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液相色谱串联质谱分析中降低基质效应的系统全面策略

Systematic and comprehensive strategy for reducing matrix effects in LC/MS/MS analyses.

作者信息

Chambers Erin, Wagrowski-Diehl Diane M, Lu Ziling, Mazzeo Jeffrey R

机构信息

Chemistry Applied Technology, Waters Corporation, 34 Maple Street, Milford, MA 01757, USA.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2007 Jun 1;852(1-2):22-34. doi: 10.1016/j.jchromb.2006.12.030. Epub 2007 Jan 3.

Abstract

A systematic, comprehensive strategy that optimizes sample preparation and chromatography to minimize matrix effects in bioanalytical LC/MS/MS assays was developed. Comparisons were made among several sample preparation methods, including protein precipitation (PPT), liquid-liquid extraction (LLE), pure cation exchange solid-phase extraction (SPE), reversed-phase SPE and mixed-mode SPE. The influence of mobile phase pH and gradient duration on the selectivity and sensitivity for both matrix components and basic analytes was investigated. Matrix effects and overall sensitivity and resolution between UPLC technology and HPLC were compared. The amount of specific matrix components, or class of matrix components, was measured in the sample preparation extracts by LC/MS/MS with electrospray ionization (ESI) using both precursor ion scanning mode and multiple reaction monitoring (MRM). PPT is the least effective sample preparation technique, often resulting in significant matrix effects due to the presence of many residual matrix components. Reversed-phase and pure cation exchange SPE methods resulted in cleaner extracts and reduced matrix effects compared to PPT. The cleanest extracts, however, were produced with polymeric mixed-mode SPE (both reversed-phase and ion exchange retention mechanisms). These mixed-mode sorbents dramatically reduced the levels of residual matrix components from biological samples, leading to significant reduction in matrix effects. LLE also provided clean final extracts. However, analyte recovery, particularly for polar analytes, was very low. Mobile phase pH was manipulated to alter the retention of basic compounds relative to phospholipids, whose retention tends to be relatively independent of pH. In addition to the expected resolution, speed and sensitivity benefits of UPLC technology, a paired t-test demonstrated a statistically significant improvement with respect to matrix effects when this technology was chosen over traditional HPLC. The combination of polymeric mixed-mode SPE, the appropriate mobile phase pH and UPLC technology provides significant advantages for reducing matrix effects resulting from plasma matrix components and in improving the ruggedness and sensitivity of bioanalytical methods.

摘要

我们开发了一种系统、全面的策略,该策略优化了样品制备和色谱分析,以尽量减少生物分析液相色谱/串联质谱(LC/MS/MS)检测中的基质效应。我们比较了几种样品制备方法,包括蛋白沉淀法(PPT)、液液萃取法(LLE)、纯阳离子交换固相萃取法(SPE)、反相固相萃取法和混合模式固相萃取法。研究了流动相pH值和梯度持续时间对基质成分和碱性分析物的选择性及灵敏度的影响。比较了超高效液相色谱(UPLC)技术和高效液相色谱(HPLC)之间的基质效应以及整体灵敏度和分离度。使用电喷雾电离(ESI)的LC/MS/MS在前体离子扫描模式和多反应监测(MRM)模式下测定了样品制备提取物中特定基质成分或基质成分类别的含量。PPT是效果最差的样品制备技术,由于存在许多残留基质成分,常常会导致显著的基质效应。与PPT相比,反相和纯阳离子交换固相萃取法能得到更纯净的提取物,并减少基质效应。然而,最纯净的提取物是用聚合物混合模式固相萃取法(同时具有反相和离子交换保留机制)制备的。这些混合模式吸附剂显著降低了生物样品中残留基质成分的水平,从而大幅降低了基质效应。LLE也能提供纯净的最终提取物。然而,分析物回收率,尤其是极性分析物的回收率非常低。通过调节流动相pH值来改变碱性化合物相对于磷脂的保留情况,磷脂的保留往往相对不受pH值影响。除了UPLC技术预期的分离度、速度和灵敏度优势外,配对t检验表明,与传统HPLC相比,选择该技术时在基质效应方面有统计学上的显著改善。聚合物混合模式固相萃取法、合适的流动相pH值和UPLC技术的结合,在减少血浆基质成分产生的基质效应以及提高生物分析方法的耐用性和灵敏度方面具有显著优势。

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