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用于定量测定加兰他敏的酶免疫测定法。

Enzyme immunoassay for the quantitative determination of galanthamine.

作者信息

Poulev A, Deus-Neumann B, Zenk M H

机构信息

Lehrstuhl für Pharmazeutische Biologie, Universität München, Karlstraße 29, D-80333 München, Federal Republic of Germany.

出版信息

Planta Med. 1993 Oct;59(5):442-6. doi: 10.1055/s-2006-959728.

Abstract

An enzyme immunoassay for the quantitation of fmol amounts of the therapeutically important Amaryllidaceae alkaloid, galanthamine, was established. The antiserum was raised against a conjugate of galanthamine-2- O-hemisuccinate-bovine serum albumin. The antibodies used were isolated and purified by Rivanol treatment with subsequent (NH (4)) (2)SO (4) precipitation. The measuring range of the assay extends from 2 to lOO pg of galanthamine, and as little as 3.5 fmol may be detected. The antibodies are highly specific for galanthamine, showing no cross reactivity with several Amaryllidaceae alkaloids. This assay allows the rapid, sensitive and precise quantitation of galanthamine in unpurified plant extracts as well as biological fluids. The galanthamine content in a variety of herbarium material as well as the frequency distribution of galanthamine in 1000 LEUCOJUM AESTIVUM plants from various origins in South Bulgaria have been investigated. The preliminary results demonstrate that the galanthamine-specific enzyme immunoassay can be a useful tool in medicinal plant breeding, for screening programs, as well as for taxonomic and pharmacokinetic studies.

摘要

建立了一种酶免疫分析法,用于定量测定治疗上重要的石蒜科生物碱加兰他敏的飞摩尔量。抗血清是针对加兰他敏-2-O-半琥珀酸酯-牛血清白蛋白的偶联物产生的。所使用的抗体通过利凡诺处理并随后用硫酸铵沉淀进行分离和纯化。该分析方法的测量范围为2至100 pg加兰他敏,最低可检测到3.5飞摩尔。这些抗体对加兰他敏具有高度特异性,与几种石蒜科生物碱无交叉反应。该分析方法可对未纯化的植物提取物以及生物体液中的加兰他敏进行快速、灵敏和精确的定量。研究了各种标本馆材料中的加兰他敏含量以及来自保加利亚南部不同产地的1000株夏水仙植物中加兰他敏的频率分布。初步结果表明,加兰他敏特异性酶免疫分析法可成为药用植物育种、筛选计划以及分类学和药代动力学研究的有用工具。

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引用本文的文献

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Influence of plant origin on propagation capacity and alkaloid biosynthesis during long-term cultivation of L.
In Vitro Cell Dev Biol Plant. 2009;45(4):458-465. doi: 10.1007/s11627-008-9178-2. Epub 2008 Dec 6.

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