Rathod Dhiraj M, Patel Keyur R, Mistri Hiren N, Jangid Arvind G, Shrivastav Pranav S, Sanyal Mallika
Department of Chemistry, Kadi Sarva Vishwavidyalaya, Gandhinagar, Ahmedabad 382015, India.
Bioanalytical Research Department, Accutest Research Lab, Bodakdev, Ahmedabad 380059, India.
J Pharm Anal. 2016 Aug;6(4):226-234. doi: 10.1016/j.jpha.2016.02.002. Epub 2016 Feb 24.
An improved high performance liquid chromatography--tandem mass spectrometry (LC-MS/MS) method has been developed for sensitive and rapid determination of albendazole (ABZ) and its active metabolite, albendazole sulfoxide (ABZSO), in the positive ionization mode. The method utilized solid phase extraction (SPE) for sample preparation of the analytes and their deuterated internal standards (ISs) from 100 µL human plasma. The chromatography was carried out on Hypurity C column using acetonitrile-2.0 mM ammonium acetate, pH 5.0 (80:20, v/v) as the mobile phase. The assay exhibited a linear response over the concentration range of 0.200-50.0 ng/mL for ABZ and 3.00-600 ng/mL for ABZSO. The recoveries of the analytes and ISs ranged from 86.03%-89.66% and 89.85%-98.94%, respectively. Matrix effect, expressed as IS-normalized matrix factors, ranged from 0.985 to 1.042 for the both analytes. The method was successfully applied for two separate studies in healthy subjects using single dose of 400 mg conventional tablets and 400 mg chewable ABZ tablets, respectively.
已开发出一种改进的高效液相色谱-串联质谱(LC-MS/MS)方法,用于在正离子模式下灵敏、快速地测定阿苯达唑(ABZ)及其活性代谢物阿苯达唑亚砜(ABZSO)。该方法采用固相萃取(SPE)从100 μL人血浆中制备分析物及其氘代内标(ISs)。色谱分析在Hypurity C柱上进行,使用乙腈-2.0 mM醋酸铵,pH 5.0(80:20,v/v)作为流动相。该测定法在0.200-50.0 ng/mL的阿苯达唑浓度范围和3.00-600 ng/mL的阿苯达唑亚砜浓度范围内呈现线性响应。分析物和内标的回收率分别为86.03%-89.66%和89.85%-98.94%。以IS归一化基质因子表示的基质效应,两种分析物的范围均为0.985至1.042。该方法已成功应用于两项分别针对健康受试者的研究,分别使用单剂量400 mg常规片剂和400 mg咀嚼片阿苯达唑。