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基于荧光开启-关闭-开启策略的亮锰掺杂碳点用于测定高锰酸盐和 L-抗坏血酸。

Bright Mn-doped carbon dots for the determination of permanganate and L-ascorbic acid by a fluorescence on-off-on strategy.

机构信息

Guangxi Key Laboratory of Natural Polymer Chemistry and Physics, College of Chemistry and Materials, Nanning Normal University, Nanning, 530001, People's Republic of China.

出版信息

Mikrochim Acta. 2020 Nov 17;187(12):659. doi: 10.1007/s00604-020-04604-0.

Abstract

A one-pot hydrothermal synthesis of manganese-doped carbon dots (Mn-CDs) is reported for fluorescent "on-off-on" determination of Mn(VII) and L-ascorbic acid (L-AA) in aqueous solution and living cells. Mn-CDs were prepared by using sulfanilic acid, tetrakis(hydroxymethyl)phosphonium chloride, and Mn(II) chloride as precursors. Mn-CDs were characterized by several spectroscopic methods and microscopic techniques. Mn-CDs show distinctly long fluorescence lifetime (12.39 ± 0.07 ns) and high absolute fluorescence quantum yield (around 37%) with excitation and emission wavelengths of 362 and 500 nm, respectively. Mn-CDs exhibit no significant cytotoxicity to human cervical carcinoma HeLa cells and human embryonic kidney HEK-293T cells at 200 μg mL level after 48 h incubation. The fluorescence of Mn-CDs at 500 nm (excited at 362 nm) is quenched efficiently by Mn(VII) and can be further recovered after the addition of L-AA, resulting in a fluorescent "on-off-on" assay for the determination of Mn(VII) and L-AA. Under optimal experimental conditions, the linear response covers the 3 to 150 μM Mn(VII) concentration range and the 3 to 140 μM L-AA concentration range. This method offers relatively low detection limits of 0.66 μM for Mn(VII) and 0.90 μM for L-AA. This strategy was applied to visual determination of Mn(VII) and L-AA in living HeLa cells with satisfying results. Graphical abstract Schematic presentation of bright Mn-CD-based fluorescence "on-off-on" assay for both Mn(VII) and L-AA. This fluorescent assay possessed low detection limit of 0.66 μM for Mn(VII) and 0.90 μM for L-AA. This strategy was applied for visual determination of Mn(VII) and L-AA in living HeLa cells with satisfying results.

摘要

一种一锅水热法合成了锰掺杂碳点(Mn-CDs),用于荧光“开-关-开”测定水溶液和活细胞中的 Mn(VII)和 L-抗坏血酸(L-AA)。Mn-CDs 是用磺胺酸、四羟甲基氯化磷和 Mn(II)氯化物作为前体制备的。Mn-CDs 采用多种光谱方法和显微镜技术进行了表征。Mn-CDs 具有明显长的荧光寿命(12.39±0.07ns)和高的绝对荧光量子产率(约 37%),激发和发射波长分别为 362nm 和 500nm。Mn-CDs 在 200μg mL 水平孵育 48 小时后对人宫颈癌 HeLa 细胞和人胚肾 HEK-293T 细胞无明显细胞毒性。在 500nm(362nm 激发)处的 Mn-CDs 荧光被 Mn(VII)有效猝灭,加入 L-AA 后可进一步恢复,从而实现了 Mn(VII)和 L-AA 的荧光“开-关-开”测定。在最佳实验条件下,线性响应范围覆盖 3 至 150μM Mn(VII)浓度范围和 3 至 140μM L-AA 浓度范围。该方法对 Mn(VII)的检测限低至 0.66μM,对 L-AA 的检测限低至 0.90μM。该策略用于活 HeLa 细胞中 Mn(VII)和 L-AA 的可视化测定,结果令人满意。

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