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首页> 外文期刊>Microchemical Journal: Devoted to the Application of Microtechniques in all Branches of Science >Determination of thiol-containing drugs in human plasma by stable isotope labeling coupled with high performance liquid chromatography-electrospray ionization-tandem mass spectrometry analysis
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Determination of thiol-containing drugs in human plasma by stable isotope labeling coupled with high performance liquid chromatography-electrospray ionization-tandem mass spectrometry analysis

机译:用稳定同位素标记耦合高性能液相色谱 - 电喷雾电离 - 串联质谱分析,测定人血浆中含硫醇的药物

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摘要

A pair of stable isotope labeling (SIL) reagents, N-(4-(carbazole-9-yl)-phenyl)-N-maleimide (NCPM-d(0)) and its heavy analogue NCPM-d(2), were used for labeling thiol-containing drugs. On basis of SIL, a global isotope internal standard quantitative method for the detection of five thiol-containing drugs by high-performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS) was developed. The NCPM-d(0) and NCPM-d(2) can easily label thiol-containing drugs under mild conditions within 10 min at 40 degrees C. The NCPM-d(0) and NCPM-d(2) labeled thiol-containing drugs can generate two characteristic product ions (m/z at 372.5 and 374.5) under collision induced dissociation, respectively, which is used to establish the multiple reaction monitoring (MRM) based detection. The NCPM labeling combined with MRM analysis not only allowed trace detection of thiol-containing drugs due to the extremely high sensitivity, but also efficiently corrected the matrix effects during HPLC-MS/MS and the instrument fluctuation in the MS/MS signal intensity. The detection sensitivities of thiol-containing drugs improved by 14.5-650.5-fold due to NCPM-labeling, while the matrix and ion suppression effects were markedly minimized by the SIL strategy. The limits of detection (LODs) and the limits of quantitation (LOQs) were in the range 10.0-15.0 ng.mL(-1) and 31.0-50.0 ng.mL(-1), respectively. The proposed method was used for the simultaneous determination of five thiol-containing drugs in plasma samples with satisfactory recoveries in the range of 95.0-97.5%.
机译:一对稳定同位素标记(SIL)试剂,N-(4-(咔唑-9-基) - 苯基)-N-马来酰亚胺(NCPM-D(0))及其重型类似NCPM-D(2)是用于标记含硫醇的药物。在SIL的基础上,通过高效液相色谱 - 串联质谱(HPLC-MS / MS)开发了一种用于检测五种含硫醇药物的全局同位素内标定量方法。 NCPM-D(0)和NCPM-D(2)可以在40℃下在10分钟内容易地在60分钟内在温和条件下标记硫醇的药物。NCPM-D(0)和NCPM-D(2)标记含硫醇的在碰撞诱导的解离,药物可以在碰撞诱导的解离中产生两种特征产物离子(372.5和374.5),用于建立基于多反应监测(MRM)的检测。 NCPM标记与MRM分析相结合,而不仅允许由于极高的灵敏度捕获含硫醇的药物,而且还有效地校正了在HPLC-MS / MS期间的基质效应以及MS / MS信号强度中的仪器波动。由于NCPM标记,含硫醇的药物的检测敏感性提高了14.5-650.5倍,而SIL策略显着最小化了基质和离子抑制效应。检测限(LOD)和定量限的限制(LOQs)分别为10.0-15.0 ng.ml(-1)和31.0-50.0ng.ml(-1)。所提出的方法用于同时测定血浆样品中的五种硫醇药物,令人满意的回收率在95.0-97.5%的范围内。

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