KR880004312A - 특정 표적 세포의 검출 및 치사용 친화력 증강 면역학적 시약 - Google Patents
특정 표적 세포의 검출 및 치사용 친화력 증강 면역학적 시약 Download PDFInfo
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- A61K47/68—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 the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A61K2123/00—Preparations for testing in vivo
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Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (42)
- a) 적합한 합텐에 대하여 결합 친화력을 가진 모노클로날 항체 또는 소편에 접합된 적합한 항원에 대하여 결합 친화력을 가진 모노클로날 항체 또는 소편, b) 제1a)항이 접합체에 대하여 결합 친화력을 가진 적어도 2개의 합텐 ; 방사성 표지화, 또는 안정한 상자성 금속을 사용하여 표지화시키거나 또는 약품 또는 독소를 공유결합시키는데 적합한 적어도 1개의 부위, 및 이들 기능기를 공유결합시키는 화학적 구조로 되는 합성 분자로 되는 면역학적 시약.
- a) 2개의 상이한 접합체(여기서, 접합체는 각각 제1a)항에서와 같이 적합한 항원 및 합텐에 대하여 결합 친화력을 가짐)의 혼합물, b) 2개의 상이한 합텐(여기서, 합텐은 각각 제2a)항의 혼합물의 2개의 접합체 중 하나에 대하여 결합 친화력을 가짐) ; 방사성 표지화, 또는 안정한 상자성 금속을 사용하여 표지화시키거나 또는 약품 또는 독소를 공유 결합시키는데 적합한 적어도 1개의 부위 ; 및 이들 기능기를 공유 결합시키는 화학적 구조로 되는 합성 분자로 되는 면역학적 시약.
- 제1항에 있어서, 모노클로날 항체가 생쥐 항체인 시약.
- 제2항에 있어서, 모노클로날 항체가 생쥐 항체인 시약.
- 제3항에 있어서, 모노클로날 항체가 IgG 부류인 시약.
- 제4항에 있어서, 모노클로날 항체가 IgG 부류인 시약.
- 제5항에 있어서, 소편이 Fab'2또는 Fab' 또는 Fab인 시약.
- 제6항에 있어서, 소편이 Fab'2또는 Fab' 또는 Fab인 시약.
- 제1항에 있어서, 합텐이 2,4-디니트로페놀의 유도체인 시약.
- 제2항에 있어서, 합텐중 하나가 2,4-디니트로페놀의 유도체인 시약.
- 제1항 또는 제9항에 있어서, 생리학적 조건 하에서 접합체와 합텐 사이의 결합 작용의 해리 상수가 10-9-10-7M인 시약.
- 제2항 또는 제10항에 있어서, 생리학적 조건 하에서 접합체와 이 접합체에 대하여 특이적인 합텐 사이의 결합 작용의 해리 상수가 10-9-10-7M인 시약.
- 제1항에 있어서, 합성 분자에 금속 양이온으로 표지화시키는 데 적합한 킬레이트제가 함유된 시약.
- 제2항에 있어서, 합성 분자에 금속 양이온으로 표지화시키는 데 적합한 킬레이트제가 함유된 시약.
- 제9항 또는 제13항에 있어서, 합성 분자가 다음 구조식으로 표시되는 시약.
- 제2항에 있어서, 합성 분자에 할로겐으로 표지화시키는 데 적합한 페놀기가 함유된 시약.
- 제1항에 있어서, 합성 분자에 할로겐으로 표지화시키는 데 적합한 페놀기가 함유된 시약.
- 제2항에 있어서, 화합 결합 구조가 펩티드인 시약.
- 제1항에 있어서, 화합 결합 구조가 펩티드인 시약.
- 제9항, 제17항 또는 제19항에 있어서, 합성분자가 다음 구조식으로 표시되는 시약.
- 제19항에 있어서, 펩티드에 1개 또는 수개의 D-아미노산이 함유된 시약.
- 제18항에 있어서, 펩티드에 1개 또는 수개의 D-아미노산이 함유된 시약.
- 제1항에 있어서, 표지화된 부위가 합텐이고 그리하여, 제1a) 항의 접합체가 표지화된 합성 분자에 대하여 표지화되지 않은 부위보다 더 큰 결합 친화력을 가진 시약.
- 제2항에 있어서, 1개의 표지화된 부위가 2개의 합텐 중 1개 이고 그리고하여, 제2a) 항의 혼합물 중의 1개의 접합체가 표지화되지 않은 합텐 보다 표지화된 합텐에 대하여 더 큰 결합 친화력을 가진 시약.
- 제1항에 있어서, 적합한 항원이 종양과 관련된 항원인 시약.
- 제1항에 있어서, 적절한 항원이 세포와 관련된 항원인 시약.
- 제1항에 있어서, 적합한 항원이 조직과 관련된 항원인 시약.
- 제2항에 있어서, 1개의 적합한 항원이 종양과 관련된 항원이고 다른 1개의 항원이 종양, 세포 또는 조직과 관련된 항원인 시약.
- 제25항 또는 28항에 있어서, 종양이 흑종 또는 임파종, 또는 유방, 폐 또는 결장직장 종양인 시약.
- 제26항 또는 제28항에 있어서, 세포와 관련된 항원이 미오신 또는 빌린인 시약.
- 제27항 또는 제28항에 있어서, 조직과 관련된 항원이 피브린인 시약.
- 합성 분자를 표지화시킨후, 시약을 동시에 또는 계속적으로 주입시키고 형상을 선행 기술에 공지된 검출기를 사용하여 기록하는 것을 특징으로 하는 제1항 내지 31항 중 어느 하나의 항의 시약을 사용하여 생체내에서 목적 세포를 표적화시키는 방법.
- 제32항에 있어서, 합성 분자를 방사성이 측정된 적합한 방사성 동위원소로 표지화시키는 방법.
- 제33항에 있어서, 방사성 동위원소가18F,76Br,77Br,123I135I,131I,221At,57Co,67Ga,68Ga,67Cu,99Y,97Ru,99mTc,111In,203Pb 또는213Bi인 시약.
- 합성 분자를 상자성 금속 이온으로 표지화시킨 후, 시약을 동시에 또는 계속적으로 주입시키고 국재 부위에서의 증가된 자기 공명 완화를 적합한 MRI 장치에 의하여 검출하는 것을 특징으로 하는 제1항 내지 31항 중 어느 하나의 항의 시약을 사용하여 생체 내에서 목적세포를 표적화하는 방법.
- 제35항에 있어서, 상자성 금속이 Gd, Mn 또는 Fe인 방법.
- 합성 분자를 표지화시킨 후, 시약을 동시에 또는 계속적으로 주입시키고 이 시약을 표적 세포를 치사시키는 데 사용하는 것을 특징으로 하는 제1항 내지 31항 중 어느 하나의 항의 시약을 사용하여 생체내에서 목적 세포를 표적화시키는 방법.
- 제37항에 있어서, 합성분자를 방사성 동위원소로 표지화시키는 방법.
- 제38항에 있어서, 동위원소가131I,211At,99Y 또는212Bi인 방법.
- 1개 또는 수개의 세포독성 약품, 또는 1개 또는 수개의 세균성 또는 식물성 독소 분자를 합성 분자에 결합시킨 후, 시약을 동시에 또는 계속적으로 주입시키는 것을 특징으로 하는 제1항 내지 31항 중 어느 하나의 항의 시약을 사용하여 생체 내에서 목적 세포를 표적화하는 방법.
- 제40항에 있어서, 약품이 메토트렉세이트, 항 종양 빈카(Vinca) 알칼로이드 유도체, 백금 착물, 안트라시클린 또는 이들의 임의의 조합물질인 방법.
- 제41항에 있어서, 독소가 리신, 아브린, 겔로닌, 아메리카자리공 항비루스성 단백질, 디프테리아 독소 또는 이들의 임의의 조합 물질인 방법.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
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FR86.13146 | 1986-09-19 | ||
FR8613146 | 1986-09-19 | ||
FR8613146A FR2604092B1 (fr) | 1986-09-19 | 1986-09-19 | Immunoreactifs destines a cibler les cellules animales pour leur visualisation ou leur destruction in vivo |
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KR880004312A true KR880004312A (ko) | 1988-06-07 |
KR900005622B1 KR900005622B1 (ko) | 1990-07-31 |
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US (1) | US5256395A (ko) |
EP (1) | EP0263046B1 (ko) |
JP (1) | JP2612454B2 (ko) |
KR (1) | KR900005622B1 (ko) |
AT (1) | ATE74769T1 (ko) |
AU (1) | AU613318B2 (ko) |
CA (1) | CA1306414C (ko) |
DE (1) | DE3778281D1 (ko) |
ES (1) | ES2032468T3 (ko) |
FR (1) | FR2604092B1 (ko) |
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-
1986
- 1986-09-19 FR FR8613146A patent/FR2604092B1/fr not_active Expired - Lifetime
-
1987
- 1987-09-10 US US07/096,829 patent/US5256395A/en not_active Expired - Lifetime
- 1987-09-16 EP EP87430031A patent/EP0263046B1/en not_active Expired - Lifetime
- 1987-09-16 ES ES198787430031T patent/ES2032468T3/es not_active Expired - Lifetime
- 1987-09-16 AT AT87430031T patent/ATE74769T1/de not_active IP Right Cessation
- 1987-09-16 DE DE8787430031T patent/DE3778281D1/de not_active Expired - Lifetime
- 1987-09-17 CA CA000547184A patent/CA1306414C/en not_active Expired - Lifetime
- 1987-09-18 AU AU78656/87A patent/AU613318B2/en not_active Ceased
- 1987-09-18 JP JP62234680A patent/JP2612454B2/ja not_active Expired - Lifetime
- 1987-09-18 KR KR1019870010382A patent/KR900005622B1/ko not_active IP Right Cessation
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1992
- 1992-06-11 GR GR920401264T patent/GR3004914T3/el unknown
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FR2604092A1 (fr) | 1988-03-25 |
DE3778281D1 (de) | 1992-05-21 |
AU7865687A (en) | 1988-04-21 |
CA1306414C (en) | 1992-08-18 |
KR900005622B1 (ko) | 1990-07-31 |
GR3004914T3 (ko) | 1993-04-28 |
JPS63159327A (ja) | 1988-07-02 |
ES2032468T3 (es) | 1993-02-16 |
JP2612454B2 (ja) | 1997-05-21 |
EP0263046A1 (en) | 1988-04-06 |
US5256395A (en) | 1993-10-26 |
ATE74769T1 (de) | 1992-05-15 |
AU613318B2 (en) | 1991-08-01 |
EP0263046B1 (en) | 1992-04-15 |
FR2604092B1 (fr) | 1990-04-13 |
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