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公开(公告)号:US20050065066A1
公开(公告)日:2005-03-24
申请号:US10825995
申请日:2004-04-16
申请人: Niels Kaarsholm , Peter Madsen , Morten Schlein , Helle Olsen , Svend Havelund , Dorte Steensgaard , Svend Ludvigsen , Palle Jakobsen , Anders Petersen , Gerd Schluckebier
发明人: Niels Kaarsholm , Peter Madsen , Morten Schlein , Helle Olsen , Svend Havelund , Dorte Steensgaard , Svend Ludvigsen , Palle Jakobsen , Anders Petersen , Gerd Schluckebier
IPC分类号: A61K31/416 , A61K31/4192 , A61K38/00 , A61K38/28 , C07D249/06 , C07D249/18 , C07D277/34 , C07D403/04 , C07D413/12 , C07D417/12 , C07K14/62
CPC分类号: C07D403/04 , A61K31/416 , A61K31/4192 , A61K38/28 , C07D249/06 , C07D249/18 , C07D277/34 , C07D413/12 , C07D417/12 , C07K14/62 , A61K2300/00
摘要: The present invention provides pharmaceutical compositions comprising insulin and novel ligands for the HisB10 Zn2+ sites of the R-state insulin hexamer. The resulting preparations have improved physical and chemical stability.
摘要翻译: 本发明提供包含胰岛素和R状态胰岛素六聚体的His B> Zn 2+位点的新配体的药物组合物。 所得制剂具有改善的物理和化学稳定性。
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公开(公告)号:US20060258561A1
公开(公告)日:2006-11-16
申请号:US11226870
申请日:2005-09-09
申请人: Per Balschmidt , Helle Olsen , Niels Kaarsholm , Peter Madsen , Palle Jakobsen , Svend Ludvigsen , Gerd Schluckebier , Dorte Steensgaard , Anders Petersen
发明人: Per Balschmidt , Helle Olsen , Niels Kaarsholm , Peter Madsen , Palle Jakobsen , Svend Ludvigsen , Gerd Schluckebier , Dorte Steensgaard , Anders Petersen
IPC分类号: A61K38/28 , A61K31/522 , A61K31/513 , A61K31/426 , A61K31/4196 , A61K31/4184 , A61K31/4166 , A61K33/32
CPC分类号: A61K31/4166 , A61K31/4184 , A61K31/4196 , A61K31/426 , A61K31/513 , A61K31/522 , A61K33/30 , A61K38/28 , A61K45/06
摘要: This invention relates to NPH-insulin (crystalline preparations) that are prepared in the presence of certain high-affinity ligands for the HisB10 Zn2+-sites of the R-state insulin hexamer. Preparation of NPH-insulin in the presence of high-affinity ligand results in crystalline NPH-insulin suspensions that are absorbed more slowly from subcutis than regular NPH-insulin. Hence the resulting action profile is longer and the spike is less pronounced than observed with regular NPH-insulin
摘要翻译: 本发明涉及在R状态胰岛素六聚体的HisB10 Zn 2+ 2+的某些高亲和力配体存在下制备的NPH-胰岛素(结晶制剂)。 在高亲和力配体的存在下制备NPH-胰岛素导致结晶NPH-胰岛素悬浮液比皮下组织比常规NPH-胰岛素更慢吸收。 因此,所得到的作用谱更长,并且峰值不如用常规NPH-胰岛素观察到的
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公开(公告)号:US20060069013A1
公开(公告)日:2006-03-30
申请号:US11227760
申请日:2005-09-12
申请人: Soren Ostergaard , Helle Olsen , Niels Kaarsholm , Peter Madsen , Palle Jakobsen , Svend Ludvigsen , Gerd Schluckebier , Dorte Steensgaard , Anders Petersen
发明人: Soren Ostergaard , Helle Olsen , Niels Kaarsholm , Peter Madsen , Palle Jakobsen , Svend Ludvigsen , Gerd Schluckebier , Dorte Steensgaard , Anders Petersen
IPC分类号: A61K38/28 , A61K31/555
CPC分类号: A61K38/28 , A61K9/0019 , A61K31/41 , A61K31/555
摘要: Novel ligands for the HisB10 Zn2+ sites of the R-state insulin hexamer that are capable of prolonging the action of insulin preparations are disclosed.
摘要翻译: 公开了能够延长胰岛素制剂作用的R状态胰岛素六聚体的HisB10 Zn 2+ 2 +位点的新配体。
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