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采用高效前沿分析结合混合胶束液相色谱法同时测定血浆中游离蛋白和总正电子发射断层扫描放射性配体浓度:在人血浆中[11C]PBR28 的应用。

Simultaneous determination of protein-free and total positron emission tomography radioligand concentrations in plasma using high-performance frontal analysis followed by mixed micellar liquid chromatography: application to [11C]PBR28 in human plasma.

机构信息

Department of Clinical Neuroscience, Center for Psychiatric Research, Karolinska Institute , Stockholm, Sweden.

出版信息

Anal Chem. 2013 Sep 17;85(18):8728-34. doi: 10.1021/ac401742v. Epub 2013 Sep 5.

Abstract

A two-dimensional liquid chromatographic (LC) system was developed for the determination of protein-free and total (free + bound forms) positron emission tomography (PET) radioligand concentrations in plasma by direct plasma injection. The unbound PET radioligand was first analyzed by high-performance frontal analysis using a short gel-filtration column and phosphate buffered saline solution as the mobile phase. All the collected effluent from the gel-filtration column was then transferred to the second dimension consisting of a monolithic C-18 column and mixed (anionic and nonionic surfactants) micellar eluent for determination of the total PET radioligand concentration. The simultaneous analysis of protein binding and radiometabolism of [(11)C]PBR28 was completed within 11 min without any pretreatment of plasma and employing a single analytical system. This system allowed highly sensitive analysis of total [(11)C]PBR28 with a limit of detection (LOD) of 1.6 becquerel (Bq). The LOD for the determination of unbound [(11)C]PBR28 was 21 Bq. Finally, simultaneous measurements of protein binding and radiometabolism of [(11)C]PBR28 in human plasma were achieved for up to 50 min after radioligand administration.

摘要

建立了二维液相色谱(LC)系统,用于直接血浆进样测定血浆中无蛋白和总(游离加结合形式)正电子发射断层扫描(PET)放射性配体浓度。首先通过使用短凝胶过滤柱和磷酸盐缓冲盐水作为流动相的高效前沿分析来分析游离的 PET 放射性配体。然后将凝胶过滤柱的所有洗脱液转移到第二维,由整体 C-18 柱和混合(阴离子和非离子表面活性剂)胶束洗脱液组成,用于测定总 PET 放射性配体浓度。无需对血浆进行任何预处理,仅使用单个分析系统,即可在 11 分钟内完成 [11C]PBR28 的蛋白结合和放射性代谢的同时分析。该系统允许对总 [11C]PBR28 进行高灵敏度分析,检测限(LOD)为 1.6 贝克勒尔(Bq)。游离 [11C]PBR28 的测定 LOD 为 21 Bq。最后,在放射性配体给药后长达 50 分钟内实现了人血浆中 [11C]PBR28 的蛋白结合和放射性代谢的同时测量。

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