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机构地区:[1]浙江省药品检验所,杭州310004 [2]浙江大学医学院附属邵逸夫医院,杭州310016 [3]浙江中医药大学,杭州310053
出 处:《中国抗生素杂志》2007年第7期414-418,共5页Chinese Journal of Antibiotics
摘 要:目的采用反相高效液相色谱法测定阿奇霉素软胶囊中阿奇霉素的含量。方法用耐碱性的十八烷基硅烷键合硅胶柱为固定相,以水∶0.01mol/L磷酸氢二钠溶液(用氢氧化钠试液调节pH值至10.3)∶乙腈(16.7∶23.3∶60)为流动相,流速1.5ml/min,柱温40℃,检测波长210nm。结果阿奇霉素主成分峰与相邻杂质峰分离状况良好;空白辅料植物油不干扰阿奇霉素主成分的分离检测。阿奇霉素在0.2052~1.9207μg/ml的浓度范围内质量与峰面积呈良好的线性关系;在添加了空白油辅料的体系中在0.1995~2.0147μg/ml的浓度范围内质量与峰面积呈良好的线性关系。在添加了空白油辅料的体系中阿奇霉素的最低检测浓度为1.0483~2.0966μg/ml,最低定量浓度为4.1932~10.483μg/ml。准确性试验的平均回收率为101.4%,RSD为0.2%(n=9);重复性试验的平均含量为98.0%,RSD为1.0%(n=9)。结论方法专属性强,精密、准确、耐用,可替代抗生素微生物检定法作为阿奇霉素软胶囊的含量测定方法。Objective To established a high performance liquid chromatography method for determination of azithromycin soft capsules. Methods A high pH stability column (Agilent Zorbax Extend-C18, 4.6mm× 150mm, 5μm) was used; the mobile phase consisted of water : 0. 01mol/L dibasic sodium phosphate buffer solution (the pH value was adjusted to 10.3 by sodium hydroxide T. S. ): acetonitrile (16.7 : 23.3 : 60) ; the flow rate was 1.5ml/min; and the UV detection wavelength was at 210nm. Results The good resolution between peaks of azithromycin and of the adjacent purity was obtained. The blank excipient soybean oil did not interfere with the detection of azithromycin. The linear range for azithromycin was 0. 2052- 1. 9207 μg/ml, and the actual linear range for azithromycin in simulated samples spiked with soybean oil excipient was 0. 1995-2. 0147 μg/ml. The LOD of azithromycin in simulated samples spiked with soybean oil excipient was 1. 0483-2. 0966 μg/ml, and the LOQ was 4. 1932-10.483 μg/ml. The average recovery 101.4% was obtained with a RSD of 0.2%; and the average content 98.0% was obtained from the precision test; and the RSD was 1.0% (n=9). Conclusion The method is specific, precise, accurate and robust. It's suitable for the content determination of azithromycin soft capsules.
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