| Literature DB >> 24309556 |
Yoshinari Yokoyama1, Miho Tomatsuri1, Hideki Hayashi1, Keita Hirai2, Yasuo Ono3, Yuto Yamada1, Kenichiro Todoroki4, Toshimasa Toyo'oka4, Hiroshi Yamada5, Kunihiko Itoh6.
Abstract
A simultaneous, selective, sensitive, and rapid liquid chromatography/tandem mass spectrometry (LC-MS/MS) method was developed and validated for the quantification of bosentan, ambrisentan, sildenafil, and tadalafil in 50μL of human blood plasma. Diluted plasma samples were extracted using a solid-phase extraction procedure with 2% formic acid and methanol. The four drugs were separated by high-performance liquid chromatography using a C18 column and an isocratic mobile phase running at a flow rate of 0.2mL/min for 5min. The drugs were detected by a tandem mass spectrometer with electrospray ionization using deuterated compounds as internal standards. Calibration curves were generated over the linear concentration range of 2-1000ng/mL in plasma with a lower limit of quantification of 2ng/mL for all compounds. Finally, this validated method was applied to a clinical pharmacokinetic study in pediatric patients with pulmonary arterial hypertension (PAH) following the oral administration of PAH drugs. These results indicate that this method is suitable for assessing the risk/benefit of combination therapy in the pediatric population and useful for therapeutic drug monitoring for PAH treatment.Entities:
Keywords: Ambrisentan; Bosentan; LC–MS/MS; Sildenafil; Tadalafil
Mesh:
Substances:
Year: 2013 PMID: 24309556 DOI: 10.1016/j.jpba.2013.11.007
Source DB: PubMed Journal: J Pharm Biomed Anal ISSN: 0731-7085 Impact factor: 3.935