METHODS AND ARTICLES FOR KEEPING FOOD FRESHER FOR LONGER AND SHELF-LIFE EXTENSION TO ENHANCE FOOD SECURITY AND SAFETY
20230097707 · 2023-03-30
Assignee
Inventors
Cpc classification
A01N25/34
HUMAN NECESSITIES
A01N25/34
HUMAN NECESSITIES
A01N55/00
HUMAN NECESSITIES
A01N59/00
HUMAN NECESSITIES
A01P1/00
HUMAN NECESSITIES
A01N55/00
HUMAN NECESSITIES
A01N59/00
HUMAN NECESSITIES
International classification
Abstract
Disclosed is technology to solve the problem in a world that is inundated with microbes of keeping food fresher for longer and shelf-life extension to enhance food security and safety without refrigeration/freezing, chemical preservatives integrated into the food product and/or physically/chemically altering the food product. Aspects of the technology are directed at the three levels of the food delivery system; namely, supermarket style display ware, bulk packaging and overseas container. This technological problem is solved by situating on food contacting/abutting surfaces of display ware, bulk packaging and oversees containers an antimicrobe agent formulated as a composition comprised of (i) between about 0.25% (w/w) to about 0.75% (w/w) benzalkonium chloride; (ii) between about 0.02% (w/w) to about 1.00% (w/w) of a kill agent selected from the group consisting of hydrogen peroxide and phenoxyethanol; (iii) between about 0.25% (w/w) to about 0.75% (w/w) 3-(tri-methoxysilyl)propyldimethyl octadecyl ammonium chloride and (iv) between about 97.50% (w/w) to about 99.48% deionized water.
Claims
1. An antimicrobe supermarket style display ware comprised of: a) a supermarket style display ware having food contacting surfaces and b) situated on at least a portion of the food contacting surfaces is an antimicrobe agent formulated as a composition comprised of: i) between about 0.25% (w/w) to about 0.75% (w/w) benzalkonium chloride; ii) between about 0.02% (w/w) to about 1.00% (w/w) of a kill agent selected from the group consisting of hydrogen peroxide and phenoxyethanol; iii) between about 0.25% (w/w) to about 0.75% (w/w) 3-(tri-methoxysilyl)propyldimethyl octadecyl ammonium chloride and iv) between about 97.50% (w/w) to about 99.48% deionized water, with the sum of the percentage of all ingredients equaling 100%.
2. The antimicrobe supermarket style display ware of claim 1 where the supermarket style display ware is selected from the group consisting of open cell expanded polystyrene foam trays, closed cell expanded polystyrene foam trays, high impact polystyrene trays, absorbent pads, high oxygen flexible barrier vacuum bags, low oxygen flexible barrier vacuum bags, pouches, polyethylene terephthalate bottles, polyethylene terephthalate bottles pouches and overwrap films.
3. A method for making an antimicrobe supermarket style display ware comprised of: a) taking possession of a supermarket style display ware having food contacting surfaces; b) taking possession of a supply of antimicrobe agent comprised of: i) between about 0.25% (w/w) to about 0.75% (w/w) benzalkonium chloride; ii) between about 0.02% (w/w) to about 1.00% (w/w) of a kill agent selected from the group consisting of hydrogen peroxide and phenoxyethanol; iii) between about 0.25% (w/w) to about 0.75% (w/w) 3-(tri-methoxysilyl)propyldimethyl octadecyl ammonium chloride and iv) between about 97.50% (w/w) to about 99.48% deionized water, with the sum of the percentage of all ingredients equaling 100% and c) situating antimicrobe agent on least a portion of the food contacting surfaces.
4. A method for keeping food fresher for longer and shelf-life extension to enhance food security and safety comprised of: a) taking possession of a food in a configuration suitable for packaging in a supermarket style display ware; b) taking possession of an antimicrobe supermarket style display ware of claim 1 and c) packaging the food into the antimicrobe supermarket style display ware.
5. An antimicrobe active cardboard comprised of two surfaces and a peripheral edge having situated on at least a portion of the surface an antimicrobe agent formulated as a composition comprised of: i) between about 0.25% (w/w) to about 0.75% (w/w) benzalkonium chloride; ii) between about 0.02% (w/w) to about 1.00% (w/w) of a kill agent selected from the group consisting of hydrogen peroxide and phenoxyethanol; iii) between about 0.25% (w/w) to about 0.75% (w/w) 3-(tri-methoxysilyl)propyldimethyl octadecyl ammonium chloride and iv) between about 97.50% (w/w) to about 99.48% deionized water, with the sum of the percentage of all ingredients equaling 100%, whereby said planar surface is designated as an antimicrobe active surface.
6. The antimicrobe active cardboard of claim 5 were said antimicrobe activate cardboard is fashioned as a container for bulk packaging food having a holding space where at least a portion of the antimicrobe active surface faces the holding space, whereby said container is designated an antimicrobe container for bulk packaging food.
7. A manufacturing phase method of making an antimicrobe active cardboard comprised of: a) taking possession of a supply of antimicrobe agent comprised of: i) between about 0.25% (w/w) to about 0.75% (w/w) benzalkonium chloride; ii) between about 0.02% (w/w) to about 1.00% (w/w) of a kill agent selected from the group consisting of hydrogen peroxide and phenoxyethanol; iii) between about 0.25% (w/w) to about 0.75% (w/w) 3-(tri-methoxysilyl)propyldimethyl octadecyl ammonium chloride and iv) between about 97.50% (w/w) to about 99.48% deionized water, with the sum of the percentage of all ingredients equaling 100%; b) utilizing a corrugated cardboard plant having a gantry adapted with a mist system where cover paper passes and is misted with antimicrobe agent and c) misting at least a portion of the cover paper with antimicrobe agent, whereby said misted cover paper is designated as an antimicrobe active surface.
8. The manufacturing phase method of claim 7 where the mist system is comprised of an about 5 micron to an about 20 micron nozzle spray assembly across the corrugated cardboard plant delivering a fine mist to the cover paper.
9. The manufacturing phase method claim 7 with the additional phase of configuring the antimicrobe active cardboard into a container for bulk packaging food having a holding space where at least a portion of the active surface faces the holding space, whereby said container is designated an antimicrobe container for bulk packaging food.
10. A method for keeping food fresher for longer and shelf-life extension to enhance food security and safety comprised of: a) taking possession of a food; b) taking possession of an antimicrobe container for bulk packaging of food of claim 6 and c) packing the food into the antimicrobe container for bulk packing.
11. The method for keeping food fresher for longer and shelf-life extension to enhance food security and safety of claim 10 where the food is a food packaged into an antimicrobe super market style tray according to claim 4.
12. A method for transforming a container used in containerized shipping having a holding space defined by interior surfaces of the container into an antimicrobe container used in containerized shipping comprised of the steps of: a) receiving a shipping container utilized in containerized shipping that is of a clean and empty nature so as to be suitable for loading; b) taking possession of a supply of antimicrobe agent comprised of: i) between about 0.25% (w/w) to about 0.75% (w/w) benzalkonium chloride; ii) between about 0.02% (w/w) to about 1.00% (w/w) of a kill agent selected from the group consisting of hydrogen peroxide and phenoxyethanol; iii) between about 0.25% (w/w) to about 0.75% (w/w) 3-(tri-methoxysilyl)propyldimethyl octadecyl ammonium chloride and iv) between about 97.50% (w/w) to about 99.48% deionized water, with the sum of the percentage of all ingredients equaling 100% and c) applying antimicrobe agent to at least a portion of the interior surfaces of said shipping container.
13. The method of claim 12 for transforming a container used in containerized shipping into an antimicrobe container used in containerized shipping where the applying is done by a method selected from the group of methods consisting of ULV cold fogging and electrostatic spraying.
14. A method for keeping food fresher for longer and shelf-life extension to enhance food security and safety comprised of: a) taking possession of a food; b) taking possession of an antimicrobe transformed container used in containerized shipping according to claim 12; c) packing the food into the antimicrobe transformed container used in containerized shipping.
15. The method for keeping food fresher for longer and shelf-life extension to enhance food security and safety of claim 14 where the food is a food packed into an antimicrobe container for bulk packing according to claim 10.
16. The method for keeping food fresher for longer and shelf-life extension to enhance food security and safety of claim 14 where the food is a food packaged into an antimicrobe super market style tray which is packed into an antimicrobe container for bulk packing according to claim 11.
17. An antimicrobe supermarket style display ware comprised of: c) a supermarket style display ware having food contacting surfaces and d) situated on at least a portion of the food contacting surfaces is an antimicrobe agent formulated as a composition comprised of: i) about 0.50% (w/w) benzalkonium chloride; ii) about 0.49% (w/w) of a kill agent selected from the group consisting of hydrogen peroxide and phenoxyethanol); iii) about 0.50% (w/w) 3-(tri-methoxysilyl)propyldimethyl octadecyl ammonium chloride and iv) about 98.51% (w/w) deionized water.
18. The antimicrobe supermarket style display ware of claim 17 where the supermarket style display ware is selected from the group consisting of open cell expanded polystyrene foam trays, closed cell expanded polystyrene foam trays, high impact polystyrene trays, absorbent pads, high oxygen flexible barrier vacuum bags, low oxygen flexible barrier vacuum bags, pouches, polyethylene terephthalate bottles, polyethylene terephthalate bottles pouches and overwrap films.
19. A method for making an antimicrobe supermarket style display ware comprised of: a) taking possession of a supermarket style display ware having food contacting surfaces; b) taking possession of a supply of antimicrobe agent comprised of: i) about 0.50% (w/w) benzalkonium chloride; ii) about 0.49% (w/w) of a kill agent selected from the group consisting of hydrogen peroxide and phenoxyethanol); iii) about 0.50% (w/w) 3-(tri-methoxysilyl)propyldimethyl octadecyl ammonium chloride and iv) about 98.51% (w/w) deionized water and c) situating antimicrobe agent on least a portion of the food contacting surfaces.
20. A method for keeping food fresher for longer and shelf-life extension to enhance food security and safety comprised of: a) taking possession of a food in a configuration suitable for packaging in a supermarket style display ware; b) taking possession of an antimicrobe supermarket style display ware of claim 17 and c) packaging the food into the antimicrobe supermarket style display ware.
21. An antimicrobe active cardboard comprised of two surfaces and a peripheral edge having situated on at least a portion of the surface an antimicrobe agent formulated as a composition comprised of: i) about 0.50% (w/w) benzalkonium chloride; ii) about 0.49% (w/w) of a kill agent selected from the group consisting of hydrogen peroxide and phenoxyethanol); iii) about 0.50% (w/w) 3-(tri-methoxysilyl)propyldimethyl octadecyl ammonium chloride and iv) about 98.51% (w/w) deionized water, whereby said planar surface is designated as an antimicrobe active surface.
22. The antimicrobe active cardboard of claim 21 were said antimicrobe activate cardboard is fashioned as a container for bulk packaging food having a holding space where at least a portion of the antimicrobe active surface faces the holding space, whereby said container is designated an antimicrobe container for bulk packaging food.
23. A manufacturing phase method of making an antimicrobe active cardboard comprised of: a) taking possession of a supply of antimicrobe agent comprised of: i) about 0.50% (w/w) benzalkonium chloride; ii) about 0.49% (w/w) of a kill agent selected from the group consisting of hydrogen peroxide and phenoxyethanol); iii) about 0.50% (w/w) 3-(tri-methoxysilyl)propyldimethyl octadecyl ammonium chloride and iv) about 98.51% (w/w) deionized water; b) utilizing a corrugated cardboard plant having a gantry adapted with a mist system where cover paper passes and is misted with antimicrobe agent and c) misting at least a portion of the cover paper with antimicrobe agent, whereby said misted cover paper is designated as an antimicrobe active surface.
24. The manufacturing phase method of claim 23 where the mist system is comprised of an about 5 micron to an about 20 micron nozzle spray assembly across the corrugated cardboard plant delivering a fine mist to the cover paper.
25. The manufacturing phase method claim 23 with the additional phase of configuring the antimicrobe active cardboard into a container for bulk packaging food having a holding space where at least a portion of the active surface faces the holding space, whereby said container is designated an antimicrobe container for bulk packaging food.
26. A method for keeping food fresher for longer and shelf-life extension to enhance food security and safety comprised of: a) taking possession of a food; b) taking possession of an antimicrobe container for bulk packaging of food of claim 22 and c) packing the food into the antimicrobe container for bulk packing.
27. The method for keeping food fresher for longer and shelf-life extension to enhance food security and safety of claim 26 where the food is a food packaged into an antimicrobe super market style tray according to claim 20.
28. A method for transforming a container used in containerized shipping having a holding space defined by interior surfaces of the container into an antimicrobe container used in containerized shipping comprised of the steps of: a) receiving a shipping container utilized in containerized shipping that is of a clean and empty nature so as to be suitable for loading; b) taking possession of a supply of antimicrobe agent comprised of: i) about 0.50% (w/w) benzalkonium chloride; ii) about 0.49% (w/w) of a kill agent selected from the group consisting of hydrogen peroxide and phenoxyethanol); iii) about 0.50% (w/w) 3-(tri-methoxysilyl)propyldimethyl octadecyl ammonium chloride and iv) about 98.51% (w/w) deionized water and c) applying antimicrobe agent to at least a portion of the interior surfaces of said shipping container.
29. The method of claim 28 for transforming a container used in containerized shipping into an antimicrobe container used in containerized shipping where the applying is done by a method selected from the group of methods consisting of ULV cold fogging and electrostatic spraying.
30. A method for keeping food fresher for longer and shelf-life extension to enhance food security and safety comprised of: a) taking possession of a food; b) taking possession of an antimicrobe transformed container used in containerized shipping according to claim 28; c) packing the food into the antimicrobe transformed container used in containerized shipping.
31. The method for keeping food fresher for longer and shelf-life extension to enhance food security and safety of claim 30 where the food is a food packed into an antimicrobe container for bulk packing according to claim 26.
32. The method for keeping food fresher for longer and shelf-life extension to enhance food security and safety of claim 30 where the food is a food packaged into an antimicrobe super market style tray which is packed into an antimicrobe container for bulk packing according to claim 27.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
[0048] These and other features, aspects and advantages of the present invention will become better understood with reference to the following description, appended claims and accompanying drawings where:
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DETAILED DESCRIPTION OF THE INVENTION
[0065] The present invention is described more fully in the following disclosure. In this disclosure, there is a discussion of embodiments of the invention and references to the accompanying drawings in which embodiments of the invention are shown. These specific embodiments are provided so that this invention will be understood by those skilled in the art. This invention is not limited to the specific embodiments set forth herein below and in the drawings. The invention is embodied in many different forms—including all permutations and combinations of all, or less than all, of the disclosed elements with points of data being support for the beginning, middle and/or end of a range for a parameter—and should be construed as such with reference to the appended claims as filed and as amended in prosecution.
[0066] Referring to the drawings collectively, in general terms and for an overview, embodiments of the antimicrobe agent of the present invention are comprised of the following major components or subassemblies: benzalkonium chloride; hydrogen peroxide or phenoxyethanol; 3-(tri-methoxysilyl)propyldimethyl octadecyl ammonium chloride and deionized water. In the discussion that follows, each of these major components or subassemblies is discussed, along with other structures in the embodiments of this invention. Thereafter, there is a discussion on how to use embodiments of the invention.
[0067] In the discussion that follows, “(w/w)” stands for the percent by weight of an ingredient in a composition and is based on the weight of the ingredient divided by the total weight of all ingredients in a composition with the dividend multiplied by 100. A percent by weight (w/w) range is inclusive of the endpoints and includes all points therebetween. IUPAC is an international federation that develops and maintains a naming system and nomenclature for molecules using terminology based upon constituent components. IUPAC naming is general used and has meaning to persons in the art. A CAS Number is a unique numerical identifier assigned by the Chemical Abstracts Service (CAS) to every chemical substance described in the open scientific literature. CAS numbers are general used and have meaning to persons in the art.
[0068] In general terms and for an overview, embodiments of the antimicrobe agent are comprised of the following major components: benzalkonium chloride, hydrogen peroxide, 3 Tri-Methoxysilyl)propyldimethyl octadecyl ammonium chloride, and deionized water. In the discussion that follows, each of these major components is discussed, along with other components/structures in the embodiments of this invention. Thereafter, there is a discussion on how to use the antimicrobe agent.
[0069] Benzalkonium chloride is one of two immediate kill agents in the antimicrobe agent. The other being hydrogen peroxide which is discussed herein below. Benzalkonium chloride (BZK) is a quaternary ammonium compound. The molecule has the chemical structure shown below:
##STR00001##
where n=8, 10, 12, 16 and 18. The molecule has IUPAC names of N-Alkyl-N-benzyl-N,N-dimethylammonium chloride and Alkyldimethylbenzylammonium chloride.
[0070] Preferably, the benzalkonium chloride is that of the same which meets the description of Chemical Abstracts Service No. 68424-85-1. That is, quaternary ammonium compounds, benzyl-C12-16-alkyldimethyl, chlorides. As of the filing of the application for this patent, such benzalkonium chlorides are listed substances with the United States Environmental Protection Agency (EPA) and assigned tracking number 429654. Therefore, compounding with the same bodes well for getting regulatory approval and registration of a antimicrobe agent. More preferably, the alkyl component is C12 (dodecyl), C14 (Myristyl), a blend of 40% C12, 50% C14 and 10% C10.
[0071] As introduced above, benzalkonium chloride is a fast-acting microbicidal agent having have both bactericidal and virucidal activity, as well as being active against fungi and protozoa. A postulated mode of action is that benzalkonium chloride is a cationic surfactant that dissociates a microbial cellular membrane and thereby compromising cellular permeability controls and inducing leakage of cellular contents. Also postulated is that benzalkonium chloride disrupts/dissociates intermolecular interactions and denatures the tertiary structure of proteins. The result being the deactivation of enzymes essential to microbe respiratory and metabolic activities.
[0072] The concentration of the benzalkonium chloride in the antimicrobe agent ranges from about 0.25% percent by weight (w/w) to about 0.75% percent by weight (w/w). In a more preferred embodiment, the concentration of the benzalkonium chloride is about 0.50%. The benzalkonium chloride at the above concentrations in combination with the hydrogen peroxide (discussed below), and perhaps with other ingredients, at the concentrations and relative concentrations as taught herein below, is believed to act in a synergistic manner with disinfection that is heightened from that which can be expected based on the prior art.
[0073] Hydrogen peroxide is one of two immediate kill agents in the antimicrobe agent. The other being benzalkonium chloride which is discussed herein above. Hydrogen peroxide is a molecule with an oxygen-oxygen single bond and a single hydrogen bounded to each of the oxygens. Hydrogen peroxide has the chemical formula H.sub.2O.sub.2 or H2O2 and the chemical structure shown below:
##STR00002##
Hydrogen peroxide has a molecular weight in grams per mole of 34.01. Other names for hydrogen peroxide are perhydroxic acid and dihydrogen dioxide.
[0074] Preferably, the hydrogen peroxide is that of the same which meets the description of Chemical Abstracts Service No. 7722-84-1. As of the filing of the application for this patent, such hydrogen peroxide is a listed substance with the United States Environmental Protection Agency (EPA) and assigned tracking number 153015. Therefore, compounding with the same bodes well for getting regulatory approval and registration of a antimicrobe agent.
[0075] Hydrogen peroxide is a strong disinfectant which possesses bactericidal, virucidal, sporicidal and fungicidal activity. This toxicity is attributed to hydrogen peroxide being an oxidizing agent under acidic conditions, including physiological acidic conditions. In particular, the hydrogen peroxide oxidizes in a microbe its proteins, membrane lipids, deoxynucleic acids (DNA) and ribonucleic acids rendering them nonfunctional.
[0076] The concentration of hydrogen peroxide in the antimicrobe agent ranges from about 0.02% percent by weight (w/w) to about 1.00% percent by weight (w/w). In a more preferred embodiment, the concentration of the hydrogen peroxide is about 0.49%. The combination of hydrogen peroxide in the foregoing concentrations and relative concentrations with respect to the benzalkonium chloride in the above taught concentrations and relative concentrations is believed to act in a synergistic manner with disinfection that is heightened from that which can be expected based on the prior art. Further, the combination of hydrogen peroxide in the foregoing concentrations and relative concentrations with respect to the concentrations and relative concentrations of 3-(tri-methoxysilyl)propyldimethyl octadecyl ammonium (discussed below), and perhaps other ingredients, is believed to act in a synergistic manner to enhance condensation/polymerization and binding of a formed micro-coating (discussed below) that is heightened from that which can be expected based on the prior art.
[0077] The phenoxyethanol is a microbicidal agent/preservative, emulsifier and fixative for a fragrance. The chemical formula is C.sub.8H.sub.10O.sub.2 or C8H10O2. The molecule has the chemical structure shown below:
##STR00003##
The molecular weight in grams per mole is 138.166. The molecule has the IUPAC name of 2-Phenoxyethanol. Preferably, the phenoxyethanol is that of the same which meets the description of Chemical Abstracts Service No. 122-99-6.
[0078] The phenoxyethanol is believed to perform the function of a microbicidal agent/preservative and active against Gram negative bacteria, Gram positive bacteria and yeast. The phenoxyethanol is also believed to be an emulsifier effective against local phases forming within the composition and keeping all ingredients in solution. The phenoxyethanol is also believed to have activity as a fixative for a fragrance.
[0079] The phenoxyethanol is an alternative ingredient to hydrogen peroxides. The concentration of a phenoxyethanol is the same as what would be the concentration hydrogen peroxide if it were in the antimicrobe agent. That is, the concentration of phenoxyethanol ranges from about 0.02% percent by weight (w/w) to about 1.00% percent by weight (w/w). In a more preferred embodiment, the concentration of the phenoxyethanol is about 0.49%. The combination of phenoxyethanol in the foregoing concentrations and relative concentrations with respect to the benzalkonium chloride in the above taught concentrations and relative concentrations is believed to act in a synergistic manner with disinfection that is heightened from that which can be expected based on the prior art. Further, the combination of hydrogen peroxide in the foregoing concentrations and relative concentrations with respect to the concentrations and relative concentrations of 3-(tri-methoxysilyl)propyldimethyl octadecyl ammonium (discussed below), and perhaps other ingredients, is believed to act in a synergistic manner to enhance condensation/polymerization and binding of a formed micro-coating (discussed below) that is heightened from that which can be expected based on the prior art.
[0080] The quaternary ammonium silane 3-(tri-methoxysilyl)propyldimethyl octadecyl ammonium chloride is the long lasting protect agent of the antimicrobe agent. The molecule has the chemical structure shown below:
##STR00004##
The molecule has the IUPAC name of 1-Octadecanaminium, N,N-dimethyl-N-[3-(trimethoxysilyl)propyl]-, chloride (1:1). The molecular formula is C26H58NO3Si.Cl and the molecular weight is 496.29.
[0081] Preferably, the quaternary ammonium silane 3-(tri-methoxysilyl)propyldimethyl octadecyl ammonium chloride is that of the same which meets the description of Chemical Abstracts Service No. 27668-52-6. As of the filing of the application for this patent, such quaternary ammonium silane 3-(tri-methoxysilyl)propyldimethyl octadecyl ammonium chloride is a listed substances with the United States Environmental Protection Agency (EPA) and assigned tracking number 246561. Therefore, compounding with the same bodes well for getting regulatory approval and registration of a antimicrobe agent.
[0082] The believed mode of action of the 3-(tri-methoxysilyl)propyldimethyl octadecyl ammonium chloride is as follows. The following discourse on the believed mode of action necessarily overlaps with a discourse on method of use the antimicrobe agent and there is a further discourse on method of use below. The antimicrobe agent containing methoxysilyl)propyldimethyl octadecyl ammonium is applied to an inanimate surface. When the composition dries, a condensation reaction occurs where there is the formation of a micro thin coating of polymerized monomers of 3-(tri-methoxysilyl)propyldimethyl octadecyl ammonium with strong covalent bonds between the monomers. The octadecyl alkyl side chain lineup pointing away from the surface. This can be likened to having millions of sword-shaped “road spikes” on the surface. At the base of each of these “swords” is a positively charged quaternary carbon unit.
[0083] Each of positively charged quaternary carbon units performs a dual function. One function is to attach the micro-coating to commonly found surfaces which bear a negative charge. The other is to attract/trap microbes with a negatively charged outer membrane. Typically, microbes have an outer membrane comprised of lipoproteins which have long chain fatty acids and glycerides that are anionic in nature.
[0084] The alkyl side chain then pierces the outer membrane of the attracted/trapped microbe with organism lysis. The microbe is killed via a form of electrostatic electrocution. The same monomer in the polymerized micro-coating is capable of attacking a new microbe again and again with only a single application. Because it does not kill the organisms by poisoning with toxic chemicals, they cannot adapt to it so there is no possibility of mutation and consequently no possibility of superbugs forming.
[0085] In more detail, the 3-(tri-methoxysilyl)propyldimethyl octadecyl ammonium chloride first undergoes an hydrolysis in conjunction with the deionized water (discussed below) to enter into an equilibrium with 3-(tri-hydroxysilyl)propyldimethyl octadecyl ammonium chloride. This hydrolysis is depicted in the chemical drawing and chemical equation shown below:
##STR00005## ##STR00006##
The condensation/polymerization reaction is depicted in the chemical drawing and chemical equation shown below:
##STR00007##
[0086] The concentration of 3-(tri-methoxysilyl)propyldimethyl octadecyl ammonium in the antimicrobe agent ranges from about 0.25% percent by weight (w/w) to about 0.75% percent by weight (w/w). In a more preferred embodiment, the concentration of the 3-(tri-methoxysilyl)propyldimethyl octadecyl ammonium is about 0.50%. The 3-(tri-methoxysilyl)propyldimethyl octadecyl ammonium in combination in the foregoing concentrations and relative concentrations with respect to the hydrogen peroxide in the above taught concentrations and relative concentrations is believed to act in a synergistic manner to enhance the bonding of the micro-coating onto surfaces that is heightened from that which can be expected based on the prior art. Also believed enhanced by the concentrations and relative concentrations of 3-(tri-methoxysilyl)propyldimethyl octadecyl ammonium and hydrogen peroxide as taught herein from that which can be expected based on the prior art is the durability of the micro-coating on various surfaces.
[0087] Deionized water is the base/solvent. Water is a molecule with an oxygen atom and two hydrogen atoms singling bounded to the oxygen atom. Water has the chemical formula H.sub.2O or H2O. The molecule has the chemical structure shown below:
##STR00008##
Water has a molecular weight in grams per mole of 18.01528. Being deionized, as a to-be-added ingredient to the composition, the concentration of the water approaches 100%. Accordingly, the melting point of deionized water approaches 0° C. (degrees Celsius) and the boiling point approaches 100° C. At 20° C., deionized water has a vapor pressure of 17.5 Torr. Preferably, the deionized water is that of the same which meets the description of Chemical Abstracts Service No. 7732-18-5.
[0088] As introduced above, the deionized water is a base/solvent into which the other ingredients are dissolved. The deionized water is also reactant in the hydrolysis discussed above 3-(tri-methoxysilyl)propyldimethyl octadecyl ammonium. The evaporation of the deionized water is integral with the condensation/polymerization of the 3-(tri-methoxysilyl)propyldimethyl octadecyl ammonium into a microcoating, as discussed above.
[0089] The concentration of deionized water in the antimicrobe agent ranges from about 97.75% percent by weight (w/w) to about 99.25% percent by weight (w/w). The particular concentration of deionized water is a function of the concentration of all other ingredients so that total of every ingredient, including deionized water, is 100%. Accordingly, concentrations are set for 3-(tri-methoxysilyl)propyldimethyl octadecyl ammonium chloride between about 0.25% (w/w) to about 0.75% (w/w), benzalkonium chloride between about 0.25% (w/w) to about 0.75% (w/w) and hydrogen peroxide between about 0.25% (w/w) to about 0.75% (w/w) with deionized water being present in a concentration to achieve the concentrations set for the other ingredients. In a more preferred embodiment, where the concentration of 3-(tri-methoxysilyl)propyldimethyl octadecyl ammonium chloride is about 0.50% (w/w), the concentration all benzalkonium chloride is about 0.50% (w/w) and the concentration of hydrogen peroxide hydrogen peroxide about 0.50% (w/w), the concentration of deionized water is about 98.5% (w/w).
[0090] The antimicrobe agent is manufactured by mixing and blending using standard equipment for chemical mixing and blending. That is, the compositions are made using for examples, liquid storage containers, ingredient and product handlers, in-line mixers, co-rotating twin-screw mixers, homogenizers, bottling operations, automation, electronic control and product storage, in the manner in accordance with that prescribed by the manufacturer(s) of the equipment.
[0091] The methoxysilyl)propyldimethyl octadecyl ammonium, as discussed above, will react with oxides and hydroxyls on the surface of the surface through the above-described condensation reaction. The bonds formed are covalent and are resistant to re-hydration. On evaporation of the water solvent, a durable bonded coating is produced which last at least about 30 days.
[0092] The antimicrobe agent is believed, as a general proposition, but not necessarily to every listed species, to be active against:
[0093] (1) Gram Positive Bacteria, e.g., Cacillus sp. (vegetative cell), Corynebacterium diphtheriae, Micrococcus lutea, Micrococcus sp., Mycobacterium tuberculosis, Mycobacterium smegmatis, Propionibacterium acnes, Staphylococcus aureus, Staphylococcus epidermidis, Streptococcus faecalis, Streptococcus mutans, Streptococcus pneumonia, Streptococcus pyogenes;
[0094] (2) Gram Negative Bacteria, e.g., Acinetobacter calcoaceticus, Aeromonas hydrophilia, Citrobacter deversus, Citrobacter freundi, Enterobacter aerogenes, Enterobacter aglomerans, Enterobacter cloacae, Enterococcus, Escherichia coli, Klebsiella oxytoca, Klebsiella pneumoniae, Klebsiella terriena, Legionella pneumophila, Morganella morganii, Proteus mirabilis, Proteus vulgaris, Pseudomonas aeruginosa, Pseudomonas fluorescens, Salmonella cholera suis, Salmonella typhi, Salmonella typhimurium, Serratia liquifaciens, Serratia marcescens, Xanthomonas campestris;
[0095] (3) Viruses. e.g., adenovirus Type II & IV, bovine adenovirus Type I & IV, corona virus, COVID-19 (SARS-Cov-2), feline pneumonitis, herpes simplex Type I, herpes simplex Type II, human immunodeficiency virus HIV-1 (AIDS), influenza A2 (Aichi), influenza A2 (Asian), influenza B, mumps, parinfluenza (Sendai), rous Sarcoma, reovirus Type I, SARS-Cov-2 (COVID-19), simian virus 40, vaccinia, MS2, PRD1, H1N1 (Swine Flu), norovirus, Middle East Respiratory Syndrome (MFRS);
[0096] (4) Fungi, Algae, Mould, Yeast and Spores, e.g., Alternaria alternate, Aphanizomenon sp., Aspergillus flavus, Aspergillus niger, Aspergillus sydowii, Aspergillus terreus, Aspergillus versicolor, Aspergillus verrucaria, Aureobasidium pullans, Candida albicans, Candida pseudotropocalis, Chaetomium globsum, Cladosporium cladosporioides, Chlorella vulgaris, Drechslera australiensis Epidermophyton sp., Gliomastix cerealis, Gloeophyllum trabeum microsporum sp., Microsporum audouinii, Monilia grisea, Oscillatoria, Penicillium chrysogenum, Pencillium commune, Penicillium funiculosum, Penicillium pinophilium, Penicillium variable, Phoma fimeti, Pithomyces chartarum, Poria placenta, Scenedesmus, Saccharomyces cerevisiae, Scolecobasidium humicola Selenastrum sp., Trichoderma viride, Trichophyton interdigitale Trichophyton maidson, Trichophyton mentogrophytes, Trichophyton sp. 9 and
[0097] (5) Protozoa Parasites, e.g., Cryptosporidium parvum (oocysts).
[0098] Referring to
[0099] Referring to
[0100] Referring to
[0101] The antimicrobe supermarket style display ware (10) is used in a conventional manner; except, that refrigeration, freezing and other prior art food preservation methods, see, supra, may be completely obviated and unnecessary or reduced in intensity. In most all cases, the antimicrobe supermarket style display ware (12) was found to have lowered microbial counts to achieve the result of keeping food fresher for longer and shelf-life extension to enhance food security and safety. The antimicrobe supermarket style display ware (12) is durable with a retention of activity. For example, referring to
[0102] Referring to
[0103] Referring to
[0104] Continuing to refer to
[0105] Further continuing to refer to
[0106] 2 nozzles (34)=0.062 per meter @ 60 minutes=3.72 Liters/Hour and
[0107] 4 nozzles (34)=0.124 per metre @ 60 minutes=7.44 liters/Hour.
[0108] Referring to
[0109] Referring to
[0110] Referring to
[0111] 20 ft shipping container—1-1.5 liters (L) and
[0112] 40 ft shipping container—2-2.5 liters (L).
[0113] Continuing to refer
[0114] The previously described versions of the present invention have many advantages. At the highest level, the present invention enhances food security and food safety. The articles and methods advantageously can be applied to a variety of substrates to deliver the combination function of shelf-life extension and to keep food fresher for longer. Another advantage is a broad-spectrum antimicrobial agent that kills and inactivates bacteria, viruses, fungi and molds. Another advantage is an antimicrobial agent that cannot to any significance diminish in strength and is long lasting. Another advantage is an antimicrobial agent that cannot to any significance leave the surface to which it is applied. Another advantage is an antimicrobial agent that cannot to any significance encourage resistance by microorganisms to become resistant. Another advantage is the ability to reduce total bacterial count populations by up to about 90% in food packaging, including food poisoning pathogens. Another advantage is increased food safety across a broad range of packaged foods. Another advantage is contributing to extended shelf life in the market for storage and display.
EXAMPLES
[0115] The following examples further describe and demonstrate embodiments within the scope of the present invention. The examples are given solely for the purpose of illustration and are not to be construed as limitations or restrictions of the present invention, as persons skilled in the art will quickly realize many variations thereof are possible that are all within the spirit and scope of the invention.
Example 1
Oral Toxicity of 3-(Tri-Methoxysilyl)Propyldimethyl Octadecyl Ammonium Chloride
[0116] Example 1 is a small animal oral toxicity test of 3-(tri-methoxysilyl)propyldimethyl octadecyl ammonium chloride in aqueous solutions derived from concentrate. The small animal was an albino rat (EPA/MRID.) The result acute oral LD50 at 12.27 g (grams) per kg (kilogram.) That is, the lethal dose in 50% of the test subjects 12.27 grams per kilogram of body weight. This translates to a 100 kg person ingesting 1.227 kg of the raw material (or 1723 liters) at one time. The monomer poses no ingestion hazard.
Example 2
PET Water Containers
[0117] Example 2 is study of the affect on Escherichia coli (E. coli) growth in polyethylene terephathalate (PET) water containers. PET water containers were treated in the manner provided above. Referring to
Example 3
Supermarket Style Display Ware Trial
[0118] Example 3 is a supermarket style display ware trial. Referring to
[0119] Referring to the 4A, graphically shown is the results of the trial for beef (rump steak) surface, 21 day series and log APC cfu/cm.sup.2 (colony forming units per centimeter square.) Product was stored for 21 days @ −1.5° C. plus 7 days display @ 2° C. Treated trays demonstrate lower bacterial counts and are less contaminated than untreated. Product tested as cfu/g (grams) followed similar trends in growth curve. Upper bacterial limits set at 1×107 or 10,000,000 cfu/cm2 (untreated reaches first). Extension in bacterial storage and display life indicated.
[0120] Referring to the 4B, graphically shown is the results of the trial for chicken surface 14 days series, tissue APC cfu/cm at &/g. Treated is less contaminated than untreated over 14 days at −1.5° C. plus 5 to 7 days display at 2° C. Growth curves demonstrate potential for extended bacterial display life for treated vs untreated trays.
[0121] Referring to the 4C, graphically shown is results from the percent surface skill trial, CRSA OCT; i.e., percent microbial reduction. Results show reduced bacterial count for all 6 product types under trial. The percent meat surface bacterial reduction at the product interface with the tray ranged from 50-92%. Tissue sample results as cfu/g demonstrated comparable reduction profiles These results reflect the aggregate results over each trial storage and display protocol.
[0122] Organoleptic/Sensory evaluations were undertaken. All trial product was evaluated throughout for: (i) Color, (ii) Odor, (iii) Taste and (iv) Texture. The results were generally found to conform satisfactorily to the microbiological enumerations and other records and observations made.
[0123] All in all, the trials have shown significant reduction in product microbial populations as APC cfu/cm.sup.2 and APC cfu/g at the contact surface when packaged with microbial agent treated packaging materials. The trials have been successfully undertaken with beef, pork, lamb, chicken, offals and sausages. Significant micobiological count reductions have been achieved within the trial periods from some samples. These results indicate that an increase in food storage shelf/display life may be possible downstream using antimicrobe agent and particularly where a greater surface area can be kept in direct contact with the food. In most all cases treated product was found to have lower microbial counts than untreated and the tissue samples generally reflected the trending of the surface Log APC cfu/cm2 results.
Example 4
Long Lasting Effect with Antimicrobe Supermarket Style Display Ware
[0124] Example 4 is a long-lasting efficacy in production trial. The trial is in the poultry industry interrogating effect against Salmonella typhimurium on plastic tray surfaces. The trial involved commercial treatments. Referring to
Example 5
Case Studying a Shipment from South Africa to Australia
[0125] Example 5 is a case study of a shipment from South Africa to Australia of food packed in antimicrobe active cardboard boxes according to the present invention which were loaded into an overseas shipping containers having antimicrobe agent applied to interior surfaces according to the present invention. Antimicrobe agent was applied to cover paper during a manufacturing phase of cardboard in a cardboard plant. Antimicrobe agent was applied to the overseas shipping containers via an ULV cold fogger and Electrostatic backpack sprayer. The overseas shipping containers were treated with a volume of antimicrobe agent
[0126] Contamination upon arrival and Australia was assessed via visible observation and readings taken in ATP Swab testings. An ATP swab test is a process of rapidly measuring actively growing microorganisms through detection of adenosine triphosphate (ATP). The ATP test is premised on ATP being a molecule found in and around living cells. As such it gives a direct measure of biological concentration and health. ATP is quantified by measuring the light produced through its reaction with the naturally occurring firefly enzyme luciferase using a luminometer. The amount of light produced is directly proportional to the amount of ATP present in a tested sample. The results of the ATP swab test were evaluated according to the below for grade scale:
TABLE-US-00001 Considered Food Safe (A) 0-30 Considered dean (B) 31-100 Caution! (C) 101-200 Contaminated (D) 201-500 High Contamination Risk (E) 501-1000 and Extreme Contamination Risk (F) 1000+.
[0127] On arrival at Australia, contamination assessments by visual inspection were negative for both the food packed in antimicrobe active cardboard boxes and the overseas shipping containers treated with antimicrobe agent. The test results for ATP swab testing of antimicrobe active cardboard boxes are set out in
[0128] Although the present invention has been described in considerable detail with reference to certain preferred versions thereof, other versions are possible with substituted, varied and/or modified materials and steps are employed—including all permutations and combinations of all, or less than all, of the disclosed elements with points of data being support for the beginning, middle and/or end of a range for a parameter. These other versions do not depart from the invention. Therefore, the spirit and scope of the appended claims should not be limited to the description of the preferred versions contained herein.