Zhang Qiang, Li Zheng, Qu Hai-Bin, Li Wen-Long
School of Pharmaceutical Engineering of Traditional Chinese Medicine, Tianjin University of Traditional Chinese Medicine Tianjin 300193, China.
Pharmaceutical Informatics Institute, School of Pharmaceutical Sciences, Zhejiang University Hangzhou 310058, China.
Zhongguo Zhong Yao Za Zhi. 2020 Apr;45(8):1918-1923. doi: 10.19540/j.cnki.cjcmm.20200221.310.
To compare the quality of Fufang Danshen Pian, the dissolution behaviors of 7 index components in Fufang Danshen Pian in different batches and from different manufacturers in 4 kinds of dissolution mediums, and evaluate by multiple dissolution curves. The dissolution test was carried out by the paddle method, with pH 1.2 hydrochloride buffer, pH 4.0 acetate buffer, distilled water and pH 6.8 phosphate buffer as dissolution medium. The rotation speed was 75 r·min~(-1). The content of 7 index components at each sampling point was measured by HPLC. The accumulative dissolution rate was calculated, the cumulative dissolution curve was drawn, and the dissolution models were fitted. The dissolution behaviors and the dissolution curve fitting equations of Fufang Danshen Pian in different batches and from different manufacturers in different dissolution mediums were quite different. The dissolution of the same preparation from different manufactures was different in the same dissolution medium, and the dissolution of different index components from the same manufacturer was not synchronized in the same dissolution medium; the dissolution behaviors of Fufang Danshen Pian in different batches and from different manufacturers in the same dissolution medium were different and greatly affected by pH value, indicating differences in the quality of Fufang Danshen Pian in different batches and from different manufacturers. This study provides scientific basis for the improvement in preparation process and the evaluation of batch consistency of Fufang Danshen Pian.
为比较复方丹参片的质量,考察不同批次、不同厂家的复方丹参片中7种指标成分在4种溶出介质中的溶出行为,并通过多条溶出曲线进行评价。采用桨法进行溶出试验,以pH 1.2盐酸盐缓冲液、pH 4.0醋酸盐缓冲液、蒸馏水和pH 6.8磷酸盐缓冲液作为溶出介质。转速为75 r·min-1。采用高效液相色谱法测定各取样点7种指标成分的含量。计算累积溶出率,绘制累积溶出曲线,并拟合溶出模型。不同批次、不同厂家的复方丹参片在不同溶出介质中的溶出行为及溶出曲线拟合方程差异较大。同一溶出介质中,不同厂家同一制剂的溶出情况不同,同一厂家不同指标成分在同一溶出介质中的溶出也不同步;不同批次、不同厂家的复方丹参片在同一溶出介质中的溶出行为存在差异,且受pH值影响较大,表明不同批次、不同厂家的复方丹参片质量存在差异。本研究为复方丹参片制备工艺的改进及批次一致性评价提供了科学依据。