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Oncol Ther (2016) 4:117–128 DOI 10.1007/s40487-016-0022-2 ORIGINAL RESEARCH Liquid Chromatography–Mass Spectrometry/Mass Spectrometry Analysis and Pharmacokinetic Assessment of Ponatinib in Sprague–Dawley Rats . . . . Pei Wang Ying Peng Xiaolan Zhang Fei Fei . . . . Shuyao Wang Siqi Feng Jingqiu Huang Hongbo Wang Jiye Aa Guangji Wang Received: March 15, 2016 / Published online: June 6, 2016 The Author(s) 2016. This article is published with open access at Springerlink.com Methods: The method was verified and ABSTRACT successfully applied to evaluate the Introduction: By means of liquid–liquid pharmacokinetics of ponatinib in extraction with ethyl acetate, a rapid, Sprague–Dawley rats. sensitive, and specific LC–MS/MS method was Results: Ponatinib showed dose-dependent developed and validated for assaying ponatinib exposure in the circulation system, and the and the internal standard, warfarin. absolute bioavailabilities of ponatinib were 43.95 ± 2.40%, 47.69 ± 5.08% and 55.02 ± Enhanced Content To view enhanced content for this article go to www.medengine.com/Redeem/ 2.50% after intragastric administration of 7.5, 53D4F060083D3591. 15.0 and 30.0 mg/kg ponatinib in rats, Electronic supplementary material The online respectively. After consecutive administration version of this article (doi:10.1007/s40487-016-0022-2) at 3.75 mg/kg for 7 days, there was distinct contains supplementary material, which is available to authorized
Oncology and Therapy – Springer Journals
Published: Jun 6, 2016
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