具有hxl拓扑的胺模板N,O-Linked Co(II)-MOF用于肿瘤生物标志物GSH和工业毒物HCHO的“开启”检测:双靶标方法

IF 2.9 Q2 CHEMISTRY, ANALYTICAL
Udayan Mondal, Rajeshwari Pal, Bappaditya Goswami, Priyabrata Banerjee
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引用次数: 0

摘要

荧光功能材料,特别是发光金属有机框架(LMOFs),在过去十年中一直是材料科学研究的核心。在此,我们报道了一种溶剂热合成的Co- mof [Co(phen)(5-aipa)]∞(phen: 1,10-菲罗啉,5-aipa: 5-氨基间苯二甲酸),用于基于发光的,可回收的,“开启”检测“肿瘤生物标志物”谷胱甘肽(GSH)和工业污染物甲醛(FA)。复杂的表征,包括XRD, XPS, TGA, FESEM, FT-IR和Hirshfeld分析,证明了高相纯度,热稳定性,鲁强性,存在π -π堆叠和弱h键。MOF对GSH (60.37 nM)和FA (9.77 μM)的检出限低,响应时间快(GSH为25 s, FA为2 min)。在复杂的生物样品中检测到生物标志物谷胱甘肽,包括胎牛血清、蔬菜和人尿,回收率在81%至89%之间。通过几种传感器分析物加合物的RGB颜色变化,提出了一种智能手机辅助gsh传感平台。基于传感器对不同GSH浓度的光谱响应,还演示了一个5输入4输出的分子逻辑门。将FA检测范围扩展到鱼类、肉类和废水样品中,回收率为91 ~ 107%。DFT计算表明,分析物相互作用限制了MOF中光诱导的电子转移,增强了荧光现象。这些发现为基于mof的传感器技术开辟了新的可能性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Amine-Templated N,O-Linked Co(II)-MOF with hxl Topology for “Turn-On” Detection of Tumor Biomarker GSH and Industrial Toxicant HCHO: A Dual-Target Approach

Amine-Templated N,O-Linked Co(II)-MOF with hxl Topology for “Turn-On” Detection of Tumor Biomarker GSH and Industrial Toxicant HCHO: A Dual-Target Approach

Amine-Templated N,O-Linked Co(II)-MOF with hxl Topology for “Turn-On” Detection of Tumor Biomarker GSH and Industrial Toxicant HCHO: A Dual-Target Approach

Fluorescent functional materials, particularly luminescent metal–organic frameworks (LMOFs), have been central to material science research over the past decade. Herein, we report a Co-MOF [Co(phen)(5-aipa)] (phen: 1,10-phenanthroline, 5-aipa: 5-aminoisophthalic acid), synthesized solvothermally, for luminescence-based, recyclable, “turn-on” detection of “tumor biomarker” glutathione (GSH), and industrial pollutant formaldehyde (FA). Sophisticated characterizations, including XRD, XPS, TGA, FESEM, FT-IR, and Hirshfeld analysis, demonstrate high phase purity, thermal stability, robustness, presence of ππ stacking, and weak H-bonding in the framework. The MOF shows low detection limits for GSH (60.37 nM) and FA (9.77 μM) with fast response times (25 s for GSH, <2 min for FA). Biomarker GSH was detected in complex biological samples, including fetal bovine serum, vegetable, and human urine, with recovery rates between 81% and 89%. A smartphone-assisted GSH-sensing platform was proposed via RGB color variations of several sensor-analyte adducts. A 5-input, 4-output molecular logic gate was also demonstrated based on the sensor's spectroscopic response to varying GSH concentrations. FA detection was extended to fish, meat, and wastewater samples, with recoveries of 91–107%. DFT calculations revealed that analyte interactions restricted photo-induced electron transfer in the MOF, enhancing fluorescence phenomenon. These findings open new possibilities for MOF-based sensor technologies.

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