A thiourea dihydropyridine as a highly selective and sensitive “turn-on” fluorescent chemosensor for mercury(II) ion in water and its application for cell imaging

IF 4.1 Q1 CHEMISTRY, ANALYTICAL
Islah Muttaqin , Waroton Paisuwan , Thitiporn Pattarakankul , Tanapat Palaga , Mongkol Sukwattanasinitt , Anawat Ajavakom
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引用次数: 0

Abstract

The existence of extremely toxic mercury contaminants in the environment, even at very low concentrations, poses severe human health issues. Mercury exposure may lead to various diseases, such as prenatal brain damage, cognitive severe, motion disorders, and Minamata diseases. Hence, developing an effective and selective method to detect Hg2+ in the environment and biological samples is of great interest. Amongst various Hg2+ detection techniques, fluorescent chemosensors offer more convenient procedures, affordable cost, high selectivity, and the capability to perform cell imaging for Hg2+ detection. Herein, a novel "turn-on" fluorescent chemosensor, Thiourea-DHP derivative (TUD), highly selective to Hg2+, was successfully developed. TUD was synthesized by cyclotrimerization of β-amino acrylate, followed by the thioacylation of the resulting dihydropyridine (DHP) with dimethylamino thiocarbonyl chloride. The Hg2+ detection by TUD displayed an astonishing naked-eye blue fluorescence signal under blacklight, exhibiting an LOD of 69 nM or 14 ppb at pH 7.4 in the HEPES buffer. Hg2+-induced hydrolytic desulfurization of the low fluorescent TUD to produce the strongly fluorescent urea-DHP (UD) is proposed as a mechanism for this fluorescence enhancement. The formation of UD was confirmed by 1H NMR, 13C NMR, and HRMS. This detecting system of TUD provided excellent percentage recovery (>97 %) for the analysis of Hg2+ contaminants in real-environmental water samples. Besides, the TUD probe showed nontoxic properties in living cells towards RAW264.7 murine macrophage cell line even at high concentrations (100 µM). Our proposed TUD probe demonstrated superior sensitivity in pure aqueous media compared to current mercury-desulfurization fluorescent chemosensors. This sensing system proved effective for analysing Hg2+ contaminants in real-environmental water samples. Additionally, the nontoxic TUD probe successfully revealed the remarkable biocompatibility for Hg2+ detection in living cells.

Abstract Image

硫脲二氢吡啶作为水中汞(II)离子的高选择性、高灵敏度 "开启 "荧光化学传感器及其在细胞成像中的应用
环境中存在毒性极强的汞污染物,即使浓度很低,也会对人类健康造成严重危害。接触汞可能会导致各种疾病,如产前脑损伤、严重的认知障碍、运动障碍和水俣病。因此,开发一种有效且具有选择性的方法来检测环境和生物样本中的 Hg2+ 是非常有意义的。在各种 Hg2+ 检测技术中,荧光化学传感器具有操作简便、成本低廉、选择性高、可进行细胞成像等优点。本研究成功开发了一种新型 "开启式 "荧光化学传感器--硫脲-DHP 衍生物(TUD),它对 Hg2+ 具有高选择性。TUD 是由β-氨基丙烯酸酯环化合成的,然后用二甲基氨基硫代羰酰氯对生成的二氢吡啶(DHP)进行硫代酰化。在黑光灯下,TUD 对 Hg2+ 的检测显示出惊人的裸眼蓝色荧光信号,在 pH 值为 7.4 的 HEPES 缓冲液中,检测限为 69 nM 或 14 ppb。Hg2+ 诱导的低荧光 TUD 水解脱硫产生强荧光脲-DHP(UD)被认为是这种荧光增强的机制。1H NMR、13C NMR 和 HRMS 证实了 UD 的形成。这种 TUD 检测系统对实际环境水样中 Hg2+ 污染物的分析具有极高的回收率(97%)。此外,即使在高浓度(100 µM)下,TUD 探针在活细胞中对 RAW264.7 鼠巨噬细胞系也显示出无毒性。与目前的汞脱硫荧光化学传感器相比,我们提出的 TUD 探针在纯水介质中表现出更高的灵敏度。事实证明,这种传感系统能有效分析实际环境水样中的 Hg2+ 污染物。此外,无毒 TUD 探针成功揭示了在活细胞中检测 Hg2+ 的显著生物相容性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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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