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Simultaneous determination of asiaticoside and its novel metabolites in culture of Aspergilus niger by SPE-HPLC

机译:固相萃取-高效液相色谱法同时测定黑曲霉培养物中积雪草苷及其新代谢产物

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When cultured with Aspergillus niger, asiaticoside, purified from Centella Asiatica (L.) Urban, was metabolized into four metabolites including one novel alkaloid. A simple and rapid SPE-HPLC method for simultaneous determination of asiaticoside and its four metabolites in culture of A. niger was developed. The chromatographic separation was achieved on a Dikma Diamonsi C18 ODS column (200×4.6 mm i.d.) by gradient elution with 0.1% phosphoric acid in water and 0.1% phosphoric acid in methanol as the gradient mixtures. The flow rate was 1 mL/min, the detection wavelength was 204 nm and the column temperature was kept at 28°C. The retention times of asiaticoside, asiatic acid, M1, M2, and M3 were 11.3, 9.4 and 17.1, 19.3 and 7.9 min, respectively. The mean recoveries of five analysts were all over 99%. Quantification limits were 0.02 µg/mL for all tested compounds. The method was sucessively applied to the quantification of the biotransformation of asiaticoside.
机译:用黑曲霉培养时,从积雪草(L.)Urban纯化的积雪草苷被代谢为四种代谢物,其中包括一种新型生物碱。建立了同时测定黑曲霉培养物中积雪草苷及其四种代谢物的简单,快速的SPE-HPLC方法。在Dikma Diamonsi C18 ODS色谱柱(200×4.6 mm i.d.)上进行色谱分离,方法是使用0.1%的磷酸水溶液和0.1%的甲醇磷酸溶液作为梯度混合物进行梯度洗脱。流速为1 mL / min,检测波长为204 nm,柱温保持在28°C。积雪草苷,积雪草酸,M 1 ,M 2 和M 3 的保留时间分别为11.3、9.4和17.1、19.3和7.9分钟, 分别。五位分析师的平均回收率均超过99%。所有测试化合物的定量限为0.02 µg / mL。该方法成功地应用于积雪草苷生物转化的定量分析。

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