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J Pharm Biomed Anal ; 100: 230-235, 2014 Nov.
Article in English | MEDLINE | ID: mdl-25173108

ABSTRACT

A sensitive and accurate liquid chromatography method with mass spectrometry detection was developed and validated for the quantification of dabigatran (Pradaxa(®)) and rivaroxaban (Xarelto(®)). (13)C6-dabigatran and (13)C6-rivaroxaban were used as the internal standard. A single-step protein precipitation was used for plasma sample preparation. This method was validated with respect to linearity, selectivity, inter- and intra-day precision and accuracy, limit of quantification and stability. The lower limit of quantification was 2.5ng/mL for both drugs in plasma.


Subject(s)
Antithrombins/blood , Benzimidazoles/blood , Chromatography, High Pressure Liquid , Drug Monitoring/methods , Factor Xa Inhibitors/blood , Morpholines/blood , Tandem Mass Spectrometry , Thiophenes/blood , beta-Alanine/analogs & derivatives , Calibration , Chromatography, High Pressure Liquid/standards , Cold Temperature , Dabigatran , Drug Monitoring/standards , Drug Stability , Humans , Limit of Detection , Linear Models , Molecular Structure , Reference Standards , Reproducibility of Results , Rivaroxaban , Tandem Mass Spectrometry/standards , Time Factors , beta-Alanine/blood
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