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高压液相色谱法测定谷物和动物饲料中的黄天精

High pressure liquid chromatographic determination of xanthomegnin in grains and animal feeds.

作者信息

Carman A S, Kuan S S, Francis O J, Ware G M, Gaul J A, Thorpe C W

出版信息

J Assoc Off Anal Chem. 1983 May;66(3):587-91.

PMID:6863178
Abstract

A high pressure liquid chromatographic (HPLC) method is described for the determination of xanthomegnin in grains and mixed animal feeds at levels ranging from 150 to 1200 ng/g. This is equivalent to actual amounts of xanthomegnin injected on the HPLC system at from 15 to 120 ng/injection. Xanthomegnin is extracted with chloroform and 0.1M phosphoric acid. An aliquot of the crude extract is purified by column chromatography using a commercially available silica gel cartridge. Xanthomegnin is then separated from the remaining interferences by HPLC with a reverse phase C-8 column, and subsequently determined by absorbance detection at 405 nm. Elapsed time for the method from initial extraction to final HPLC determination is approximately 1 h. Recoveries of xanthomegnin added to grains and animal feeds at levels from 150 to 1200 ng/g averaged 82% with a coefficient of variation of 10.2%.

摘要

描述了一种高压液相色谱(HPLC)方法,用于测定谷物和混合动物饲料中含量范围为150至1200 ng/g的黄天精。这相当于在HPLC系统上每次进样15至120 ng的黄天精实际量。黄天精用氯仿和0.1M磷酸提取。粗提取物的一份等分试样通过使用市售硅胶柱进行柱色谱纯化。然后用反相C-8柱通过HPLC将黄天精与其余干扰物分离,随后通过在405 nm处的吸光度检测进行测定。该方法从初始提取到最终HPLC测定的耗时约为1小时。添加到谷物和动物饲料中含量为150至1200 ng/g的黄天精的回收率平均为82%,变异系数为10.2%。

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