In-source CID mass spectral libraries for the “general unknown” screening of drugs and toxicants

P. Marquet, N. Venisse, E. Lacassie, G. Lachâtre
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引用次数: 80

Abstract

A “general unknown” screening procedure for drugs and toxicants using LC-ES-MS was developed. It involved in-source collision induced dissociation of the molecular ions (in the negativeion mode) or protonated molecules (in the positive-ion mode) generally obtained from electrospray sources. Spectra were reconstructed by adding, on one hand, a pair of positive spectra, one without and one with fragmentation, and on the other a pair of negative spectra acquired in similar conditions. These reconstructed spectra showed at least as many fragments as MS/MS spectra, and sometimes as many as electron-ionisation spectra. They were repeatable and reproducible enough to be used for the specific identification of hundreds of molecules. Libraries of about 1100 positive spectra and 500 negative spectra were constructed and are used routinely, together with chromatographic separation involving a Nucleosil C18, 5 µm column (150 〈 1m m i.d.) and a gradient of acetonitrile in 2 mM, pH 3 ammonium formate as a screening technique complementary to GC-MS and HPLC-DAD.
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用于“一般未知”药物和毒物筛选的源内CID质谱库
开发了一种使用LC-ES-MS进行药物和毒物“一般未知”筛选的程序。它涉及通常从电喷雾源获得的分子离子(处于负离子模式)或质子化分子(处于正离子模式)的源内碰撞诱导解离。通过添加一对无破碎和有破碎的正光谱和一对在相似条件下获得的负光谱来重建光谱。这些重建的光谱显示的片段至少与质谱/质谱一样多,有时与电子电离谱一样多。它们是可重复和可复制的,足以用于数百种分子的特定鉴定。构建了约1100个阳性光谱库和500个阴性光谱库,并常规使用,同时采用色谱分离,涉及核sil C18, 5µm柱(150 < 1m m .d)和乙腈在2 mM, pH 3甲酸铵中梯度,作为与GC-MS和HPLC-DAD互补的筛选技术。
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