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Development of self-micellizing solid dispersion system employing amphipathic copolymer for the improvement of dissolution and oral bioavailability of cyclosporine A
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作者 Hiroki Suzuki Hideyuki Sato +5 位作者 Yoshiki Kojo takahiro mizumoto Kayo Yuminoki Naohumi Hashimoto Yoshiki Seto Satomi Onoue 《Asian Journal of Pharmaceutical Sciences》 SCIE CAS 2016年第1期50-51,共2页
The main objective of the present study is to develop a selfmicellizing solid dispersion(SMSD)system of cyclosporine A(CsA)using an amphiphilic copolymer,poly[MPC-co-BMA](pMB)to improve the biopharmaceutical propertie... The main objective of the present study is to develop a selfmicellizing solid dispersion(SMSD)system of cyclosporine A(CsA)using an amphiphilic copolymer,poly[MPC-co-BMA](pMB)to improve the biopharmaceutical properties of CsA(Fig.1A).Unlike conventional carrier compounds,pMB would perform the bifunctional ability as both polymeric carrier of solid dispersion system and solubilizer derived from a high micellizing property,which could be considered beneficial for the production of highly water soluble formulation of poorly water soluble compound[1].Improvement in the aqueous solubility has been believed to be a key consideration for acquiring potent pharmacological effects of BCS class II drug like CsA. 展开更多
关键词 CYCLOSPORINE A AMPHIPATHIC COPOLYMER Self-micellizing solid dispersion Oral BIOAVAILABILITY
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