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通过高压液相色谱法分离黄曲霉毒素B1、B2、G1和G2。

Resolution of aflatoxins B1, B2, G1, and G2 by high-pressure liquid chromatography.

作者信息

Pons W A

出版信息

J Assoc Off Anal Chem. 1976 Jan;59(1):101-5.

PMID:175044
Abstract

Aflatoxins were completely resolved as sharp peaks in the order BU-B2-G1-G2 by high-pressure liquid chromatography on a small particle (10 mum) porous silica gel column in 7-13 min (B1 through G2) by a water-saturated chloroform-cyclohexane-acetonitrile elution solvent (25+7.5+1.0), with detection by ultraviolet absorbance at 360 nm. The relationship between peak height and amount injected was linear over a 5-400 ng range for each aflatoxin. Both retention times and peak heights were highly reproducible, multiple injections of mixed standards giving coefficients of variation of 1.0-1.4% (retention time) and 1.6-2.8% (peak height) for the 4 aflatoxins. Detection was highly sensitive, with mean peak height, mm/ng, of 7.1 (B1), 6.4 (B2), 4.5 (G1), and 4.1(G2), allowing detection of 1-2 ng of each aflatoxin.

摘要

黄曲霉毒素在粒径为10微米的多孔硅胶柱上,通过高压液相色谱法,以水饱和的氯仿 - 环己烷 - 乙腈(25 + 7.5 + 1.0)为洗脱溶剂,在7 - 13分钟内(从B1到G2),按照BU - B2 - G1 - G2的顺序完全分离为尖锐的峰,通过在360纳米处的紫外吸光度进行检测。对于每种黄曲霉毒素,在5 - 400纳克范围内,峰高与进样量之间的关系呈线性。保留时间和峰高都具有高度的重现性,混合标准品多次进样时,4种黄曲霉毒素的保留时间变异系数为1.0 - 1.4%,峰高变异系数为1.6 - 2.8%。检测灵敏度很高,B1、B2、G1和G2的平均峰高(毫米/纳克)分别为7.1、6.4、4.5和4.1,每种黄曲霉毒素的检测限为1 - 2纳克。

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