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非芳香族发光聚合物的比色 pH 传感、光物理和细胞成像。

Ratiometric pH Sensing, Photophysics, and Cell Imaging of Nonaromatic Light-Emitting Polymers.

机构信息

Advanced Polymer Laboratory, Department of Polymer Science and Technology, Government College of Engineering and Leather Technology (Post Graduate), Maulana Abul Kalam Azad University of Technology, Salt Lake City, Kolkata, West Bengal 700106, India.

Department of Chemistry, University of Gour Banga, Mokdumpur, Malda, West Bengal 732103, India.

出版信息

ACS Appl Bio Mater. 2022 Jun 20;5(6):2990-3005. doi: 10.1021/acsabm.2c00297. Epub 2022 May 17.

Abstract

Here, four nontraditional fluorescent polymers (s) of varying ,-dimethyl-2-propenamide (DMPA) and butyl prop-2-enoate (BPE) mole ratios, i.e., 2:1 (), 4:1 (), 8:1 (), and 16:1 (), are prepared via random polymerization in water. The maximum fluorescence enhancement of makes it suitable for ratiometric pH sensing, Cu(II) sensing, and pH-dependent cell imaging of Madin-Darby canine kidney (MDCK) cells. The oxygen donor functionalities of involved in binding and sensing with Cu(II) ions are studied by absorption, emission, electron paramagnetic resonance, Fourier transform infrared (FTIR), and O1s/Cu2p X-ray photoelectron spectroscopies (XPS). The spectral responses of the ratiometric pH sensor within 1.5-11.5 confirm 22 and 44 nm red shifts in absorption and ratiometric emission, respectively. The striking color changes from blue (436 nm) to green (480 nm) via an increase in pH are thought to be the stabilization of the charged canonical form of tertiary amide, i.e., -C(O)═N(CH), realized from the changes in the absorption/fluorescence spectra and XPS/FTIR analyses. The through-space -π* interactions in the aggregate, N-branching-associated rigidity, and nonconventional intramolecular hydrogen bondings of adjacent moieties in the aggregate contribute to aggregation-enhanced emissions (AEEs). Here, structures of , aggregate, and Cu(II)-; absorption; -π* interactions; hydrogen bondings; AEEs; and binding with Cu(II) are ascertained by density functional theory, time-dependent density functional theory, and reduced density gradient calculations. The excellent limits of detection and Stern-Volmer constants of are 2.24 nM/0.14234 ppb and 4.26 × 10 M at pH = 6.5 and 0.95 nM/0.06037 ppb and 4.90 × 10 M at pH = 8.0, respectively. Additionally, the Stokes shift and binding energy of are 13,636 cm/1.69 eV and -4.64 eV, respectively. The pH-dependent MDCK cell imaging ability of noncytotoxic is supported via fluorescence imaging and 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay.

摘要

这里,通过在水中的随机聚合制备了四种不同摩尔比的 - 二甲基-2-丙烯酰胺(DMPA)和丁基丙-2-烯酸酯(BPE)的非传统荧光聚合物(s),即 2:1()、4:1()、8:1()和 16:1()。最大荧光增强使 适用于比率 pH 感应、Cu(II)感应和 Madin-Darby 犬肾(MDCK)细胞的 pH 依赖性细胞成像。通过吸收、发射、电子顺磁共振、傅里叶变换红外(FTIR)和 O1s/Cu2p X 射线光电子能谱(XPS)研究了与 Cu(II)离子结合和感应的氧供体功能。比率 pH 传感器在 1.5-11.5 范围内的光谱响应分别确认了吸收和比率发射的 22 和 44nm 红移。通过 pH 值增加从蓝色(436nm)到绿色(480nm)的显著颜色变化被认为是稳定的三级酰胺的带电经典形式,即 -C(O)═N(CH)3,从吸收/荧光光谱和 XPS/FTIR 分析的变化中实现。在 聚集物中,通过空间 -π相互作用、N-支化相关的刚性以及相邻 基团在 聚集物中的非常规分子内氢键,有助于聚集增强发射(AEEs)。这里,通过密度泛函理论、含时密度泛函理论和简化密度梯度计算确定了、聚合体、和 Cu(II)-;吸收;-π相互作用;氢键;AEEs;和与 Cu(II)的结合。在 pH = 6.5 时,检测限和 Stern-Volmer 常数分别为 2.24 nM/0.14234 ppb 和 4.26 × 10 M,在 pH = 8.0 时,检测限和 Stern-Volmer 常数分别为 0.95 nM/0.06037 ppb 和 4.90 × 10 M。此外,的斯托克斯位移和结合能分别为 13,636cm/1.69eV 和-4.64eV。通过荧光成像和 3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四唑溴化物测定,支持非细胞毒性的 pH 依赖性 MDCK 细胞成像能力。

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