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一种将固定化技术应用于膜分离和荧光光谱法定量测定药物样品中阿米洛利和呋塞米的新方法。

A novel application of immobilization on membranes for the separation and spectrofluorimetric quantification of amiloride and furosemide in pharmaceutical samples.

机构信息

Instituto de Química de San Luis (INQUISAL-CONICET), Chacabuco y Pedernera, 5700-San Luis, Argentina.

出版信息

Anal Chim Acta. 2010 Feb 19;661(1):85-90. doi: 10.1016/j.aca.2009.12.015. Epub 2009 Dec 21.

DOI:10.1016/j.aca.2009.12.015
PMID:20113719
Abstract

A new, simple and highly sensitive method for spectrofluorimetric determination of amiloride (AMI) and furosemide (FUR) in pharmaceuticals is presented. The proposed method is based on the separation of AMI from FUR by solid-phase extraction using a nylon membrane, followed by spectrofluorimetric determination of both drugs, on the solid surface and the filtered aqueous solution, respectively. AMI shows low native fluorescence, but its separation-preconcentration by immobilization (solid-phase extraction) on nylon membrane surface provides a considerable enhancement in fluorescence intensity. The fluorescence determination is carried out at lambda(ex)=237, lambda(em)=415 nm for FUR; and lambda(ex)=365, lambda(em)=406 nm for AMI. The calibration graphs are linear in the range 3.20 x 10(-4) to 0.8 microg mL(-1) and 1.33 x 10(-3) to 4.0 microg mL(-1), for AMI and FUR, respectively, with a detection limit of 9.62 x 10(-5) and 4.01 x 10(-4) microg mL(-1) (S/N=3). The commonly found excipients in commercial pharmaceutical formulations do not interfere. The developed method is successfully applied to the determination of both drugs in pharmaceutical formulations.

摘要

一种新的、简单且高灵敏度的荧光分光光度法用于测定药物中的阿米洛利(AMI)和呋塞米(FUR)。该方法基于尼龙膜固相萃取分离 AMI 和 FUR,然后分别在固相中对两种药物进行荧光分光光度测定,以及在过滤后的水溶液中进行荧光分光光度测定。AMI 本身荧光强度较弱,但通过在尼龙膜表面固定化(固相萃取)可显著增强其荧光强度。FUR 的荧光测定在 lambda(ex)=237,lambda(em)=415nm 进行;AMI 的荧光测定在 lambda(ex)=365,lambda(em)=406nm 进行。对于 AMI 和 FUR,校准曲线在 3.20 x 10(-4) 至 0.8 microg mL(-1) 和 1.33 x 10(-3) 至 4.0 microg mL(-1) 范围内呈线性,检测限分别为 9.62 x 10(-5) 和 4.01 x 10(-4) microg mL(-1)(S/N=3)。常见的商业药物制剂赋形剂不干扰测定。该方法成功应用于药物制剂中两种药物的测定。

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