首页> 外文期刊>Natural medicines =: 生薬学雜誌 >Simple and rapid analysis of aristolochic acid contained in crude drugs and Kampo formulations with solid-phase extraction and HPLC photodiode-array detection.
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Simple and rapid analysis of aristolochic acid contained in crude drugs and Kampo formulations with solid-phase extraction and HPLC photodiode-array detection.

机译:固相萃取和HPLC光电二极管阵列检测可对粗药物和Kampo制剂中的马兜铃酸进行简单,快速的分析。

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摘要

Simple and rapid analysis of aristolochic acid (AA) in crude drugs and Kampo extracts using a solid-phase extraction method and HPLC-PDA analysis was investigated. Extraction of AA from samples was accomplished by adding methanol containing 1% ammonia. The addition of ammonia ionized the AA of acidic substances so that they adhered to an acrylamide copolymer of a strong anion exchange resin (Sep-Pak QMA) coupled to diol silica easily. Furthermore, a mixture of acetonitrile-water-phosphoric acid (75:25:2, v/v) was effective in isolating AA from its carrier. Since almost all interfering peaks originating from contaminants in crude drugs and Kampo extract formulations could be removed, a satisfactory HPLC chromatogram of AA was obtained. A good result was also obtained when Aristolochiaceae and crude drugs containing AA were tested. Particularly in the case of the medicinal parts of Asarum, several interfering peaks and a ghost peak detected near the AA peak were eliminated. The AA contents of two Kampo extract formulations, tokishigyakukagoshuyushokyoto and ryutanshakanto, were calculated by HPLC analysis. The AA content (the sum of AA-I and AA-II) was 1.25-6.13 mg per daily dose. From an additional recovery experiment for Kampo formulations, high recovery rates of AA were obtained. Neither LC/MS nor special instrumentation was necessary. Our results suggest that this simple, quick, and sensitive analytical method to detect AA in crude drugs and Kampo extract formulations would be valuable in safety inspections of AA in crude drugs and their products.
机译:研究了使用固相萃取方法和HPLC-PDA分析方法对粗药和甘草提取物中的马兜铃酸(AA)进行简单,快速的分析。通过添加含1%氨的甲醇从样品中提取AA。氨的加入使酸性物质的AA离子化,从而使它们粘附到与二醇二氧化硅偶联的强阴离子交换树脂(Sep-Pak QMA)的丙烯酰胺共聚物上。此外,乙腈-水-磷酸的混合物(75:25:2,v / v)可有效地从其载体中分离出AA。由于几乎可以去除所有来自粗药和坎波提取物制剂中污染物的干扰峰,因此获得了令人满意的AA HPLC色谱图。当测试马兜铃科和含有AA的粗制药物时,也获得了良好的结果。特别是在细辛的药用部位中,消除了几个干扰峰和在AA峰附近检测到的重影峰。通过HPLC分析来计算两种汉方提取物制剂tokishigyakukagoshuyushokyoto和ryutanshakanto的AA含量。 AA含量(AA-I和AA-II之和)为每日剂量1.25-6.13 mg。从针对甘宝制剂的另一回收实验中,获得了较高的AA回收率。无需LC / MS或特殊仪器。我们的结果表明,这种简单,快速,灵敏的分析方法可检测粗药物和汉方提取物制剂中的氨基酸,这对粗药物及其产品中的AA的安全性检查非常有价值。

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