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作 者:郑伊琳 郑付春[2] 李春泉 李妙霞 陈潮升 叶丹彦[1] 陈沛洪 陈一村[1]
机构地区:[1]汕头大学医学院药理教研室,广东汕头515041 [2]汕头大学医学院第一附属医院药剂科,广东汕头515041 [3]广东汇群中药饮片股份有限公司,广东汕头515041
出 处:《癌变.畸变.突变》2016年第4期310-313,328,共5页Carcinogenesis,Teratogenesis & Mutagenesis
基 金:汕头市科技局科技计划项目[汕市财教(2014)242号];广东汇群特派员工作站建设(20150905)
摘 要:目的:采用高效液相色谱法测定余甘子中没食子酸的含量,优化色谱条件,比较3个来源余甘子中没食子酸的含量差异。方法:分别对来自云南大理(2个批号)和福建漳州的余甘子中没食子酸进行含量测定,色谱条件为十八烷基硅烷键合硅胶色谱柱(粒径25μm,柱直径4.6 mm,柱长250 mm);流动相乙腈-0.2%磷酸水溶液(5∶95);等度洗脱;流速1.000 m L/min;检测波长2273nm;柱温30℃,标准曲线外标法。结果:没食子酸在13.010~130.104μg/m L范围内与峰面积有明显线性关系(R=0.999 4);精密度良好[相对标准偏差(RSD)=0.08%];稳定性良好(RSD=0.29%);重现性一般(RSD=4.23%)。对3批来自不同产地批号的余甘子药材进行了没食子酸含量评价,结果显示3个批次(福建20150304、云南20150205、云南20150304)的余甘子中没食子酸含量分别为2.60%、3.38%和2.82%,3个批次的余甘子中没食子酸含量均高于《中国药典》国家标准1.2%。结论:本方法测定余甘子中的没食子酸含量专属性强、精密度好、结果准确可靠。OBJECTIVE: To optimize chromatographic conditions for determination of gallic acid contents inPhyllanthus emblica L. from different regions. METHODS:Determination of gallic acid in Phyllanthus emblica L. indifferent regions was performed on an Eclipse plus C18 (25 μm,4.6 mm×250 mm). The mobile phase was Acetonitrile-0.2% phosphoric acid solution (5∶ 95). The elution was in same degree. The current speed was 1.000 mL/min. Thedetection wave length was 273 nm and the determination of linear regression equation used standard curve method. Thecolumn temperature was 30 degrees Celsius. RESULTS:Gallic acid had a good linear relationship in the range of2 13.010-130.104 g/mL (R =0.999 4). It also had good precision (RSD=0.08%),good stability (RSD=0.29%) and generalreproducibility (RSD=4.23%). The content of gallic acid in the three batches of Phyllanthus emblica L. were higher thanChinese Pharmacopoeia national standard of 1.2%. CONCLUSION:The method for the determination of gallic acid inPhyllanthus emblica showed strong specificity and good precision. In addition,the results were accurate and reliable.
分 类 号:R917[医药卫生—药物分析学]
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