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Preparation of itraconazole/2-hydroxypropyl-? -cyclodextrin inclusion complexform supercritical antisolvent method and in vitro dissolution behavior

机译:伊曲康唑/ 2-羟丙基-α的制备-环糊精包合物的超临界反溶剂方法及体外溶出行为

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摘要

An inclusion complex of an antifungal drug,itraconazol, with 2-hydroxypropyl-?-cyclodextrin(HP-?-CD) were prepared using a supercriticalantisolvent (SAS) process at temperatures of35~65?And at pressures of 83~140 bar.According to the results of this study, the SASprocess appears to be a promising method for thepreparation of water-insoluble drug/cyclodextrininclusion complexes.
机译:在35〜65℃,压力为83〜140 bar的条件下,采用超临界抗溶剂(SAS)工艺制备了抗真菌药伊曲康唑与2-羟丙基-α-环糊精(HP-α-CD)的包合物。根据这项研究的结果,SAS工艺似乎是制备水不溶性药物/环糊精包合物的有前途的方法。

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  • 会议地点 Honolulu, HI(US)
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    Department of Chemical and Biochemical Engineering The University of Suwon KoreaDepartment of Chemical Engineering Yonsei University Korea gblim@suwon.ac.kr;

    Department of Chemical and Biochemical Engineering The University of Suwon Korea;

    Department of Chemical Engineering Yonsei University Korea;

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