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采用反相色谱C18的超高效液相色谱-质谱联用法定量分析卤离子的首个特定分析方法。

First Specific Analytical Method for Quantification of Halide Ions by UHPLC-MS Using Reverse Phase Chromatography C18.

作者信息

Bonert Steven, Sayer Hervé, Tabone Ghislaine, Robert Benoit

机构信息

Global CMC Development/CMC Synthetics Plateform/Early Development France, Sanofi-Aventis R&D, 13 Quai Jules Guesde, Vitry sur Seine F-94400, France.

出版信息

ACS Omega. 2025 Aug 26;10(35):39463-39470. doi: 10.1021/acsomega.4c10817. eCollection 2025 Sep 9.

Abstract

In the pharmaceutical industry, optimizing methods for trace detection and stoichiometry determination of salts is highly sought after, particularly for studies on pharmaceutical compounds in the development phase. Current methods for halide ion detection are commonly carried out using ion chromatography (IC) due to the high specificity and sensitivity of this technique, which allows the detection of various ions at very low concentrations. Advanced techniques such as mass spectrometry, which offers significantly higher sensitivity thanks to its specificity, can be particularly advantageous in analytical applications both for trace detection with a view to quantification and for its accuracy in stoichiometric calculations, allowing the precise determination of the ratio between the compound of interest and the counterion. To our knowledge, no LC-MS methods using a reverse-phase polarity chromatographic system (C18), commonly employed in high-performance liquid chromatography (HPLC) or ultrahigh-performance liquid chromatography (UHPLC), currently exist that allow for sufficiently effective halogen separation for accurate quantification. We present a new rapid and efficient method compliant with (ICH) standards using a C18 reverse phase, which enables optimal separation of three halogens in order to precisely quantify analytes through mass spectrometry. This method will be illustrated with a relevant application, dedicated to the stoichiometry investigation of pharmaceutical compounds in the form of salts or halide ion residues.

摘要

在制药行业,优化盐类的痕量检测和化学计量测定方法备受关注,尤其是在药物化合物研发阶段的研究中。由于离子色谱(IC)技术具有高特异性和灵敏度,能够检测极低浓度的各种离子,因此目前卤离子检测方法通常采用离子色谱法。质谱等先进技术由于其特异性而具有显著更高的灵敏度,在分析应用中尤其有利,既可以用于痕量检测以进行定量,也因其在化学计量计算中的准确性,能够精确测定目标化合物与抗衡离子之间的比例。据我们所知,目前不存在使用高效液相色谱(HPLC)或超高效液相色谱(UHPLC)中常用的反相极性色谱系统(C18)的液相色谱 - 质谱(LC - MS)方法,能够实现足够有效的卤素分离以进行准确的定量分析。我们提出了一种符合国际人用药品注册技术协调会(ICH)标准的新型快速高效方法,该方法使用C18反相柱,能够实现三种卤素的最佳分离,以便通过质谱法精确量化分析物。本文将通过一个相关应用对该方法进行说明,该应用专门用于盐类形式的药物化合物或卤离子残留的化学计量研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10df/12423822/139ad7725940/ao4c10817_0001.jpg

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