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Solid Phase Microextraction-Based Miniaturized Probe and Protocol for Extraction of Neurotransmitters from Brains in Vivo

机译:基于固相微萃取的小型化探针及其在体内从大脑中提取神经递质的方案

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摘要

Despite the importance of monitoring and correlating neurotransmitter concentrations in the brain with observable behavior and brain areas in which they act, in vivo measurement of multiple neurochemicals in the brain remains a challenge. Here, we propose an alternative solid phase microextraction-based (SPME) chemical biopsy approach as a viable method for acquirement of quantitative information on multiple neurotransmitters by one device within a single sampling event, with multisite measurement capabilities and minimized invasiveness, as no tissue is removed. The miniaturized SPME probe developed for integrated in vivo sampling/sample preparation has been thoroughly optimized with respect to probe shape, desorption solvent, and extracting phase tailored for extraction of small hydrophilic molecules via synthesis and functionalization of coating. Experimental evaluations of sampling time and storage strategy led to achieving appropriate temporal resolution versus recovery balance as well as little or no analyte loss, respectively. Validation of the developed SPME-HPLC-MS/MS protocol in a surrogate brain matrix yielded satisfactory accuracies of 80-100%, precision below 17%, as well as linear dynamic range and limits of quantitation suitable for determining neurochemicals at physiologically relevant levels. Finally, we present a proof-of concept in vivo application in macaque brain, where several target neurotransmitters were extracted simultaneously from three brain areas. The developed probe and protocol are herein presented as a potential powerful addition to the existing in vivo toolbox for measurements of local levels of neurochemicals in multiple brain systems implicated in the neuropathology of psychiatric disorders.
机译:尽管监测和关联大脑中神经递质浓度的重要性,但在其行为的可观察行为和脑区,仍然是大脑中多种神经化素的测量仍然是挑战。在这里,我们提出了一种替代的固相微萃取基(SPME)化学活检方法,作为一种可行的方法,用于在单个采样事件中通过一个设备在单个采样事件中获取多个神经递质的定量信息,具有多态测量能力和最小化的侵入性,因为没有组织删除了。用于集成体内采样/样品制剂的小型化SPME探针已经相对于探针形状,解吸溶剂和萃取阶段通过合成和涂层官能化而彻底地优化。采样时间和储存策略的实验评估导致实现适当的时间分辨率与恢复余额以及少数或没有分析物损失。在替代脑基质中验证的SPME-HPLC-MS / MS协议产生令人满意的令人满意的80-100%,精度低于17%,以及适合在生理相关水平确定神经化学的线性动态范围和定量限制。最后,我们在猕猴的体内施用中呈现了一种概念,其中几种靶神经递质从三个脑区域同时提取。本文介绍了发育的探针和方案作为存在于体内工具箱中存在的潜在的强力补充,用于测量涉及精神病疾病神经病理学中的多种脑系统中的神经化学水平的局部水平。

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  • 来源
    《Analytical chemistry》 |2019年第7期|共10页
  • 作者单位

    Univ Waterloo Dept Chem 200 Univ Ave West Waterloo ON N2L 3G1 Canada;

    Vanderbilt Univ Dept Psychol PMB 407817 2301 Vanderbilt Pl Nashville TN 37240 USA;

    Univ Waterloo Dept Chem 200 Univ Ave West Waterloo ON N2L 3G1 Canada;

    Univ Waterloo Dept Chem 200 Univ Ave West Waterloo ON N2L 3G1 Canada;

    Vanderbilt Univ Dept Psychol PMB 407817 2301 Vanderbilt Pl Nashville TN 37240 USA;

    Univ Waterloo Dept Chem 200 Univ Ave West Waterloo ON N2L 3G1 Canada;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 分析化学;
  • 关键词

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