Suppr超能文献

培养细胞中谷胱甘肽的快速液相色谱测定法。

Rapid liquid chromatographic assay of glutathione in cultured cells.

作者信息

Leroy P, Nicolas A, Thioudellet C, Oster T, Wellman M, Siest G

机构信息

Laboratoire de Chimie Analytique et Bromatologie, URA CNRS 597, Faculté des Sciences Pharmaceutiques et Biologiques, Nancy, France.

出版信息

Biomed Chromatogr. 1993 Mar-Apr;7(2):86-9. doi: 10.1002/bmc.1130070208.

Abstract

A rapid, sensitive and selective method for the assay of glutathione in cultured cells has been developed using ion-pair reversed phase rapid high performance liquid chromatography. The use of a 4 micron particle, 5 cm long column (Superspher 100 RP 18 end-capped) allowed complete analysis of glutathione within 3 min. A postcolumn derivatization reaction with o-phthalaldehyde and fluorometric detection made the assay fully selective with regard to other endogenous thiols and sensitive (the detection limit was 0.5 ng of glutathione injected). The linearity range was between 0.1 and 2.0 microgram/mL with good repeatability (relative standard deviation less than 5% for the lowest concentration quantitated). Recoveries of GSH from cultured cell samples were above 98%. The rapid analysis enabled the processing of a large number of samples in a short time (up to 20 per hour). The method was applied to the measurement of the intracellular glutathione amount in V79 fibroblasts along cell growth in culture.

摘要

已开发出一种使用离子对反相快速高效液相色谱法测定培养细胞中谷胱甘肽的快速、灵敏且选择性高的方法。使用一根4微米粒径、5厘米长的色谱柱(Superspher 100 RP 18封端柱)可在3分钟内完成谷胱甘肽的完整分析。与邻苯二甲醛的柱后衍生反应及荧光检测使该测定方法对其他内源性硫醇具有完全选择性且灵敏(检测限为进样0.5纳克谷胱甘肽)。线性范围为0.1至2.0微克/毫升,具有良好的重复性(最低定量浓度的相对标准偏差小于5%)。培养细胞样品中谷胱甘肽的回收率高于98%。这种快速分析能够在短时间内处理大量样品(每小时最多20个)。该方法应用于测定培养的V79成纤维细胞在细胞生长过程中的细胞内谷胱甘肽含量。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验