用共价有机骨架和聚吡咯复合吸附剂在填充注射器中微萃取联合高效液相色谱/紫外分光光度法测定尿样中的阿片类药物

IF 4.1 Q1 CHEMISTRY, ANALYTICAL
Fatemeh Zanganeh , Yadollah Yamini , Mohammad Mahdi Khataei , Mahboube Shirani
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引用次数: 3

摘要

本研究旨在建立在包装注射器(MEPS)中微萃取测定尿液样品中三种阿片类药物的方法。合成了共价有机骨架-聚吡咯-十六烷基三甲基溴化铵(cof - py - ctab)纳米复合材料,作为一种合适的高效吸附剂,并应用于MEPS工艺。分析物通过π堆积、疏水和主客体相互作用在吸附剂的固相表面分离和提取,然后用解吸溶剂洗脱。合成该复合材料,在注射器中作为分析物吸附底物,对影响分析物提取的参数进行优化,并根据最佳条件获得校准曲线。结果在0.5 ~ 1000 μg L−1浓度范围内呈线性关系,测定系数大于0.9945。检测限和定量限分别在(0.1 ~ 1.0)和(0.5 ~ 5.0)μ L-1范围内。在一天内、天之间以及注射器与注射器之间的工作精度分别为4.4-6.1%、6.5-8.1%和7.8-10.1%。可待因、罂粟碱和纳曲酮的预富集因子分别为17、20和16。尿液样品中可待因的相对回收率为94.4 ~ 100.6%,罂粟碱的相对回收率为99.3 ~ 103.1%,纳曲酮的相对回收率为95.0 ~ 98.9%。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Determination of opiates in urine samples using a composite of covalent organic framework and polypyrrole as a sorbent for microextraction in a packed syringe combined with HPLC/UV

Determination of opiates in urine samples using a composite of covalent organic framework and polypyrrole as a sorbent for microextraction in a packed syringe combined with HPLC/UV

This study aimed to develop microextraction in a packed syringe (MEPS) method for the determination of the three opiates in urine samples. Covalent organic framework-polypyrrole- cetyltrimethylammonium bromide (COF-PPy-CTAB) nanocomposite, as an appropriate and highly efficient adsorbent, was synthesized and applied to the MEPS process. The analytes were separated and extracted on the solid phase surface of the adsorbent through π stacking, hydrophobic, and host-guest interaction and then eluted by a desorbing solvent. After synthesizing the composite and using it in the syringe as a substrate for analyte adsorption, the parameters affecting the extraction of the analytes were optimized and the calibration curve was obtained according to the optimum conditions. The results were linear in the concentration range of 0.5–1000 μg L  1 with a coefficient of determination greater than 0.9945. The limits of detection and quantification were obtained in the range of (0.1–1.0) and (0.5–5.0) μg L‒1, respectively. The precision of the work was obtained for a syringe in a day and between days and also syringe to syringe in the range of 4.4–6.1%, 6.5–8.1%, and 7.8–10.1%, respectively. The preconcentration factors of 17, 20, and 16 were obtained for codeine, papaverine, and naltrexone, respectively. Relative recoveries of the drugs from urine samples were in acceptable range of 94.4–100.6% for codeine, 99.3–103.1% for papaverine and 95.0–98.9% for naltrexone.

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来源期刊
Talanta Open
Talanta Open Chemistry-Analytical Chemistry
CiteScore
5.20
自引率
0.00%
发文量
86
审稿时长
49 days
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