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液相色谱流动相缓冲液含量对液相色谱/离子喷雾串联质谱测定中分析物电离和碎裂的影响

Effects of liquid chromatography mobile phase buffer contents on the ionization and fragmentation of analytes in liquid chromatographic/ionspray tandem mass spectrometric determination.

作者信息

Zhao Jamie J, Yang Amy Y, Rogers J Douglas

机构信息

Department of Drug Metabolism, Merck Research Laboratories, WP75A-303, West Point, Pennsylvania 19486, USA.

出版信息

J Mass Spectrom. 2002 Apr;37(4):421-33. doi: 10.1002/jms.299.

Abstract

The effects of liquid chromatography mobile phase buffer contents on the ionization and fragmentation of drug molecules in liquid chromatographic/ionspray tandem mass spectrometric (LC/MS/MS) determination were evaluated for simvastatin (SV) and its hydroxy acid (SVA). The objective was to improve further the sensitivity for SV by overcoming the unfavorable condition caused by the formation of multiple major adduct ions and multiple major fragment ions when using ammonium as LC mobile phase buffer. Mobile phases (70:30 acetonitrile-buffer, 2 mM, pH 4.5) with buffers made from ammonium, hydrazine or alkyl (methyl, ethyl, dimethyl or trimethyl)-substituted ammonium acetate were evaluated. Q1 scan and product ion scan spectra were obtained for SV in each of the mobile phases under optimized conditions. The results showed that, with the alkylammonium buffers, the alkylammonium-adducted SV was observed as the only major molecular ion, while the formation of other adduct ions (M + H, M + Na and M + K) was successfully suppressed. On the other hand, product ion spectra with a single major fragment ion were not observed for any of the alkylammonium-adducted SVs. The affinity of the alkylammoniums to SV and the basicity of the alkylamines are believed to be factors influencing the formation and abundance of molecular and fragment ions, respectively. Methylammonium acetate provided the most favorable condition among all the buffers evaluated and improved the sensitivity several-fold for SV in LC/MS/MS quantitation compared with that obtained using ammonium acetate buffer. Better precision for SV in both Q1 and SRM scans was observed when using methylammonium buffer compared with those using ammonium buffer. The mobile phase buffer contents did not seem to affect the ionization, fragmentation and chromatography of SVA. The results of this evaluation can be applied to similar situations with other organic molecules in ionspray LC/MS/MS determination.

摘要

在液相色谱/离子喷雾串联质谱(LC/MS/MS)测定中,针对辛伐他汀(SV)及其羟酸(SVA)评估了液相色谱流动相缓冲液成分对药物分子电离和裂解的影响。目的是通过克服使用铵作为液相色谱流动相缓冲液时因形成多个主要加合离子和多个主要碎片离子而导致的不利条件,进一步提高对SV的灵敏度。评估了由铵、肼或烷基(甲基、乙基、二甲基或三甲基)取代的醋酸铵制成缓冲液的流动相(70:30乙腈 - 缓冲液,2 mM,pH 4.5)。在优化条件下,针对每种流动相中的SV获得了Q1扫描和产物离子扫描光谱。结果表明,使用烷基铵缓冲液时,烷基铵加合的SV被观察为唯一的主要分子离子,而其他加合离子(M + HM + NaM + K)的形成被成功抑制。另一方面,对于任何烷基铵加合的SV,均未观察到具有单个主要碎片离子的产物离子光谱。烷基铵与SV的亲和力以及烷基胺的碱性分别被认为是影响分子离子和碎片离子形成及丰度的因素。在所有评估的缓冲液中,醋酸甲基铵提供了最有利的条件,与使用醋酸铵缓冲液相比,在LC/MS/MS定量中对SV的灵敏度提高了几倍。与使用铵缓冲液相比,使用甲基铵缓冲液时在Q1和SRM扫描中SV的精密度更高。流动相缓冲液成分似乎不影响SVA的电离、裂解和色谱行为。该评估结果可应用于离子喷雾LC/MS/MS测定中其他有机分子的类似情况。

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