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一种基于双位点识别的用于检测咖啡酸的水溶性硼酸传感器。

A water-soluble boronic acid sensor for caffeic acid based on double sites recognition.

作者信息

Bian Zhancun, Fang Guiqian, Wang Ran, Zhan Dongxue, Yao Qingqiang, Wu Zhongyu

机构信息

School of Medicine and Life Sciences, University of Jinan, Shandong Academy of Medical Sciences Jinan 250200 Shandong China.

Institute of Materia Medica, Shandong First Medical University, Shandong Academy of Medical Sciences Jinan 250062 Shandong China

出版信息

RSC Adv. 2020 Jul 27;10(47):28148-28156. doi: 10.1039/d0ra00980f.

Abstract

Due to reversibly and covalently binding with Lewis bases and polyols, boronic acid compounds as fluorescent sensors have been widely reported to recognize carbohydrates, ions, hydrogen peroxide, and so on. However, boronic acid sensors for highly selective recognition of caffeic acid rather than catechol or catechol derivatives have not been reported yet. Herein a novel water-soluble sensor 5c with double recognition sites based on a boronic acid was reported. When 2.3 × 10 M of caffeic acid was added, the fluorescence intensity of sensor 5c decreased by 99.6% inner filter effect (IFE) because its excitation spectrum well overlaps with the absorption spectrum of caffeic acid under neutral condition, while the fluorescence increased or did not change obviously after binding with other analytes including carbohydrates and other catechol derivatives. In addition, the response time to caffeic acid is fast at room temperature, and a high binding constant (9245.7 ± 348.3 M) and low LOD (1.81 × 10 M) was calculated. Moreover, determination of caffeic acid content in caffeic acid tablets was studied, and the recovery rate is sufficient. Therefore, sensor 5c can be used as a potential tool for detecting biologically significant caffeic acid in real samples.

摘要

由于硼酸化合物能与路易斯碱和多元醇发生可逆和共价结合,作为荧光传感器的硼酸化合物已被广泛报道可用于识别碳水化合物、离子、过氧化氢等。然而,尚未有关于硼酸传感器对咖啡酸具有高度选择性识别而不是对儿茶酚或儿茶酚衍生物的报道。在此报道了一种基于硼酸的具有双识别位点的新型水溶性传感器5c。当加入2.3×10⁻⁶ M的咖啡酸时,传感器5c的荧光强度因内滤效应(IFE)降低了99.6%,因为在中性条件下其激发光谱与咖啡酸的吸收光谱很好地重叠,而与包括碳水化合物和其他儿茶酚衍生物在内的其他分析物结合后荧光增强或无明显变化。此外,在室温下对咖啡酸的响应时间很快,计算得到高结合常数(9245.7±348.3 M⁻¹)和低检测限(1.81×10⁻⁷ M)。而且,研究了咖啡酸片中咖啡酸含量的测定,回收率良好。因此,传感器5c可作为检测实际样品中具有生物学意义的咖啡酸的潜在工具。

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