College of Pharmacy, Catholic University of Daegu, Kyoungbuk 712-702, South Korea.
J Pharm Biomed Anal. 2011 Feb 20;54(3):568-71. doi: 10.1016/j.jpba.2010.10.007. Epub 2010 Oct 16.
A novel T-type calcium channel blocker, 4-amino-1-{4-[(4-chloro-phenyl)-phenyl-methyl]-piperazin-1-yl}-butan-1-one (HYP-10) has been synthesized, and the compound has shown promise as both a nociceptive and inflammatory pain reliever as well as an analgesic in a rat neuropathic pain model. A quantification method was developed for the determination of HYP-10 in rat plasma. After simple protein precipitation with methanol, HYP-10 and the internal standard, methaqualone were chromatographed on a reversed-phase column and detected by liquid chromatography/tandem mass spectrometry with electrospray ionization. The accuracy and precision of the assay were in accordance with FDA regulations for validation of bioanalytical methods. This method was applied to measure the plasma HYP-10 concentration after a single intravenous administration of the compound in rats.
一种新型的 T 型钙通道阻滞剂,4-氨基-1-({4-[(4-氯苯基)-苯基甲基]-哌嗪-1-基}-丁-1-酮(HYP-10)已被合成,该化合物已显示出作为痛觉和炎症性疼痛缓解剂以及在大鼠神经性疼痛模型中的镇痛剂的潜力。已经开发了一种用于测定大鼠血浆中 HYP-10 的定量方法。用甲醇进行简单的蛋白沉淀后,HYP-10 和内标,甲喹酮在反相柱上进行色谱分离,并用液相色谱/串联质谱法(电喷雾电离)检测。该测定的准确性和精密度符合 FDA 对生物分析方法验证的规定。该方法应用于测量大鼠单次静脉给予该化合物后血浆中 HYP-10 的浓度。