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作 者:朱迪[1] 谭丹[1] 向文英[2] 孙佳[2,3] 李勇军[1,2] 王爱民[1,3]
机构地区:[1]贵州医科大学民族药与中药开发应用教育部工程研究中心,贵州贵阳550004 [2]贵州医科大学贵州省药物制剂重点实验室,贵州贵阳550004 [3]贵州医科大学药学院,贵州贵阳550004
出 处:《贵阳医学院学报》2015年第8期843-847,共5页Journal of Guiyang Medical College
摘 要:目的:建立中药饮片中黄曲霉毒素(AF)B1、B2、G1、G2含量测定的方法。方法:收集中药饮片87批,用免疫亲和柱进行AF的分离处理,采用高液相色谱(HPLC)柱后光化学衍生化法测定中药饮片中AFB1、AFB2、AFG1、AFG2含量并进行方法学分析。结果:被测定的AFB1、AFB2、AFG1、AFG2的检出限分别为0.7、0.3、0.6和0.3μg/kg,在选定的范围内线性关系良好(r≥0.999),精密度试验、重复性试验、准确度试验及标准样品验证试验结果均良好,87批中药饮片均未检出黄曲霉毒素。结论:免疫亲和柱-HPLC柱后光化学衍生化法操作简便,专属性强、灵敏度高,检测中药饮片中AFB1、AFB2、AFG1及AFG2的含量准确可靠。Objective:To establish a method for determination of aflatoxins in Chinese medicinal de-coction pieces and to promote quality control of Chinese medicinal decoction pieces. Methods:Eighty-seven batches of Chinese medicinal decoction pieces were collected and immunoaffinity column and HPLC with post column photochemical derivatization was adopted to measure aflatoxins content,inclu-ding aflatoxin B1,aflatoxin B2,aflatoxin G1,aflatoxin G2 in all samples. Results:The detection lim-it of aflatoxin B1 ,aflatoxin B2 ,aflatoxin G1 ,aflatoxin G2 was 0 . 7 ,0 . 3 ,0 . 6 and 0 . 3 μg/kg respec-tively. There was a a good linear relationship(r≥0. 999)in selected range of content. The results of precision test,repeatability test,accuracy test were good as well. In 87 different batches of Chinese medicinal decoction pieces,aflatoxins were not detected. Conclusion:The mothod of Immunoaffinity column and HPLC with post column photochemical derivatization is convenient,specific,sensitive,ac-curate and reliable in measuring aflatoxins content of Chinese medicinal decoction pieces.
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