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酶催化的迈克尔加成法合成华法林及其通过 l-色氨酸的荧光猝灭法测定。

Enzyme-catalyzed Michael addition for the synthesis of warfarin and its determination via fluorescence quenching of l-tryptophan.

机构信息

Key Laboratory of Luminescent and Real-Time Analytical Chemistry (Southwest University), Ministry of Education, College of Chemistry and Chemical Engineering, Southwest University, Chongqing 400715, China.

College of Chemical and Environmental Engineering, Chongqing Three Gorges University, Wanzhou, Chongqing 404100, China.

出版信息

Spectrochim Acta A Mol Biomol Spectrosc. 2017 Apr 5;176:183-188. doi: 10.1016/j.saa.2017.01.014. Epub 2017 Jan 9.

Abstract

A sensitive fluorescence sensor for warfarin was proposed via quenching the fluorescence of l-tryptophan due to the interaction between warfarin and l-tryptophan. Warfarin, as one of the most effective anticoagulants, was designed and synthesized via lipase from porcine pancreas (PPL) as a biocatalyst to catalyze the Michael addition of 4-hydroxycoumarin to α, β-unsaturated enones in organic medium in the presence of water. Furthermore, the spectrofluorometry was used to detect the concentration of warfarin with a linear range and detection limit (3σ/k) of 0.04-12.0μmolL (R=0.994) and 0.01μmolL, respectively. Herein, this was the first application of bio-catalytic synthesis and fluorescence for the determination of warfarin. The proposed method was applied to determine warfarin of the drug in tablets with satisfactory results.

摘要

通过酶促迈克尔加成反应,利用猪胰脂肪酶作为生物催化剂,在水相存在的条件下,于有机相中催化 4-羟基香豆素与α,β-不饱和烯酮的迈克尔加成反应,设计并合成了华法林。由于华法林与 l-色氨酸之间的相互作用,导致 l-色氨酸的荧光猝灭,从而构建了一种对华法林敏感的荧光传感器。此外,采用荧光光谱法检测华法林的浓度,线性范围和检测限(3σ/k)分别为 0.04-12.0μmol·L(R=0.994)和 0.01μmol·L。这是首次将生物催化合成与荧光法应用于华法林的测定。该方法用于测定片剂中的华法林,结果令人满意。

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