Xia Binfeng, Wang Ting, Fox Laura M, Wang Desuo
Department of Basic Pharmaceutical Sciences, South Carolina College of Pharmacy, University of South Carolina, Columbia, SC 29208, USA.
J Chromatogr B Analyt Technol Biomed Life Sci. 2009 Jul 1;877(20-21):1867-72. doi: 10.1016/j.jchromb.2009.05.011. Epub 2009 May 15.
Chemically synthesized 3-carbamyl-4-methylpyrroles were characterized as a group of antihypertensive agents with dual-targeting mechanism to simultaneously inhibit type 4 phosphodiesterase (PDE4) and L-type calcium channels. A 5-butyl analog of the pyrrole family, MNP001, was found to have high potency in reducing animal blood pressure and heart rate. A method for measuring MNP001 using high performance liquid chromatography combined with tandem mass spectrometry (HPLC/MS/MS) was developed. The calibration curve for MNP001 showed good linearity with the value of correlation coefficient greater than 0.987 over the range of 0.25-500 ng/mL. The results for inter-day and intra-day precision as well as accuracy were acceptable according to the criteria established by FDA. The lower limit of quantification was 0.25 ng/mL. This method was quick, sensitive and sufficient for in vivo pharmacokinetic and pharmacodynamic studies on this novel antihypertensive pyrrole compound.
化学合成的3-氨甲酰基-4-甲基吡咯被表征为一类具有双重靶向机制的抗高血压药物,可同时抑制4型磷酸二酯酶(PDE4)和L型钙通道。吡咯家族的一种5-丁基类似物MNP001在降低动物血压和心率方面具有高效能。开发了一种使用高效液相色谱结合串联质谱(HPLC/MS/MS)测定MNP001的方法。MNP001的校准曲线在0.25 - 500 ng/mL范围内显示出良好的线性,相关系数大于0.987。根据美国食品药品监督管理局(FDA)制定的标准,日间和日内精密度以及准确度的结果是可接受的。定量下限为0.25 ng/mL。该方法对于这种新型抗高血压吡咯化合物的体内药代动力学和药效学研究来说快速、灵敏且足够。