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HPMCAS/PVP K30胡椒碱双载体无定型固体分散体的制备及其体外溶出测定
引用本文:梁淇,朱成豪,邓月义,高飞龙,周振芳,方裕丹,张磊,高升.HPMCAS/PVP K30胡椒碱双载体无定型固体分散体的制备及其体外溶出测定[J].广西科学院学报,2019,35(1):71-77.
作者姓名:梁淇  朱成豪  邓月义  高飞龙  周振芳  方裕丹  张磊  高升
作者单位:桂林医学院药学院,广西桂林,541004;桂林医学院药学院,广西桂林 541004;广西壮族自治区中国科学院广西植物研究所,广西桂林 541006
基金项目:广西壮族自治区自然科学基金项目(2014GXNSFBA118052,2016GXNSFAA380266)资助。
摘    要:为提高胡椒碱(Piperine,Pip)的体外溶出,本文对Pip的双载体无定型态固体分散体制备技术进行研究。将醋酸羟丙基甲基纤维素琥珀酸酯(HPMC-AS)的3种异构体(HPMC-AS-HF、HPMC-AS-MF、HPMCAS-LF,分别简称为HF、MF和LF)和聚乙烯吡咯烷酮PVP K30(K30)按一定比例混合作为载体,并通过超饱和测试测定其对Pip溶液超饱和度的影响。使用溶剂法制备Pip双载体无定型态固体分散体,并运用差示扫描量热法(DSC)和红外光谱(IR)对Pip双载体固体分散体进行表征。实验结果显示K30/HF、K30/LF、K30/MF 3种组合均对Pip有一定的增溶作用,HF与MF可以提高溶液的超饱和度。当双载体固体分散体载药量为10%时,其溶出速度和稳定性按比例顺序为K30/HFK30/MFK30/LF。当MF/HF比例为1∶1或4∶1时效果最佳。随着MF占比增大,双载体固体分散体的溶出速度加快,稳定性下降。因此,双载体无定型态固体分散体对于维持胡椒碱的超饱和作用和提高体外溶出度都有显著效果。

关 键 词:胡椒碱  无定型固体分散体  稳定性  体外溶出

Preparation of HPMCAS/PVP K30 Double Carrier Amorphous Solid Dispersion and Determination of Its Dissolution in Vitro
LIANG Qi,ZHU Chenghao,DENG Yueyi,GAO Feilong,ZHOU Zhenfang,FANG Yudan,ZHANG Lei and GAO Sheng.Preparation of HPMCAS/PVP K30 Double Carrier Amorphous Solid Dispersion and Determination of Its Dissolution in Vitro[J].Journal of Guangxi Academy of Sciences,2019,35(1):71-77.
Authors:LIANG Qi  ZHU Chenghao  DENG Yueyi  GAO Feilong  ZHOU Zhenfang  FANG Yudan  ZHANG Lei and GAO Sheng
Institution:College of Pharmacy, Guilin Medical University, Guilin, Guangxi, 541004, China,College of Pharmacy, Guilin Medical University, Guilin, Guangxi, 541004, China;Guangxi Institute of Botany, Chinese Academy of Sciences, Guilin, Guangxi, 541006, China,College of Pharmacy, Guilin Medical University, Guilin, Guangxi, 541004, China,College of Pharmacy, Guilin Medical University, Guilin, Guangxi, 541004, China,College of Pharmacy, Guilin Medical University, Guilin, Guangxi, 541004, China,College of Pharmacy, Guilin Medical University, Guilin, Guangxi, 541004, China,College of Pharmacy, Guilin Medical University, Guilin, Guangxi, 541004, China and College of Pharmacy, Guilin Medical University, Guilin, Guangxi, 541004, China
Abstract:In order to improve the in vitro dissolution of piperine (Pip), the preparation technology of Pip doublecarrier amorphous solid dispersion was studied. Three isomers of hydroxypropyl methylcellulose acetate succinate (HPMC-AS) (HPMC-AS-HF, HPMC-AS-MF, HPMC-AS-LF, referred to as HF, MF and LF, respectively) and polyvinyl pyrrolidone PVP K30 (K30) were mixed as a carrier in a certain ratio, and its effect on the super saturation of Pip solution was determined by super saturation test. The Pip dual-carrier amorphous solid dispersion was prepared by solvent method, and the Pip dual-carrier solid dispersion was characterized by differential scanning calorimetry (DSC) and infrared spectroscopy (IR). The experiment results showed that the combination of K30/HF, K30/LF and K30/MF all had a certain solubilization effect on Pip, and HF and MF could increase the super saturation of the solution. When the dual carrier solid dispersion was loaded at 10%, the dissolution rate and stability were in the order of K30/HF > K30/MF > K30/LF. When the MF/HF ratio was 1:1 or 4:1, the effect was the best. As the MF ratio increased, the dissolution rate of the dual carrier solid dispersion increased and the stability decreased. Therefore, the dual-carrier amorphous solid dispersion has a significant effect on maintaining the super saturation of pip and improving the dissolution in vitro.
Keywords:piperine  amorphous solid dispersion  stability  in vitro dissolution
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