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采用液液萃取和 GC-MS 法测定水溶性 API 中间体中低 ppm 级别的二甲基硫酸酯。

Determination of low ppm levels of dimethyl sulfate in an aqueous soluble API intermediate using liquid-liquid extraction and GC-MS.

机构信息

Dept. R45T, GPRD, Abbott Laboratories, North Chicago, IL 60064, USA.

出版信息

J Pharm Biomed Anal. 2009 Dec 5;50(5):1054-9. doi: 10.1016/j.jpba.2009.06.022. Epub 2009 Jun 17.

Abstract

Dimethyl sulfate (DMS) is an alkylating reagent commonly used in organic syntheses and pharmaceutical manufacturing processes. Due to its potential carcinogenicity, the level of DMS in the API process needs to be carefully monitored. However, in-process testing for DMS is challenging because of its reactivity and polarity as well as complex matrix effects. In this short communication, we report a GC-MS method for determination of DMS in an API intermediate that is a methyl sulfate salt. To overcome the complex matrix interference, DMS and an internal standard, d6-DMS, were extracted from the matrix with methyl tert-butyl ether. GC separation was conducted on a DB-624 column (30 m long, 0.32 mm ID, 1.8 microm film thickness). MS detection was performed on a single-quad Agilent MSD equipped with an electron impact source while the MSD signal was acquired in selected ion monitoring mode. This GC/MS method showed a linear response for DMS equivalent from 1.0 to 60 ppm. The practical quantitation limit for DMS was 1.0 ppm and the practical detection limit was 0.3 ppm. The relative standard derivation for analyte response was found as 0.1% for six injections of a working standard equivalent to 18.6 ppm of DMS. The spike recovery was ranged from 102.1 to 108.5% for a sample of API intermediate spiked with 8.0 ppm of DMS. In summary, the GC/MS method showed adequate specificity, linearity, sensitivity, repeatability and accuracy for determination of DMS in the API intermediate. This method has been successfully applied to study the efficiency of removing DMS from the process.

摘要

二甲亚砜(DMS)是一种常用的有机合成和制药制造过程中的烷基化试剂。由于其潜在的致癌性,需要仔细监测 API 过程中的 DMS 水平。然而,由于其反应性和极性以及复杂的基质效应,DMS 的过程中测试具有挑战性。在本简短通讯中,我们报告了一种用于测定 API 中间体中 DMS 的 GC-MS 方法,该 API 中间体是一种硫酸甲酯盐。为了克服复杂的基质干扰,DMS 和内标 d6-DMS 用甲基叔丁基醚从基质中提取。GC 分离在 DB-624 柱(30 m 长,0.32 mm ID,1.8 微米膜厚)上进行。MS 检测在配备电子轰击源的单四极 Agilent MSD 上进行,而 MSD 信号在选择的离子监测模式下采集。该 GC/MS 方法对 1.0 至 60 ppm 等效的 DMS 显示出线性响应。DMS 的实际定量限为 1.0 ppm,实际检测限为 0.3 ppm。对于相当于 18.6 ppm DMS 的工作标准的六个进样物,分析物响应的相对标准偏差为 0.1%。用 8.0 ppm DMS 对 API 中间体进行加标,加标回收率在 102.1%至 108.5%之间。总之,GC/MS 方法对 API 中间体中 DMS 的测定表现出足够的特异性、线性、灵敏度、重复性和准确性。该方法已成功应用于研究从工艺中去除 DMS 的效率。

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