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采用高效液相色谱法测定激发后的人白细胞制剂中的组胺。

The determination of histamine in challenged human leukocyte preparations by high-performance liquid chromatography.

作者信息

Leino L, Juhakoski A, Lauren L

机构信息

Department of Biochemistry, Turku University, Finland.

出版信息

Agents Actions. 1990 Nov;31(3-4):178-82. doi: 10.1007/BF01997605.

Abstract

A highly sensitive and rapid method was developed for the determination of histamine in challenged human leukocyte preparations by high-performance liquid chromatography. The assay is based on the Shore's OPT-reaction of the unpurified sample and on a specific separation of the derivate with analytical reversed phase phenyl column combined with spectrofluorometric detection. The detection limit of histamine by this method was 0.07 pmol (signal to noise ratio 2:1) and the within-day variation for peak height was 3.6% and for retention time 0.8%. A good linear standard curve ranging from 12.5 pg to 500 pg (0.07 pmol-2.7 pmol) was obtained with correlation coefficient of 0.998. The histamine release from human basophils in mixed leukocyte preparation was induced by the calcium ionophore A 23187. A concentration of 0.4 micrograms/ml ionophore was required for 50% histamine release with a Ca2(+)-concentration of 1.8 mmol/l. The measured total histamine content was 1.5 pg/basophil.

摘要

建立了一种高灵敏度、快速的高效液相色谱法,用于测定激发后的人白细胞制剂中的组胺。该测定基于未纯化样品的肖尔OPT反应,以及使用反相苯基分析柱结合荧光检测对衍生物进行特异性分离。该方法对组胺的检测限为0.07皮摩尔(信噪比2:1),日内峰高变化为3.6%,保留时间变化为0.8%。获得了良好的线性标准曲线,范围为12.5皮克至500皮克(0.07皮摩尔至2.7皮摩尔),相关系数为0.998。混合白细胞制剂中人类嗜碱性粒细胞的组胺释放由钙离子载体A 23187诱导。在钙离子浓度为1.8毫摩尔/升的情况下,50%组胺释放需要0.4微克/毫升的离子载体浓度。测得的总组胺含量为1.5皮克/嗜碱性粒细胞。

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