Dept of Pharmacy Practice, University of Nebraska Medical Center, Omaha, NE 68198, United States.
Centre Suisse de Recherches Scientifiques en Côte d'Ivoire (CSRS), 01 BP1303 Abidjan 01, Cote d'Ivoire.
J Pharm Biomed Anal. 2018 Mar 20;151:84-90. doi: 10.1016/j.jpba.2017.12.037. Epub 2017 Dec 24.
Combination therapy with anti-filarial drugs is now widely used for treatment of lymphatic filariasis. A rapid, selective, and sensitive liquid chromatography coupled with tandem mass spectrometry (LC-MS/MS) method was developed and validated for simultaneous quantitation of diethylcarbamazine (DEC), albendazole (ABZ) and albendazole metabolites in human plasma. Separation and detection of analytes were achieved on a reversed phase column (Acquity UPLCBEH C18 column (100 × 2.1 mm, 1.7 μm) with gradient elution using 0.05% formic acid in methanol and 0.05% formic acid as mobile phase. Solid phase extraction was utilized for elution of analytes from the matrix. Thereafter, analytes were monitored by using MS/MS with electrospray ionization source in positive multiple reaction monitoring mode. The MS/MS response was linear over the concentration range from 0.1-200 ng/mL for ABZ and ABZ-ON, 0.5-1000 ng/mL for ABZ-OX and 1-2000 ng/mL for DEC with a correlation coefficient (r) of 0.998 or better. The within- and between-batch precisions (relative standard deviation, % RSD) and the accuracy (% bias) were within the acceptable limits as per FDA guideline. The validated method was successfully applied to the clinical pharmacokinetic study. Due to high sensitivity and low requirement of sample volume, the method will be applicable for therapeutic drug monitoring of this regimen.
联合抗丝虫药物治疗目前广泛用于治疗淋巴丝虫病。本研究建立并验证了一种快速、选择性和灵敏的液相色谱串联质谱(LC-MS/MS)法,用于同时定量检测人血浆中的乙胺嗪(DEC)、阿苯达唑(ABZ)及其代谢物。采用反相色谱柱(Acquity UPLC BEH C18 柱,100×2.1mm,1.7μm),以甲醇中 0.05%甲酸和 0.05%甲酸为流动相进行梯度洗脱,实现了分析物的分离和检测。采用固相萃取法从基质中洗脱分析物。然后,采用电喷雾离子源在正离子多反应监测模式下进行 MS/MS 监测。ABZ 和 ABZ-ON 的浓度范围为 0.1-200ng/mL、ABZ-OX 的浓度范围为 0.5-1000ng/mL、DEC 的浓度范围为 1-2000ng/mL 时,ABZ 和 ABZ-ON 的 MS/MS 响应呈线性,相关系数(r)均大于 0.998。根据 FDA 指南,批内和批间精密度(相对标准偏差,%RSD)和准确度(%偏差)均在可接受范围内。该验证方法成功应用于临床药代动力学研究。由于灵敏度高,样品体积要求低,该方法将适用于该方案的治疗药物监测。