发明名称 |
METHOD FOR PREPARATION OF NANOSTRUCTURED COMPLEX OF HYDROPHOBIC DRUG |
摘要 |
PURPOSE: A method for preparing an insoluble drug nanocomplex is provided to enhance manufacture yield of the insoluble drug nanocomplex. CONSTITUTION: A method for preparing an insoluble drug nanocomplex comprises: a step of dissolving insoluble drug in a solvent containing surfactant; a step of adding apolipoprotein in the solution; a step of heating the solution; and a step of removing surfactant and solvent from the solution. The insoluble drug is dissolved with phospholipid. The phospholipid is phosphatidylcholine. The insoluble drug is coenzyme Q10, ursodeoxycholic acid, ilaprazole, paclitaxel or imatinib mesylate. The surfactant is cholic acid or salt thereof. The apolipoprotein is apolipotprotein A-I.
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申请公布号 |
KR20100096038(A) |
申请公布日期 |
2010.09.01 |
申请号 |
KR20100016400 |
申请日期 |
2010.02.23 |
申请人 |
SUNGKYUNKWAN UNIVERSITY FOUNDATION FOR CORPORATE COLLABORATION;AP TECHNOLOGY CO., LTD. |
发明人 |
KWEON, DAE HYUK;SHIN, CHUL SOO;SHIN, JAE YOON |
分类号 |
A61K9/127;A61K31/122;A61K31/575;A61K47/48 |
主分类号 |
A61K9/127 |
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