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引用本文:孙婷,姜建国,郭永辉.HPLC测定比沙可啶肠溶片体外释放度[J].中国现代应用药学,2017,34(1):81-84.
SUN Ting,JIANG Jianguo,GUO Yonghui.Determination of the in Vitro Release of Bisacodyl Enteric-coated Tablets by HPLC[J].Chin J Mod Appl Pharm(中国现代应用药学),2017,34(1):81-84.
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HPLC测定比沙可啶肠溶片体外释放度
孙婷, 姜建国, 郭永辉
河北省药品检验研究院, 石家庄 050011
摘要:
目的 建立高效液相色谱法测定比沙可啶肠溶片的体外释放度。方法 采用Agilent ZORBAX SB-C18色谱柱(4.6 mm×150 mm,5 μm),以20 mmol·L-1的乙酸铵溶液(冰醋酸调节pH 5.0)-乙腈(45:55)为流动相,检测波长为265 nm。结果 比沙可啶在1.0~15 μg·mL-1内线性关系良好;平均回收率为100.4%,RSD为0.8%。A企业3批样品45 min内比沙可啶肠溶片的释放度分别为83%,81%,79%;B企业3批样品45 min内比沙可啶肠溶片的释放度分别为56%,59%,61%。结论 该释放度实验条件可以较客观地反映产品的内在质量,为不同厂家同一制剂质量的区分提供可靠依据。
关键词:  比沙可啶肠溶片  高效液相色谱法  体外释放度
DOI:10.13748/j.cnki.issn1007-7693.2017.01.019
分类号:
基金项目:
Determination of the in Vitro Release of Bisacodyl Enteric-coated Tablets by HPLC
SUN Ting, JIANG Jianguo, GUO Yonghui
Hebei Institute for Drug Control, Shijiazhuang 050011, China
Abstract:
OBJECTIVE To establish an HPLC method for the determination of the release rate of bisacodyl enteric-coated tablets. METHODS Agilent ZORBAX SB-C18 column(4.6 mm×150 mm, 5 μm) was used with the mobile phase of 20 mmol·L-1 ammonium acetate (acetic acid adjust pH 5.0)-acetonitrile(45:55), at the detection wavelength of 265 nm. RESULTS The calibration curve of bisacodyl was linear in the range of 1.0-15 μg·mL-1. The average recovery was 100.4%, with RSD of 0.8%. The bisacodyl release rate at 45 min of three batches of A samples were 83%, 81% and 79%; the bisacodyl release rate at 45 min of three batches of B samples were 56%, 59% and 61%. CONCLUSION The inherent quality of the product can be objectively reflected in the above conditions. Furthermore, it has a significant distinction of the same agents from different sources.
Key words:  bisacodyl enteric-coated tablet  HPLC  in vitro release
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