MXPA00004481A - Improved film-forming compositions for protecting animal skin - Google Patents
Improved film-forming compositions for protecting animal skinInfo
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- MXPA00004481A MXPA00004481A MXPA/A/2000/004481A MXPA00004481A MXPA00004481A MX PA00004481 A MXPA00004481 A MX PA00004481A MX PA00004481 A MXPA00004481 A MX PA00004481A MX PA00004481 A MXPA00004481 A MX PA00004481A
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- 239000000203 mixture Substances 0.000 title claims abstract description 125
- 210000003491 Skin Anatomy 0.000 title claims abstract description 24
- 230000002633 protecting Effects 0.000 title claims abstract description 6
- 239000000020 Nitrocellulose Substances 0.000 claims abstract description 23
- 229920001220 nitrocellulos Polymers 0.000 claims abstract description 23
- 229920002635 polyurethane Polymers 0.000 claims abstract description 14
- 239000004814 polyurethane Substances 0.000 claims abstract description 14
- 239000000969 carrier Substances 0.000 claims abstract description 13
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 11
- 239000003722 gum benzoin Substances 0.000 claims abstract description 11
- 239000002904 solvent Substances 0.000 claims abstract description 11
- 239000004721 Polyphenylene oxide Substances 0.000 claims abstract description 10
- 230000002070 germicidal Effects 0.000 claims abstract description 10
- 229920000570 polyether Polymers 0.000 claims abstract description 10
- 229960001884 Chlorhexidine diacetate Drugs 0.000 claims abstract description 5
- WDRFFJWBUDTUCA-UHFFFAOYSA-N [amino-[(E)-[amino-(4-chloroanilino)methylidene]amino]methylidene]-[6-[amino-[(E)-[amino-(4-chloroanilino)methylidene]amino]methylidene]azaniumylhexyl]azanium;diacetate Chemical compound CC(O)=O.CC(O)=O.C=1C=C(Cl)C=CC=1NC(N)=NC(N)=NCCCCCCN=C(N)N=C(N)NC1=CC=C(Cl)C=C1 WDRFFJWBUDTUCA-UHFFFAOYSA-N 0.000 claims abstract description 5
- 230000001681 protective Effects 0.000 claims description 18
- WYURNTSHIVDZCO-UHFFFAOYSA-N tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 18
- 241000283690 Bos taurus Species 0.000 claims description 12
- 239000000975 dye Substances 0.000 claims description 9
- 210000004080 Milk Anatomy 0.000 claims description 7
- 239000003795 chemical substances by application Substances 0.000 claims description 7
- 235000013336 milk Nutrition 0.000 claims description 7
- 239000008267 milk Substances 0.000 claims description 7
- -1 alkylene glycols Chemical class 0.000 claims description 5
- 238000001035 drying Methods 0.000 claims description 4
- YXFVVABEGXRONW-UHFFFAOYSA-N toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 4
- 150000001298 alcohols Chemical class 0.000 claims description 2
- 229940027983 antiseptics and disinfectants Quaternary ammonium compounds Drugs 0.000 claims description 2
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 2
- 239000000194 fatty acid Substances 0.000 claims description 2
- 150000004665 fatty acids Chemical class 0.000 claims description 2
- 150000002576 ketones Chemical class 0.000 claims description 2
- 150000003856 quaternary ammonium compounds Chemical class 0.000 claims description 2
- 229920002413 Polyhexanide Polymers 0.000 claims 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 claims 1
- 150000002170 ethers Chemical class 0.000 claims 1
- 239000001048 orange dye Substances 0.000 claims 1
- 239000001044 red dye Substances 0.000 claims 1
- 239000001043 yellow dye Substances 0.000 claims 1
- 208000004396 Mastitis Diseases 0.000 abstract description 6
- 238000004040 coloring Methods 0.000 abstract 1
- 210000002445 Nipples Anatomy 0.000 description 11
- 239000004615 ingredient Substances 0.000 description 6
- 241000894006 Bacteria Species 0.000 description 5
- 210000000481 Breast Anatomy 0.000 description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- 201000009910 diseases by infectious agent Diseases 0.000 description 4
- 230000014759 maintenance of location Effects 0.000 description 4
- ISAOCJYIOMOJEB-UHFFFAOYSA-N Benzoin Chemical compound C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 description 3
- 229960002130 Benzoin Drugs 0.000 description 3
- 240000008975 Styrax benzoin Species 0.000 description 3
- 235000000126 Styrax benzoin Nutrition 0.000 description 3
- 235000008411 Sumatra benzointree Nutrition 0.000 description 3
- 206010052428 Wound Diseases 0.000 description 3
- 238000004140 cleaning Methods 0.000 description 3
- 238000007598 dipping method Methods 0.000 description 3
- 235000019382 gum benzoic Nutrition 0.000 description 3
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 2
- 206010059837 Adhesion Diseases 0.000 description 2
- WWZKQHOCKIZLMA-UHFFFAOYSA-N Caprylic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 2
- GHVNFZFCNZKVNT-UHFFFAOYSA-N Decanoic acid Chemical compound CCCCCCCCCC(O)=O GHVNFZFCNZKVNT-UHFFFAOYSA-N 0.000 description 2
- 241000238631 Hexapoda Species 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 244000144992 flock Species 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 2
- 229910052740 iodine Inorganic materials 0.000 description 2
- 239000011630 iodine Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- OKKJLVBELUTLKV-UHFFFAOYSA-N methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N n-butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- DNIAPMSPPWPWGF-UHFFFAOYSA-N propylene glycol Chemical group CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 2
- 238000002791 soaking Methods 0.000 description 2
- ATJFFYVFTNAWJD-UHFFFAOYSA-N tin hydride Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 200000000019 wound Diseases 0.000 description 2
- GTEOJYGNMFDLPG-KCRKGURFSA-N (4E)-2-methyl-4-[(4-phenyldiazenylphenyl)hydrazinylidene]cyclohexa-2,5-dien-1-one Chemical compound C1=CC(=O)C(C)=C\C1=N\NC1=CC=C(N=NC=2C=CC=CC=2)C=C1 GTEOJYGNMFDLPG-KCRKGURFSA-N 0.000 description 1
- AZXGXVQWEUFULR-UHFFFAOYSA-N 2',4',5',7'-tetrabromofluorescein Chemical compound OC(=O)C1=CC=CC=C1C1=C2C=C(Br)C(=O)C(Br)=C2OC2=C(Br)C(O)=C(Br)C=C21 AZXGXVQWEUFULR-UHFFFAOYSA-N 0.000 description 1
- JHIVVAPYMSGYDF-UHFFFAOYSA-N Cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 1
- 210000004907 Glands Anatomy 0.000 description 1
- 210000002264 Mammary Glands, Animal Anatomy 0.000 description 1
- 210000004293 Mammary Glands, Human Anatomy 0.000 description 1
- FBUKVWPVBMHYJY-UHFFFAOYSA-N Nonanoic acid Chemical compound CCCCCCCCC(O)=O FBUKVWPVBMHYJY-UHFFFAOYSA-N 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- XNCOSPRUTUOJCJ-UHFFFAOYSA-N diguanide Chemical compound NC(N)=NC(N)=N XNCOSPRUTUOJCJ-UHFFFAOYSA-N 0.000 description 1
- 230000000916 dilatatory Effects 0.000 description 1
- LCGLNKUTAGEVQW-UHFFFAOYSA-N dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 1
- ROSDSFDQCJNGOL-UHFFFAOYSA-O dimethylaminium Chemical class C[NH2+]C ROSDSFDQCJNGOL-UHFFFAOYSA-O 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 230000035876 healing Effects 0.000 description 1
- 244000144980 herd Species 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 239000000367 immunologic factor Substances 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 230000002757 inflammatory Effects 0.000 description 1
- KFZMGEQAYNKOFK-UHFFFAOYSA-N iso-propanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 1
- 244000144972 livestock Species 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000006396 nitration reaction Methods 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- 230000002085 persistent Effects 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propanol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 239000000565 sealant Substances 0.000 description 1
- AXMCIYLNKNGNOT-UHFFFAOYSA-M sodium;3-[[4-[(4-dimethylazaniumylidenecyclohexa-2,5-dien-1-ylidene)-[4-[ethyl-[(3-sulfonatophenyl)methyl]amino]phenyl]methyl]-N-ethylanilino]methyl]benzenesulfonate Chemical compound [Na+].C=1C=C(C(=C2C=CC(C=C2)=[N+](C)C)C=2C=CC(=CC=2)N(CC)CC=2C=C(C=CC=2)S([O-])(=O)=O)C=CC=1N(CC)CC1=CC=CC(S([O-])(=O)=O)=C1 AXMCIYLNKNGNOT-UHFFFAOYSA-M 0.000 description 1
- QMFYDAZWMAZXKO-UHFFFAOYSA-O sodium;pyridin-1-ium Chemical compound [Na+].C1=CC=[NH+]C=C1 QMFYDAZWMAZXKO-UHFFFAOYSA-O 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 150000005219 trimethyl ethers Chemical class 0.000 description 1
- 239000004034 viscosity adjusting agent Substances 0.000 description 1
Abstract
Improved film-forming skin protectant compositions are provided which are capable of forming a long-lasting elastic barrier film when applied to skin;the compositions have particular utility as barrier teat dips, for protecting cows against mastitis, especially during their susceptible non-lactating periods. The compositions include a film-forming component (preferably a mixture of polyether polyurethane and benzoin gum) dispersed in a compatible carrier and further having a minor amount of nitrocellulose incorporated therein in order to increase the time of adherence of the compositions to skin, as compared with an otherwise identical composition without nitrocellulose. The compositions may also include a germicide (e.g., chlorhexidine diacetate), and a coloring dye. The most preferred compositions include polyether polyurethane, benzoin gum, a solvent system made up of tetrahydrafuran and a lower alcohol, and chlorhexidine diacetate.
Description
IMPROVED FILM COMPOSITIONS FOR THE PROTECTION OF ANIMAL SKIN
Field of Invention
The present invention concerns skin protective compositions in the form of improved films capable of forming an elastic film when applied to the skin and include a film-like component dispersed in a carrier, and wherein the compositions of the invention are improved by the condition of an amount of nitrocellulose dispersed in the carrier; Nitrocellulose is used to create a larger resistant film capable of protecting the skin (for example, the skin of the tits of bovines) for relatively long periods of time. More particularly, the preferred forms of the invention concern compositions in film form which include in them effective amounts of polyurethane polyether and benzoin gum dispersed in tetrahydrofuran solvent (THF), with a minor amount of nitrocellulose therein.
Ref: 119227 Background of the invention.
A significant problem for farmers is the incidence of mastitis in livestock. It is known that up to 40-50% of inflammatory infections are contracted in dry cows or in periods when they do not produce milk, with large percentages of these infections occurring in the first and the last two weeks of the dry period. At this time, the mammary gland is the state of transition where the immunological factors are worrying or suppressed, the milk does not flow along the gland, and the breast pressure is increased by dilating the breast, thus allowing an easy penetration of the breast. bacteria through the milk channel.
It is known to apply protective compositions to the tits of bovines, especially during or notably in the period in which milk is not produced, in order to minimize the occurrence of mastitis. The first point in such mastitis treatment is to minimize exposure to the bacteria at the ends of the teats.
U.S. Patent No. 5,192,536 discloses protective compositions containing polyurethane polyether dissolved in tetrahydrofuran. The compositions of this patent can be applied to the animal skin to form a fast-drying elastic film, which has protective qualities. Patent No. 5,688,498 further describes compositions of this general nature, but which are improved by the condition of benzoin gum (benzoin resinoid). It has been found that benzoin gum significantly increases the adhesion time of the protective compositions and renders the appropriate compositions for soaking to improve the coverage of the compositions and to facilitate use.
The pending application for U: S Patent Letter. S / N 08 / 644,009, filed on February 14, 1997, refers to the -498 patent and discloses additional compositions made to use a variety of different solvents and additional ingredients such as germicides, dyes and optional ingredients, for example fillers, perfumes, viscosity modifiers.
In addition to mastitis control, skin protective compositions also find utility as wound dressings to be applied over open wounds to protect against infection from dirt, insects or other sources of bacteria.
In order to increase the protection of the protective compositions of the skin of the past types, it is desirable that these remain intact in the skin for as long as possible. This not only provides an added measure of protection against infection, but also reduces the time and expense involved in repeating applications of the compositions again.
This is consequently a need in the art for improving skin protective compositions that maintain the ease-of-use and protection capabilities of the polyurethane polyurethane / benzoin gum compositions while giving an integrity and longevity of increased strength.
Brief description of the invention.
The present invention overcomes the problems outlined above, and provides largely improved skin protective compositions capable of forming an elastic film when applied to the skin; such compositions broadly include a film forming component dispersed in a carrier wherein the improvement of the invention comprises the addition of an amount of nitrocellulose dispersed in the carrier in an amount sufficient to increase the adherence time of the compositions to the skin, as compared to the opposite with an identical composition that does not include nitrocellulose.
In preferred forms, the nitrocellulose is present at a level of about 0.2-15% by weight in the protective compositions forming a film of the invention, and more preferably about 1.5-5% by weight. Nitrocellulose is commercially available in various grades that vary in the degree of polymerization and nitration. Essentially all such commercially available nitrocellulose products are useful in the context of the present invention, however the amounts for use for respective degrees may vary.
The component forming a preferred film of the present invention is made in a mixture of polyurethane polyether and benzoin gum. The film forming component is generally preferably present at a level of about 5-50% by weight, and more preferably from about 7-25% by weight in the compositions of the invention. In more detail, the polyurethane polyether is typically used at a level of from about 5-25% by weight, more preferably from about 5-15% by weight; on the other hand, benzoin gum normally occurs at a level from about 2-20% by weight, and more preferably at a level from about 2-10% by weight. The carrier portion of the compositions is preferably a solvent for the film forming component. The most preferred solvent is a mixture of tetrahydrofuran and alcohol, with the last component being present at a level of from about 0.1-30% by weight, and more preferably at a level from about 5-25% by weight. In addition to the foregoing, a wide variety of other solvents can be used for the entire general composition is stable at room temperature and has a sufficiently rapid drying time (preferably up to about 20 minutes, and more preferably up to about 10 minutes after the application to the skin). Suitable solvents can therefore be selected from the group consisting of THF, cyclohexanone, toluene, acetone, alkylene glycols (for example propylene or ethylene glycol) and C? -C4 ether, ketones and alcohols (trimethyl ether, dimethyl ether, me t) ilet ilé ter, acetone, methyl ethyl ketone, diethyl itolone, methanol, ethanol, propanol, isopropanol or butanol).
The compositions of the invention may also have a germicidal agent dispersed in the carrier, which is normally used at a level of from about 0.01-2% by weight, and more preferably at a level from about 0.05-1% by weight. The germicidal agent can be selected from a wide variety of effective agents, such as those taken from the group consisting of straight or branched chain fatty acids (octanoic acid, nonanoic acid, decanoic acid), sodium pyridinium, polyhexamethylene, biguanide, chlorhexidine diacetate and quaternary ammonium compounds such as the alkyl dimethyl-ilbenzyl ammonium salts, dialkyl dimethyl ammonium compounds and benztonium. Combinations of such germicides can also be used, such as the germicides themselves, and in combination with the other ingredients, for compatible compositions that are physically and chemically at ambient temperatures.
The dyes can also be added to the skin protective compositions of the invention in order to improve the visualization of the barrier film in the area to be treated. Acceptable dyes include those that are soluble or dispersible in the liquid compositions of the invention. Preferred dyes provide easy viewing of the water film from a distance of at least 20 feet (6.096 meters) and can be used at relatively low concentrations. The dyes can also be used at a level from about 0.001-0.5% by weight in the compositions, and more preferably at a level from about 0.005-0.2% by weight. The dyes are normally selected from the group consisting of the red D & amp;; C 19, 43 yellow solvent, yellow fluoride naphthyl acid amide, yellow plastic TGH key, red FD &C 3, red FD &C 22, red FD &C 28, red FD &C 39, red FD &C 19, green FD &C 6, orange 5, orange 10, orange 17, red 17, red 21, red, 27, red 31, violet 2, yellow 7, and yellow 11.
In order to make the compositions of the invention more useful, they can have a desirable viscosity level to create optimal protective films. Generally, the viscosity may be at a level from about 50-2000 cPs. More preferably from about 100-1500 cPs. As previously indicated, the compositions can have a drying time at about 72 ° F (22.2 ° C) of room temperature of more than about 20 minutes and more preferably more than about 10 minutes.
The composition is used in a typical teat dipping product manner, that is, bovine tits are immersed in the liquid compositions in order to create the long-lasting protective films of the invention.
However, if desired, the compositions thereof can be applied by other means, such as by cleaning or atomizing to create elastic films that are vapor permeable, resistant to water, wind, dirt, and insects and that present a barrier to bacterium. The film protects the skin from damage or exposure during the healing process (in the case of wound treatment) or the entry of bacteria that causes mastitis when used as a teat dip.
Detailed description of the invention.
The following examples illustrate the preferred film protective compositions according to the invention, and demonstrate the long-lasting nature of the elastic films using such compositions. It will be understood, however, that the examples are provided by way of illustration only, and should not be taken as a limitation on the general scope of the invention.
EXAMPLES
The following compositions (Table 1) were prepared and tested for adherence to cow tits. In each case, the compositions were prepared by dissolving the polyether polyurethane / benzoin gum forming component in THF and an ethanol solvent system which is subsequently added to the nitrocellulose and other ingredients. The mixing is carried out at ambient conditions.
Table 1
In the first adhesion experiment, in the dry mid-season the cows were initially immersed with a commercially available iodine-based teat immersion (Quarter Mate sold by West Agro, Inc.) to clean the tits of the cows. The tits were submerged dried clean and submerged with the test teat protective composition of Table 1. All four tits of each cow were submerged with a different product. Adherence was evaluated every 24 hours. Positive adhesions were determined if the sealed teat still covered the orifice of the teat. The results shown below confirm that the incorporation of nitrocellulose improves the adhesion of the sealant.
Table 2
In the second experiment using cows that were completely dry, the tits of 21 cows were treated as described above. The adhesion results shown below further confirm that the composition supplemented in nitrocellulose has much better adhesion characteristics.
Table 3
In a third experiment comprising compositions A, B and E, the tits of 12 cows that do not produce milk were immersed in an iodine-based dip, dried thoroughly and then soaked in the test compositions. The four test compositions were used in a complete randomized design in and around the cows. The persistent film or protection of the end of the tit was evaluated every 12 hours. Composition A was used on two tits of each cow.
Table 4
"Retention time - When the ends of the tits are the last ones that are visualized with the test composition.
2 Complete peeling by soaking due to the milk sample needed for another experiment.
Composition E supplemented with nitrocellulose gave the best results. This was taken at the maximum (or almost to the maximum) in the
9/12 cows' and had the highest percentage of protected tits in 48, 72 and 100 hours.
Compositions F and G were prepared as previously described and compared with composition A of Table 1.
Table 5
The following Table 6 places the results of the comparison between compositions F and G of Table 5 and composition A of Table 1. TABLE 6
The compositions were tested by dipping one teat of each cow with the respective test composition. The retention time was measured at 12 hour intervals until the composition did not very effectively cover the teat duct.
The compositions in Table 7 were prepared as described above. The samples contained different ratios of polyurethane polyether, benzoin and nitrocellulose. The total solids were adjusted to give a viscosity of 298 to 334 cps. The adherence of the formulations was tested on 31 dry cows from a herd developed at the University of Guelph. The H-K products were randomly applied to the four tits of a group of cows. Samples L-0 were tested in a second group of cows. The adhesion was determined for each product in each tit. The average retention is reported in Table 7. Due to the great variation between cow and cow in adherence, the number of times the product had the highest adherence is also reported. In the H-K group, product H gave the best adhesion. In group L-0, M, N and O were similar and were better than sample L.
Table 7
Table 8 shows seven formulations that were tested for adherence in 99 cows in five flocks in Canada. The formulations were prepared as described above and containing variations in the type of nitrocellulose, type of polyurethane, and benzoin resinoid supplier. The compositions were tested in four separate groupings of four compositions as shown in Table 9. The number of times that a composition had the highest adhesion in a given cow is indicated. The control composition without nitrocellulose had the lowest number of "gains" in each of the four treatment groups. Sample Q, made with tin 5707 polyurethane polyester, gave a lower adhesion than the same composition made with Tin 5714 (sample P). Table 8 shows the combined adhesion averages for the four group of experiments. Sample U provides 1.4 days of better adhesion than control samples without nitrocellulose.
Four of the samples in Table 8, A, S, T, and U were also tested on an udder designed part of the flock developed at Iowa State University. The results are shown in Table 10. The three samples with nitrocellulose had better adhesions than the control sample without nitrocellulose.
Table 8
Table 9
Table 10
The compositions were tested by dipping one teat of each cow with the respective test composition. The retention time was measured at 12 hour intervals until the composition did not very effectively cover the teat duct.
It can be seen in this manner, that the compositions of the invention provide a significant degree of protective film over a substantial period of unequal time in prior compositions of this character. It will be further apparent that a wide variety of specific ingredients can be used in the formulations of the invention and at various novel uses. The following Table 11 shows the approximate spectrum and preferred ranges for the essential and preferred ingredients used in the formulations, and also shows the important critical properties.
Table 11
'Brookfield Viscosity @ 24 ° C (60 rpm, axis # 3) It is noted that in relation to this date, the best method known to the applicant to carry out the aforementioned invention, is that which is clear from the present description of the invention.
Having described the invention as above, the content of the following is claimed as property.
Claims (29)
1. A skin protective composition that forms a film capable of forming an elastic film when applied to the skin including a film forming component dispersed in a carrier, the improvement characterized in that it comprises an amount of nitrocellulose dispersed in the carrier in a amount to increase the time of adherence of the composition to the skin, as compared to the opposite with an identical composition without nitrocellulose.
2. The composition according to claim 1, characterized in that the nitrocellulose is present at a level from about 0.2-15% by weight in the composition.
3. The composition according to claim 2, characterized in that the level is from about 1-10% by weight.
4. The composition according to claim 1, characterized in that the component comprises a mixture of polyurethane polyether and benzoin gum.
5. The composition according to claim 4, characterized in that the polyurethane polyether is present at a level of about 5-25% by weight in the composition.
6. The composition according to claim 5, characterized in that the level is from about 5-15% by weight.
7. The composition according to claim 4, characterized in that the benzoin gum is present at a level of about 2-20% by weight in the composition.
8. The composition according to claim 7, characterized in that the level is from about 2-10% by weight.
9. The composition according to claim 1, characterized in that the carrier is a solvent for the component that forms a film.
10. The composition according to claim 9, characterized in that the solvent is selected from the group consisting of THF, cyclohexane, toluene, C? -C4 ethers, ketones and alcohols, alkylene glycols and mixtures thereof.
11. The composition according to claim 1, characterized in that it includes a germicidal agent dispersed in the carrier.
12. The composition according to claim 11, characterized in that the germicidal agent is present at a level of about 0.01-2% by weight in the composition.
13. The composition according to claim 12, characterized in that the level is from about 0.05-1% by weight.
14. The composition according to claim 11, characterized in that the germicidal agent is selected from the group consisting of straight or branched chain fatty acids, polyhexamethylene biguanide, chlorhexidine diacetate, quaternary ammonium compounds and mixtures thereof.
15. The composition according to claim 14, characterized in that the germicidal agent comprises chlorhexidine diacetate.
16. The composition according to claim 1, characterized in that it includes a dye dispersed in the carrier.
17. The composition according to claim 16, characterized in that the dye is selected from the group consisting of the red, orange and yellow dyes and mixtures thereof.
18. The composition according to claim 16, characterized in that the dye is present at a level from about 0.001-0.5% by weight in the composition.
19. The composition according to claim 18, characterized in that the level is from about 0.005-0.2% by weight.
20. The composition according to claim 1, characterized in that the carrier comprises respectively quantities of THF and an alcohol of C? -C4.
21. The composition according to claim 2, characterized in that the alcohol is present at a level of about 0.1-30% by weight, with the THF making the balance of the composition.
22. The composition according to claim 21, characterized in that the level is from about 5-20% by weight.
23. The composition according to claim 21, characterized in that the alcohol is ethanol.
24. The composition according to claim 1, characterized in that the composition has a viscosity from about 50-2000 cPs.
25. The composition according to claim 24, characterized in that the viscosity is present from about 100-1500 cPs.
26. The composition according to claim 1, characterized in that it has a skin drying time of about 72 ° F (22.2 ° C) of room temperature of more than about 20 minutes.
27. The composition according to claim 26, characterized in that the time is up to 10 months.
28. A method to protect the tits of bovines, characterized in that it comprises the step of applying to the tits the composition of claim 1, and allowing the applied composition to dry on it and form a protective, elastic teat film.
29. The method according to claim 28, characterized in that the tits are the tits of cows that do not produce milk.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US09080509 | 1998-05-18 |
Publications (1)
Publication Number | Publication Date |
---|---|
MXPA00004481A true MXPA00004481A (en) | 2002-02-26 |
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