Obando María Antonieta, Estela José Manuel, Cerdà Víctor
Analysis and Quality Department, Faculty of Pharmacy, Los Andes University, Mérida, Venezuela.
J Pharm Biomed Anal. 2008 Sep 10;48(1):212-7. doi: 10.1016/j.jpba.2008.05.016. Epub 2008 May 21.
In this paper, a combination of multi-syringe chromatography analysis technique with extraction disks sorbents for the pre-concentration and determination of hydrochlorothiazide and losartan potassium in superficial water, groundwater and wastewater outlet samples has been developed. The system developed was proved for the determination of hydrochlorothiazide and losartan potassium in spiked water samples with recoveries ranging from 95 to 118%. The method involves the on-line enrichment of the targeted analytes from spiked water samples onto a Cation-SR sorbent material. The analytes are subsequently eluted and transported to the monolithic column, Chromolith Flash RP-18e column (25 mmx4.6 mm i.d.). The mobile phase used was 10 mM potassium dihydrogen phosphate (pH 3.0):acetonitrile:methanol (60:30:10 v/v/v), flow-rate 0.8 mL min(-1). UV detection is carried out at 226 nm. Under the optimized chemical and physical variables, the detection limit for hydrochlorothiazide and losartan potassium calculated as 3Syx/b was 0.07 and 0.09 mgL(-1), respectively, for a sample loading volume of 1.0 mL.
本文开发了一种将多注射器色谱分析技术与萃取盘吸附剂相结合的方法,用于地表水、地下水和废水排放口样品中氢氯噻嗪和氯沙坦钾的预浓缩和测定。所开发的系统已被证明可用于测定加标水样中的氢氯噻嗪和氯沙坦钾,回收率在95%至118%之间。该方法包括将加标水样中的目标分析物在线富集到阳离子SR吸附剂材料上。随后将分析物洗脱并输送到整体柱,即Chromolith Flash RP - 18e柱(25 mm×4.6 mm内径)。所用流动相为10 mM磷酸二氢钾(pH 3.0):乙腈:甲醇(60:30:10 v/v/v),流速0.8 mL min(-1)。在226 nm处进行紫外检测。在优化的化学和物理变量下,对于1.0 mL的进样体积,按3Syx/b计算的氢氯噻嗪和氯沙坦钾的检测限分别为0.07和0.09 mgL(-1)。