Thermally reversible polyurethane hydrogels and cosmetic, biological and medical uses

• US 5,000,955 A
• Filed: 07/23/1990
• Issued: 03/19/1991
• Est. Priority Date: 07/29/1988
• Status: Expired due to Term

• Current Assignee: Tyndale Plains-Hunter, Ltd.
• Original Assignee: Tyndale Plains-Hunter, Ltd.
• Inventors: Seems, George E., Johnston, Christian W., Gould, Francis E.
• Primary Examiner(s): IVY, C WARREN
• Application Number:
  US07/559,513
• Time in Patent Office: 239 Days
• Field of Search: 524/591, 524/916, 523/105, 424/409, 424/422, 424/486
• US Class Current: 424/497
• CPC Class Codes: A61K 47/34 Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyesters, polyamino acids, polysiloxanes, polyphosphazines, copolymers of polyalkylene glycol or poloxamers A61K47/10 takes precedence
• CPC Class Codes: A61K 8/042 Gels
• CPC Class Codes: A61K 8/87 Polyurethanes
• CPC Class Codes: A61K 9/2031 obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyethylene glycol, polyethylene oxide, poloxamers
• CPC Class Codes: A61Q 1/10 for eyes, e.g. eyeliner, mascara
• CPC Class Codes: A61Q 13/00 Formulations or additives for perfume preparations essential oils or perfumes per se C11B9/00
• CPC Class Codes: A61Q 15/00 Anti-perspirants or body deodorants deodorisation of air A61L9/00
• CPC Class Codes: A61Q 17/00 Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
• CPC Class Codes: A61Q 19/00 Preparations for care of the skin
• CPC Class Codes: A61Q 19/007 Preparations for dry skin
• CPC Class Codes: A61Q 19/08 Anti-ageing preparations
• CPC Class Codes: C08G 18/4833 Polyethers containing oxyethylene units
• CPC Class Codes: C08G 18/6674 with compounds of group C08G18/3203
• CPC Class Codes: C08G 18/73 acyclic
• CPC Class Codes: C08G 18/758 containing two or more cycloaliphatic rings
• CPC Class Codes: C08G 2210/00 Compositions for preparing hydrogels
• CPC Class Codes: C12N 1/20 Bacteria; Culture media therefor
• CPC Class Codes: Y10S 524/916 Hydrogel compositions

Abstract

Thermally reversible polyurethane hydrogels are formed by adding water to a gel forming hydrophilic polyurethane polymer produced by reacting under anhydrous conditions a non-aromatic organic diisocyanate with a glycol component in an NCO/OH mole weight ratio of from about 0.900/1 to about 0.980/1, the glycol component having a number average molecular weight of from about 1000 to 3500 wherein the percentage by weight of the diisocyanate in the reaction mixture is from about 7% to about 20%. The hydrogels are solids at room temperature but liquify at higher temperatures such as body temperature and therefore are useful as carriers for the protection, delivery and sustained release of a variety of active agents including pharmaceuticals, cosmetics, living cells and organisms.

Claims

1. A thermally reversible hydrogel, comprising water and a gel forming hydrophilic polyurethane polymer, produced by reacting under anhydrous conditions an alkylene diisocyanate, bicycloalkane diisocyanate in which the rings are connected via ring carbon atoms by a single bond, or dicycloalkylalkane diisocyanate in which the rings are connected via ring carbon atoms through an alkylene chain, with a glycol component comprising one or more polyoxyethylene glycols, optionally mixed with one or more lower molecular weight ethylene glycols, in a mole weight ratio of NCO/OH of from about 0.900/1 to about 0.980/1, the total glycol component having a number average molecular weight of from about 1000 to about 3500 and wherein the amount by weight of the diisocyanate in the anhydrous reaction mixture is from about 7% to about 20%, mixing the reaction product in an aqueous medium, heating the mixture with stirring until homogeneous, and cooling the mixture.

2. The hydrogel of claim 1 wherein the amount by weight of the diisocyanate is from about 10% to about 15%.

3. The hydrogel of claim 1 wherein the concentration by weight of the polyurethane polymer is from about 1% to about 15%.

4. The hydrogel of claim 1 wherein the concentration of the polyurethane polymer is from about 3% to about 7%.

5. The hydrogel of claim 1 wherein the glycol component is a mixture of a lower molecular weight ethylene glycol and a polyoxyethylene glycol having a number average molecular weight of up to about 10,000.

6. The hydrogel of claim 1 wherein the glycol component is a mixture of diethylene glycol and at least one polyoxyethylene glycol having a number average molecular weight of from about 1450 to about 8000.

7. The hydrogel of claim 1 wherein the diisocyanate is 4,4'"'"'-dicyclohexylmethane diisocyanate or hexamethylene diisocyanate.

8. The hydrogel of claim 1 wherein the diisocyanate is 4,4'"'"'-dicyclohexylmethane diisocyanate.

9. The hydrogel of claim 6 wherein the glycol component is a mixture of diethylene glycol and a polyoxyethylene glycol having a number average molecular weight of about 1450.

10. The hydrogel of claim 6 wherein the glycol component is a mixture of diethylene glycol and a polyoxyethylene glycol having a number average molecular weight of about 4500.

11. The hydrogel of claim 6 wherein the glycol component is a mixture of diethylene glycol and a polyoxyethylene glycol having a number average molecular weight of about 8000.

12. The hydrogel of claim 6 wherein the glycol component is a mixture of diethylene glycol, a polyoxyethylene glycol having a number average molecular weight of about 1450 and a polyoxyethylene glycol having a number average molecular weight of about 8000.

19. A skin protectant film produced by applying to the skin the thermally reversible hydrogel of claim 1.

13. An active agent carrier system comprising an active agent and as the carrier vehicle therefore a hydrophilic, thermally reversible hydrogel comprising water and a gel forming polyurethane polymer produced by reacting under anhydrous conditions an alkylene diisocyanate, bicycloalkane diisocyanate in which the rings are connected via ring carbon atoms by a single bond, or dicycloalkylalkane diisocyanate in which the rings are connected via ring carbon atoms through an alkylene chain, with a glycol component comprising one or more polyoxyethylene glycols, optionally mixed with one or more lower molecular weight ethylene glycols, in a mole weight ratio of NCO/OH of from about 0.900/1 to about 0.980/1, the total glycol component having a number average molecular weight of from about 1000 to about 3500 and the percentage by weight of the diisocyanate in the anhydrous reaction mixture is from about 7% to about 20%, mixing the reaction product in an aqueous medium, heating the mixture with stirring until homogeneous, and cooling the mixture.

14. The carrier system of claim 13 wherein the percentage of the diisocyanate is from about 10% to about 15%.

15. The active agent carrier system of claim 13 wherein the active agent is a pharmaceutical.

16. The active agent carrier system of claim 13 wherein the pharmaceutical is an anti-cancer drug.

17. The active agent carrier system of claim 13 wherein the active agent is a cosmetic agent.

18. The active agent carrier system of claim 17 wherein the cosmetic agent is a fragrance, deodorant or mixture thereof.

20. A method of delivering an active agent to a treatment zone comprising the steps of:

(1) mixing the active agent with a thermally reversible hydrogel in its liquid state, the said hydrogel comprising water and a hydrophilic polyurethane polymer produced by reacting under anhydrous conditions, an alkylene diisocyanate, bicycloalkane diisocyanate in which the rings are connected via ring carbon atoms by a single bond, or dicycloalkylalkane diisocyanate in which the rings are connected via ring carbon atoms through an alkylene chain, with a glycol component comprising one or more polyoxyethylene glycols, optionally mixed with one or more lower molecular weight ethylene glycols, in a mole weight NCO/OH ratio of from about 0.900/1 to about 0.980/1, the total glycol component having a number average molecular weight of from about 1000 to 3500 and the percentage by weight of the diisocyanate in the anhydrous reaction mixture is from about 10% to about 15%, mixing the reaction product in an aqueous medium, heating the mixture with stirring until homogeneous,

(2) lowering the temperature of the liquid hydrogel to convert it into the solid gel form with concomitant encapsulation therein of the active agent;

(3) introducing the solid hydrogel containing the encapsulated active agent to the treatment zone; and

(4) raising the temperature of the solid hydrogel to convert it to the liquid form, thereby freeing the active agent to exert its therapeutic effect at the treatment zone.

21. The method of claim 20 wherein the hydrogel contains by weight from about 1% to about 15% of the polyurethane polymer.

22. The method of claim 20 wherein the hydrogel contains by weight from about 3% to about 7% of the polyurethane polymer.

23. The method of claim 20 wherein the glycol component is a mixture of a lower molecular weight ethylene glycol and a polyoxyethylene glycol having a number average molecular weight of up to about 10,000.

24. The method of claim 20 wherein the glycol component is a mixture of diethylene and at least one polyoxyethylene glycol having a number average molecular weight of from about 1450 to about 8000.

25. The method of claim 20 wherein the diisocyanate is selected from the class consisting of 4,4'"'"'-dicyclohexylmethane diisocyanate and hexamethylene diisocyanate.

26. The method of claim 20 wherein the diisocyanate is 4,4'"'"'-dicyclohexylmethane diisocyanate.

27. The method of claim 20 wherein the glycol component is a mixture of a diethylene glycol and a polyoxyethylene glycol having a number average molecular weight of about 1450.

28. The method of claim 20 wherein the glycol component is a mixture of a diethylene glycol and a polyoxyethylene glycol having a number average molecular weight of about 4500.

29. The method of claim 20 wherein the glycol component is a mixture of a diethylene glycol and a polyoxyethylene glycol having a number average molecular weight of about 8000.

30. The method of claim 20 wherein the glycol component is a mixture of diethylene glycol, a polyoxyethylene glycol having a number average molecular weight of about 1450 and a polyoxyethylene glycol having a number average molecular weight of about 8000.