Zheng Xin, Yang Rui, Tang Xing, Zheng Liangyuan
Department of Pharmaceutics, Shenyang Pharmaceutical University, Shenyang, Liaoning, P.R.China.
Drug Dev Ind Pharm. 2007 Jul;33(7):791-802. doi: 10.1080/03639040601050213.
The purpose of this study was to prepare and characterize solid dispersions of nimodipine with hydroxypropyl methylcellulose (HPMC, Methocel E5), polyvinylpyrrolidone/vinyl acetate copolymer (PVP/VA, Plasdone S630), and ethyl acrylate, methyl methacrylate polymer (Eudragit EPO). The goal was to investigate whether the solid dispersion prepared by hot-melt extrusion can improve the dissolution rate of nimodipine. The dissolution results indicated that three polymers are suitable carriers to enhance the in vitro dissolution rate of nimodipine in pH 4.5 medium. The solubility research and solubility parameters calculation was corresponded with dissolution data. XRPD and DSC data showed that the crystallinity was not observed in hot-melt extrudates. NMD acted as a plasticizer for PVP/VA and EPO and was miscible with the polymers as well as 10% NMD-HPMC systems, because a single T(g) was observed in these extrudates. However, two T(g)s were observed in the 30 and 50% NMD-HPMC samples, indicating phase separation. The weakening and shift of the N-H stretching vibration of the secondary amine groups of nimodipine as determined by FT-IR proved hydrogen bonding between the drug and polymers in the solid dispersion.
本研究的目的是制备尼莫地平与羟丙基甲基纤维素(HPMC,美多秀E5)、聚乙烯吡咯烷酮/醋酸乙烯酯共聚物(PVP/VA,普拉斯酮S630)以及丙烯酸乙酯-甲基丙烯酸甲酯共聚物(尤特奇EPO)的固体分散体并对其进行表征。目标是研究通过热熔挤出制备的固体分散体是否能提高尼莫地平的溶出速率。溶出结果表明,这三种聚合物是提高尼莫地平在pH 4.5介质中体外溶出速率的合适载体。溶解度研究和溶解度参数计算与溶出数据相符。X射线粉末衍射(XRPD)和差示扫描量热法(DSC)数据表明,在热熔挤出物中未观察到结晶度。尼莫地平对PVP/VA和EPO起到增塑剂的作用,并且与聚合物以及10%尼莫地平-HPMC体系互溶,因为在这些挤出物中观察到单一的玻璃化转变温度(T(g))。然而,在30%和50%尼莫地平-HPMC样品中观察到两个T(g),表明发生了相分离。傅里叶变换红外光谱(FT-IR)测定显示,尼莫地平仲胺基团的N-H伸缩振动减弱并发生位移,这证明了固体分散体中药物与聚合物之间存在氢键。