WO2011123949A1 - Edible coating composition and uses thereof - Google Patents
Edible coating composition and uses thereof Download PDFInfo
- Publication number
- WO2011123949A1 WO2011123949A1 PCT/CA2011/000392 CA2011000392W WO2011123949A1 WO 2011123949 A1 WO2011123949 A1 WO 2011123949A1 CA 2011000392 W CA2011000392 W CA 2011000392W WO 2011123949 A1 WO2011123949 A1 WO 2011123949A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- solution
- polysaccharide
- food product
- edible coating
- anyone
- Prior art date
Links
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- 238000000576 coating method Methods 0.000 claims abstract description 208
- 239000011248 coating agent Substances 0.000 claims abstract description 185
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- IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical group CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 claims description 91
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Classifications
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- A—HUMAN NECESSITIES
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Definitions
- the present relates to an edible coating for food products. More particularly, the present relates to an edible coating comprising a layer of a cross-linked polysaccharide.
- Edible coatings create a physical barrier between the fruit or vegetable and the surrounding environment, and reduce ripening reactions such as color and aroma changes, desiccation and degradation of the product. Edible coatings are thus effective in creating a micro-environment for each individual fruit or part thereof, thereby retaining humidity and reducing respiration and oxidation and extending shelf life of the products.
- edible coatings were also envisioned to serve as vehicles for adding functional ingredients to the fresh product.
- Known functional ingredients include antimicrobial agents (e.g. essential oils), antioxidants (e.g. organic acids), texture enhancers (e.g. glycerol) and nutraceuticals (e.g. probiotics, prebiotics and omega-3), which are embodied in the coating to promote health benefits and provide added nutritive value to the coated product.
- antimicrobial agents e.g. essential oils
- antioxidants e.g. organic acids
- texture enhancers e.g. glycerol
- nutraceuticals e.g. probiotics, prebiotics and omega-3
- Edible coatings known in the art include polysaccharide-, protein- and lipid-based edible coatings.
- Protein-based edible coatings typically include whey protein, soy protein, gluten, corn protein and/or sodium caseinate. While being efficient, the use of protein- based coating may be limited by current concerns with food allergies since many of the protein ingredients trigger allergic responses. Further, vegetarians and vegans may tend to avoid products coated with protein-based coating because they are derived from an animal source.
- Lipid ingredients used for the production of edible coatings include shellac, beeswax, candelilla wax, carnauda wax and fatty acids. Again, some of the lipid-based coatings are from animal sources and tend to be avoided by vegetarians and vegans, which makes them unsuitable for coating products that are, at least partially, destined to this market segment.
- polysaccharides from plant, seaweed and/or bacteria origin have thus been studied for their jellification capacities.
- the polysaccharides most commonly used are cellulose derivatives, alginate, carrageenan, chitosan, pectin, starch derivates and other gums.
- Sodium alginate and carrageenan are both derived from seaweed whereas gellan is produced by a bacteria, Sphingomonas elodea.
- polysaccharide coatings tend to be good microbial culture mediums. Because fresh-cut fruits (e.g. pineapple slices, etc.) are more subject to microbial spoilage than whole fruits (e.g. grapes, apples, pears) and product deterioration and food safety issues are more likely to occur (Brecht 1995; Thunberg et al. 2002), polysaccharide-based edible coatings known in the art have therefore not all proven effective.
- an edible coating for a food product comprises a polysaccharide layer including at least one cross-linked polysaccharide.
- the at least one cross-linked polysaccharide is selected from the group consisting of carrageenan, gellan, alginate and pectin, and is cross- linked with a cross-linking agent.
- the at least one cross-linked polysaccharide is an alginate, and preferably sodium alginate.
- the least one cross-linked polysaccharide solution is pectin, and preferably pectin LM.
- the at least one cross-linked polysaccharide comprises sodium alginate and pectin LM.
- the cross-linking agent is a calcium cross-linking agent, and preferably calcium ascorbate.
- the edible coating further comprises an antimicrobial agent, preferably vanillin or an essential oil.
- the edible coating further comprises a flavoring agent, preferably a vanilla essence.
- the edible coating further comprises antioxidant agent, and preferably at least one of a citric acid and an ascorbic acid.
- the edible coating further comprises a nutraceutical agent and preferably at least one probiotic, and more preferably a probiotic is selected from the Our re : 282351.00005
- Lactobacillus acidophilus Lactobacillus casei and, Bifidobacterium lactis.
- the edible coating comprises an immune response enhancer, and more preferably a yeast gluco polysaccharide.
- the edible coating comprises at least one element selected from the group consisting of a coloring agent, a protein, an amino acid and a vitamin.
- the coating has a pH above 3, and preferably a pH ranging between about 4 and about 9, and more preferably a pH ranging between about 5 and about 8.
- the food product is a fruit or a vegetable.
- a method for coating a food product with an edible coating comprises: (1 ) coating the food product with a polysaccharide solution to substantially cover the food product, the polysaccharide solution including at least one polysaccharide selected from the group consisting of carrageenan, gellan, alginate and pectin; (2) cross-linking said polysaccharide solution by immersing said food product in a cross-linking agent solution to obtain a polysaccharide layer substantially covering said food product; and (3) reducing the moisture content of said polysaccharide layer to obtain said edible coating.
- the polysaccharide solution is an alginate solution, and preferably a sodium alginate solution.
- the polysaccharide solution preferably comprises between about 0.1 % (w/w) and about 8% (w/w) sodium alginate, more preferably between about 0.5% (w/w) and 4% (w/w) sodium alginate, even more preferably between about 0.7% (w/w) and about 3% (w/w) sodium alginate, and still even more preferably between about 1 % (w/w) and about 2% (w/w) sodium alginate.
- the polysaccharide solution is a pectin solution, and preferably a pectin LM solution.
- the pectin LM solution preferably comprises between about 2% (w/w) and about 15% (w/w) pectin LM, and more preferably between about 5% (w/w) and about 10% (w/w) pectin LM.
- the polysaccharide solution comprises sodium alginate and pectin LM.
- the polysaccharide solution preferably comprises between about Our re : 282351.00005
- the cross-linking agent solution comprises a calcium cross- linking agent solution, and preferably a calcium ascorbate solution.
- the calcium ascorbate solution comprises between about 0.5% (w/w) and about 35% (w/w) calcium ascorbate, more preferably between about 1% (w/w) and about 30% (w/w) calcium ascorbate, even more preferably between about 13% (w/w) and about 27% (w/w) calcium ascorbate and still even more preferably about 15% (w/w) calcium ascorbate.
- the polysaccharide solution further comprises a flavoring agent, where the flavoring agent is preferably a vanilla essence.
- the polysaccharide solution further comprises an antimicrobial agent, and preferably vanillin or an essential oil.
- the polysaccharide solution further comprises an antioxidant agent.
- the antioxidant preferably comprises at least one of citric acid and ascorbic acid.
- the polysaccharide solution further comprises a nutraceutical agent.
- the nutraceutical agent preferably includes at least one probiotic, where the probiotic is preferably selected from the group consisting of Lactobacillus acidophilus, Lactobacillus casei and , Bifidobacterium lactis.
- the polysaccharide solution further comprises an immune response enhancer, and preferably a yeast gluco polysaccharide.
- the polysaccharide solution further comprises at least one element selected from the group consisting of a coloring agent, a protein, an amino acid and a vitamin.
- the step of coating of the food product with a polysaccharide solution to substantially cover the food product is carried out by immersing the food product in the polysaccharide solution.
- the step of coating the food product with a polysaccharide solution to substantially cover the food product is carried out by spraying the polysaccharide solution on the food product.
- the step of immersing the food product in the cross-linking agent solution for a period of time to obtain the polysaccharide layer ranges from about 1 second to about 15 minutes, preferably from about 10 seconds to about 10 minutes, and more preferably from about 10 seconds to about 4 minutes.
- the polysaccharide solution and the cross-linking agent solution have a temperature below 37 Celsius degrees, and preferably have a temperature ranging from about -5 Celsius degrees to about 20 Celsius degrees, and more preferably a temperature ranging from about 4 Celsius degrees to about 10 Celsius degrees, and even more preferably a temperature ranging from about 4 Celsius degrees to about 7 Celsius degrees.
- the edible coating has a pH above 3, preferably a pH ranging between about 4 and about 9, and more preferably a pH ranging between about 5 and about 8.
- the moisture content of the polysaccharide layer is reduced from about 30% to about 97% to obtain the edible coating.
- reducing the moisture content of the polysaccharide layer to obtain said edible coating is carried out using a drying process that minimize thermoshocks to the food product, and preferably one process selected from the group consisting of a compression process, a desiccation process and a surface lyophilisation process.
- the method further comprises a step of sprinkling a food additive on a surface of the edible coating.
- the food additive comprises granules of at least one dried fruit, and more preferably at least one dried fruit selected from the group consisting of a dried apple, a dried strawberry and a dried raspberry.
- the food product is preferably at least one of a fruit and a vegetable.
- a method for obtaining clusters of food products comprises: (1) coating the food product Our ref.: 282351.00005 7
- the polysaccharide solution including at least one polysaccharide selected from the group consisting of carrageenan, gellan, alginate and pectin; (2) grouping the food products to form clusters thereof; (3) cross-linking the polysaccharide solution by immersing the food product in a cross-linking agent solution to obtain a polysaccharide layer substantially covering the food product; and (4) reducing the moisture content of the polysaccharide layer to obtain the edible coating.
- the method comprises: (1) grouping the food products to form clusters thereof; (2) coating the food product with a polysaccharide solution to substantially cover the food product, the polysaccharide solution including at least one polysaccharide selected from the group consisting of carrageenan, gellan, alginate and pectin; (3) cross-linking the polysaccharide solution by immersing the food product in a cross-linking agent solution to obtain a polysaccharide layer substantially covering the food product; and (4) reducing the moisture content of the polysaccharide layer to obtain the edible coating.
- a food product comprising the edible coating described hereinabove.
- the food product further comprises a food additive sprinkled on the surface of the edible coating.
- the food additive preferably comprises granules of at least one dried fruit, and more preferably at least one dried fruit is selected from the group consisting of a dried apple, a dried strawberry and a dried raspberry.
- a kit for a snack comprises a package of a food product, the food comprising the edible coating described hereinabove; and a package of a food additive suitable for being sprinkle on a surface of said edible coating.
- the food additive of the snack kit comprises granules of at least one dried fruit, and more preferably at least one dried fruit is selected from the group consisting of a dried apple, a dried strawberry and a dried raspberry.
- the snack kit further comprises a tool for allowing a user to eat the food product, where the tool is preferably selected from the group consisting of a fork and a toothpick.
- Figure 1 shows the difference in appearance between uncoated and coated grapes after 2 days of storage.
- Figure 2 shows the difference in appearance between uncoated (control) and coated pineapple tidbits after storage at 4°C.
- Figure 3 shows the difference in appearance between uncoated (control) and coated blueberries after storage at 4°C.
- Figure 4 shows the formation of lowbush blueberries clusters.
- Figure 5 shows the difference in appearance between uncoated (control) and coated apple clusters after storage at 4°C.
- Figure 6 shows the difference in appearance between uncoated (control) and coated vegetables of a first mix of fresh cut vegetables after storage at 4°C.
- Figure 7 shows the difference in appearance between uncoated (control) and coated vegetables of a second mix of fresh cut vegetables after storage at 4°C.
- Figure 8 shows the difference in appearance between uncoated (control) and coated vegetables of a third mix of fresh cut vegetables after storage at 4°C.
- an edible coating for a food product is provided.
- the edible coating is typically used for coating a perishable food product such as a fruit or a Our ret: 282351.00005 9
- Exemplary food products for use with the edible coating include, but are not limited to, whole and fresh cut fruits such as strawberries, grapes, blueberries, mangoes, papayas, apples, kiwis, cantaloupes, pineapples, honeydew melons, watermelons, and whole and fresh cut vegetables, such as bell peppers, carrots, turnips, onions (e.g. red and yellow onions), celery, leeks, broccolis, cauliflowers, potatoes, sweet potatoes, cabbages, zucchinis and the like.
- the edible coating may find use with any other product intended for animal or human consumption.
- the edible coating could be used for coating meat or fish products, as well as bakery meals such as bakery patties.
- the edible coating is used to extend or prolong the shelf-life of fruits and vegetables.
- extending shelf-life shall be interpreted broadly so as to include any gain in product conservation. This would include, for instance maintaining or preserving, at least partially, one or several of the appearance (e.g. color), texture or taste, or reducing desiccation (i.e. juice losses) of the product.
- the edible coating comprises polysaccharide layer including at least one cross-linked polysaccharide.
- the at least one cross-linked polysaccharide is preferably selected from the group consisting of carrageenan, gellan, alginate and pectin, and has been cross-linked using a cross-linking agent.
- the cross-linked polysaccharide is alginate, and preferably sodium alginate. As it will become apparent below, experiments have shown that sodium alginate is capable of forming thin gels that are firm or very firm and yet be easy to masticate.
- the cross-linked polysaccharide is pectin, and more preferably pectin LM.
- pectin displayed better coating properties on food products having higher contents of juices or syrups (e.g. fruit salads) than sodium alginate, carrageenan and gellan (see Example 1 below). Accordingly, in instances where the food product to be coated is prone to exude substantial amounts of juice, the use of pectin would be preferred. In some other instances, it may be desirable to use an edible coating comprising a combination of cross-linked polysaccharides, such as, for instance, a combination of Our ref.: 282351.00005
- sodium alginate and pectin LM sodium alginate and pectin LM.
- a person skilled in the art would nevertheless recognize that any combination of sodium alginate, pectin, carrageenan and gellan may work.
- the cross-linking agent used for cross-linking the polysaccharide is a calcium cross-linking agent, and more preferably calcium ascorbate.
- the use of calcium ascorbate is desirable because this cross-linking agent tends to avoid the off-flavor, bitter taste, salty taste and/or chlorine taste associated with calcium and potassium sources known in the art (e.g. CaC or KCI), or with calcium lactate and calcium citrate, as described below in Example 1.
- the term "off-flavor" is used to describe a flavor (and an odor) generally associated with the degradation of a perishable food product.
- off- flavor excludes a flavor or an odor conferred to the edible coating by the presence of an additional ingredient such as, for example, a probiotic, as it will become apparent below.
- ascorbate is an ion of ascorbic acid (i.e. Vitamin C) and thus, the use of calcium ascorbate as cross-linking agent confers antioxidant properties to the edible coating, which may also make its use desirable.
- the edible coating has a moisture content ranging from about 3% to about 70%.
- the moisture content of the cross-linked polysaccharide layer is preferably reduced by about 30% to about 97% during a drying step, as it will become apparent below.
- the reduction of the moisture content of the edible coating matrix makes it less susceptible to microbial proliferation since the water is sequestered in the polysaccharide matrix, which in turn tends to expand the shelf-life of the coated food product. Further, the reduction of the moisture content tends to minimize the unpleasant mouth feel generally associated with the edible coatings of the prior art.
- the edible coating may further comprise an antimicrobial agent.
- an antimicrobial agent may be beneficial to further enhance the conservation properties of the edible coating.
- the use of vanillin as microbial agent is desirable because vanillin also contribute to mask the taste associated with some polysaccharides (e.g. the very mild algae taste associated with sodium alginate) or other elements that may be added to the edible coating (e.g. probiotics), and also enhance sweetness of products such as fruits.
- any other antimicrobial agent suitable for consumption may be used to replace, or in combination with vanillin. For example, one may opt for using Our ref.: 282351.00005
- essential oils such as citrus essential oil, which are also known for their antimicrobial properties.
- the edible coating may also comprise an antioxidant agent, such as, for example, citric acid, ascorbic acid or a combination thereof.
- an antioxidant agent such as, for example, citric acid, ascorbic acid or a combination thereof.
- these antioxidants are known to have anti-browning properties.
- their concentration in the edible coating should not significantly lower its pH since, as it will become apparent in the examples below, a low pH may cause a premature jellification or cross- linking of the polysaccharide during the coating process, which in turn affect the uniformity of the coating on the food product.
- the pH of the edible coating is above 3, and preferably ranges between about 4 and about 9, and more preferably ranges between about 5 and about 8.
- the nutraceutical agent typically comprises at least one probiotic, examples of which include Lactobacillus acidophilus, Lactobacillus casei and, Bifidobacterium lactic.
- An example of immune response enhancer includes a yeast gluco polysaccharide, such as, for instance, Wellmune WGP®.
- a flavoring agent such as a vanilla essence can be used to provide a sweet taste to the coating.
- the edible coating could comprise at least one element selected from the group consisting of a coloring agent, a protein, an amino acid and a vitamin.
- the method for coating a food product comprises: (1) coating the food product with a polysaccharide solution to substantially cover said food product, the polysaccharide solution including at least one polysaccharide selected from the group consisting of carrageenan, gellan, alginate and pectin; (2) cross-linking the polysaccharide solution by immersing the food product in a cross-linking agent solution to obtain a polysaccharide layer substantially covering said food product; and (3) reducing the moisture content of the polysaccharide layer to obtain the edible coating.
- the method described herein is typically carried out as described in Examples 1 to 5 below.
- the polysaccharide solution comprises sodium alginate.
- the polysaccharide solution typically comprises between about 0.1% (w/w) and about 8% (w/w) sodium alginate, and more typically between between about 0.5% (w/w) and 4% (w/w) sodium alginate, even more typically between about 0.7% (w/w) and about 3% (w/w) sodium alginate, and further even more typically between about 0.7% and about 2% sodium alginate.
- concentration of polysaccharide used in solution may be selected based on the capacity to uniformly and rapidly coat the surface of the products, without compromising the ability to form a gel having a proper firmness.
- the polysaccharide solution may comprise pectin, and more typically pectin LM.
- pectin concentration in the solution used for the coating process may vary.
- the polysaccharide solution comprises between about 2% (w/w) to about 15% (w/w) pectin LM, and more typically between about 5% (w/w) to about 10% (w/w) pectin LM.
- the polysaccharide solution may comprise a combination of sodium alginate and pectin LM.
- the polysaccharide solution would typically comprise between about 0.1% (w/w) to about 3% (w/w) sodium alginate and between 0.1% (w/w) to about 7% (w/w) pectin LM.
- a person skilled in the art would acknowledge that many combinations of sodium alginate, pectin, carrageenan and gellan are possible, including a combination of at least one of those with other polysaccharides.
- coating the food product with the polysaccharide solution is carried out by immersing the food product in the polysaccharide solution.
- immersion time required for substantially covering the food product with the polysaccharide solution will depend upon the consistency of the solution and the size of the fruit.
- coating the food product with the polysaccharide solution to substantially cover said food product can be carried out by Our ref.: 282351.00005 13
- the food product coated with the polysaccharide solution is immersed in the cross-linking agent solution.
- the cross-linking agent solution comprises between about 0.5% (w/w) and about 35% (w/w) calcium ascorbate, and typically between about 1% (w/w) and about 30% (w/w) calcium, and more typically between about 13% (w/w) and about 27% (w/w) calcium ascorbate, and even more typically about 15% (w/w) calcium ascorbate.
- concentrations above 35% (w/w) would also work.
- a calcium ascorbate solution at saturation may be used. Saturation of a calcium ascobrate solution typically occurs at a calcium ascorbate concentration of 50% (w/w), but the person skilled in the art will appreciated that concentration at saturation will vary based on the temperature of the solution.
- Immersion of the food product in the cross-linking agent solution is typical since it allows a simultaneous contact of all surfaces of the food product coated with the cross- linking agent solution and thus a uniform jellification or cross-linking of the polysaccharide on the food product.
- immersion time for allowing cross-linking of the polysaccharide solution will be based upon the concentration of cross-linking agent in the solutions and the thickness of the polysaccharide layer to be cross-linked (i.e. generally, the thicker is the layer of polysaccharide to be cross-linked, the longer is the immersion time) .
- an immersion time of about 15-20 seconds in a solution comprising 15% calcium ascorbate would be sufficient to allow proper gel formation while the use of a 0.5% calcium ascorbate solution would require an immersion time of 5 to 8 minutes.
- the food product is typically immersed in the cross-linking agent solution for a period of time ranging from about 1 second to about 15 minutes, and more typically for a period of time ranging from about 10 seconds to about 10 minutes, and even more typically from about 10 seconds to about 4 minutes.
- the food product is coated with a generally uniform polysaccharide layer.
- polysaccharide layer would tend to affect the "mouth feel" of the coated food product and to provide unpleasant sensations to customers. Further, the polysaccharide layer would be more subject to microbial proliferation and would reduce the effectiveness of the coating. Therefore, in one embodiment, the moisture content of the polysaccharide layer is reduced to obtain the edible coating.
- a low temperature e.g. at 4°C
- the moisture content is reduced by drying the food product by using a drying process that minimize thermoshocks to the food product.
- the drying process is a process selected from the group consisting of a compression process, a desiccation process and a surface lyophilisation process.
- the moisture content of the polysaccharide layer is reduced by about 30% to about 97% or, in other words, such that the moisture content of the edible coating ranges from about 3% to about 70%.
- the polysaccharide solution and the cross-linking agent solutions have a temperature below 37 Celsius degrees during the coating process, and preferably a temperature ranging from about -5 Celsius degrees and 20 Celsius degrees, and more preferably between about 4 Celsius degrees and 10 Celsius degrees, and even more preferably between about 4 Celsius degrees and 7 Celsius degrees.
- the drying step of the polysaccharide layer to obtain the edible coating is carried out by drying the food product by using a drying process that minimize thermoshocks to the food product.
- the edible coating may further comprise a flavoring agent, an antimicrobial agent, an antioxidant agent, a nutraceutical agent, an immune response enhancer, a coloring agent, a protein, an amino acid, a vitamin or others food additives.
- a flavoring agent an antimicrobial agent, an antioxidant agent, a nutraceutical agent, an immune response enhancer, a coloring agent, a protein, an amino acid, a vitamin or others food additives.
- these agents are added in the polysaccharide solution prior to the cross-linking step.
- these agents could alternatively be added to the cross-linking agent solution.
- the addition of components such as antioxidants to the polysacharride solution or to the cross-linking solution may cause a premature jellification or cross-linking of the polysaccharide during the coating process, which in turn affect the uniformity of the coating on the food product.
- the pH of the polysaccharide solution and the cross-linking agent solution is maintained above 3, and preferably ranges between about 4 and about 9, and more preferably ranges between about 5 and about 8.
- the edible coating described herein be used for purposes other that product conservation.
- the edible coating may be used for clusters of small, imperishable food products such as, for example, clusters of dry grapes, dry papaya and the like, and for clusters of perishable food product such as blueberries and pomegranates.
- a person skilled in the art may also use the edible coating to coat and/or form clusters of product and objects that are not aimed at human or animal consumption.
- the method comprises (1) coating the food product with the polysaccharide solution to substantially cover said food product, the polysaccharide solution including at least one polysaccharide selected from the group consisting of carrageenan, gellan, alginate and pectin; (2) grouping the food products to form clusters thereof; (3) cross-linking the polysaccharide solution by immersing the food product in the cross-linking agent solution to obtain a polysaccharide layer substantially covering the food product; and (4) reducing the moisture content of said polysaccharide layer to obtain the edible coating.
- the method for obtaining clusters of food products could be carried out by inverting steps (1) and (2), i.e. by grouping the food products to form clusters prior to coating the same with the polysaccharide solution.
- steps (1) and (2) i.e. by grouping the food products to form clusters prior to coating the same with the polysaccharide solution.
- a person skilled in the art would appreciate that the various coating conditions or parameters described above may also apply to the methods for obtaining clusters of food products.
- a snack comprising a food product coated with the edible coating described above.
- the snack kit comprises a first package comprising the coated food product and a second package comprising a food additive capable of being sprinkle by the consumer on the food product (i.e. on the surface of the edible coating) at the time of consumption.
- the food additive comprises a powder or granules of at least one dried fruit, and typically the at least one dried fruit is selected from the group consisting of a dried apple, a dried strawberry and a dried raspberry.
- the food additive comprises a mixture of dried fruits.
- dried fruits can be obtained according to different methods, such as, for instance, drum drying and freeze drying.
- any other food additive could be used, such as for instance sugar, cinnamon, condiments and the like.
- the package of food additive is wrapped with the package of food product using a plastic membrane.
- the food additive package could be placed inside the package of food product prior to sealing the same.
- the first package i.e. the package of food product
- the second package i.e. the food additive package
- the first package is a plastic tray heat sealed with a microperforated membrane, as described in the examples below
- the second package is a plastic pouch or bag impermeable to humidity.
- the snack kit may further comprise a tool for allowing a user to eat said food product.
- a tool for allowing a user to eat said food product examples include a fork and a toothpick.
- the tool is packaged inside the first package or is wrapped with the first and second packages using a plastic membrane.
- a first selection was made based on the known characteristics of the different agents.
- Protein-based compositions were avoided because of current concerns with food allergens and because many of these ingredients are isolated from animal sources. Further to the screening based on the known characteristic of each component, polysaccharide compositions were selected.
- Sodium alginate, carrageenan, gellan and/or pectin were solubilized in stainless steel tanks with tap water at 50°C.
- concentrations jellifying agents were based on the type of fruit to be coated and typically ranged from 1% to 1.5% w/w for sodium alginate, carrageenan and gellan and from about 5% to about 10% for pectin.
- a lower sodium alginate concentration (of 1% w/w for acid fruits) was used with fresh-cut fruits such as pineapple tidbit since sodium alginate jellifies at acid pH and fresh-cut fruits tend to release acidic juice. The juice released tends to acidify the solution and contributes to unwanted, premature gel formation. Accordingly, a gel having expected characteristics (i.e. firmness and resistance) can be obtained using a lower sodium alginate concentration.
- the sodium alginate, carrageenan, gellan and/or pectin solutions were refrigerated at 10°C and kept at this temperature throughout the coating of the fruits.
- natural vanilla essence 0.1 % and/or other agents were added in some instances.
- the purpose of the natural vanilla extract was to mask the mild algae taste associated with the use of sodium alginate, to enhance the natural sweetness taste of the fruits (sweetness enhancer), to act as an antimicrobial agent and to provide a new taste to the consumers.
- strawberries, grapes, blueberries and blackberries were used as whole fruits models while, papayas, apples, kiwis, cantaloupes, pineapples, melon dews and watermelons were used as fresh-cut models.
- the various coatings tested were assessed for their capability to retain the fruit's inherent juices, for their transparency, flexibility, taste and texture, ability to cover the whole fruit and mechanical resistance through storage time and handling.
- sodium alginate as sole polysaccharide source, in combination with calcium ascorbate, provides the best gel texture, resistance and a complete fruit coverage, without off-flavor. Further, the combination of sodium alginate and calcium ascorbate provided the best results with the broader variety of fruits or, in other words, appeared to be the more polyvalent combinations. Pectin showed better results than sodium alginate with fruits in syrup such as, for instance, fruit salad. Carrageenan and gellan provided weaker yet acceptable gel properties.
- Vanilla extract was effective to mask the mild algae taste associated with the use of sodium alginate and to enhance the natural sweetness taste of the fruits.
- Antioxidants citric and ascorbic acids
- Probiotic bacterias added to the edible coating composition showed a good survival rate for the whole duration of the experiments, which corresponds to the products' shelf-life.
- the addition of probiotic bacterias brought mild yogurt odor and taste to the composition.
- Fresh table grapes were used as a model to fresh fruits that conserve their natural peel such as blueberries, cherries, and the like. Grapes (Flames, Crimson or Red Globe cultivars) were cultivated in California, Mexico or Chile and were purchased from Margi- Fruit, Quebec, Canada. Grapes were imported from California to Canada in monitored refrigerated containers. Transportation took approximately 5 to 7 days. Table grape preparation
- Grapes were divided into first control grapes (kept in their original package for the whole duration of the experiment), uncoated control grapes and coated grapes.
- whole table grape clusters were immersed in a peracetic acid and hydrogen peroxide solution kept at 4°C Chinook® (Sani Marc, Quebec, Canada) or Tsunami 100®, (Ecolab, Quebec, Canada) for 15 seconds. While in immersion, grape clusters were gently agitated to ensure thorough washing. Grapes were detached from the stems and sorted out to discard the damaged and/or rotten grapes.
- sodium alginate (1.5% w/w) was solubilized in a tank with tap water at 50°C. Natural vanilla essence was added to the sodium alginate solution in a concentration of 0.1% (Ingredient #33282, David Michael Ingredients, AZ, USA). The final concentration of sodium alginate used for table grapes was 1.5% w/w since the gel formed by the crosslinking action of calcium ascorbate appeared to be optimal at this concentration.
- the sodium alginate/vanilla solution was refrigerated a 10°C and kept at this temperature until before the coating of the fruits.
- Grapes were individually enrobed in the in the sodium alginate solution for 0 seconds. Grapes were held on a conveyor belt and excess solution was drained for 10 seconds. Grapes were then immersed individually in the calcium ascorbate solution (15% w/w) for 15 to 20 seconds and then held on a conveyor belt to allow excess solution to drain. Grapes were later air dried for 6 min with a domestic hair dryer (20-24 km/hr) on a conveyor belt.
- Uncoated and coated grapes were packaged (first control grapes remained in their original package).
- the packaging was designed for the coated fruits aims to prevent produce dehydration and maintain optimal CO2/O2 ratios inside the packaging to respect produce respiration (controlled atmosphere). Accordingly, grapes were packaged in PETE 3.7 oz plastic trays.
- the trays were heat-sealed with a microperforated PET based film (Ultraperf, Quebec, Canada). The permeability of the film allowed for a maximum buildup of 15% CO 2 and 5% O 2 .
- the headspace within the trays accounted for 50% of the total volume. All sealed containers were refrigerated at 4°C, in the dark, for 21 days.
- edible coating and packaging also contributed to preserve the original color and texture of the test grapes throughout the storage time.
- the natural vanilla extract present in the edible coating enhanced the grape's sweetness.
- the sensory attributes of appearance, texture and taste were evaluated on a scale of 1 to 5, where a ranking of 1 suggests poor quality and unacceptability whereas a ranking of 5 suggests excellent quality and acceptability. These three quality attributes were evaluated for the grapes throughout the storage period of 21 days.
- First control grapes i.e. kept in the original commercial package
- ranking 1 i.e. the lowest possible rank
- the control, uncoated grapes scored 3 for appearance, texture and taste.
- the PETE packaging heat-sealed with micro- perforated PET film thus appeared to significantly contribute to increase the shelf-life of grapes.
- the inherent oxygen and carbon dioxide ratio inside each package thus appeared to reduce microbial spoilage.
- the coated grapes displayed the best characteristics, scoring a 5 for appearance, texture and taste.
- the coating, in combination with packaging thus contributed to maintain the initial quality of the grapes throughout 21 days and notably increased the shelf-life of grapes.
- Pineapple tidbits were used as model for fresh-cut fruits for which the interior of the fruit is exposed to environmental conditions. As such, pineapple results obtained with pineapple tidbits may be expanded to other cut fruits such as apples, papaya, kiwi, pomegranates, Clementines, pears, melon dew, cantaloupe and the like. Pineapples were cultivated in Costa Rica and were purchased from Margi-Fruits, Quebec, Canada. Pineapples were carried from Costa Rica to Canada in monitored refrigerated containers in 5 to 10 days.
- the pineapple segments obtained were sanitized in a new solution of peracetic acid and hydrogen peroxide. Still on a sanitized surface, the pineapple segments were then cut into tidbits using a sanitized knife.
- Sodium alginate (1.0% w/w) and calcium ascorbate (15% w/w, H&A Canada Industrial inc., Ontario, Canada) solutions were prepared as described above. Natural vanilla essence was added to the sodium alginate solution in a concentration of 0.1% (Ingredient #33282, David Michael Ingredients, PA, USA). The sodium alginate/vanilla solution was refrigerated at 10°C and kept at this temperature until before the coating of the fruits. The calcium ascorbate solution was kept between 4°C and 7°C for the duration of the experiments.
- Pineapple tidbits were divided into control tidbits and test tidbits, where control tidbits remained uncoated.
- Test tidbits were individually enrobed in the in the sodium alginate solution.
- Test pineapple tidbits were held on a conveyor belt and excess solution was drained for 10 seconds. Tidbits were then immersed individually in the calcium ascorbate solution for 15 to 20 seconds and then again held on a conveyor belt to allow excess solution to drain. Pineapple tidbits were later air dried for 8 min with a domestic hair dryer (20-24 km/hr) on a conveyor belt.
- Control and test pineapple tidbits were packaged in PETE 3.7 oz plastic trays heat- sealed with a microperforated PET based film, as described above. The headspace within the trays accounted for 50% of the total volume. All sealed containers were refrigerated at 4°C, in the dark, for 5 days.
- the natural vanilla essence present in the edible coating enhanced the fruit's sweetness.
- the sensory attributes of appearance, texture and taste were evaluated on a scale of 1 to 5, as described above. These three quality attributes were evaluated for the pineapple throughout the storage period of 15 days.
- Blueberries were soaked in a peracetic acid and hydrogen peroxide solution (Chinook® or Tsunami 100®) for 15 seconds. The temperature of the solution was kept at 4°C.
- Blueberries were divided into a control portion and a test portion.
- test blueberries were individually coated in the sodium alginate solution for 10 seconds. Blueberries were held on a conveyor belt and excess solution was drained for 10 seconds. Our ref.: 282351.00005
- the blueberries were immersed in the calcium ascorbate solution for 15 to 20 seconds. Once the blueberries had jellified in the calcium ascorbate solution, they were held on a conveyor belt to allow excess solution to drain. Blueberries were later air dried for 8 min with a domestic hair dryer (20-24 km/hr) on a conveyor belt. Coated blueberries clusters conditioning
- Control blueberries and coated blueberries were later packaged in PETE 3.7 oz plastic trays heat-sealed with a microperforated PET based film, as described above.
- the headspace within the trays accounts for 50% of the total volume. All sealed containers were refrigerated at 4°C for 21 days. Results
- the sensory attributes of appearance, texture and taste were evaluated on a scale of 1 to 5, as described above. These three quality attributes were evaluated for the blueberries throughout the storage period of 21 days.
- Lowbush blueberries from the Lac St-Jean region were purchased from a local market. These blueberries are generally much smaller than imported highbush blueberries. Because they have a thinner peel, lowbush blueberries also tend to be more fragile. Since they are frequently damaged, lowbush blueberries are generally used as Our ref.: 282351.00005
- ingredients for the manufacture of transformed products e.g. pies, jams, etc.
- consumed as fresh fruits e.g. pies, jams, etc.
- Lowbush blueberries were soaked in a peracetic acid and hydrogen peroxide solution (Chinook® or Tsunami 100®) for 15 seconds. The temperature of the solution was kept at 4°C.
- Blueberries were coated in the sodium alginate solution for 10 seconds and clusters were formed manually by grouping gently handfuls of blueberries. Blueberries clusters were held on a conveyor belt and excess solution was drained for 10 seconds.
- the blueberries clusters were then gently immersed in the calcium ascorbate solution for 15 to 20 seconds. Once the blueberries clusters had jellified in the calcium ascorbate solution, they were held on a conveyor belt to allow excess solution to drain. Blueberries were later air dried for 8 min with a domestic hair dryer (20-24 km/hr) on a conveyor belt.
- Blueberries clusters were packaged in PETE 3.7 oz plastic trays heat-sealed with a microperforated PET based film, as described above. The headspace within the trays accounts for 50% of the total volume. All sealed containers were refrigerated at 4°C for 21 days.
- Figure 4 shows the formation of clusters using the method and the edible coating described above. Our ref.: 282351.00005
- the use of the edible coating to create blueberry clusters contributes to prevent mechanical damage associated to handling and transportation. Further, fruit clusters are fun and interactive healthy snacks.
- Apple pieces were individually coated in the sodium alginate solution for 10 seconds. Apple pieces were held on a conveyor belt and excess solution was drained for 10 seconds. Coated apple cluster were then manually formed before immersing the apple cluster in the calcium ascorbate solution for 15 to 20 seconds. Once the apple clusters had jellified in the calcium ascorbate solution, the clusters were held on a conveyor belt to allow excess solution to drain. Apple clusters were later air dried for 8 min with a domestic hair dryer (20-24 km/hr) on a conveyor belt. Our ref.: 282351.00005
- Control uncoated chopped apple pieces were packed in the same packaging as coated apple clusters.
- the apple pieces were previously washed, cored and cut into fine pieces.
- the control apple pieces were kept in the same controlled atmosphere packaging as the apple clusters in order to compare the relative importance of the edible coating as a mean to extend produce shelf-life.
- Coated apple clusters were later packaged in PETE 3.7 oz plastic trays heat-sealed with a microperforated PET based film obtained, as described above. The headspace within the trays accounts for 50% of the total volume. All sealed containers were refrigerated at 4°C for 21 days.
- Apple clusters kept their original color and texture throughout the storage time.
- the edible coating contributed to significantly preserve the natural juices of the apples for a longer period than the control.
- the natural vanilla essence present in the edible coating enhanced the fruits sweetness.
- the sensory attributes of appearance, texture and taste were evaluated on a scale of 1 to 5, as described above. These three quality attributes were evaluated for the apple clusters throughout the storage period of 21 days. Control apple bits became dehydrated and oxidized within 10 days, rendering a score of 2 for each quality attribute while coated apple clusters maintained initial quality throughout storage time of 21 days. A score of 5 was attributed for appearance, texture and taste.
- the first mix comprises carrots, turnips, onions, and celery.
- the second mix comprised carrots, onions, celery and bell peppers.
- the third mix comprised carrots, red onions, celery, leeks, zucchinis and cabbage. Our ref.: 282351.00005
- Vegetables were soaked in a peracetic acid and hydrogen peroxide solution (Chinook® or Tsunami 100®) for 15 seconds. The temperature of the solution was kept at 4°C.
- the first mix trivially called the “Soup mix” comprised carrots, turnips, onions (red and yellow) and celery.
- the second mix trivially called the “Spaghetti mix” comprised carrots, turnips, onions (red and yellow), celery and peppers.
- the third mix comprised carrots, turnips, onions (red and yellow), celery and leeks
- Each vegetable mix was divided into a control portion and a test portion.
- test vegetables were coated in the sodium alginate solution for 10 seconds. Vegetables were held on a conveyor belt and excess solution was drained for 10 seconds.
- the vegetables were immersed in the calcium ascorbate solution for 15 to 20 seconds. Once the blueberries had jellified in the calcium ascorbate solution, they were held on a conveyor belt to allow excess solution to drain. Blueberries were later air dried for 8 min with a domestic hair dryer (20-24 km/hr) on a conveyor belt.
- Control vegetables and coated vegetables were later packaged in PETE 3.7 oz plastic trays heat-sealed with a microperforated PET based film, as described above.
- the headspace within the trays accounts for 50% of the total volume. All sealed containers were refrigerated at 4°C for 21 days.
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Abstract
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Priority Applications (11)
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DK11764991.3T DK2555640T3 (en) | 2010-04-09 | 2011-04-08 | EDIBLE COATING COMPOSITION AND APPLICATIONS THEREOF |
BR112012025866A BR112012025866A2 (en) | 2010-04-09 | 2011-04-08 | edible coating composition and uses thereof. |
ES11764991T ES2699272T3 (en) | 2010-04-09 | 2011-04-08 | Edible coating composition and uses thereof |
EP11764991.3A EP2555640B1 (en) | 2010-04-09 | 2011-04-08 | Edible coating composition and uses thereof |
US13/497,156 US20130029012A1 (en) | 2010-04-09 | 2011-04-08 | Edible coating composition and uses thereof |
PL11764991T PL2555640T3 (en) | 2010-04-09 | 2011-04-08 | Edible coating composition and uses thereof |
AU2011238387A AU2011238387B2 (en) | 2010-04-09 | 2011-04-08 | Edible coating composition and uses thereof |
IL222316A IL222316A0 (en) | 2010-04-09 | 2012-10-09 | Edible composition and uses thereof |
US14/500,014 US20150017223A1 (en) | 2010-04-09 | 2014-09-29 | Edible coating composition and uses thereof |
US15/645,269 US20170303575A1 (en) | 2010-04-09 | 2017-07-10 | Edible coating composition and uses thereof |
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Cited By (16)
Publication number | Priority date | Publication date | Assignee | Title |
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WO2013049928A1 (en) | 2011-10-07 | 2013-04-11 | Fruitsymbiose Inc. | Composition and methods for improving organoleptic properties of food products |
WO2014052241A1 (en) * | 2012-09-25 | 2014-04-03 | Cal Poly Corporation | Improved antibrowning compositions |
WO2015097335A1 (en) * | 2013-12-27 | 2015-07-02 | Production And Innovation On Edible Coatings, S.L. | Edible coating for preserving fruit pieces, manufacturing and application method thereof |
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Also Published As
Publication number | Publication date |
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CA2800944A1 (en) | 2011-10-13 |
CA2769776A1 (en) | 2011-10-13 |
AU2011238387B2 (en) | 2015-05-07 |
ZA201307826B (en) | 2015-09-30 |
PL2555640T3 (en) | 2019-07-31 |
CA2769776C (en) | 2013-06-11 |
US20130029012A1 (en) | 2013-01-31 |
EP2555640A1 (en) | 2013-02-13 |
ES2699272T3 (en) | 2019-02-08 |
IL222316A0 (en) | 2012-12-31 |
AU2017203346A1 (en) | 2017-06-08 |
EP2555640A4 (en) | 2014-04-02 |
DK2555640T3 (en) | 2018-12-17 |
AU2011238387A1 (en) | 2012-11-15 |
US20150017223A1 (en) | 2015-01-15 |
BR112012025866A2 (en) | 2015-09-22 |
US20170303575A1 (en) | 2017-10-26 |
PT2555640T (en) | 2018-12-14 |
AU2015205911A1 (en) | 2015-08-20 |
EP2555640B1 (en) | 2018-09-05 |
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