KR960704578A - 모노글리세리드/락테이트 에스테르 투과 촉진제(Monoglyceride/Lactate Ester Permeation Enhancer) - Google Patents

모노글리세리드/락테이트 에스테르 투과 촉진제(Monoglyceride/Lactate Ester Permeation Enhancer)

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KR960704578A
KR960704578A KR1019960701610A KR19960701610A KR960704578A KR 960704578 A KR960704578 A KR 960704578A KR 1019960701610 A KR1019960701610 A KR 1019960701610A KR 19960701610 A KR19960701610 A KR 19960701610A KR 960704578 A KR960704578 A KR 960704578A
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skin
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리나 톨먼 타스코비치
수 일 염
은 수 이
니베스 마르잔 크리솔로고
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에드워드 엘. 만델
앨자 코포레이션
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Abstract

투여될 약물의 치료 유효량; 및 모노글리세리드 또는 모노글리세리드의 혼합물, 및 락테이트 에스테르 또는 락테이트 에스테르의 혼합물로 이루어지는 투과-촉진 혼합물의 조합으로 이루어지는 체표면이나 막을 통한 투과에 의해 약물을 투여하기 위한 체표면 또는 막에 작용하는 물질의 조성물.

Description

모노글리세리드/락테이트 에스테르 투과 촉진제(Monoglyceride/Lactate Ester Permeation Enhancer)
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음

Claims (46)

  1. (a) 투여될 약물의 치료 유효량 및 (b) (ⅰ) 15 내지 25중량%의 모노글리세리드 또는 모노글리세리드의 혼합물 및 (ⅱ) 8 내지 25중량%의 락테이트 에스테르 또는 락테이트 에스테르의 혼합물로 이루어지는 투과-촉진 혼합물의 조합으로 이루어지는 체표면이나 막을 통한 투과에 의해 약물을 투여하기 위한 체표면 또는 막에 작용하는 물질의 조성물.
  2. 제1항에 있어서, 모노글리세리드 또는 모노글리세리드의 혼합물이 조성물의 20중량%를 이루며, 락테이트 에스테르 또는 락테이트 에스테르의 혼합물이 조성물의 12중량%를 이루는 것인 조성물.
  3. 제1항에 있어서, 락테이트 에스테르가 라우릴 락테이트인 조성물.
  4. 제1항에 있어서, 락테이트 에스테르가 에틸 락테이트인 조성물.
  5. 제1항에 있어서, 락테이트 에스테르가 미리스틸 락테이트인 조성물.
  6. 제1항에 있어서, 락테이트 에스테르가 세틸 락테이트인 조성물.
  7. 제1항에 있어서, 락테이트 에스테르의 혼합물이 에틸 락테이트 및 라우릴 락테이트인 조성물.
  8. 제3 내지 7항 중 어느 한 항에 있어서, 모노글리세리드가 글리세롤 모노라우레이트인 조성물.
  9. 제8항에 있어서, 글리세롤 모노라우레이트가 조성물의 20중량%를 이루며, 락테이트 에스테르가 조성물의 12중량%를 이루는 것인 조성물.
  10. 제1항에 있어서, 약물이 벤조디아제핀, 항무스카린 제제, 부신피질 스테로이드, 에스트로겐, 안드로겐 또는 프로게스틴으로 이루어지는 군으로부터 선택되는 것인 조성물.
  11. 제10항에 있어서, 부신피질 스테로이드가 알클로메타존, 알도스테론, 암시노니드, 베클로메타존, 디프로피오네이트, 베타메타존, 클로베타졸, 클로코르톨론, 코르티졸, 코르티존, 코르티코스테론, 데소니드, 데속시메타존, 11-데속시코르티코스테론, 11-데속시코르티졸, 덱사메타존, 디플로라존, 플루드로코르티존, 플루니솔리드, 플루오시놀론, 플루오시노니드, 플루오메톨론, 플루르안드레놀리드, 할시노니드, 히드로코르티존, 메드리존, 6α-메틸프레드니졸론, 모메타존, 파라메타존, 프레드니졸론, 프레드니존, 테트라히드로코르티졸 또는 트리암시놀론으로 이루어지는 군으로부터 선택되는 것인 조성물.
  12. 제10항에 있어서, 안드로겐이 다나졸, 플루옥시메스테론, 메트안드로스테놀론, 메틸테르토스테론, 난드롤론 데카노에이트, 난드롤론 펜프로피오네이트, 옥산드롤론, 옥시메톨론, 스타노졸론, 테스톨락톤, 테스토스테론, 테스토스테론 시피오네이트, 테스토스테론 에난테이트 또는 테스토스테론 프로피오네이트로 이루어지는 군으로부터 선택되는 것인 조성물.
  13. 제10항에 있어서, 에스트로겐이 클로로트리아니센, 디에틸스틸베스트롤, 에스트라디올, 에스트라디올 시피오네이트, 에스트라디올 발러레이트, 에스토론, 황산나트륨 에스트론, 에스트로피페이트, 에티닐 에스트라디올, 메스트라놀, 퀸에스트롤 또는 나트륨 이퀄린 술페이드로 이루어지는 군으로부터 선택되는 것인 조성물.
  14. 제10항에 있어서, 프로게트틴이 에티노디올 디아세테이트, 게스토덴, 히드록시프로게스테론 카프로에이트, 레보노르게스트렐, 메드록시프로게스테론 아세테이트, 메게스트롤 아세테이트, 노르에틴드론, 노르에틴드론 아세테이트, 노르에티노드렐, 노르게스트렐 또는 프로게스테론으로 이루어지는 군으로부터 선택되는 것인 조성물.
  15. 제10항에 있어서, 항무스카린 제제가 아니소트로핀, 아트로핀, 클리디늄, 시클로펜톨레이트, 디시클로민, 플라복세이트, 글리코피롤레이트, 헥소시클륨, 호마트로핀, 이프라트로퓸, 이소프로프아미드, 메펜졸레이트, 메탄텔린, 옥시펜시클리민, 피렌제핀, 프로판텔린, 스코폴아민, 텔렌제핀, 트리디헥스에틸 또는 트로픽 아미드로 이루어지는 군으로부터 선택되는 것인 조성물.
  16. (a) 치료 유효량의 약물 및 (ⅰ) 15 내지 25중량%의 모노글리세리드 또는 모노글리세리드의 혼합물 및 (ⅱ) 8 내지 25중량%의 락테이트 에스테르 또는 락테이트 에스테르의 혼합물로 이루어지는 피부 투과-촉진량의 투과 혼합물로 이루어지는 저장고; (b) 저장고의 피부 반대편 상의 배면; 및 (c) 저장고를 피부와의 약물- 및 투과 촉진 혼합물-이동 관계로 유지시켜 주는 수단으로 이루어지는, 치료 유효 속도에서의 약물의 경피 투여용 장치.
  17. (a) 치료 유효량의 약물 및 (ⅰ) 15 내지 25중량%의 모노글리세리드 또는 모노글리세리드의 혼합물 및 (ⅱ) 8 내지 25중량%의 락테이트 에스테르 또는 락테이트 에스테르의 혼합물로 이루어지는 피부 투과-촉진량의 투과 혼합물로 이루어지는 제1저장고; (b) 과량의 투과 촉진 혼합물 및 포화 이하의 약물로 이루어지는 제2저장고; (c) 제1저장고 및 제2저장고 사이의 속도-조절막; (d) 저장고의 피부 반대편 상의 배면; 및 (e) 저장고를 피부와의 약물- 및 투과 촉진 혼합물-이동 관계로 유지시켜 주는 수단으로 이루지는, 치료 유효 속도에서의 약물의 경피 투여용 장치.
  18. 제16 또는 17항에 있어서, 모노글리세리드가 글리세롤 모노라우레이트인 장치.
  19. 제16 또는 17항에 있어서, 락테이트 에스테르가 라우릴 락테이트인 장치.
  20. 제16 또는 17항에 있어서, 락테이트 에스테르가 에틸 락테이트인 장치.
  21. 제16 또는 17항에 있어서, 락테이트 에스테르가 세틸 또는 미리스틸 락테이트인 장치.
  22. 제16 또는 17항에 있어서, 락테이트 에스테르의 혼합물이 에틸 및 라우릴 락테이트인 장치.
  23. 제16 또는 17항에 있어서, 모노글리세리드가 글리세롤 모노라우레이트이며, 락테이트 에스테르가 에틸 락테이트 또는 라우릴 락테이트 또는 그의 혼합물인 장치.
  24. 제16 또는 17항에 있어서, 약물이 벤조디아제핀, 항무스카린 제제, 에스트로겐, 안드로겐 또는 프로게스틴으로 이루어지는 군으로부터 선택되는 것인 장치.
  25. 제16 또는 17항에 있어서, 약물이 알클로메타존, 알도스테론, 암시노니드, 베클로메타존, 디프로피오네이트, 베타메타존, 클로베타졸, 클로코르톨론, 코르티졸, 코르티존, 코르티코스테론, 데소니드, 데속시메타존, 11-데속시코르티코스테론, 11-데속시코르티졸, 덱사메타존, 디플로라존, 플루드로코르티존, 플루니솔리드, 플루오시놀론, 플루오시노니드, 플루오메톨론, 플루르안드레놀리드, 할시노니드, 히드로코르티존, 메드리존, 6α-메틸프레드니졸론, 모메타존, 파라메타존, 프레드니졸론, 프레드니존, 테트라히드로코르티졸 또는 트리암시놀론으로 이루어지는 군으로부터 선택되는 것인 장치.
  26. 제16 또는 17항에 있어서, 약물이 다나졸, 플루옥시메스테론, 메트안드로스테놀론, 메틸테르토스테론, 난드롤론 데카노에이트, 난드롤론 펜프로피오네이트, 옥산드롤론, 옥시메톨론, 스타노졸론, 테스톨락톤, 테스토스테론, 테스토스테론 시피오네이트, 테스토스테론 에난테이트 또는 테스토스테론 프로피오네이트로 이루어지는 군으로부터 선택되는 것인 장치.
  27. 제16 또는 17항에 있어서, 약물이 클로로트리아니센, 디에틸스틸베스트롤, 에스트라디올, 에스트라디올 시피오네이트, 에스트라디올 발러레이트, 에스토론, 황산 나트륨 에스트론, 에스트로피페이트, 에티닐 에스트라디올, 메스트라놀, 퀸에스트롤 또는 나트륨 이퀄린 술페이드로 이루어지는 군으로부터 선택되는 것인 장치.
  28. 제16 또는 17항에 있어서, 프로게트틴이 에티노디올 디아세테이트, 게스토덴, 히드록시프로게스테론 카프로에이트, 레보노르게스트렐, 메드록시프로게스테론 아세테이트, 메게스트롤 에세테이트, 노르에틴드론, 노르에틴드론 아세테이트, 노르에티노드렐, 노르게스트렐 또는 프로게스테론으로 이루어지는 군으로부터 선택되는 것인 장치.
  29. 제16 또는 17항에 있어서, 약물이, 아니소트로핀, 아트로핀, 클리디늄, 시클로펜톨레이트, 디시클로민, 플라복세이트, 글리코피롤레이트, 헥소시클륨, 호마트로핀, 이프라트로퓸, 이소프로프아미드, 메펜졸레이트, 메탄텔린, 옥시펜시클리민, 피렌제핀, 프로판텔린, 스코폴아민, 텔렌제핀, 트리디헥스에틸 또는 트로픽아미드로 이루어지는 군으로부터 선택되는 것인 장치.
  30. 제16항에 있어서, 저장고와 피부 사이의 관계를 유지시켜주는 수단이 저장고의 피부 인접면 상의 인-라인(in-line) 접착층으로 이루어지는 것인 장치.
  31. 제17항에 있어서, 저장고와 피부 사이의 관계를 유지시켜주는 수단이 제1저장고의 피부 인접면 상의 인-라인(in-line) 접착층으로 이루어지는 것인 장치.
  32. 제17항에 있어서, 제1저장고 또한 저장고와 피부 사이의 관계를 유지시켜주는 수단으로서 기능하는 접착층인 장치.
  33. 제19 내지 22항 중 어느 한 항에 있어서, 모노글리세리드가 글리세롤 모노라우레이트인 장치.
  34. 제33항에 있어서, 글리세롤 모노라우레이트 및 락테이트 에스테르가 약물 함유 저장고의 각각 20중량% 및 12중량%를 이루는 것인 장치.
  35. (a) 연장된 시간 주기 동안 치료 효과를 제공하기에 충분한 양의 약물 및 피부 투과-촉진량의 (ⅰ) 15 내지 25중량%의 모노글리세리드 또는 모노글리세리드의 혼합물 및 (ⅱ) 8 내지 25중량%의 락테이트 에스테르 또는 락테이트 에스테르의 혼합물로 이루어지는 피부 투과-촉진량의 투과 혼합물로 이루어지는 저장고; (b) 저장고의 피부 반대편 상의 배면; 및 (c) 저장고를 피부와의 약물- 및 투과 촉진 혼합물-이동 관계로 유지시켜 주는 수단으로 이루어지는 경피 전달 장치를 환자의 피부 상에 올려 놓는 단계로 이루어지는 약물의 경피 투여 방법.
  36. (a) 연장된 시간 주기 동안 치료 효과를 제공하기에 충분한 양의 약물 및 (ⅰ) 15 내지 25중량%의 모노글리세리드 또는 모노글리세리드의 혼합물 및 (ⅱ) 8 내지 25중량%의 락테이트 에스테르 또는 락테이트 에스테르의 혼합물로 이루어지는 피부 투과-촉진량의 투과 혼합물로 이루어지는 저장고; (b) 저장고의 피부 반대편 상의 배면; 및 (c) 저장고를 피부와의 약물- 및 투과 촉진 혼합물-이동 관계로 유지시켜 주는 수단으로 이루지는 경피 약물 전달 장치를 환자의 피부 상에 올려 놓는 단계로 이루어지는 약물의 경피 투여 방법.
  37. (a) 치료 유효량의 약물 및 (ⅰ) 15 내지 25중량%의 모노글리세리드 또는 모노글리세리드의 혼합물 및 (ⅱ) 8 내지 25중량%의 락테이트 에스테르 또는 락테이트 에스테르의 혼합물로 이루어지는 피부 투과-촉진량의 투과 혼합물로 이루어지는 제1저장고; (b) 과량의 투과 촉진 혼합물 및 포화 이하의 약물로 이루어지는 제2저장고; (c) 제1저장고 및 제2저장고 사이의 속도-조절막; (d) 저장고의 피부 반대편 상의 배면; 및 (e) 저장고를 피부와의 약물- 및 투과 촉진 혼합물-이동 관계로 유지시켜 주는 수단으로 이루지는 경피 전달 장치를 환자의 피부 상에 올려 놓는 단계로 이루어지는 약물의 경피 투여 방법.
  38. 제35 또는 37항 중 어느 한 항에 있어서, 모노글리세리드가 글리세롤 모노라우레이트인 방법.
  39. 제35 또는 37항 중 어느 한 항에 있어서, 락테이트 에스테르가 라우릴 락테이트인 방법.
  40. 제35 또는 37항 중 어느 한 항에 있어서, 락테이트 에스테르가 에틸 락테이트인 방법.
  41. 제35 또는 37항 중 어느 한 항에 있어서, 락테이트 에스테르가 세틸 또는 미리스틸 락테이트인 방법.
  42. 제35 또는 37항 중 어느 한 항에 있어서, 락테이트 에스테르가 에틸 및 라우릴 락테이트인 방법.
  43. 제35 또는 37항 중 어느 한 항에 있어서, 모노글리세리드가 글리세롤 모노라우레이트이며, 락테이트 에스테르가 에틸 락테이트 또는 라우릴 락테이트 또는 그의 혼합물인 방법.
  44. 제35 또는 37항 중 어느 한 항에 있어서, 약물이 벤조디아제핀, 항무스카린 제제, 에스트로겐, 안드로겐 또는 프로게스틴으로 이루어지는 군으로부터 선택되는 것인 방법.
  45. 제36 또는 37항에 있어서, 모노글리세리드가 글리세롤 모노라우레이트이며, 글리세롤 모노라우레이트 및 락테이트 에스테르가 약물 함유 저장고의 각각 20중량% 및 12중량%를 이루어지는 것인 방법.
  46. 제35항에 있어서, 모노글리세리드가 글리세롤 모노라우레이트이며 글리세롤 모노라우레이트 및 락테이트 에스테르가 약물 및 투과 촉진제 혼합물의 각각 20중량% 및 12중량%를 이루는 것인 방법.
    ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
KR1019960701610A 1993-09-29 1994-09-29 모노글리세리드/락테이트 에스테르 투과 촉진제(Monoglyceride/Lactate Ester Permeation Enhancer) KR960704578A (ko)

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US12949493A 1993-09-29 1993-09-29
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PCT/US1994/011120 WO1995009006A1 (en) 1993-09-29 1994-09-29 Monoglyceride/lactate ester permeation enhancer

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KR1019960701611A KR960704579A (ko) 1993-09-29 1994-09-29 옥시부티닌용 모노글리세리드/락테이트 에스테르 투과 촉진제(Monoglyceride/lactate Ester Permeation Enhancer for Oxybutynin)

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ATE183926T1 (de) 1999-09-15
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US5686097A (en) 1997-11-11
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