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环境水体中米托蒽醌的测定:一种采用分子印迹聚合物通过盐饱和移液器吸头微固相萃取进行预富集的分光光度法。

Determination of mitoxantrone in environmental waters: a spectrophotometric method with preconcentration by salt saturated pipette-tip micro solid phase extraction using molecularly imprinted polymer.

作者信息

Hashemi Sayyed Hossein, Kaykhaii Massoud, Jamali Keikha Ahmad, Esmailiun Mina

机构信息

Department of Marine Chemistry, Faculty of Marine Science, Chabahar Maritime University, Chabahar, Iran.

Department of Analytical Chemistry, Faculty of Natural Sciences, Comenius University in Bratislava, Bratislava, Slovak Republic.

出版信息

Turk J Chem. 2025 Apr 4;49(3):267-278. doi: 10.55730/1300-0527.3728. eCollection 2025.

Abstract

In this research, a fast and simple spectrophotometric method is presented for mitoxantrone determination in various aqueous samples. It utilizes preconcentration by salt saturated pipette-tip micro solid phase extraction with a selective molecularly imprinted polymer adsorbent packed in a micropipette tip. Prior to sample loading, they were saturated with a mixture of NaCl, Mg (NO).6HO and KNO salts, enhancing extraction efficiency by 27.5% compared to salt-free conditions. Key microextraction parameters (amount of molecularly imprinted polymer, sample pH, eluent type/volume, and adsorption/desorption cycles) were optimized using response surface methodology and one-variable-at-a-time methods. The method achieves a low detection limit (0.2 μg L) and a wide linear range (1-1000 μg L). An enrichment factor of 49 is obtained with excellent accuracy (relative standard deviation <4.4%). The method was validated by comparing it to a standard high performance liquid chromatography protocol, as well as spiking real samples in three concentration levels. The method successfully detected low levels of mitoxantrone in various water samples.

摘要

本研究提出了一种快速简便的分光光度法,用于测定各种水性样品中的米托蒽醌。该方法采用盐饱和移液器吸头微固相萃取进行预富集,使用填充在微量移液器吸头中的选择性分子印迹聚合物吸附剂。在加载样品之前,先用氯化钠、六水合硝酸镁和硝酸钾的混合物使其饱和,与无盐条件相比,萃取效率提高了27.5%。使用响应面法和一次变量法对关键微萃取参数(分子印迹聚合物的量、样品pH值、洗脱液类型/体积以及吸附/解吸循环)进行了优化。该方法实现了低检测限(0.2 μg/L)和宽线性范围(1 - 1000 μg/L)。获得了49的富集因子,具有出色的准确度(相对标准偏差<4.4%)。通过与标准高效液相色谱法进行比较以及对三个浓度水平的实际样品进行加标,对该方法进行了验证。该方法成功检测了各种水样中低水平的米托蒽醌。

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