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用于氟喹诺酮类药物磁性固相萃取的高度氟化卟啉基共价有机框架修饰FeO纳米球的制备

Fabrication of highly fluorinated porphyrin-based covalent organic frameworks decorated FeO nanospheres for magnetic solid phase extraction of fluoroquinolones.

作者信息

Zhang Juan, Chen Zhipeng, Tang Furong, Wu Fengshou, Luo Xiaogang, Liu Genyan

机构信息

School of Chemistry and Environmental Engineering, Hubei Key Laboratory of Novel Reactor and Green Chemical Technology, Key Laboratory for Green Chemical Process of Ministry of Education, Wuhan Institute of Technology, Wuhan, 430205, China.

School of Chemical Engineering and Pharmacy, Key Laboratory of Novel Biomass-Based Environmental and Energy Materials in Petroleum and Chemical Industry, Wuhan Institute of Technology, Wuhan, 430205, China.

出版信息

Mikrochim Acta. 2022 Nov 17;189(12):449. doi: 10.1007/s00604-022-05541-w.

Abstract

A highly fluorinated porphyrin-based covalent organic frameworks magnetic adsorbent (FPy-COF@PDA@FeO) was fabricated by using polydopamine (PDA) grafting FeO nanospheres as magnetic core and FPy-COF as shell for magnetic solid phase extraction (MSPE) of fluoroquinolones (FQs). FPy-COF was constructed by using 5,15-bis(4-aminophenyl)-10,20-bis(perfluorophenyl)porphyrin and 4,4'-biphenyldicarboxaldehyde as two building blocks. PDA as a bridge grafting on the surface of FeO nanospheres facilitated the growth of FPy-COF. The morphology and structure of FPy-COF@PDA@FeO adsorbent were characterized in detail. The prepared magnetic adsorbent exhibited good extraction capability to amphiphilic FQs due to their superior chemical affinities such as fluorophilic interaction and hydrogen-bond interaction from nitrogen-rich skeleton. Under the optimized conditions, the MSPE method combined with high performance liquid chromatography with ultraviolet detection (HPLC-UV) was developed to sensitively quantify trace level of six FQs in milk samples. The developed MSPE-HPLC method showed good linearity with wide concentration range, precision, and low limits of detection (S/N = 3) for six FQs as low as 2.3 ngꞏmL in milk. The extraction recoveries of different spiked concentrations were in the range 77.8-110.4% for milk samples with RSD less than 9.7%.

摘要

通过使用聚多巴胺(PDA)接枝FeO纳米球作为磁核以及FPy - COF作为壳层,制备了一种高度氟化的基于卟啉的共价有机框架磁性吸附剂(FPy - COF@PDA@FeO),用于氟喹诺酮类药物(FQs)的磁性固相萃取(MSPE)。FPy - COF是由5,15 - 双(4 - 氨基苯基)- 10,20 - 双(全氟苯基)卟啉和4,4'-联苯二甲醛作为两个构建单元构建而成。PDA作为桥接物接枝在FeO纳米球表面,促进了FPy - COF的生长。对FPy - COF@PDA@FeO吸附剂的形态和结构进行了详细表征。所制备的磁性吸附剂对两亲性FQs表现出良好的萃取能力,这归因于它们具有卓越的化学亲和力,如来自富氮骨架的氟ophilic相互作用和氢键相互作用。在优化条件下,开发了结合高效液相色谱 - 紫外检测(HPLC - UV)的MSPE方法,用于灵敏定量牛奶样品中痕量水平的六种FQs。所开发的MSPE - HPLC方法对六种FQs在牛奶中具有宽浓度范围的良好线性、精密度和低检测限(S/N = 3),低至2.3 ng·mL。对于牛奶样品,不同加标浓度的萃取回收率在77.8 - 110.4%范围内,相对标准偏差小于9.7%。

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