory polymer in a slow release fashion. The agent may include a cooling agent, a fragrance, a heating agent, a visual indicator or aid, an antibiotic, a drug, a medicinal agent, a noise-making agent, or a combination thereof. For example, the agent may include a salt capable of producing an exothermic reaction when dissolved in water, a salt capable of producing an endothermic reaction when dissolved in water, an essential oil, pressurized carbon dioxide, or a combination thereof.
[0017] In some embodiments, the agent is disposed on the surface of a shape memory polymer. In an embodiment shown in Figure 1, the agent 102 may be stored in a core 101 of a shape memory polymer 100. The shape memory polymer 100 may be shaped as a bulk polymer rod and the agent 102 released upon exposure to a stimulus by actuation into a hydrophilic matrix. For example, the bulk polymer rod can open upon exposure to the stimulus and release the agent 102, such as a cooling agent, a fragrance, a heating agent, a visual indicator or aid, an antibiotic, a drug, a medicinal agent, a noise-making agent, or a combination thereof, in order to create a sensory experience. In an alternate embodiment, shown in Figure 2, the agent 201 may be stored in a material encapsulant and coated on a sheet surface 203 of a shape memory polymer 200. In Figure 2, the agent 201 may be released by rupturing a capsule 204 that encapsulates the shape memory polymer 200 when the shape memory polymer contracts 202, going from a flat shape to a spiral shape upon exposure to a stimulus, such as a change in temperature. As shown in Figure 3, the shape memory polymer may be shaped as a food garnish 300, such as food garnishes in the shape of a leaf (Figure 3 A to 3D) or a flower (Figure 3E), and the shape change may be engineered such that it provides a decorative "origami" effect when the shape memory polymer transitions from one shape to another shape.
[0018] In some embodiments, the agent may be a salt capable of producing an endo thermic reaction when dissolved in water. In some embodiments, the agent may be selected from ammonium nitrate, lithium chloride, potassium chloride, ammonium nitrite, potassium thiocyanate, ammonium thiocyanate, potassium iodide, ammonium chloride, sodium nitrite, sodium nitrate, sodium acetate, sodium carbonate, sodium chloride, sodium sulfate, sodium thiosulfate, sodium phosphate, urea, xylitol, sorbitol, glycerol, maltitol, sucrose, glucose, salivary amylase, lipase, mannose, a sugar, a carbohydrate, and a combination thereof.
[0019] In some embodiments, the agent may be a salt capable of producing an exothermic reaction when dissolved in water. For example, the agent may be selected from lithium chloride, magnesium chloride, potassium carbonate, magnesium sulfate, calcium sulfate, calcium chloride, calcium oxide, aluminum chloride, aluminum sulfate, potassium aluminum sulfate, and a combination thereof.
[0020] In some embodiments, the agent may be an essential oil selected from agar oil, ajwain oil, angelica root oil, anise oil, asafetida, balsam oil, basil oil, bay oil, bergamot oil, black pepper essential oil, buchu oil, birch oil, camphor, cannabis flower essential oil, caraway oil, cardamom seed oil, carrot seed oil, cedarwood oil, chamomile oil, calamus root, cinnamon oil, cistus oil, citronella oil, clary sage oil, clove oil, coriander oil, coffee, coriander, costmary oil, costus root, cranberry seed oil, cubeb, cumin oil, cypress, cypriol, curry leaf, davana oil, dill oil, elecampane, eucalyptus oil, fennel seed oil, fenugreek oil, fir, frankincense oil, galangal, galbanum, geranium oil, ginger oil, goldenrod, grapefruit oil, henna oil, helichrysum, limonene, hickory nut oil, horseradish oil, hyssop, Idaho tansy, jasmine oil, juniper berry oil, lavender oil, lemon oil, lemongrass, lime, Litsea cubeba oil, mandarin, marjoram, melaleuca, tea tree oil, Melissa oil, mint oil, mountain savory, mustard oil, mugwort oil, myrrh oil, myrtle, neem oil, neroli, nutmeg, orange oil, oregano oil, orris oil, palo santo, parsley oil, patchouli oil, perilla essential oil, pennyroyal oil, peppermint oil, petitgrain, pine oil, ravensara, red cedar, roman chamomile, rose oil, rosehip oil, rosemary oil, rosewood oil, sage oil, sassafras oil, savory oil, sandalwood oil, schisandra oil, spearmint oil, spikenard, spruce, star anise oil, tangerine, tarragon oil, thyme oil, tsuga, turmeric, valerian, vetiver oil, omega-3 oil, flaxseed oil, fish oil, tallow, tung oil, banana oil, western red cedar, wintergreen, yarrow oil, ylang-ylang, zedoary, and any combinations thereof.
[0021] As used herein, shape memory polymers are polymers that have the ability to "memorize" a macroscopic (permanent) shape, be manipulated and fixed to a temporary and dormant shape under certain temperature and stress conditions, and relax to the macroscopic shape upon exposure to a stimulus. Compared to shape memory alloys (for example, metal alloys such as Ni-Ti), the shape memory polymers described herein may advantageously possess high elastic deformation (elastic deformity up to more than 200% for most of the materials), low density, biodegradability and biocompatibility, and may be low cost. Such polymers may also be tailored for different applications and may be easily processed. The high elastic deformation of such shape memory polymers allows for large contractions when stimulated. In some embodiments, a prerequisite for stabilizing a temporary shape is the temporary fixation of the chain segments' conformation in the deformed shape. In some embodiments, the temporary, reversible crosslinks may be covalent bonds or physical crosslinks. In some embodiments, the physical crosslinks may be crystallites that reform to a viscous state.
[0022] In some embodiments, the deformation causes the shape memory polymer to be fixed in a second, temporary shape. This temporary shape may be retained until the shaped body is exposed to an appropriate stimulus, which induces the recovery of the original shape. In some embodiments, the temporary shape may recover its original shape as soon as a stimulus is terminated. The movement that occurs during recovery may be predefined as it reverses the mechanical deformation which led to the temporary shape. Shape memory polymers of embodiments herein have the advantages of being lightweight and permitting high elongations. The varying structural parameters of the molecular architecture may enable tailoring shape memory polymers to demands for specific food and beverage packaging applications, such as adjusting a transition temperature (Ttrans) to initiate shape change allowing the shape memory polymer to burst release a cooling agent enclosed within. For example, for a shape memory polymer that is sensitive to temperature where certain chain segments of the shape memory polymer function as molecular switches (switching segments), Ttrans is the thermal transition temperature of the switching phase. Figures 8A-8C illustrate the molecular architecture of a thermally induced shape memory polymer in which the switching segments are initially relaxed (Figure 8A) and become elongated and fixed when the polymer is cooled (Figure 8B). As used herein, switching segments are the functional groups or stimuli-sensitive domains that facilitate shape change. When heated, the shape memory polymer reverts back to its original shape (Figure 8C), and the switching segments become relaxed once more.
[0023] In some embodiments, a shape memory polymer may be adapted to undergo a shape change to release the agent in response to the stimulus. For example, the shape memory polymer may undergo a shape change from a flat shape to a coiled shape, from a coiled shape to a flat shape, from a tubular shape to a spiral shape, from a spiral shape to a tubular shape or a combination thereof. In some embodiments, the shape memory polymer may change from a closed configuration to an open configuration in response to the stimulus. In some embodiments, shape memory polymer may contract. In some embodiments, at least a portion of the shape memory polymer may rupture. For example, the shape change may cause a capsule comprising the agent to rupture where the capsule is formed from the shape memory polymer. In some embodiments, the shape change may be reversible or irreversible. In some embodiments, the shape change may be temporary or permanent.
[0024] In some embodiments, the shape memory polymer may include cinnamic acid, starch, a polyetherurethane matrix, triphenylmethane leuco derivatives, azobenzene, biopolymers, poly(2-methyl-2-oxazoline), poly(silsesquioxane), high impact polystyrene, cross-linked polyethylene and polyethylene/nylon 6 graft copolymer, trans-polyisoprene, cross-linked ethylene-vinyl acetate copolymer, styrene-based polymers, acrylate -based polymers, polynorbornene, cross-linked polycyclooctene, epoxy-based polymers, thio-ene- based polymers, segmented polyurethane, segmented polyurethane ionomers, poly(3- hydroxyalkanoate), copolymers comprising dodecanedioic acid or sebacic acid monomers and bile acid-based polyesters, or a combination thereof. [0025] In some embodiments, the shape memory polymer includes an edible polymer. Edible polymers may include starch, oligo epsilon-caprolactone-co-glycolide- dimethacrylates, or other biopolymers.
[0026] As used herein, a shape recovery ratio, Rr, quantifies the ability of the shape memory polymer to memorize its permanent shape. The shape memory polymer may have a shape recovery ratio of about 80% to about 1000%. In some embodiments, the shape recovery ratio may be about 80% to about 900%, about 80% to about 800%, about 80% to about 700%, about 80% to about 600%, about 80% to about 500%, about 80% to about 400%, about 80% to about 300%, about 80% to about 250%, about 80% to about 200%, about 80% to about 150%, about 80% to about 100%, about 100% to about 900%, about 100% to about 800%, about 100% to about 700%, about 100% to about 600%, about 100% to about 500%, about 100% to about 400%, about 100% to about 300%, about 100% to about 250%, about 100% to about 200%, about 100% to about 150%, about 150% to about 1000%, about 200% to about 1000%, about 250% to about 1000%, about 300% to about 1000%, about 400% to about 1000%, or a combination thereof. In some embodiments, the shape recovery ratio may be about 100%, about 150%, about 200%, about 250%, about 300%, about 400%, about 500%, about 600%, about 700%, about 800%, about 900%, about 1000%, or a range between any of these values.
[0027] The shape recovery ratio of a strain-controlled protocol is: ffr (N) = £m £ W where £ js the nominal strain, Sm is the default strain in a cyclic,
£m £ (N— 1)
thermomechanical experiment, Sp is the recovered strain in a cyclic, thermomechanical experiment, N is the number of cycles, and Rr is the shape recovery ratio. The shape recovery ratio of a stress-controlled test protocol is: Rr(N) = g^^ g ^^ where Sx is the strain after cooling to a temperature Tlow, Sp is the recovered strain in a cyclic, thermomechanical experiment, N is the number of cycles, and Rr is the shape recovery ratio. In a strain-controlled protocol, the strain that occurs during the programming step in the N* cycle Sm - Sp (N -1) is related to the change in strain that occurs during the present shape memory effect ("SME") Sm - Sp (N). The strain of the samples in two successively passed cycles in the stress-free state before application of yield stress is represented by Sp (N -1) and Sp (N). In the case of a stress-controlled programming and stress-free recovery after cooling to a temperature, Tlow, of the Nth cycle E1 (N) the shape recovery ratio Rr quantifies the ability of the material to memorize its permanent shape. For this purpose the change in strain that occurs during the programming step in the Nth cycle Sx (N)- £p (N) is compared to the change in strain, which occurs as a result of the SME E1 (N)- £p (N -1).
[0028] As used herein, a shape fixity ratio may be used to quantify the ability of the shape memory polymer to fix a deformation (such as, an elongation) resulting in a temporary shape. In some embodiments, the shape memory polymer may have a shape fixity ratio of about 100% to about 1000%. In some embodiments, the shape fixity ratio may be about 100% to about 900%, about 100% to about 800%, about 100% to about 700%, about 100% to about 600%, about 100% to about 500%, about 100% to about 400%, about 100% to about 300%, about 100% to about 250%, about 100% to about 200%, about 100% to about 150%, about 150% to about 1000%, about 200% to about 1000%, about 250% to about 1000%, about 300% to about 1000%, about 400% to about 1000%, or a combination thereof. In some embodiments, the shape fixity ratio may be about 100%, about 150%, about 200%, about 250%, about 300%, about 400%, about 500%, about 600%, about 700%, about 800%, about 900%, about 1000%, or a range between any of these values.
[0029] The shape fixity ratio of a strain controlled protocol is: ff QV) = Eu^N where Su is the fixed strain after unloading in a cyclic, thermomechanical experiment, Sm is the default strain in a cyclic, thermomechanical experiment, N is the number of cycles, and Rf is the shape fixity ratio. The shape fixity ratio of a stress-controlled protocol is Rf (N) = - , where Sx is the strain after cooling to a temperature Tlow, m is the default strain in a cyclic, thermomechanical experiment, N is the number of cycles, and Rf is the shape fixity ratio. In a strain-controlled programming protocol Rf is given by the ratio of the strain in the stress-free state after the withdrawal of the tensile stress in the Nth cycle Eu (N) and the maximum strain £m. In the case of a stress-controlled programming protocol, Rf is given by the ratio of the tensile strain after unloading, Su (N), to the maximum strain at σ = om after cooling to a temperature Tlow, E1 (N)
[0030] In some embodiments, the stimulus may include an increase in temperature, a decrease in temperature, ultraviolet (UV) light exposure, infrared (IR) light exposure, altering a magnetic field, pH change, change in ionic concentration, change in water concentration, change in electric field, or a combination thereof.
[0031] In some embodiments, shape memory polymers may undergo a photoreversible reaction to create reversible chemical crosslinks effectuating a shape change to fix the temporary shape. In some embodiments, the photoreversible stimulus may be light of suitable wavelengths, such as ultraviolet (UV) light or infrared (IR) light. Light-sensitive groups may include triphenylmethane leuco- derivatives, azobenzene, or a combination thereof. For example, a triphenylmethane leuco-derivative may be stimulated by UV light having a wavelength of at least about 270 nm. An azobenzene group may be stimulated by UV light having a wavelength of about 330 nm to about 380 nm for a trans-cis transition or at least about 420 nm for a cis-trans transition. Figure 7 illustrates the molecular mechanism of light- induced SME of a grafted polymer network (Behl et al., Shape Memory Polymers and Shape-Changing Polymers, Advances in Polymer Science, Vol. 226, 2010, pp.1-40). The photosensitive groups (open triangles) are covalently linked to the permanent polymer network (filled circles, permanent crosslinks) shown in Figure 7 A, forming photoreversible crosslinks (filled diamonds) shown in Figure 7B. Fixation shown in Figure 7C and recovery shown in Figure 7D of the temporary shape are realized by UV light irradiation of suitable wavelengths. Incorporation of light-sensitive groups such as molecular switches in the polymer networks may enable the development of light-induced SMPs. In this way, SME could be induced independently from any temperature effect. Instead of increasing the sample's temperature, light of different wavelength ranges can be used for the fixation of the temporary and the recovery of the permanent shape. CA or cinnamyliden acetic acid (CAA) may be used as photosensitive molecular switches on the molecular level as they are able to form covalent crosslinks with each other in a [2+2] cycloaddition reaction when irradiated with light of suitable wavelengths. These bonds could be cleaved again when irradiated with light of different suitable wavelengths. The programming cycle may include deforming the samples to the maximum strain £m and irradiating with UV-light of λ>260ηιη afterwards so that the strained polymer chain segments can be fixed in their uncoiled conformation by the new covalent bonds created. The permanent shape could be recovered when the sample was irradiated with light having wavelengths λ<260ηιη and the newly formed covalent bonds were cleaved.
[0032] In some embodiments, the shape change may be induced by a magnetic field. In some embodiments, magnetic nanoparticles may be added to a polymer. In some embodiments, the polymer may be a polyetherurethane matrix. In some embodiments, the stimulus may be an alternating magnetic field. In some embodiments, the alternating magnetic field may have a frequency of about 150 kHz to about 400 kHz, In some embodiments, the alternating magnetic field may have a magnetic field strength (H) of about 7 kAm"1 to about 30 kAm"1, about 10 kAm"1 to about 30 kAm"1, about 15 kAm"1 to about 30 kAm"1, about 20 kAm"1 to about 30 kAm"1, about 25 kAm"1 to about 30 kAm"1, or a combination thereof. In some embodiments, the alternating magnetic field may have a magnetic field strength (H) of about 7 kAm"1, about 10 kAm"1, about 15 kAm"1, about 20 kAm"1, about 25 kAm"1, about 30 kAm"1, or a range between any two of these values. Magnetic fields of different strength and/or frequencies may also be used within the scope of this disclosure.
[0033] The shape memory polymer may be coated with an encapsulant. In some embodiments, the encapsulant may break when the shape memory polymer undergoes a shape change. In some embodiments, the agent may be encapsulated. In some embodiments, the encapsulant may be selected from starch, poly (urea-formaldehyde), amino resin, polyamide, polyurethane, gelatin, cellulose, polyvinyl acetate, urea-resourcinol formaldehyde, or a combination thereof.
[0034] The shape memory polymer may be disposed within a hydrophilic matrix. In some embodiments, the agent may be released into the hydrophilic matrix. In some embodiments, the agent may react with the hydrophilic matrix upon release from the shape memory polymer. In some embodiments, the agent may react with the hydrophilic matrix in an exothermic process. In alternate embodiments, the agent may react with the hydrophilic matrix in an endothermic process.
[0035] In some embodiments, the hydrophilic matrix may include a polymer with bound water. In some embodiments, release of the agent into the hydrophilic polymer matrix triggers an endothermic or exothermic reaction. In an embodiment, the polymer may be polyvinyl alcohol. In some embodiments, the hydrophilic matrix may form a portion of the packaging. For example, the hydrophilic matrix may form one layer of a 'leaf or flower petal in an exemplary package shaped like a flower. In some embodiments, the hydrophilic matrix may include hydroxypropyl methylcellulose (HPMC), hydroxypropylcellulose (HPC), polyethylene oxide (PEO), polyvinyl alcohol, or a combination thereof. [0036] Some embodiments are directed to a method of making packaging including disposing at least one agent within a shape memory polymer, wherein the shape memory polymer is adapted to release the agent in response to a stimulus. The agent, as described above, may be released from the shape memory polymer in a burst release fashion or a slow release fashion. In some embodiments, the method further includes shaping the shape memory polymer around the at least one agent. In some embodiments, the shape memory polymer may be shaped around the at least one agent to form a capsule. In some embodiments, the method further includes coating the shape memory polymer with an encapsulant. In some embodiments, the encapsulant may be adapted to break when the shape memory polymer undergoes a shape change. In some embodiments, the method further includes encapsulating the agent. The agent may be encapsulated before disposing the agent in the shape memory polymer. In some embodiments, the method further includes disposing the shape memory polymer encasing the agent within a hydrophilic matrix, such that the agent reacts with the hydrophilic matrix upon release from the shape memory polymer as described above.
[0037] Some embodiments are directed to a method of using packaging including providing packaging having at least one agent disposed within a shape memory polymer; and providing a stimulus to deform the shape memory polymer. Upon application of the stimulus, the agent may be released from the shape memory polymer. The method may further include providing a hydrophilic matrix, whereby the agent reacts with the hydrophilic matrix upon release from the shape memory polymer.
[0038] In some embodiments, providing a stimulus may include increasing a temperature, decreasing a temperature, exposing the packaging to ultraviolet (UV) light, exposing the packaging to infrared (IR) light, altering a magnetic field, changing pH, changing an ion concentration, changing water concentration, changing an electric field, or a combination thereof. In some embodiments, providing a stimulus to deform the shape memory polymer may result in a shape change.
EXAMPLES
Example 1 : Cooling Decorative Food Packaging.
[0039] Food packaging having potassium chloride disposed within a flower bud shaped polyesterurethane matrix is prepared. Upon exposure to a target temperature of 20°C, the flower bud bursts open to release the potassium chloride into a hydrophilic gel matrix having hydroxypropylcellulose. The endothermic reaction between the potassium chloride and the hydroxypropylcellulose is expected to cool the food. The burst release may occur subsequent to purchase and removal from a refrigerator.
Example 2: Warming Olfactory Food Packaging.
[0040] A pasta dish is disposed in a dual layered plastic tray having a shape memory polymer composed of cross-linked polyethylene and polyethylene/nylon- 6 graft copolymer disposed between the two plastic layers. A hydrophilic matrix composed of hydroxypropylcellulose is disposed on the layer above the shape memory polymer and calcium sulfate, lemongrass fragrance, and pressurized carbon dioxide capsules disposed beneath the shape memory polymer. During microwave heating, the shape memory polymer undergoes a shape change to a temporary shape and the calcium sulfate is released into the hydrophilic matrix. The exothermic reaction of the calcium sulfate and hydroxycellulose is expected to maintain a warm temperature for the food. The burst release also releases a lemongrass fragrance, and popping (crackling) noises due to the release of the pressurized carbon dioxide capsules in order to contribute a pleasant sensory experience for the consumer. Example 3: Heat-Detecting Packaging.
[0041] Packaging having ammonium nitrate disposed in high impact polystyrene is used for storage and transport of a food substance. During storage and transport, when a target temperature of 40°C is reached, endothermic agents are released into a hydrophilic matrix having hydroxypropyl methylcellulose, thereby cooling the contents of the packaging. The shape change of the high impact polystyrene may also notify the recipient that excessive storage temperatures were encountered.
Example 4: Heating Food Packaging.
[0042] Food packaging having magnesium sulfate disposed in a shape memory polymer is prepared. The shape memory polymer includes azobenzene. Magnesium sulfate will be released by directing a laser scanner (infrared light), such as during purchase of the food product, towards the packaging. The infrared light will cause the burst release of the magnesium sulfate into a hydrophilic gel matrix having polyethylene oxide, and the exothermic reaction of the magnesim sulfate and polyethylene oxide is expected to heat the food.
Example 5: Color changing bowl.
[0043] A bowl includes a spiral coiled polyesterurethane having a colorant to indicate when hot foods have cooled sufficiently to eat safely. After heating a hot food, such as soup, the soup is placed in the bowl and the polyesterurethane unravels releasing a colorant into the surrounding gel matrix within the bowl causing the bowl to change color, indicating when the soup is cooled enough to drink safely. The unravelling of the spiral coiled polyesterurethane to release the colorant can be illustrated in Example 4. Figures 4A-4D illustrate a thermally-induced transition of polyesterurethane (poly(e- caprlolactone)dimethacrylate) from a spiral structure to a temporary substantially straight structure in response to an increase in temperature (Behl et al., Shape Memory Polymers and Shape-Changing Polymers, Advances in Polymer Science, Vol. 226, 2010, pp.1-40). Figure 4A depicts a shape memory polymer in a corkscrew spiral shape that slowly unravels as shown in Figure 4B when exposed to a stimulus. Figure 4C, a bent tubular shape, depicts further stages of transformation of the shape memory polymer that unravels as shown in Figure 4D to form a straight, fixed tubular shape.
[0044] In polyesterurethane, the temporary fixation of the polyester switching segments, such as poly(e-caprolactone)dimethacrylate, may cause the shape change; while the urethane provides hard segments. The oligo(e-caprolactone) segment is the switching segment. The transition temperature,
Figure imgf000018_0001
is the melting temperature, Tm> of the oligo(e- caprolactone) segments. Elasticity is provided by the soft, amorphous poly(dimethacrylate) domains. A second temporary shape is applied to a polymer by an external stress causing deformation of the polymer. The temporary shape is retained until the shaped body is exposed to an appropriate stimulus, which induces the recovery of the original shape.
Example 6: Heat-detection packagaing.
[0045] Figures 5A-5C illustrate a thermally-induced transition of a shape memory polymer from a temporary bar shape to a permanent cork-screw-like spiral (Behl et al., Shape Memory Polymers and Shape-Changing Polymers, Advances in Polymer Science, Vol. 226, 2010, pp.1-40). Figure 5 A illustrates a shape memory polymer at its temporary bar shape which when exposed to a rise in temperature, starts to curl inward as seen in Figure 5B, yielding a permanent corkscrew shape as seen in Figure 5C. The recovery process took 35 seconds at 60°C. As the shape memory polymer curls inward an endothermic agent is released into a hydrophilic matrix having hydroxypropyl methylcellulose, thereby cooling the contents of the packaging. The shape change of the shape memory polymer may also notify the recipient that excessive storage temperatures were encountered. Example 6: Magnetically-induced packaging.
[0046] Figures 9A-9E illustrate the magnetically-induced uncoiling of a corkscrew-like spiral of a composite from an aliphatic polyetherurethane (TFX) and 10 wt magnetic nanoparticles (Behl et al., Soft Matter, Actively Moving Polymers, 2007, 3:58-67). Behl discloses a remote actuation of the thermally-induced shape-memory effect in an alternating magnetic field is realized in composites of shape-memory thermoplasts and magnetic nanoparticles. In Behl, inductive heating of the nanoparticles in an alternating magnetic field (f = 258 kHz, H = 30 kA m21) increased the sample temperature. The thermoplastic material consisted either of a biodegradable multiblock copolymer (PDC), with poly(p-dioxanone) as the hard segment and poly(e-caprolactone) as the switching segment, or an aliphatic polyetherurethane (TFX) from methylene bis(p-cyclohexyl isocyanate), butanediol and polytetrahydrofuran. Magnetic nanoparticles of iron(III)oxide cores in a silica matrix were incorporated in both polymers. While TFX has an amorphous switching phase, PDC has a crystallizable switching segment. The shape memory effect could be triggered in both samples by exposure to an alternating magnetic field. The Rr values of indirectly heated samples were comparable to samples where the environmental temperature has been increased. As the composite uncoils, an exothermic agent is released into a hydrophilic matrix having hydroxypropyl methylcellulose, thereby heating the contents of the packaging.
Example 8: Soup packaging with enhanced aroma.
[0047] A soup container includes extruded potato starch coated on the inside of the container. As the soup is heated the extruded potato starch curls and peels from the walls of the container, revealing and releasing essential oils underneath the starch coating that enhance the aroma of the soup. Figure 6 illustrates the shape changing properties of extruded potato starch from spiral to flat shape (Sjong, Chaunier, L., Lourdin, S., The shape memory of starch, Starch/Starke 61 (2009) 116-118). The edible polymer begins with a spiral shape at an initial temperature, and was subjected to a cycle of a decrease in temperature followed by an increase in temperature back to its initial temperature. The changes in the temperature resulted in the edible polymer switching from the spiral shape to the flat shape after the cycle completes. When subjected to another cycle of temperature changes, the edible polymer switches from the flat shape back to the spiral shape.
[0048] The present disclosure is not to be limited in terms of the particular embodiments described in this application, which are intended as illustrations of various aspects. Many modifications and variations can be made without departing from its spirit and scope, as will be apparent to those skilled in the art. Functionally, equivalent methods and apparatuses within the scope of the disclosure, in addition to those enumerated in this document, will be apparent to those skilled in the art from the foregoing descriptions. Such modifications and variations are intended to fall within the scope of the appended claims. The present disclosure includes the full scope of equivalents to which the claims are entitled. It is to be understood that this disclosure is not limited to particular methods, reagents, compounds, compositions or biological systems, which can, of course, vary. It is also to be understood that the terminology used in this document is for the purpose of describing particular embodiments only, and is not intended to be limiting.
[0049] With respect to the use of substantially any plural and/or singular terms in this document, those having skill in the art can translate from the plural to the singular and/or from the singular to the plural as is appropriate to the context and/or application. The various singular/plural permutations may be expressly set forth in this document for sake of clarity.
[0050] It will be understood by those within the art that, in general, terms used in this document, and especially in the appended claims (for example, bodies of the appended claims) are generally intended as "open" terms (for example, the term "including" should be interpreted as "including but not limited to," the term "having" should be interpreted as "having at least," the term "includes" should be interpreted as "includes but is not limited to," etc.). It will be further understood by those within the art that if a specific number of an introduced claim recitation is intended, such an intent will be explicitly recited in the claim, and in the absence of such recitation no such intent is present. For example, as an aid to understanding, the following appended claims may contain usage of the introductory phrases "at least one" and "one or more" to introduce claim recitations. However, the use of such phrases should not be construed to imply that the introduction of a claim recitation by the indefinite articles "a" or "an" limits any particular claim containing such introduced claim recitation to embodiments containing only one such recitation, even when the same claim includes the introductory phrases "one or more" or "at least one" and indefinite articles such as "a" or "an" (for example, "a" and/or "an" should be interpreted to mean "at least one" or "one or more"); the same holds true for the use of definite articles used to introduce claim recitations. In addition, even if a specific number of an introduced claim recitation is explicitly recited, those skilled in the art will recognize that such recitation should be interpreted to mean at least the recited number (for example, the bare recitation of "two recitations," without other modifiers, means at least two recitations, or two or more recitations). Furthermore, in those instances where a convention analogous to "at least one of A, B, and C, etc." is used, in general such a construction is intended in the sense one having skill in the art would understand the convention (for example, "a system having at least one of A, B, and C" would include but not be limited to systems that have A alone, B alone, C alone, A and B together, A and C together, B and C together, and/or A, B, and C together, etc.). It will be further understood by those within the art that virtually any disjunctive word and/or phrase presenting two or more alternative terms, whether in the description, claims, or drawings, should be understood to contemplate the possibilities of including one of the terms, either of the terms, or both terms. For example, the phrase "A or B" will be understood to include the possibilities of "A" or "B" or "A and B."
[0051] In addition, where features or aspects of the disclosure are described in terms of Markush groups, those skilled in the art will recognize that the disclosure is also thereby described in terms of any individual member or subgroup of members of the Markush group.
[0052] As will be understood by one skilled in the art, for any and all purposes, such as in terms of providing a written description, all ranges disclosed in this document also encompass any and all possible subranges and combinations of subranges thereof. Any listed range can be easily recognized as sufficiently describing and enabling the same range being broken down into at least equal halves, thirds, quarters, fifths, tenths, etc. As a non-limiting example, each range discussed in this document can be readily broken down into a lower third, middle third and upper third, etc. As will also be understood by one skilled in the art all language such as "up to," "at least," and the like include the number recited and refer to ranges which can be subsequently broken down into subranges as discussed above. Finally, as will be understood by one skilled in the art, a range includes each individual member. Thus, for example, a group having 1-3 bonds refers to groups having 1, 2, or 3 bonds. Similarly, a group having 1-5 bonds refers to groups having 1, 2, 3, 4, or 5 bonds, and so forth.
[0053] From the foregoing, it will be appreciated that various embodiments of the present disclosure have been described in this document for purposes of illustration, and that various modifications may be made without departing from the scope and spirit of the present disclosure. Accordingly, the various embodiments disclosed in this document are not intended to be limiting, with the true scope and spirit being indicated by the following claims.

Claims

CLAIMS What Is Claimed Is:
1. A packaging comprising: at least one agent disposed within a shape memory polymer, wherein the shape memory polymer is adapted to release the agent in response to a stimulus.
2. The packaging of claim 1, wherein the agent is released from the shape memory polymer in a burst release fashion.
3. The packaging of claim Error! Reference source not found., wherein the agent comprises a cooling agent, a fragrance, a heating agent, a visual indicator or aid, an antibiotic, a drug, a medicinal agent, a noise-making agent, or a combination thereof.
4. The packaging of claim Error! Reference source not found., wherein the agent comprises a salt capable of producing an exothermic reaction when dissolved in water, a salt capable of producing an endothermic reaction when dissolved in water, an essential oil, pressurized carbon dioxide, or a combination thereof.
5. The packaging of claim Error! Reference source not found., wherein the agent comprises a salt capable of producing an endothermic reaction when dissolved in water selected from ammonium nitrate, lithium chloride, potassium chloride, ammonium nitrite, potassium thiocyanate, ammonium thiocyanate, potassium iodide, ammonium chloride, sodium nitrite, sodium nitrate, sodium acetate, sodium carbonate, sodium chloride, sodium sulfate, sodium thiosulfate, sodium phosphate, urea, xylitol, sorbitol, glycerol, salivary amylase, lipase, maltitol, sucrose, glucose, mannose, a sugar, a carbohydrate, and a combination thereof.
6. The packaging of claim Error! Reference source not found., wherein the agent comprises a salt capable of producing an exothermic reaction when dissolved in water selected from lithium chloride, magnesium chloride, potassium carbonate, magnesium sulfate, calcium sulfate, calcium chloride, calcium oxide, aluminum chloride, aluminum sulfate, potassium aluminum sulfate, and a combination thereof.
7. The packaging of claim Error! Reference source not found., wherein the agent comprises an essential oil selected from agar oil, ajwain oil, angelica root oil, anise oil, asafetida, balsam oil, basil oil, bay oil, bergamot oil, black pepper essential oil, buchu oil, birch oil, camphor, cannabis flower essential oil, caraway oil, cardamom seed oil, carrot seed oil, cedarwood oil, chamomile oil, calamus root, cinnamon oil, cistus oil, citronella oil, clary sage oil, clove oil, coriander oil, coffee, coriander, costmary oil, costus root, cranberry seed oil, cubeb, cumin oil, cypress, cypriol, curry leaf, davana oil, dill oil, elecampane, eucalyptus oil, fennel seed oil, fenugreek oil, fir, frankincense oil, galangal, galbanum, geranium oil, ginger oil, goldenrod, grapefruit oil, henna oil, helichrysum, limonene, hickory nut oil, horseradish oil, hyssop, Idaho tansy, jasmine oil, juniper berry oil, lavender oil, lemon oil, lemongrass, lime, Litsea cubeba oil, mandarin, marjoram, melaleuca, tea tree oil, Melissa oil, mint oil, mountain savory, mustard oil, mugwort oil, myrrh oil, myrtle, neem oil, neroli, nutmeg, orange oil, oregano oil, orris oil, palo santo, parsley oil, patchouli oil, perilla essential oil, pennyroyal oil, peppermint oil, petitgrain, pine oil, ravensara, red cedar, roman chamomile, rose oil, rosehip oil, rosemary oil, rosewood oil, sage oil, sassafras oil, savory oil, sandalwood oil, schisandra oil, spearmint oil, spikenard, spruce, star anise oil, tangerine, tarragon oil, thyme oil, tsuga, turmeric, valerian, vetiver oil, omega-3 oil, flaxseed oil, fish oil, tallow, tung oil, banana oil, western red cedar, wintergreen, yarrow oil, ylang-ylang, zedoary, and any combinations thereof.
8. The packaging of claim Error! Reference source not found., wherein the shape memory polymer comprises cinnamic acid, starch, a polyetherurethane matrix, triphenylmethane leuco derivatives, azobenzene, biopolymers, poly(2-methyl-2-oxazoline), poly(silsesquioxane), high impact polystyrene, cross-linked polyethylene and polyethylene/nylon 6 graft copolymer, trans-polyisoprene, cross-linked ethylene-vinyl acetate copolymer, styrene-based polymers, acrylate -based polymers, polynorbornene, cross-linked polycyclooctene, epoxy-based polymers, thio-ene-based polymers, segmented polyurethane, segmented polyurethane ionomers, poly(3-hydroxyalkanoate), copolymers comprising dodecanedioic acid or sebacic acid monomers and bile acid-based polyesters, or a combination thereof.
9. The packaging of claim Error! Reference source not found., wherein the shape memory polymer comprises an edible polymer.
10. The packaging of claim Error! Reference source not found., wherein the shape memory polymer has a shape recovery of about 100% to about 1000%.
11. The packaging of claim Error! Reference source not found., wherein the stimulus comprises an increase in temperature, a decrease in temperature, ultraviolet (UV) light exposure, infrared (IR) light exposure, altering a magnetic field, pH change, change in ionic concentration, change in water concentration, change in electric field, or a combination thereof.
12. The packaging of claim Error! Reference source not found., wherein the shape memory polymer is adapted to undergo a shape change to release the agent in response to the stimulus.
13. The packaging of claim 12, wherein the shape change is reversible.
14. The packaging of claim 12, wherein the shape change is from a flat shape to a coiled shape.
15. The packaging of claim 12, wherein the shape change is from a tubular shape to a spiral shape.
16. The packaging of claim 12, wherein the shape change is from a coiled shape to a flat shape.
17. The packaging of claim 12, wherein the shape change is from a spiral shape to a tubular shape.
18. The packaging of claim 12, wherein the shape change is from a closed configuration to an open configuration in response to the stimulus.
19. The packaging of claim 12, wherein the shape change is a contraction of the shape memory polymer.
20. The packaging of claim 12, wherein the shape change is a rupture of at least a portion of the shape memory polymer.
21. The packaging of claim 12, wherein the shape change ruptures a capsule comprising the agent, the capsule being formed from the shape memory polymer.
22. The packaging of claim Error! Reference source not found., wherein the shape memory polymer is coated with an encapsulant.
23. The packaging of claim 22, wherein the encapsulant breaks when the shape memory polymer undergoes a shape change.
24. The packaging of claim 22, wherein the encapsulant comprises starch, poly (urea-formaldehyde), amino resin, polyamide, polyurethane, gelatin, cellulose, polyvinyl acetate, urea-resourcinol formaldehyde, or a combination thereof.
25. The packaging of claim Error! Reference source not found., wherein the agent is encapsulated.
26. The packaging of claim 1, wherein the shape memory polymer is disposed within a hydrophilic matrix, whereby the agent reacts with the hydrophilic matrix upon release from the shape memory polymer.
27. The packaging of claim 26, wherein the agent reacts with the hydrophilic matrix in an exothermic process.
28. The packaging of claim 26, wherein the agent reacts with the hydrophilic matrix in an endothermic process.
29. The packaging of claim 1, configured to hold food or beverages.
30. A method of making a packaging, the method comprising: disposing at least one agent within a shape memory polymer, wherein the shape memory polymer is adapted to release the agent in response to a stimulus.
31. The method of claim 30, wherein the agent is released from the shape memory polymer in a burst release fashion.
32. The method of claim 30, wherein the agent comprises a cooling agent, a fragrance, a heating agent, a visual indicator or a visual aid, an antibiotic, a drug, a medicinal agent, a noise-making agent, or a combination thereof.
33. The method of claim 30, wherein the agent comprises a salt capable of producing an exothermic reaction when dissolved in water, a salt capable of producing an endothermic reaction when dissolved in water, an essential oil, pressurized carbon dioxide, or a combination thereof.
34. The method of claim 30, wherein the agent comprises a salt capable of producing an exothermic reaction when dissolved in water selected from lithium chloride, magnesium chloride, potassium carbonate, magnesium sulfate, calcium sulfate, calcium chloride, calcium oxide, aluminum chloride, aluminum sulfate, potassium aluminum sulfate, and any combinations thereof.
35. The method of claim 30, wherein the agent comprises a salt capable of producing an endothermic reaction when dissolved in water selected from ammonium nitrate, potassium chloride, ammonium nitrite, potassium thiocyanate, ammonium thiocyanate, potassium iodide, ammonium chloride, sodium chloride, sodium nitrite, sodium nitrate, sodium acetate, sodium carbonate, sodium sulfate, sodium thiosulfate, sodium phosphate, urea, xylitol, sorbitol, glycerol, salivary amylase, lipase, maltitol, sucrose, glucose, mannose, a sugar, a carbohydrate, and any combinations thereof.
36. The method of claim 30, wherein the agent comprises an essential oil selected from agar oil, ajwain oil, angelica root oil, anise oil, asafetida, balsam oil, basil oil, bay oil, bergamot oil, black pepper essential oil, buchu oil, birch oil, camphor, cannabis flower essential oil, caraway oil, cardamom seed oil, carrot seed oil, cedarwood oil, chamomile oil, calamus root, cinnamon oil, cistus oil, citronella oil, clary sage oil, clove oil, coriander oil, coffee, coriander, costmary oil, costus root, cranberry seed oil, cubeb, cumin oil, cypress, cypriol, curry leaf, davana oil, dill oil, elecampane, eucalyptus oil, fennel seed oil, fenugreek oil, fir, frankincense oil, galangal, galbanum, geranium oil, ginger oil, goldenrod, grapefruit oil, henna oil, helichrysum, limonene, hickory nut oil, horseradish oil, hyssop, Idaho tansy, jasmine oil, juniper berry oil, lavender oil, lemon oil, lemongrass, lime, Litsea cubeba oil, mandarin, marjoram, melaleuca, tea tree oil, Melissa oil, mint oil, mountain savory, mustard oil, mugwort oil, myrrh oil, myrtle, neem oil, neroli, nutmeg, orange oil, oregano oil, orris oil, palo santo, parsley oil, patchouli oil, perilla essential oil, pennyroyal oil, peppermint oil, petitgrain, pine oil, ravensara, red cedar, roman chamomile, rose oil, rosehip oil, rosemary oil, rosewood oil, sage oil, sassafras oil, savory oil, sandalwood oil, schisandra oil, spearmint oil, spikenard, spruce, star anise oil, tangerine, tarragon oil, thyme oil, tsuga, turmeric, valerian, vetiver oil, omega-3 oil, flaxseed oil, fish oil, tallow, tung oil, banana oil, western red cedar, wintergreen, yarrow oil, ylang-ylang, zedoary, and any combinations thereof.
37. The method of claim 30, wherein the shape memory polymer comprises cinnamic acid, starch, a polyetherurethane matrix, triphenylmethane leuco derivatives, azobenzene, biopolymers, poly(2-methyl-2-oxazoline), poly(silsesquioxane), high impact polystyrene, cross-linked polyethylene and polyethylene/nylon 6 graft copolymer, trans- polyisoprene, cross-linked ethylene-vinyl acetate copolymer, styrene-based polymers, acrylate -based polymers, polynorbornene, cross-linked polycyclooctene, epoxy-based polymers, thio-ene-based polymers, segmented polyurethane, segmented polyurethane ionomers, poly(3-hydroxyalkanoate), copolymers comprising dodecanedioic acid or sebacic acid monomers and bile acid-based polyesters, or a combination thereof.
38. The method of claim 30, wherein the shape memory polymer comprises an edible polymer.
39. The method of claim 30, wherein the shape memory polymer has a shape recovery of about 100% to about 1000%.
40. The method of claim 30, wherein the stimulus comprises an increase in temperature, a decrease in temperature, ultraviolet (UV) light exposure, infrared (IR) light exposure, altering a magnetic field, pH change, change in ionic concentration, change in water concentration, change in electric field, or a combination thereof.
41. The method of claim 30, wherein the shape memory polymer is adapted to undergo a shape change to release the agent in response to the stimulus.
42. The method of claim 41, wherein the shape change is reversible.
43. The method of claim 41, wherein the shape change is from a flat shape to a coiled shape.
44. The method of claim 41, wherein the shape change is from a tubular shape to a spiral shape.
45. The method of claim 41, wherein the shape change is from a coiled shape to a flat shape.
46. The method of claim 41, wherein the shape change is from a spiral shape to a tubular shape.
47. The method of claim 41, wherein the shape change is from a closed configuration to an open configuration in response to the stimulus.
48. The method of claim 41, wherein the shape change is a contraction of the shape memory polymer.
49. The method of claim 41, wherein the shape change is a rupture of at least a portion of the shape memory polymer.
50. The method of claim 41, wherein the shape change ruptures a capsule comprising the agent, the capsule being formed from the shape memory polymer.
51. The method of claim 30, wherein the shape memory polymer is coated with an encapsulant.
52. The method of claim 51, wherein the encapsulant breaks when the shape memory polymer undergoes a shape change.
53. The method of claim 51, wherein the encapsulant comprises starch, poly(urea- formaldehyde), amino resin, polyamide, polyurethane, gelatin, cellulose, polyvinyl acetate, urea-resourcinol formaldehyde, or a combination thereof.
54. The method of claim 30, wherein the agent is encapsulated.
55. The method of claim 30, wherein the shape memory polymer is disposed within a hydrophilic matrix, whereby the agent reacts with the hydrophilic matrix upon release from the shape memory polymer.
56. The method of claim 55, wherein the agent reacts with the hydrophilic matrix in an exothermic process.
57. The method of claim 55, wherein the agent reacts with the hydrophilic matrix in an endothermic process.
58. The method of claim 30, wherein the packaging is configured to hold food or beverages.
59. A method of using a packaging, the method comprising: providing a packaging comprising at least one agent disposed within a shape memory polymer; and
providing a stimulus to deform the shape memory polymer, whereby the agent is released from the shape memory polymer.
60. The method of claim 59, wherein the agent is released from the shape memory polymer in a burst release fashion.
61. The method of claim 59, further comprising providing a hydrophilic matrix, whereby the agent reacts with the hydrophilic matrix upon release from the shape memory polymer.
62. The method of claim 61, wherein the agent reacts with the hydrophilic matrix in an exothermic process.
63. The method of claim 61, wherein the agent reacts with the hydrophilic matrix in an endothermic process.
64. The method of claim 59, wherein the agent comprises a cooling agent, a fragrance, a heating agent, a visual indicator or aid, an antibiotic, a drug, a medicinal agent, a noise-making agent, or a combination thereof.
65. The method of claim 59, wherein the agent comprises a salt capable of producing an exothermic reaction when dissolved in water, a salt capable of producing an endothermic reaction when dissolved in water, an essential oil, pressurized carbon dioxide, or a combination thereof.
66. The method of claim 59, wherein the agent comprises a salt capable of producing an exothermic reaction when dissolved in water selected from lithium chloride, magnesium chloride, potassium carbonate, magnesium sulfate, calcium sulfate, calcium chloride, calcium oxide, aluminum chloride, aluminum sulfate, potassium aluminum sulfate, and any combinations thereof.
67. The method of claim 59, wherein the agent comprises a salt capable of producing an endothermic reaction when dissolved in water selected from ammonium nitrate, potassium chloride, ammonium nitrite, potassium thiocyanate, ammonium thiocyanate, potassium iodide, ammonium chloride, sodium chloride, sodium nitrite, sodium nitrate, sodium acetate, sodium carbonate, sodium sulfate, sodium thiosulfate, sodium phosphate, urea, xylitol, sorbitol, glycerol, salivary amylase, lipase, maltitol, sucrose, glucose, mannose, a sugar, a carbohydrate, and any combinations thereof.
68. The method of claim 59, wherein the agent comprises an essential oil selected from agar oil, ajwain oil, angelica root oil, anise oil, asafetida, balsam oil, basil oil, bay oil, bergamot oil, black pepper essential oil, buchu oil, birch oil, camphor, cannabis flower essential oil, caraway oil, cardamom seed oil, carrot seed oil, cedarwood oil, chamomile oil, calamus root, cinnamon oil, cistus oil, citronella oil, clary sage oil, clove oil, coriander oil, coffee, coriander, costmary oil, costus root, cranberry seed oil, cubeb, cumin oil, cypress, cypriol, curry leaf, davana oil, dill oil, elecampane, eucalyptus oil, fennel seed oil, fenugreek oil, fir, frankincense oil, galangal, galbanum, geranium oil, ginger oil, goldenrod, grapefruit oil, henna oil, helichrysum, limonene, hickory nut oil, horseradish oil, hyssop, Idaho tansy, jasmine oil, juniper berry oil, lavender oil, lemon oil, lemongrass, lime, Litsea cubeba oil, mandarin, marjoram, melaleuca, tea tree oil, Melissa oil, mint oil, mountain savory, mustard oil, mugwort oil, myrrh oil, myrtle, neem oil, neroli, nutmeg, orange oil, oregano oil, orris oil, palo santo, parsley oil, patchouli oil, perilla essential oil, pennyroyal oil, peppermint oil, petitgrain, pine oil, ravensara, red cedar, roman chamomile, rose oil, rosehip oil, rosemary oil, rosewood oil, sage oil, sassafras oil, savory oil, sandalwood oil, schisandra oil, spearmint oil, spikenard, spruce, star anise oil, tangerine, tarragon oil, thyme oil, tsuga, turmeric, valerian, vetiver oil, omega-3 oil, flaxseed oil, fish oil, tallow, tung oil, banana oil, western red cedar, wintergreen, yarrow oil, ylang-ylang, zedoary, and any combinations thereof.
69. The method of claim 59, wherein the shape memory polymer comprises cinnamic acid, starch, a polyetherurethane matrix, triphenylmethane leuco derivatives, azobenzene, biopolymers, poly(2-methyl-2-oxazoline), poly(silsesquioxane), high impact polystyrene, cross-linked polyethylene and polyethylene/nylon 6 graft copolymer, trans- polyisoprene, cross-linked ethylene-vinyl acetate copolymer, styrene-based polymers, acrylate -based polymers, polynorbornene, cross-linked polycyclooctene, epoxy-based polymers, thio-ene-based polymers, segmented polyurethane, segmented polyurethane ionomers, poly(3-hydroxyalkanoate), copolymers comprising dodecanedioic acid or sebacic acid monomers and bile acid-based polyesters, or a combination thereof.
70. The method of claim 59, wherein the shape memory polymer comprises an edible polymer.
71. The method of claim 59, wherein the shape memory polymer has a shape recovery of about 100% to about 1000%.
72. The method of claim 59, wherein providing a stimulus comprises increasing a temperature, decreasing a temperature, exposing the packaging to ultraviolet (UV) light, exposing the packaging to infrared (IR) light, altering a magnetic field, changing pH, changing an ion concentration, changing water concentration, changing an electric field, or a combination thereof.
73. The method of claim 59, wherein providing a stimulus to deform the shape memory polymer results in a shape change.
74. The method of claim 73, wherein the shape change is reversible.
75. The method of claim 73, wherein the shape change is from a flat shape to a coiled shape.
76. The method of claim 73, wherein the shape change is from a tubular shape to a spiral shape.
77. The method of claim 73, wherein the shape change is from a coiled shape to a flat shape.
78. The method of claim 73, wherein the shape change is from a spiral shape to a tubular shape.
79. The method of claim 73, wherein the shape change is from a closed configuration to an open configuration in response to the stimulus.
80. The method of claim 73, wherein the shape change is a contraction of the shape memory polymer.
81. The method of claim 73, wherein the shape change is a rupture of at least a portion of the shape memory polymer.
82. The method of claim 73, wherein the shape change ruptures a capsule comprising the agent, the capsule being formed from the shape memory polymer.
83. The method of claim 59, wherein the shape memory polymer is coated with an encapsulant.
84. The method of claim 83, wherein the encapsulant breaks when the shape memory polymer undergoes a shape change.
85. The method of claim 83, wherein the encapsulant comprises starch, poly(urea- formaldehyde), amino resin, polyamide, polyurethane, gelatin, cellulose, polyvinyl acetate, urea-resourcinol formaldehyde, or a combination thereof.
86. The method of claim 59, wherein the agent is encapsulated.
87. The method of claim 59, wherein the packaging is configured to hold food or beverages.
PCT/US2013/051594 2013-07-23 2013-07-23 Packaging materials and methods for their preparation and use WO2015012803A1 (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
CN201380078825.9A CN105555504A (en) 2013-07-23 2013-07-23 Packaging materials and methods for their preparation and use
PCT/US2013/051594 WO2015012803A1 (en) 2013-07-23 2013-07-23 Packaging materials and methods for their preparation and use
US14/907,285 US20160159551A1 (en) 2013-07-23 2013-07-23 Packaging materials and methods for their preparation and use

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PCT/US2013/051594 WO2015012803A1 (en) 2013-07-23 2013-07-23 Packaging materials and methods for their preparation and use

Publications (1)

Publication Number Publication Date
WO2015012803A1 true WO2015012803A1 (en) 2015-01-29

Family

ID=52393674

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2013/051594 WO2015012803A1 (en) 2013-07-23 2013-07-23 Packaging materials and methods for their preparation and use

Country Status (3)

Country Link
US (1) US20160159551A1 (en)
CN (1) CN105555504A (en)
WO (1) WO2015012803A1 (en)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107364635B (en) * 2017-06-30 2019-03-08 嘉兴华悦包装用品有限公司 Food packaging zippered bag with refrigerating function
CN109265981A (en) * 2018-08-06 2019-01-25 徐州奥博包装制品有限公司 A kind of polymeric packaging material
CN110463981A (en) * 2019-07-26 2019-11-19 黄安琪 Garland product and preparation method thereof
CN112009859B (en) * 2020-08-24 2022-05-17 阿克苏优能农业科技股份有限公司 Special mould-proof, dust-proof and fresh-keeping net bag for sugar-cored apples and preparation method thereof
CN112452369B (en) * 2020-11-24 2022-03-01 东南大学 Magnetic control thermoplastic shape memory polymer wrapped heating platform and method
CN115887761B (en) * 2023-02-23 2023-05-09 四川兴泰普乐医疗科技有限公司 Sinus support and preparation method thereof

Citations (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5037698A (en) * 1987-01-21 1991-08-06 Lilly Industries Limited Capsule filling employing hygroscopic components
US5170801A (en) * 1990-10-02 1992-12-15 Glaxo Inc. Medical capsule device actuated by radio-frequency (rf) signal
US20030055198A1 (en) * 1998-02-23 2003-03-20 Mnemoscience Gmbh Shape memory polymers
WO2007107378A1 (en) * 2006-03-23 2007-09-27 Mnemoscience Gmbh Use of shape memory materials for introducing and/or liberating reactants, catalysts and additives
US20070235035A1 (en) * 2005-12-06 2007-10-11 Wolfgang Petsch Method Of Producing Auto Induced Physiological Processes In A Body Cavity And A Device For Using It
US20080027199A1 (en) * 2006-07-28 2008-01-31 3M Innovative Properties Company Shape memory polymer articles with a microstructured surface
US20090043288A1 (en) * 2001-03-23 2009-02-12 Petrakis Dennis N Temperature responsive systems
US20090130391A1 (en) * 2007-11-02 2009-05-21 University Of Washington Design of shape memory alloy fibers and shape memory polymer fibers and films and their composites for reversible shape changes
EP2075273A1 (en) * 2007-12-28 2009-07-01 Mnemoscience GmbH Multiple shape memory polymer networks
US20090306767A1 (en) * 2006-05-05 2009-12-10 Mnemoscience Gmbh Shape memory devices
US20110123614A1 (en) * 2009-11-20 2011-05-26 Tyco Healthcare Group Oral Dosage Forms for Delivery of Therapeutic Agents
US20120102897A1 (en) * 2009-05-26 2012-05-03 Rousseau Ingrid A Packaging and de-packaging methods using shape memory polymers

Patent Citations (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5037698A (en) * 1987-01-21 1991-08-06 Lilly Industries Limited Capsule filling employing hygroscopic components
US5170801A (en) * 1990-10-02 1992-12-15 Glaxo Inc. Medical capsule device actuated by radio-frequency (rf) signal
US20030055198A1 (en) * 1998-02-23 2003-03-20 Mnemoscience Gmbh Shape memory polymers
US20090043288A1 (en) * 2001-03-23 2009-02-12 Petrakis Dennis N Temperature responsive systems
US20070235035A1 (en) * 2005-12-06 2007-10-11 Wolfgang Petsch Method Of Producing Auto Induced Physiological Processes In A Body Cavity And A Device For Using It
WO2007107378A1 (en) * 2006-03-23 2007-09-27 Mnemoscience Gmbh Use of shape memory materials for introducing and/or liberating reactants, catalysts and additives
US20090306767A1 (en) * 2006-05-05 2009-12-10 Mnemoscience Gmbh Shape memory devices
US20080027199A1 (en) * 2006-07-28 2008-01-31 3M Innovative Properties Company Shape memory polymer articles with a microstructured surface
US20090130391A1 (en) * 2007-11-02 2009-05-21 University Of Washington Design of shape memory alloy fibers and shape memory polymer fibers and films and their composites for reversible shape changes
EP2075273A1 (en) * 2007-12-28 2009-07-01 Mnemoscience GmbH Multiple shape memory polymer networks
US20120102897A1 (en) * 2009-05-26 2012-05-03 Rousseau Ingrid A Packaging and de-packaging methods using shape memory polymers
US20110123614A1 (en) * 2009-11-20 2011-05-26 Tyco Healthcare Group Oral Dosage Forms for Delivery of Therapeutic Agents

Also Published As

Publication number Publication date
US20160159551A1 (en) 2016-06-09
CN105555504A (en) 2016-05-04

Similar Documents

Publication Publication Date Title
US20160159551A1 (en) Packaging materials and methods for their preparation and use
Xia et al. A review of shape memory polymers and composites: mechanisms, materials, and applications
Vasile et al. Progresses in food packaging, food quality, and safety—controlled-release antioxidant and/or antimicrobial packaging
Esser-Kahn et al. Triggered release from polymer capsules
Miao et al. 4D printing of polymeric materials for tissue and organ regeneration
Bruyninckx et al. Sustainable chemistry considerations for the encapsulation of volatile compounds in laundry-type applications
CA2567138C (en) Endoprostheses and methods of making the same
AU2012301493B2 (en) Releasably encapsulated aroma
Guo et al. Entanglement-based thermoplastic shape memory polymeric particles with photothermal actuation for biomedical applications
Sukhorukov et al. Multifunctional cargo systems for biotechnology
US20050261760A1 (en) Medical devices and methods of making the same
US20190290762A1 (en) Nano-architectured colloidosomes for controlled and triggered release
WO2020195132A1 (en) Perfume microcapsules, perfume microcapsule composition, softener, and detergent
Omid et al. Self-expanding stents based on shape memory alloys and shape memory polymers
WO2014186532A1 (en) Bioabsorbable biomedical implants
US20140023688A1 (en) Encapsulated oils
Basak et al. Solvent responsive shape memory polymers‐evolution, current status, and future outlook
Boyle et al. Solvent stimulated actuation of polyurethane-based shape memory polymer foams using dimethyl sulfoxide and ethanol
EA036376B1 (en) Shape memory polymer composite for 3d printing of medical items
Basak et al. Styrene‐butadiene‐styrene‐based shape memory polymers: Evolution and the current state of art
Safranski et al. Applications of shape-memory polymers
JP2017515005A (en) Method and device for changing the characteristics of a linear element, in particular the distance separating two ends of a linear element
EP1708962B1 (en) Chlorine dioxide releasing composite article
Huang Shape memory polymers
DE102007043773A1 (en) Moisture absorbing multilayer films and packages made therefrom

Legal Events

Date Code Title Description
WWE Wipo information: entry into national phase

Ref document number: 201380078825.9

Country of ref document: CN

121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 13890157

Country of ref document: EP

Kind code of ref document: A1

NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 13890157

Country of ref document: EP

Kind code of ref document: A1