Bonato Pierina Sueli, Lanchote Vera Lucia, Takayanagui Osvaldo Massaiti
Faculdade de Ciências Farmacêuticas de Ribeirão Preto-USP, CEP 14040-903, Ribeirão Preto, Brazil.
J Chromatogr B Analyt Technol Biomed Life Sci. 2003 Jan 5;783(1):237-45. doi: 10.1016/s1570-0232(02)00665-7.
This paper describes a simple, fast, sensitive and reliable method for the simultaneous determination of albendazole sulfoxide (ASOX) and albendazole sulfone (ASON), the two most important metabolites of the drug albendazole (ABZ), in plasma samples using liquid chromatography and tandem mass spectrometry. After liquid-liquid extraction with dichloromethane, the two albendazole metabolites and the internal standard phenacetin were resolved in a CN column using the mobile phase methanol-water (4:6, v/v) acidified with 1% acetic acid. Detection by electrospray mass spectrometry was carried out in the positive ion mode. The method was linear up to 2500 and 250 ng/ml for ASOX and ASON, respectively, with mean recoveries of more than 85%. The precision and accuracy data, based on within- and between-day variations over 5 days, were lower than 15%. The quantitation limits of 0.5 and 5.0 ng/ml for ASON and ASOX are low enough for the method to be suitable for pharmacokinetic studies. Pharmacokinetic data obtained with the proposed method following oral administration of ABZ to a patient with neurocysticercosis are also reported.
本文描述了一种简单、快速、灵敏且可靠的方法,用于使用液相色谱和串联质谱法同时测定血浆样本中阿苯达唑(ABZ)的两种最重要代谢物阿苯达唑亚砜(ASOX)和阿苯达唑砜(ASON)。用二氯甲烷进行液液萃取后,两种阿苯达唑代谢物和内标非那西丁在CN柱上使用用1%乙酸酸化的甲醇-水(4:6,v/v)流动相进行分离。通过电喷雾质谱在正离子模式下进行检测。该方法对于ASOX和ASON的线性范围分别高达2500和250 ng/ml,平均回收率超过85%。基于5天内日内和日间变化的精密度和准确度数据低于15%。ASON和ASOX的定量限分别为0.5和5.0 ng/ml,低至足以使该方法适用于药代动力学研究。还报告了使用所提出的方法对一名神经囊尾蚴病患者口服ABZ后获得的药代动力学数据。