电感耦合等离子体发射光谱法测定药物样品中痕量As、Cd、Hg和Pb

IF 5.2 Q1 CHEMISTRY, ANALYTICAL Advances in Sample Preparation Pub Date : 2023-08-01 DOI:10.1016/j.sampre.2023.100084
Sergio J. Abellán-Martín , Jorge Pérez , Fernanda C. Pinheiro , Joaquim A. Nóbrega , Miguel Ángel Aguirre , Lorena Vidal , Antonio Canals
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引用次数: 1

摘要

建立了电感耦合等离子体发射光谱法同时测定药物样品中砷、镉、汞和铅的新方法。为了提高分析的灵敏度,在使用天然深共晶溶剂(NADES)作为萃取剂溶剂的分散液-液微萃取(DLLME)程序之后,使用多沸腾器进行化学蒸汽生成(CVG)。通过多元分析优化了影响分析物提取和在线化学蒸汽生成的因素。在优化的条件下,DLLME-CVG-ICP-OES与直接ICP OES分析相比,平均提高了50倍的定量限(LOQ)值,并使灵敏度(即富集因子)平均提高了25倍,是CVG-ICP OES的25倍。根据美国药典(USP)第232章,这意味着1类目标元素的LOQ值平均比各自的0.3J值低4.3倍。根据USP建议,对两种固体剂型的口服药物样品(即商业剂型片剂)进行了回收实验,以评估其真实性。此外,已使用AGREEprep指标评估了所开发方法的绿色性,显示出优异的绿色特性,因为它包括使用减少体积(即几微升)的无害萃取剂溶剂进行多元分析的样品制备程序的小型化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Synergistic combination of natural deep eutectic solvent and chemical vapor generation for trace determination of As, Cd, Hg and Pb in drug samples by inductively coupled plasma optical emission spectrometry

A new and environmentally friendly analytical method for simultaneous determination of As, Cd, Hg and Pb in drug samples by inductively coupled plasma optical emission spectrometry (ICP OES) has been developed. In order to increase the sensitivity of the analysis, a multinebulizer has been used for chemical vapor generation (CVG) after a dispersive liquid-liquid microextraction (DLLME) procedure using a natural deep eutectic solvent (NADES) as extractant solvent. The factors affecting analyte extraction and on-line chemical vapor generation have been optimized by multivariate analysis. Under optimized conditions, DLLME-CVG-ICP OES improved limit of quantitation (LOQ) values on average 50-fold higher compared with direct ICP OES analysis and afforded an increase of the sensitivity (i.e., enrichment factor) on average 25-times higher than those obtained with CVG-ICP OES analysis. According to the United States Pharmacopoeia (USP) Chapter 232, it means LOQ values are on average 4.3-times lower than their respective 0.3J values for the target-elements from class 1. Trueness has been evaluated by recovery experiments following USP recommendations for two oral drug samples in solid dosage form (i.e., commercial dosage tablets). In addition, the greenness of the developed method has been evaluated using the AGREEprep metrics, showing an excellent green character since it includes the miniaturization of the sample preparation procedure using a reduced volume (i.e., few microliters) of a non-hazardous extractant solvent for multielemental analysis.

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