n掺杂碳空心球同步荧光光谱法测定阿托伐他汀和氨氯地平

A. Hajihosseinloo, Ali Banitalebi Dehkordi, H. Vojoudi, J. Ghasemi, M. K. Rofouei, Alireza Badiei
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引用次数: 0

摘要

建立了以介孔氮掺杂中空碳球为吸附剂的分散固相纳米萃取(DSPNE)技术同时测定加标人血浆中阿托伐他汀(AT)和氨氯地平(AM)的绿色灵敏分析方法。测定方法是测定药物在恒定波长差(Δλ=40 nm)下的同步荧光强度。研究并优化了不同实验参数对两种药物提取率的影响。检出限分别为3.24、0.406 ng。Ml -1和定量限分别为10.8和1.36 ng。AT和AM分别为ml -1。验证结果表明,AT的浓度范围为11 ~ 120,AM的浓度范围为2 ~ 90 ng ml -1,两种药物的R均为2 ~ 0.993。在最佳提取条件下,AT和AM的提取率分别为94%和89%,RSD分别为3.9和4.7 (n=4)。该方法简便、经济、可重复性好,可用于生物液中两种药物的常规分析。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
N-Doped Carbon Hollow Spheres for the Simultaneous Determination of Atorvastatin and Amlodipine by Synchronous Fluorescence Spectrofluorimetry
A green and sensitive analytical procedure by dispersive solid-phase nanoextraction (DSPNE) strategy based on mesoporous nitrogen-doped hollow carbon sphere as adsorbent is developed for the simultaneous determination of atorvastatin (AT) and amlodipine (AM) in spiked human plasma. The determination method was based on measuring the synchronous fluorescence intensity of the drugs at a constant wavelength difference (Δλ=40 nm). The different experimental parameters influencing the extraction efficiency of the two drugs were studied and optimized. The limits of detection were 3.24 and 0.406 ng. ml -1 and quantification limits were 10.8 and 1.36 ng. ml -1 for AT and AM, respectively. Validation assays indicated that the concentration ranges were linear in 11-120 for AT and 2-90 ng ml -1 for AM, with R 2 >0.993 for both drugs. Under optimum conditions, extraction recovery was 94% and 89% with RSD% 3.9 and 4.7 (n=4) for AT and AM, respectively. The developed method has been found to be simple, economical, and reproducible for the routine analysis of both drugs in biological fluids.
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