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


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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.

Sobre autores

T. Rodina

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

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

E. Mel’nikov

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

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

A. Aksenov

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

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

S. Belkov

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

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

A. Sokolov

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

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

A. Prokof’ev

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

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

G. Ramenskaya

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

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


Declaração de direitos autorais © Springer Science+Business Media, LLC, part of Springer Nature, 2018

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