GB2037160A - Milk-derived products - Google Patents
Milk-derived products Download PDFInfo
- Publication number
- GB2037160A GB2037160A GB7847801A GB7847801A GB2037160A GB 2037160 A GB2037160 A GB 2037160A GB 7847801 A GB7847801 A GB 7847801A GB 7847801 A GB7847801 A GB 7847801A GB 2037160 A GB2037160 A GB 2037160A
- Authority
- GB
- United Kingdom
- Prior art keywords
- milk
- product
- bulgaricus
- fermentation
- lyophilised
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
Classifications
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23C—DAIRY PRODUCTS, e.g. MILK, BUTTER OR CHEESE; MILK OR CHEESE SUBSTITUTES; MAKING THEREOF
- A23C9/00—Milk preparations; Milk powder or milk powder preparations
- A23C9/12—Fermented milk preparations; Treatment using microorganisms or enzymes
- A23C9/123—Fermented milk preparations; Treatment using microorganisms or enzymes using only microorganisms of the genus lactobacteriaceae; Yoghurt
- A23C9/1232—Fermented milk preparations; Treatment using microorganisms or enzymes using only microorganisms of the genus lactobacteriaceae; Yoghurt in powdered, granulated or dried solid form
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K35/00—Medicinal preparations containing materials or reaction products thereof with undetermined constitution
- A61K35/12—Materials from mammals; Compositions comprising non-specified tissues or cells; Compositions comprising non-embryonic stem cells; Genetically modified cells
- A61K35/20—Milk; Whey; Colostrum
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/01—Hydrolysed proteins; Derivatives thereof
- A61K38/012—Hydrolysed proteins; Derivatives thereof from animals
- A61K38/018—Hydrolysed proteins; Derivatives thereof from animals from milk
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/46—Ingredients of undetermined constitution or reaction products thereof, e.g. skin, bone, milk, cotton fibre, eggshell, oxgall or plant extracts
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/96—Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution
- A61K8/98—Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution of animal origin
- A61K8/981—Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution of animal origin of mammals or bird
- A61K8/986—Milk; Derivatives thereof, e.g. butter
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0014—Skin, i.e. galenical aspects of topical compositions
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/80—Process related aspects concerning the preparation of the cosmetic composition or the storage or application thereof
- A61K2800/85—Products or compounds obtained by fermentation, e.g. yoghurt, beer, wine
Abstract
A lyophilised milk-derived product is described which is produced from skimmed milk by effecting protein hydrolysis thereof, the skimmed milk having been subjected to yoghurt-producing conditions. The product obtained is rich in amino acids as well as constituents of yoghurt and metabolites of bacterial strains used in production of the yoghurt and is a suitable moisturising ingredient for inclusion in creams for cosmetic and pharmaceutical use.
Description
SPECIFICATION
Lyophilised milk-derived product having cosmetic and pharmaceutical activity
This invention relates to a lyophilised milk-derived product having cosmetic and pharmaceutical activity and to a method for the production thereof.
Milk fermentation products are known to contain a number of biologically active constituents known to be effective agents in creams for skin moisturing, nourishing and assisting in recovery from skin damage. These agents are, in particular, free amino acids produced in such milk fermentation products in addition to lactic acid. However, the quantity of free amino acid present in milk which has undergone natural souring is negligible and accordingly sour milk cannot be considered to be a viable source of free amino acid. Reference is made in this connection to J. Shalichev et al, "Stock Breeding Science", 8, 1971, No. 6. Fermentation products which have a higher content of free amino acids are, however, obtainable from casein.Moreover, German Democratic Republic Patent No. 11959 refers to a decomposed milk protein and its use in the preparation of industrial barrier creams. However, there is no disclosure as to the composition and quantity of the product obtained on decomposition of milk protein.
In addition, Czechoslovakian Patent No. 98238, among others, specifically discloses protein hydrolysates obtained from casein. Such amino acid mixtures, however, are limited as to their composition by the composition of the casein starting material and in particular, lack many biologically active constituents which are obtainable from a milk starting material.
According to one aspect of the present invention, there is provided a lyophilised milk-derived product having the following composition and characteristics:
content of from 15.5 to 16.5 g of free amino acid per 100 g of dry products;
from 5 to 11% by weight of water;
from 45 to 50% by weight of lactose;
from 27 to 33% by weight in total of protein;
from 25 to 28% by weight of water soluble protein;
from 1.4 to 2% by weight of peptonic nitrogen;
from 7 to 8% ash residue on combustion;
an acidity of 130 to 150"T; a pH of from 3.8 to 4.1; and
a content of 100,000 active cells of Lactobacillus
Bulgaricus per g of lyophilised product.
Moreover, the lyophilised product preferably exhibits an antimicrobial activity with respect to Staphiloccus Aureus of 1:32 and to B. Mezentericus ofl:62.
The product of this invention is a lyophilisate of the enzyme-decomposition product of milk casein from which whey has not been separated, the milk casein/whey starting material having additionally been subjected to fermentation processes caused by the combined use of S. Thermophilus and. Bulgaricus, that is, a yoghurt product produced from skimmed milk is subjected to enzyme decomposition and subsequently lyophilised.
Thus, according to a second aspect of the invention, there is provided a method for the production of a milk-derived product having cosmetic and pharmaceutical activity, which comprises subjecting to lyophilisation a pepsin induced hydrolysate of a fermentation product of skimmed pasteurised milk containing pancreatin, fermentation having been effected employing strains of S. Thermophilus and L.
Bulgaricus in combination.
The method of this invention uses, in effect, as milk product to be subjected to hydrolysis and then lyophilisation, a form ofyoghurt. Yoghurts known to possess nutritional and bioactive properties arising out of its characteristic composition resulting from fermentation of milk using Streptococcus Thermophilus and Lactobacilus Bulgaricus in combination. Yoghurt additionally contains useful metabolites resulting from the fermentation of the microorganism combination. The novel product of the process of this invention possesses free amino acids in a substantial quantity, rendering the product an effective source of free amino acid for use in creams for both cosmetic use and pharmaceutical use.
When carrying out the process of this invention, it is preferred to employ skimmed, pasteurised milk cooled to a temperature of about 45"C. Pancreatin is then added to the cooled milk, preferably in an amount of from 0.1 to 0.3% and the milk is allowed to stand for about 30 minutes after which it is innoculated with a starter combination of S. Thermophilus and L. Bulgaricus. It is preferred to use from 1 to 3o/o of the starter combination and the strains which are employed are preferably S. Thermophilus strain 2 ST and L. Bulgaricus strain 5 SB both of which were deposited at the Bulgarian State Institute for Control of Medicine, Boulevard "VI. Zaimov", 26, Sofia, Bulgaria, under accession nos. 113 and 114 on 21st
November, 1977.Fermentation is then effected while maintaining the temperature preferably at from 44 to 46"C for three hours. At the end of fermentation, pepsin is added preferably in a quantity of from 0.1 to 0.3 /O and the temperature is allowed to drop to 20 to 250C and maintained at this value until about 24 hours have elapsed from the beginning of fermentation. Finally, the fermentation product is subjected to lyophilisation.
The following example illustrates the invention:
EXAMPLE
100 kg of skimmed cows milk was pasteurised art a temperature of 95"C for 30 minutes. The milk was then cooled to a temperature of 45"C and 0.15 kg of pancreatin were added thereto. The milk was allowed to stand at 45" for 30 minutes and then 2.5 kg of an innoculant consisting of a bacterial combination of S. Thermophilus strain 2 ST and L.
Bulgaricus strain 5 SB was added thereto. The innoculated milk was allowed to undergo fermentation for 3 hours at a temperature of 45"C until its acidity reached 75"T and its pH reached 4. 0.1 kg of pepsin was then added to the milk. The yoghurt which formed, together with the enzyme decomposed protein therein was then maintained at ambient temperature of 20"C until 24 hours had elapsed after the beginning of fermentation. The fermentation product was then subjected to lyophilisation.
9.47 kg of lyophilisation product were obtained.
This product was a white powder containing 16 kg of free amino acids per 100 kg of dry substance, 10 kg of water, 47 kg of lactose, and 29.7 kg in total of protein of which 27.15 kg was constituted by water soluble protein. The lyophilised product contained 1.9 kg of peptonic nitrogen and yielded 8% of its original weight as ash when subjected to combustion. The lyophilised product had an acidity of 147"T and a pH of 3.9. Active cells of L. Bulgaricus were present in the lyophilisate in an amount of over 100,000 per g. The lyophilisate had an antimicrobial activity with respect to S. Aureus of 1:32 and an antibacterial activity with respect to B. Mezentericus ofl:32.
The lyophilisate characteristically possessed a high content of free amino acids and in addition contained all the constituents of yoghurt, as well as metabolites resulting from the growth of S. Ther mophilus and L. Bulgaricus. This high content of biologically active free amino acids and other substances derived from milk, as well as metabolites, made the lyophilisate obtained a suitable moisturing ingredient for inclusion in creams for cosmetic and pharmaceutical use together with a topologically acceptable carrier.
Claims (13)
1. A lyophilised milk-derived product having the following composition and characteristics:
a content of from 15.5 to 16.5 g of free amino acid per 100 g of dry products;
from 5 to 11% by weight of water;
from 45 to 50% by weight of lactose;
from 27 to 33 /O by weight in total of protein;
from 25 to 28% by weight of water soluble protein;
from 1.4 to 2% by weight of peptonic nitrogen;
from 7 to 8% ash residue on combustion;
an acidity of 130 to 1 50 T; a pH offrom3.8to4.1; and
a content of 100,000 active cells of Lactobaclllus Bulgaricus per g of lyophilised product.
2. A lyophilised milk-derived product as claimed in claim 1 which exhibits an antimicrobial activity with respect to Staphilococcus Aureus of 1 :32 to B.
Mezentericus of 1:62.
3. A lyophilised milk-derived product, substantially as described in the foregoing Example.
4. A method for the production of a milk-derived product having cosmetic and pharmaceutical activity, which comprises subjecting to lyophilisation a pepsin induced hydrolysate of a fermentation product of skimmed pasteurised milk containing pancreatin, fermentation having been effected em ploy- ing strains of S. Thermophilus and L. Bulgaricus in combination.
5. A method as claimed in claim 4, wherein the
pancreatin is added to skimmed pasteurised milk at
a temperature of about 45"C in an amount of from
0.1 to 0.30/c about 30 minutes before innoculation of the milk with a starter combination of S. Ther mophilus and L. Bulgaricus is effected.
6. A method as claimed in claim 4 or 5, wherein from 1 to 3 /O of a starter combination of strains of S.
Thermophilus and L. Bulgaricus is added to the milk.
7. A method as claimed in any one of claims 4 to 6, wherein a starter combination of S. Thermophilus strain 2 ST and L. Bulgaricus strain 5 SB is added to the milk.
8. A method as claimed in any one of claims 4 to 7, wherein fermentation is effected at a temperature of 44 to 46 C for 3 hours before pepsin is added to the milk.
9. A method as claimed in any one of claims 4 to 8, wherein pepsin is added to the milk in a quantity of from 0.1 to 0.30/c.
10. A method as claimed in any one of claims 4 to 9, wherein, after addition of the pepsin, the temperature of the milk is allowed to drop to 20 to 25"C and maintained at this value until about 24 hours have elapsed from the beginning of fermentation.
11. A method for the production of a milkderived product having cosmetic and pharmaceutical activity, substantially as described in the foregoing Example.
12. A milk-derived product having cosmetic and pharmaceutical activity, whenever produced by the method claimed in any one of claims 4 to 10.
13. A pharmaceutical or cosmetic composition comprising a milk-derived product as claimed in any one of claims 1 to 3 and 11 in association with a topologically acceptable carrier.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB7847801A GB2037160B (en) | 1978-12-08 | 1978-12-08 | Milk derived products |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB7847801A GB2037160B (en) | 1978-12-08 | 1978-12-08 | Milk derived products |
Publications (2)
Publication Number | Publication Date |
---|---|
GB2037160A true GB2037160A (en) | 1980-07-09 |
GB2037160B GB2037160B (en) | 1983-02-09 |
Family
ID=10501614
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB7847801A Expired GB2037160B (en) | 1978-12-08 | 1978-12-08 | Milk derived products |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB2037160B (en) |
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4464362A (en) * | 1980-06-27 | 1984-08-07 | Estee Lauder Inc. | Topical skin repair composition |
FR2609393A1 (en) * | 1988-02-23 | 1988-07-15 | Serobiologiques Lab Sa | Composition which is useful, in particular, as a base material for the preparation of pharmaceutical, in particular dermatological and/or cosmetic, compositions, comprising a nitrogenous substance, in particular amino acids, oligo- or polypeptides, proteins, and their derivatives, and pharmaceutical or cosmetic composition thus prepared |
EP0315541A1 (en) * | 1987-11-05 | 1989-05-10 | L'oreal | Cosmetic composition based on lyophilized reproducible yoghurt or kefir |
US5269959A (en) * | 1992-09-16 | 1993-12-14 | Gary Schreibman | Liquid deep cleaning detergent composition |
US5656268A (en) * | 1995-04-21 | 1997-08-12 | Sorodsky; Michael | Biological product |
US6258355B1 (en) * | 1996-11-22 | 2001-07-10 | Vsl Pharmaceuticals Inc. | Sphingomyelinase compositions and use thereof |
USRE39118E1 (en) * | 1996-11-22 | 2006-06-06 | Vsl Pharmaceuticals, Inc. | Sphingomyelinase compositions and use thereof |
FR2913337A1 (en) * | 2007-03-08 | 2008-09-12 | Oreal | Cosmetic treatment of keratinous material comprises providing a lyophilized form of live or inactive microorganism and a medium, extemporaneously contacting lyophilized form with medium and contacting the mixture with keratinous material |
US8697051B2 (en) | 1999-06-09 | 2014-04-15 | Vsl Pharmaceuticals Inc. | Composition comprising alkaline sphingomyelinase for use as a dietetic preparation, food supplement or pharmaceutical product |
DE102015222976A1 (en) | 2015-11-20 | 2017-05-24 | Henkel Ag & Co. Kgaa | Hair care compositions containing casein hydrolyzate for improving the hair structure |
DE102016221899A1 (en) | 2016-11-08 | 2018-05-09 | Henkel Ag & Co. Kgaa | Hair dye with yoghurt protein |
-
1978
- 1978-12-08 GB GB7847801A patent/GB2037160B/en not_active Expired
Cited By (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4464362A (en) * | 1980-06-27 | 1984-08-07 | Estee Lauder Inc. | Topical skin repair composition |
EP0315541A1 (en) * | 1987-11-05 | 1989-05-10 | L'oreal | Cosmetic composition based on lyophilized reproducible yoghurt or kefir |
FR2622797A1 (en) * | 1987-11-05 | 1989-05-12 | Oreal | COSMETIC COMPOSITION BASED ON YAURT OR KEFIR |
FR2609393A1 (en) * | 1988-02-23 | 1988-07-15 | Serobiologiques Lab Sa | Composition which is useful, in particular, as a base material for the preparation of pharmaceutical, in particular dermatological and/or cosmetic, compositions, comprising a nitrogenous substance, in particular amino acids, oligo- or polypeptides, proteins, and their derivatives, and pharmaceutical or cosmetic composition thus prepared |
US5269959A (en) * | 1992-09-16 | 1993-12-14 | Gary Schreibman | Liquid deep cleaning detergent composition |
US5656268A (en) * | 1995-04-21 | 1997-08-12 | Sorodsky; Michael | Biological product |
US6962697B2 (en) | 1996-11-22 | 2005-11-08 | Vsl Pharmaceuticals Inc. | Use of sphingomyelinase to increase the levels of skin and mucosal ceramides, and dermatological and cosmetic compositions suitable for topical application containing same |
US6582695B2 (en) | 1996-11-22 | 2003-06-24 | Vsl Pharmaceuticals Inc. | Sphingomyelinase compositions and use thereof |
US6258355B1 (en) * | 1996-11-22 | 2001-07-10 | Vsl Pharmaceuticals Inc. | Sphingomyelinase compositions and use thereof |
USRE39118E1 (en) * | 1996-11-22 | 2006-06-06 | Vsl Pharmaceuticals, Inc. | Sphingomyelinase compositions and use thereof |
US8697051B2 (en) | 1999-06-09 | 2014-04-15 | Vsl Pharmaceuticals Inc. | Composition comprising alkaline sphingomyelinase for use as a dietetic preparation, food supplement or pharmaceutical product |
US9439953B2 (en) | 1999-06-09 | 2016-09-13 | Vsl Pharmacueticals, Inc. | Compositions comprising alkaline sphingomyelinases for use as a dietetic preparation, food supplement or pharmaceutical product and methods for using them |
FR2913337A1 (en) * | 2007-03-08 | 2008-09-12 | Oreal | Cosmetic treatment of keratinous material comprises providing a lyophilized form of live or inactive microorganism and a medium, extemporaneously contacting lyophilized form with medium and contacting the mixture with keratinous material |
DE102015222976A1 (en) | 2015-11-20 | 2017-05-24 | Henkel Ag & Co. Kgaa | Hair care compositions containing casein hydrolyzate for improving the hair structure |
DE102016221899A1 (en) | 2016-11-08 | 2018-05-09 | Henkel Ag & Co. Kgaa | Hair dye with yoghurt protein |
DE102016221899B4 (en) | 2016-11-08 | 2022-04-28 | Henkel Ag & Co. Kgaa | Use of yoghurt protein in a cosmetic for changing the color of keratin fibers |
Also Published As
Publication number | Publication date |
---|---|
GB2037160B (en) | 1983-02-09 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PCNP | Patent ceased through non-payment of renewal fee |