Claims for Patent: 6,132,750

Summary for Patent: 6,132,750

Title:	Particles of cross-linked proteins and polysaccharides with hydroxamic groups for chelating metals and their uses notably in cosmetics
Abstract:	The invention relates to small sized particles. These particles comprise at least on the surface thereof a wall composed of a mixture of at least one protein and at least one polysaccharide which are cross-linked, preferably by interfacial cross-linking with a polyfunctional acylating agent which forms at least amide and ester bonds, and optionally anhydride bonds with amine, hydroxyl or carboxyl functions of the protein and of the polysaccharide, and which comprise hydroxamic groups on the surface thereof for chelating metal ions. These particles can be used in cosmetics or in pharmacy notably for the chelation or release of metal ions.
Inventor(s):	Perrier; Eric (Les Cotes d\'Arey, FR), Buffevant; Chantal (Millery, FR), Bonnet; Isabelle (Lyons, FR), Levy; Marie-Christine (Reims, FR)
Assignee:	Coletica (FR)
Application Number:	09/108,670
Patent Claims:	1. A particle selected from a micro particle and/or a nanoparticle having a surface which comprises, at least on the surface thereof, a wall composed of a mixture of at least one protein and at least one polysaccharide which are cross-linked, by interfacial cross-linking with a polyfunctional acylating cross-linking agent which forms at least amide and ester bonds, and optionally anhydride bonds, with amine, or hydroxyl or carboxyl functions of the protein and of the polysaccharide, said protein and said polysaccharide being present in said at least cross-linked wall in relative weight proportions sufficient to provide to said cross-linked wall resistance to degradation by hydroxylamine in an alkaline medium, and which comprises hydroxamic groups on the surface thereof for chelating metal ions. 2. The particle of claim 1, wherein the hydroxamic groups are bound on the surface by reaction of the particles, cross-linked by the cross-linking agent, with hydroxylamine in an alkaline medium. 3. The particle of claim 1, wherein the polysaccharide is selected from the group consisting of xanthan gum, guar gum, carobe gum, karaya gum, gum Arabic, an alginate, an agar, a carrageenin, a scleroglucan, a gluco-mannan, a galacto-manan, an arabinogalactan, a pectin, a glycosaminoglycan, a pentosan, a dextran, a chitosan, a chitosan compound, a hydrosoluble starch compound, a hydrodispersible starch derivative, a hydrosoluble cellulose compound, and a hydrodispersible cellulose compound. 4. The particle of claim 3, wherein said starch compound is selected from the group consisting of an alkyl ether of starch, a hydroxyalkyl ether of starch, and a carboxyalkyl ether of starch. 5. The particle of claim 3, wherein said cellulose compound is selected from the group consisting of an alkyl ether of cellulose, a hydroxyalkyl ether of cellulose, and a carboxyalkyl ether of cellulose. 6. The particle of claim 5, wherein said hydroxyalkyl ether of cellulose is a hydroxypropyl cellulose. 7. The particle of claim 5, wherein said carboxyalkyl ether of cellulose is a carboxymethyl cellulose. 8. The particle of claim 1, wherein said protein is a protein of non-regulated use selected from the group consisting of collagen, marine collagen, atelocollagen, marine atelocollagen, a moderate hydrolysate of collagen, a marine collagen hydrolysate, a gelatine, a marine gelatine, and a plant protein. 9. The particle of claim 8, wherein said plant protein is extracted from a leguminous or proteagenous plant selected from the group consisting of lupin (genus Lupinus), soya (genus Glycine), pea (genus Pisum), chick pea (genus Cicer), lucerne (genus Medicago), bean (genus Vicea), lentil (genus Lens), bean (genus Phaseolus), sesame (genus Sesamum), rape (genus Brassica), and sunflower (genus Elientus). 10. The particle of claim 8, wherein said plant protein is extracted from a cereal selected from the group consisting of wheat, maize, barley, malt, and oats. 11. The particle of claim 8, wherein said plant protein is used in the form of a powdery preparation selected from the group consisting of a flour, a concentrate, an isolate, and a liquid preparation. 12. The particle of claim 11, wherein said liquid preparation is a soya milk. 13. The particle of claim 1, which can chelate a metal ion selected from the group consisting of calcium, iron II, iron III, copper I, copper II, chromium, nickel, cobalt, mercury, zinc, silver, aluminium, cadmium, magnesium, lead, arsenic, silicon, selenium, germanium, gadolinium, manganese, a metal ion of a radioactive metal, and a metal ion of a radioactive isotope of a metal. 14. The particle of claim 1 which is loaded with a chelated metal ion, and which is used in a medium to exert a specific role or activity, directly or by release of said chelated metal ions. 15. The particle of claim 14, wherein said metal ion is selected from the group consisting of calcium, iron II, iron III, copper I, copper II, cobalt, zinc, silver, magnesium, silicon, selenium, manganese, and germanium. 16. The particle of claim 1, which is loaded with a metal ion selected from the group consisting of a metal ion of a radioactive metal, a metal ion of a radioactive isotope of a metal, and a metal ion of a paramagnetic metal. 17. The particle of claim 16, wherein said metal ion of a paramagnetic metal is selected from the group consisting of iron, manganese, gadolinium, and their alloys. 18. The particle of claim 16, which becomes detectable by an imaging technique. 19. The particle of claim 18, wherein said imaging technique is selected from the group consisting of scintigraphy, and NMR imaging. 20. A particle selected from a micro-particle and/or a nanoparticle having a surface, which comprises, at least on the surface thereof, a wall composed of a mixture of at least one protein and of at least one polysaccharide which are cross-linked in a reaction medium by interfacial cross-linking with a polyfunctional acylating cross-linking agent which forms at least amide and ester bonds, and optionally anhydride bonds, with amine, hydroxyl or carboxyl functions of the protein and of the polysaccharide, said protein and said polysaccharide being present in said at least cross-linked wall in a relative weight ratio of at least 0.5/0.1 of reaction medium, to provide to said cross-linked wall resistance to degradation by hydroxylamine in an alkaline medium, said particles comprising hydroxamic groups on the surface thereof for chelating metal ions. 21. A particle selected from a micro particle and/or a nanoparticle having a surface, which comprises, at least on the surface thereof, a wall composed of a mixture of at least one protein and of at least one polysaccharide which are cross-linked in a reaction medium by interfacial cross-linking with a polyfunctional acylating cross-linking agent which forms at least amide and ester bonds, and optionally anhydride bonds, with amine, hydroxyl or carboxyl functions of the protein and of the polysaccharide, said protein ranging between 0.5 and 2.5 weight % and said polysaccharide ranging between 0.1 and 10 weight % with respect to the reaction medium, to provide to said cross-linked wall resistance to degradation by hydroxylamine in an alkaline medium, said particles comprising hydroxamic groups on the surface thereof for chelating metal ions. 22. A composition comprising particles of claim 1 which comprise hydroxamic groups on the surface thereof. 23. The composition of claim 22 which is selected from the group consisting of a cosmetic composition, a pharmaceutical composition, an agro-foodstuff composition, and a liquid treatment composition. 24. The composition of claim 23, wherein said liquid is water. 25. A method of preparing particles selected from micro particles and/or nanoparticles having a surface which comprises a first step wherein an interfacial cross-linking is carried out in a reaction medium comprising a mixture of at least one protein and of at least one polysaccharide, with a polyfunctional acylating cross-liking agent to obtain said particles comprising, at least on the surface thereof, amide, ester and optionally anhydride functions, said protein and said polysaccharide being present in said at least cross-linked wall in relative weight proportions sufficient to provide to said cross-linked wall resistance to degradation by hydroxylamine in an alkaline medium, and, in a second step, these cross-linked particles are reacted with hydroxylamine in an alkaline medium to cause rupture at least of ester bonds and optionally anhydride bonds with the linking of hydroxamic groups, which particles are recovered, said particles being there by capable of carrying out the chelation of metal ions. 26. The method of claim 25, wherein for the reaction with hydroxylamine, a relative proportion of hydroxylamine hydrochloride is between 10 and 400 g per kilogram of wet particles to be treated, the pH being adjusted to values between 9 and 13.5 by the addition of a strong base. 27. The method of claim 26, wherein said strong base is sodium hydroxide. 28. The method of claim 26, wherein said pH is adjusted to a value between 9 and 13.5. 29. The method of claim 26, wherein said pH is adjusted to a value between 9.5 and 13. 30. The method of claim 26, wherein said relative proportion of hydroxylamine hydrochloride is between 30 and 200 g/Kg. 31. The method of claim 25, wherein before carrying out the grafting of the hydroxamic group onto the particle, an esterification step is carried out with an alcohol. 32. The method of claim 31, wherein said alcohol is ethanol or benzyl alcohol. 33. A method of preparing particles selected from micro particles and/or nanoparticles having a surface which comprises a first step wherein an interfacial cross-linking is carried out in a reaction medium comprising a mixture of at least one protein and of at least one polysaccharide, with a polyfunctional acylating cross-linking agent to obtain said particles comprising, at least on the surface thereof amide, ester and optionally anhydride functions, said protein and said polysaccharide being present in said at least cross-linked wall in a relative weight ratio of at least 0.5/0.1 of reaction medium, and, in the second step, these cross-linked particles are reacted with hydroxylamine in an alkaline medium to cause a rupture at least of ester bonds and optionally anhydride bonds with the linking of hydroxamic groups, which particles are recovered, said particles being thereby capable of carrying out the chelation of metal ions. 34. A method of preparing particles selected from micro-particles and/or nanoparticles having a surface which comprises a first step wherein an interfacial cross-linking is carried out in a reaction medium comprising a mixture of at least one protein and of at least one polysaccharide, with a polyfunctional acylating cross-linking agent to obtain said particles comprising, at least on the surface thereof amide, ester and optionally anhydride functions, said protein ranging between 0.5 and 2.5 weight % and said polysaccharide ranging between 0.1 and 10 weight % with respect to the reaction medium, and, in a second step, these cross-linked particles are reacted with hydroxylamine in an alkaline medium to cause a rupture at least of ester bonds and optionally anhydride bonds with the linking of hydroxamic groups, which particles are recovered, said particles being thereby capable of carrying out the chelation of metal ions. 35. A method of employing or controlled releasing a metal ion in a given medium, comprising the prior preparation of particles selected from microparticles and nanoparticles having a surface of claim 1, wherein hydroxamic groups engaged in chelates with the metal ion that is desired to use or to release into the medium, and placing these particles thus loaded with this chelated metal ion to be used or to be released in contact with the medium in which this use or release must be carried out, for a sufficient period of contact in order to exert a role or a function, or even the release of the metal ion. 36. The method of claim 35 for carrying out a cosmetic treatment, wherein the medium consists of the skin of an animal. 37. The method of claim 36, wherein said animal is a human being. 38. The method of claim 36, wherein said metal to be released is selected from the group consisting of calcium, copper, selenium, zinc, silicon, and germanium. 39. A method of cosmetic treatment of an animal comprising treating said animal with particles selected from microparticles and/or nanoparticles having a surface of claim 1, wherein hydroxamic groups on the surface thereof which are free or engaged in chelates with metal ions on an area of this animal which is sought after, in order to remove these metal ions, or on the contrary, to release these metal ions in said area of the animal. 40. The method of claim 39, wherein said animal is a human being. 41. The method of claim 39 which is a method of protecting materials of the dermis by applying an effective amount of a cosmetic or dermo-pharmaceutical composition containing said particles. 42. The method of claim 39 which is a method of inhibiting enzymatic activities, including collagenase activities, involved in the degradation of the skin support tissues and the intrinsic or photo-inducing ageing of skin tissues by applying an effective amount of said particles for trapping calcium. 43. The method of claim 39 which is a method of inhibiting the activity of certain enzymes involved in the uncontrolled pigmentation of the skin tissues under the action of UV by applying an effective amount of said particles for trapping or releasing copper. 44. The method of claim 39 which is a method of improving the anti-radical defense of the skin while at the same time activating its immune functions by applying an effective amount of said particles which is loaded with a chelated metal ion, and which is used in a medium to exert a specific role or activity, directly or by release of said chelated metal ions. 45. The method of claim 39 which is a method of reducing disorders linked to the accidental presence of nickel or cobalt on the skin by applying an effective amount of said particles.

Details for Patent 6,132,750

Applicant	Tradename	Biologic Ingredient	Dosage Form	BLA	Approval Date	Patent No.	Expiredate
Smith & Nephew, Inc.	SANTYL	collagenase	Ointment	101995	06/04/1965		2018-04-14