Comparison of Approaches to Determining N-Nitrosodimethylamine Impurity in Valsartan Drug Substance By GC-MS Methods


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Methods for determining the genotoxic impurity N-nitrosodimethylamine (NDMA) in valsartan drug substance by gas chromatography (GC) with mass-spectrometric detection in SIM and MRM modes using direct introduction and vapor-phase analysis are compared. The obtained LOQ and DL differed insignificantly. The test results led to the conclusion that use of a method corresponding to the capabilities and equipment of the laboratory was advisable.

作者简介

M. Khorol’skii

I. M. Sechenov First Moscow State Medical University (Sechenov University); Scientific Center for Expert Evaluation of Medicinal Products, Ministry of Health of the Russian Federation

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Email: mkhorolski@gmail.com
俄罗斯联邦, 8/2 Trubetskaya St, Moscow, 119991; 8/2 Petrovskii Blvd, Moscow, 127051

O. Anan’ina

Scientific Center for Expert Evaluation of Medicinal Products, Ministry of Health of the Russian Federation

Email: mkhorolski@gmail.com
俄罗斯联邦, 8/2 Petrovskii Blvd, Moscow, 127051

A. Chaplenko

Scientific Center for Expert Evaluation of Medicinal Products, Ministry of Health of the Russian Federation

Email: mkhorolski@gmail.com
俄罗斯联邦, 8/2 Petrovskii Blvd, Moscow, 127051

I. Nedkov

Scientific Center for Expert Evaluation of Medicinal Products, Ministry of Health of the Russian Federation

Email: mkhorolski@gmail.com
俄罗斯联邦, 8/2 Petrovskii Blvd, Moscow, 127051

N. Maslennikova

Scientific Center for Expert Evaluation of Medicinal Products, Ministry of Health of the Russian Federation

Email: mkhorolski@gmail.com
俄罗斯联邦, 8/2 Petrovskii Blvd, Moscow, 127051

G. Ramenskaya

I. M. Sechenov First Moscow State Medical University (Sechenov University)

Email: mkhorolski@gmail.com
俄罗斯联邦, 8/2 Trubetskaya St, Moscow, 119991

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