首页> 外文期刊>Biomedical Chromatography: An International Journal Devoted to Research in Chromatographic Methodologies and Their Applications in the Biosciences >Simultaneous determination of swertiamarin and its metabolites (5Z)-5-ethylidene-8-hydroxy-3,4,5,6,7,8-hexahydro-1H-pyrano(3,4-c)pyridin-1-one and erythrocentaurin in broth of Aspergillus niger by HPLC.
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Simultaneous determination of swertiamarin and its metabolites (5Z)-5-ethylidene-8-hydroxy-3,4,5,6,7,8-hexahydro-1H-pyrano(3,4-c)pyridin-1-one and erythrocentaurin in broth of Aspergillus niger by HPLC.

机译:同时测定swertiamarin及其代谢物(5Z)-5-亚乙基-8-羟基-3,4,5,6,7,8-六氢-1H-吡喃(3,4-c)吡啶-1-酮和赤藓铁蛋白通过HPLC在黑曲霉的肉汤中提取。

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摘要

When cultivated with Aspergillus niger, swertiamarin, an important drug, is rapidly transformed into erythrocentaurin and (5Z)-5-ethylidene-8-hydroxy-3,4,5,6,7,8-hexahydro-1H-pyrano[3,4-c]pyridin-1-one (M(1)), a new compound with high anti-inflammatory activity. A simple and rapid HPLC method for simultaneous determination of swertiamarin and its two metabolites in broth of A. niger is described. The chromatographic separation was achieved on a C(18) ODS column (250 x 4.6 mm i.d.) by gradient elution with 0.04% formic acid in water and 0.04% formic acid in acetonitrile as the gradient mixtures. The flow rate was 1 mL/min, the detection wavelength was 237 nm and the column temperature was kept at 30 degrees C. The retention times of swertiamarin, erythrocentaurin and M(1) were 14.6, 16.8 and 24.8 min, respectively. The mean absolute recoveries of three analysts were over 96%. Quantification limits were 0.02 microg/mL for swertiamarin and 0.05 microg/mL for both of the two metabolites. The method was applied for the quantification of swertiamarin and its two metabolites during the fermentation process and the evaluation of the bioavailabilities in the Caco-2 monolayer.
机译:与黑曲霉一起培养时,一种重要的药物swertiamarin迅速转化为赤藓铁蛋白和(5Z)-5-亚乙基-8-羟基-3,4,5,6,7,8-六氢-1H-吡喃[3, 4-c]吡啶-1-酮(M(1)),一种具有高抗炎活性的新化合物。描述了一种同时测定黑曲霉肉汤中苦味松素及其两种代谢物的简单而快速的HPLC方法。色谱分离是在C(18)ODS色谱柱(250 x 4.6 mm i.d.)上通过以0.04%甲酸的水溶液和0.04%甲酸的乙腈溶液作为梯度混合物进行梯度洗脱而实现的。流速为1 mL / min,检测波长为237 nm,柱温保持在30摄氏度。swertiamarin,erythrocentaurin和M(1)的保留时间分别为14.6、16.8和24.8 min。三位分析师的平均绝对回收率超过96%。 Swertiamarin的定量限为0.02 microg / mL,两种代谢物的定量限均为0.05 microg / mL。该方法适用于发酵过程中的swertiamarin及其两种代谢产物的定量以及Caco-2单层生物利用度的评估。

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