Development of an HPLC-MS/MS Method for Quantitative Determination of Rivaroxaban in Human Blood Serum


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Abstract

An HPLC-MS/MS method for determination of rivaroxaban in human blood serum was developed. Sample preparation included protein precipitation by MeOH followed by centrifugation and dilution with deionized H2O. The developed procedure had simple sample preparation, a short analysis time, and a wide analytical range (1.00 to 1,000.00 ng/mL). The procedure was convenient for routine bioanalytical studies, in particular, for therapeutic drug monitoring.

About the authors

T. A. Rodina

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

Email: chem@folium.ru
Russian Federation, 8/2 Petrovskii Blvd, Moscow, 127051

E. S. Mel’nikov

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

Email: chem@folium.ru
Russian Federation, 8/2 Petrovskii Blvd, Moscow, 127051

A. A. Aksenov

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

Email: chem@folium.ru
Russian Federation, 8/2 Petrovskii Blvd, Moscow, 127051

S. A. Belkov

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

Email: chem@folium.ru
Russian Federation, 8/2 Petrovskii Blvd, Moscow, 127051

A. V. Sokolov

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

Email: chem@folium.ru
Russian Federation, 8/2 Petrovskii Blvd, Moscow, 127051

A. B. Prokof’ev

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

Email: chem@folium.ru
Russian Federation, 8/2 Petrovskii Blvd, Moscow, 127051

G. V. Ramenskaya

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

Email: chem@folium.ru
Russian Federation, 8/2 Petrovskii Blvd, Moscow, 127051


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