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Rapid determination of atropine and scopolamine content in scopolia extract powder by HPLC

机译:HPLC快速测定东determination提取物中粉末中阿托品和东pol碱的含量

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A rapid method that does not require a complicated preparation was developed for determining by HPLC the content of atropine (At) and scopolamine (Sc) in a sample of scopolia extract powder. The sample solution for HPLC was extracted using 0.1 mol/L HC1/ methanol (8:2). At and Sc were separated using a penta-fluorophenylpropyl column and detected at a wavelength of 210 nm. Acetonitrile-10 mmol/L ammonium acetate adjusted to pH 5.0 (8:2, v/v) was used as the mobile phase. The linearity was good in the 5.0-500 mug/mL range for At and 0.5-500 mug/mL range for Sc. The specificity for both At and Sc was satisfactory. The quantitation limits were 5.0 mug/mL for At and 0.5 mug/mL for Sc. The quantitative values of total alkaloid calculated using this method were higher (1.3-3.7%) than those obtained using the Japanese Pharmacopoeia Fifteenth Edition (JP15) method. The precision of this method, measured as the standard deviation, was found to be satisfactory and comparable to that of the JP15 method, determined by an analysis of 3 commercial scopolia extract powder samples.
机译:开发了一种无需复杂制备方法的快速方法,用于通过HPLC测定东poli提取物粉末样品中阿托品(At)和东pol碱(Sc)的含量。 HPLC的样品溶液用0.1 mol / L HC1 /甲醇(8:2)萃取。使用五氟苯基丙基柱分离At和Sc,并在210 nm波长处检测。将乙腈-10 mmol / L醋酸铵调节至pH 5.0(8:2,v / v)作为流动相。线性度在At的5.0-500杯/ mL范围和Sc的0.5-500杯/ mL范围内良好。 At和Sc的特异性均令人满意。 At的定量限为5.0杯/ mL,Sc的定量限为0.5杯/ mL。使用该方法计算出的总生物碱的定量值要比使用日本药典第十五版(JP15)方法获得的定量值更高(1.3-3.7%)。通过对3种商用天花粉提取物粉末样品进行分析确定,该方法的精密度(以标准偏差衡量)令人满意,可与JP15方法相媲美。

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