Su Qi-Biao, He Fan, Guan Su, Lu Yu-Jing, Gu Lian-Quan, Huang Zhi-Shu, Chen Xiao, Huang Min, Li Chun-Guang, Chowbay Balram, Zhou Shu-Feng
Institute of Clinical Pharmacology, School of Pharmaceutical Sciences, Sun Yat-Sen University, 74 Zhongshan Road, Section 2, Guangzhou, China.
J Chromatogr B Analyt Technol Biomed Life Sci. 2007 Jul 1;854(1-2):332-7. doi: 10.1016/j.jchromb.2007.03.043. Epub 2007 Apr 8.
A sensitive assay for the determination of SYUIQ-5, a novel telomerase inhibitor and anti-tumor drug, in rat liver microsomes was developed by using high-performance liquid chromatography with ultraviolet detection. SYUIQ-5 was incubated in vitro with liver microsomes from rats pre-treated with control vehicle, beta-naphthofIavone, phenobarbital, 20% ethanol or dexamethasone. The analytes were extracted with diethyl ether and separated a C(18) 5-microm analytical column. Elution was conducted with 30 mM dipotassium hydrogen phosphate (pH 8.0)-methanol-triethylamine (30:70:0.05, v/v/v) at a flow-rate of 1.0 ml/min and the detection of UV absorbance was conducted at 278 nm. Intra-day and inter-day precision and accuracy of the method were within 10%. The mean analytical recoveries of SYUIQ-5 ranged from 78.8 to 95.3%. The linearity of the calibration curve was in the range of 1.0-80.0 microM. The lower limit of quantification (LOQ) was 1.0 microM. Kinetic analysis showed that beta-naphthofIavone and dexamethasone significantly induced SYUIQ-5 metabolism, suggesting that cytochrome P450 1A and 3A are the major contributor to SYUIQ-5 metabolism in rat liver microsomes.
建立了一种灵敏的测定新型端粒酶抑制剂及抗肿瘤药物SYUIQ-5在大鼠肝微粒体中含量的方法,采用高效液相色谱-紫外检测法。将SYUIQ-5与经对照溶剂、β-萘黄酮、苯巴比妥、20%乙醇或地塞米松预处理的大鼠肝微粒体进行体外孵育。分析物用乙醚萃取,并在C(18) 5微米分析柱上分离。以30 mM磷酸氢二钾(pH 8.0)-甲醇-三乙胺(30:70:0.05,v/v/v)为流动相,流速为1.0 ml/min进行洗脱,在278 nm处检测紫外吸光度。该方法的日内和日间精密度及准确度均在10%以内。SYUIQ-5的平均分析回收率在78.8%至95.3%之间。校准曲线的线性范围为1.0 - 80.0 microM。定量下限(LOQ)为1.0 microM。动力学分析表明,β-萘黄酮和地塞米松显著诱导SYUIQ-5的代谢,提示细胞色素P450 1A和3A是大鼠肝微粒体中SYUIQ-5代谢的主要贡献者。