Gautam N, Singh R P, Pratap R, Singh S K
Pharmacokinetics and Metabolism Division, Central Drug Research Institute, Lucknow, India.
Biomed Chromatogr. 2010 Jul;24(7):692-8. doi: 10.1002/bmc.1348.
A sensitive and selective LC-MS/MS method has been developed and validated for the estimation of novel antidiabetic synthetic flavonoid S002-853 in rat plasma using centchroman as an internal standard. The method involves a simple two-step liquid-liquid extraction with diethyl ether. The analyte was chromatographed on a Pierce Spheri-5, guard cyano column (30 x 4.6 mm i.d., 5 microm) with isocratic mobile phase consisting of methanol-ammonium acetate buffer (pH 4.6, 10 mm; 90 : 10, v/v) at a flow rate of 0.75 mL/min. The API 4000 triple-quadrupole LC-MS/MS system was operated under multiple reaction-monitoring mode. The ionization was performed by electrospray ionization technique in positive ion mode. The chromatographic run time was 6 min and the weighted (1/x(2)) calibration curves were linear over the range 0.78-400 ng/mL. The limit of detection and lower limit of quantification were 0.195 and 0.78 ng/mL, respectively. The intra- and inter-batch accuracy (%bias) and precision (%RSD) were found to be less than 8.47 and 11.6% respectively. The average absolute recoveries of S002-853 and internal standard from spiked plasma samples were >90%. S002-853 was stable for 8 h at ambient temperature, 4 weeks at -60 degrees C and after three freeze-thaw cycles. The assay was successfully applied to determine the pharmacokinetic parameters in male Sprague-Dawley rats after an oral dose administration at 25 mg/kg.
已开发并验证了一种灵敏且具选择性的液相色谱-串联质谱(LC-MS/MS)方法,用于以炔诺酮为内标物测定大鼠血浆中新型抗糖尿病合成黄酮类化合物S002-853。该方法采用简单的两步乙醚液-液萃取。分析物在Pierce Spheri-5保护氰基柱(内径30×4.6 mm,5μm)上进行色谱分离,等度流动相由甲醇-醋酸铵缓冲液(pH 4.6,10 mM;90:10,v/v)组成,流速为0.75 mL/min。API 4000三重四极杆LC-MS/MS系统在多反应监测模式下运行。通过电喷雾电离技术在正离子模式下进行电离。色谱运行时间为6分钟,加权(1/x²)校准曲线在0.78 - 400 ng/mL范围内呈线性。检测限和定量下限分别为0.195和0.78 ng/mL。批内和批间准确度(%偏差)和精密度(%相对标准偏差)分别小于8.47%和11.6%。加标血浆样品中S002-853和内标的平均绝对回收率>90%。S002-853在室温下稳定8小时,在-60℃下稳定4周,且经过三次冻融循环后仍稳定。该测定法成功应用于在雄性Sprague-Dawley大鼠口服25 mg/kg剂量后测定药代动力学参数。