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荧光液相色谱法测定牛奶中8种中性β-内酰胺类青霉素的多残留方法

Multiresidue method for determination of eight neutral beta-lactam penicillins in milk by fluorescence-liquid chromatography.

作者信息

Munns R K, Shimoda W, Roybal J E, Vieira C

出版信息

J Assoc Off Anal Chem. 1985 Sep-Oct;68(5):968-71.

PMID:4055646
Abstract

A method of determining total penicillins begins with an enzymatic hydrolysis of the beta-lactam ring to form their respective penicilloate product. Acetonitrile precipitates much of the casein and protein, which are then separated from the liquid by centrifugation. The lipids are removed from the aqueous fraction with methylene chloride. Mercuric chloride is added, which reacts with the penicilloate to liberate the side chain that has a terminal aldehyde. These penilloaldehyde products are extracted with methylene chloride and are subsequently reacted with dansyl hydrazine. The resulting fluorolabeled side chains are separated by liquid chromatography on a C18 column with acetonitrile-water as mobile phase. The fluorescence is measured by the mercury line at 254 nm excitation wavelength and a 500 nm filter on the emission side. The overall average recoveries from milk spiked at 25, 50, and 100 ppb are benzyl penicillin 79.4%; phenoxymethyl penicillin 59.7%; phenethicillin 75.9%; nafcillin 87.7%; methacillin 47.5%; oxacillin 57.6%; cloxicillin 37.3%; and dicloxicillin 26.4%.

摘要

一种测定总青霉素的方法,首先是通过酶促水解β-内酰胺环以形成各自的青霉素酸盐产物。乙腈会沉淀大部分酪蛋白和蛋白质,然后通过离心将它们与液体分离。用二氯甲烷从水相中去除脂质。加入氯化汞,其与青霉素酸盐反应以释放具有末端醛的侧链。这些青霉醛产物用二氯甲烷萃取,随后与丹磺酰肼反应。所得的荧光标记侧链通过以乙腈 - 水为流动相在C18柱上进行液相色谱分离。在激发波长为254nm的汞线和发射侧的500nm滤光片下测量荧光。在25、50和100 ppb加标的牛奶中的总体平均回收率分别为:苄青霉素79.4%;苯氧甲基青霉素59.7%;苯乙青霉素75.9%;萘夫西林87.7%;甲氧西林47.5%;苯唑西林57.6%;氯唑西林37.3%;双氯西林26.4%。

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