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Inclusion Complex Formation of Water- soluble Drug, Captopril, and Peracetylated-β-Cyclodextrin in Supercritical CO_2 for Controlled Release Applications

机译:控释应用中超临界CO_2中水溶性药物,卡托普利和过乙酰化β-环糊精的包合物形成

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摘要

The inclusion complex of CO_2-soluble peracetylated-β-cyclodextrin (PAc-β-CD), heptakis(2,3,6-tri-O-acetyl)-β-cyclodextrin, and highly water-soluble drug captopril, was prepared by a chemical solvent-free method using supercritical carbon dioxide. The captopril-PAc-β-CD inclusion complex was further confirmed by DSC and XRD studies. In- vitro release of captopril from an oily suspension confirmed that the dissolution rate of captopril was much retarded from the inclusion complex as a result of the hydrophobic properties of PAc-β-CD.
机译:通过以下方法制备了CO_2可溶性全乙酰化β-环糊精(PAc-β-CD),七(2,3,6-三-O-乙酰基)-β-环糊精和高水溶性药物卡托普利的包合物一种使用超临界二氧化碳的无化学溶剂方法。通过DSC和XRD研究进一步证实了卡托普利-PAc-β-CD包涵体复合物。卡托普利从油性悬浮液中的体外释放证实,由于PAc-β-CD的疏水性,卡托普利的溶解速度大大低于包合物。

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