Methods and compositions for locally increasing body fat
원문보기
IPC분류정보
국가/구분
United States(US) Patent
등록
국제특허분류(IPC7판)
A61K-031/425
C07D-277/34
A61K-009/00
A61K-031/57
A61K-031/4439
출원번호
US-0086785
(2013-11-21)
등록번호
US-8778981
(2014-07-15)
발명자
/ 주소
Kalayoglu, Murat V.
Singer, Michael S.
출원인 / 주소
Topokine Therapeutics, Inc.
대리인 / 주소
Wolf, Greenfield & Sacks, P.C.
인용정보
피인용 횟수 :
11인용 특허 :
54
초록▼
Provided are methods for increasing fat locally in a body of a subject in need thereof comprising percutaneously administering to the subcutaneous fat of the subject a thiazolidinedione or an orexigenic compound, or a pharmaceutically acceptable salt or prodrug thereof, optionally delivered as a com
Provided are methods for increasing fat locally in a body of a subject in need thereof comprising percutaneously administering to the subcutaneous fat of the subject a thiazolidinedione or an orexigenic compound, or a pharmaceutically acceptable salt or prodrug thereof, optionally delivered as a composition comprising a pharmaceutically acceptable carrier, as described herein. In certain embodiments, the pharmaceutically acceptable carrier comprises a percutaneous carrier, as described herein. Further provided are compositions comprising a thiazolidinedione or an orexigenic compound, or a pharmaceutically acceptable salt or prodrug thereof, for use according to the invention.
대표청구항▼
1. A method for increasing subcutaneous fat locally in a body of a subject in need thereof, the method comprising topically administering to the skin of the subject a thiazolidinedione selected from the group consisting of: and pharmaceutically acceptable salts thereof, using a percutaneous carrier
1. A method for increasing subcutaneous fat locally in a body of a subject in need thereof, the method comprising topically administering to the skin of the subject a thiazolidinedione selected from the group consisting of: and pharmaceutically acceptable salts thereof, using a percutaneous carrier selected from the group consisting of ethanol, propylene glycol, oleic acid, and lauryl lactate, in order to deliver an effective amount of the thiazolidinedione to the subcutaneous fat of the subject. 2. The method of claim 1, wherein the subject suffers from a subcutaneous fat deficiency. 3. The method of claim 2, wherein the subcutaneous fat deficiency is associated with a metabolic disorder. 4. The method of claim 2, wherein the subcutaneous fat deficiency is acquired. 5. The method of claim 4, wherein the acquired subcutaneous fat deficiency is HIV-associated lipodystrophy, lipidema, acquired partial lipodystrophy, acquired generalized lipodystrophy, Parry-Romberg syndrome, juvenile dermatomyositis, centrifugal abdominal lipodystrophy, lipoatrophia annularis, or localized lipodystrophy. 6. The method of claim 2, wherein the subcutaneous fat deficiency is caused by a medication, surgery, or an injury. 7. The method of claim 1, wherein the subject suffers from wrinkles of the skin. 8. The method of claim 1, wherein the subject suffers from dissatisfaction with the size or contour of a body part. 9. The method of claim 8, wherein the body part is the face, forehead, periorbital region of the face, cheeks, chin, lips, breast, limbs, hands, trunk, hips, or buttocks. 10. The method of claim 1, wherein the subject has transplanted fat. 11. The method of claim 1, wherein the thiazolidinedione is rosiglitazone or a pharmaceutically acceptable salt thereof. 12. The method of claim 11, wherein the rosiglitazone is administered in a composition at a concentration between about 0.1 percent and about 2 percent by weight. 13. The method of claim 1, wherein the percutaneous carrier comprises oleic acid. 14. The method of claim 13, wherein the oleic acid is administered in a composition at a concentration between about 1 percent and about 5 percent by weight. 15. The method of claim 1, wherein the percutaneous carrier comprises propylene glycol. 16. The method of claim 15, wherein the propylene glycol is administered in a composition at a concentration between about 20 percent and about 40 percent by weight. 17. The method of claim 1, wherein the percutaneous carrier comprises propylene glycol and oleic acid. 18. The method of claim 1, wherein the fat is locally increased by at least 10 percent, at least 20 percent, at least 30 percent, or at least 40 percent compared to control. 19. The method of claim 1, wherein increasing fat locally occurs locally on the face, breast, limbs, hands, trunk, hips, or buttocks. 20. The method of claim 1, wherein the administering is three times a day, twice a day, once a day, every other day, or every third day.
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