探索天然环糊精纳米海绵的提取能力:从α-到γ-环糊精聚合物的改进

IF 6.5 Q1 CHEMISTRY, ANALYTICAL
Nina Felli, Davide Filardi, Riccardo Sergi, Luisa Maria Migneco, Massimo Giuseppe De Cesaris, Lorenzo Antonelli, Iolanda Francolini, Alessandra Gentili
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引用次数: 0

摘要

环糊精(CD)是一种环状低聚糖,以其与适当大小的分子形成包合物的能力而闻名。cd还可以作为多官能单体用于聚合反应,制备具有生物降解特性的专用吸附剂。在这项工作中,以天然cd (α-, β-和γ-CD)为单体,柠檬酸为交联剂,磷酸二氢钠(NaH2PO4)为催化剂,制备了不同的cd基聚合物,称为“纳米海绵”(CDNS)。红外光谱的羰基带移证实了CD的交联,热重分析证实了CDNS的降解途径比CD更复杂。扫描电镜显示CDNS具有多孔结构。研究了它们在分散固相萃取中对42种模型化合物(包括药物、激素、除草剂和杀虫剂等常见有机污染物)的吸附性能。其中,γ-CDNS效率最高,在0.5µg/L和5µg/L浓度下,平均回收率分别为67%和79%。相对标准偏差均在20%以下。检出限为0.001 ~ 0.462µg/L,定量限为0.004 ~ 1.428µg/L。合成材料易于生产,开发的程序可以分析10个样品/小时,为样品制备的新应用打开了大门。最后,不同指标的应用证明了整个分析过程的环境相容性(AGREE评分=0.55,ComplexMoGAPI评分=64)和所提出的提取方法的良好实用性(BAGI评分>;60).
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Exploring the extraction capabilities of natural cyclodextrin-nanosponges: The improvement moving from α- to γ-cyclodextrin-based polymers

Exploring the extraction capabilities of natural cyclodextrin-nanosponges: The improvement moving from α- to γ-cyclodextrin-based polymers
Cyclodextrins (CD) are cyclic oligosaccharides known for their capability to form inclusion complexes with molecules of appropriate size. CDs can also be used as polyfunctional monomers in polymerization reactions to prepare specialised sorbents with characteristics of biodegradability. In this work, different CD-based polymers, known as “nanosponges” (CDNS), were obtained using natural CDs (α-, β-, and γ-CD) as monomers, citric acid as the cross-linker and sodium dihydrogen phosphate (NaH2PO4) as the catalyst. CD cross-linking was confirmed by the carbonyl band shift in IR spectroscopy and the more complex degradation pathway in CDNS compared to CDs in thermogravimetric analysis. Scanning electron microscopy evidenced a porous structure of CDNS. Their sorption properties were investigated in the dispersive-solid phase extraction of 42 model compounds (common organic contaminants including drugs, hormones, herbicides, and pesticides) from river water samples. Among all the polymers, γ-CDNS exhibited the highest efficiency, achieving recoveries averaged on all the analytes of 67% and 79% at the concentration of 0.5 and 5 µg/L, respectively. Relative standard deviations were always below 20%. Detection limits ranged from 0.001 to 0.462 µg/L, while quantitation limits from 0.004 to 1.428 µg/L. The synthesized material is easy to produce, and the developed procedure enables the analysis of 10 samples/h, opening the door to new applications in sample preparation. Finally, the application of different metrics proved the environmental compatibility of the entire analytical procedure (AGREE score=0.55, and ComplexMoGAPI score=64) and the good practicability of the extraction method proposed (BAGI score > 60).
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3.50
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