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由硫氰酸铵衍生的硫氮二元掺杂碳点用于活细胞中多西环素的选择性检测及多色细胞成像

Sulfur and nitrogen binary doped carbon dots derived from ammonium thiocyanate for selective probing doxycycline in living cells and multicolor cell imaging.

作者信息

Xue Mingyue, Zhang Liangliang, Zhan Zhihua, Zou Mengbing, Huang Yong, Zhao Shulin

机构信息

Key Laboratory for the Chemistry and Molecular Engineering of Medicinal Resources (Ministry of Education), College of Chemistry and Pharmacy, Guangxi Normal University, Guilin 541004, China; Guilin Normal College, Guilin 541001, China.

Key Laboratory for the Chemistry and Molecular Engineering of Medicinal Resources (Ministry of Education), College of Chemistry and Pharmacy, Guangxi Normal University, Guilin 541004, China.

出版信息

Talanta. 2016 Apr 1;150:324-30. doi: 10.1016/j.talanta.2015.12.024. Epub 2015 Dec 12.

Abstract

A novel sulfur and nitrogen binary doped carbon dots (S,N-CDs) was synthesized by one-step manner through the hydrothermal treatment of citric acid (CA) and ammonium thiocyanate, and the procedures for biomedical applications, including probing doxycycline in living cells and multicolor cell imaging were developed. The obtained S,N-CDs are stable in aqueous solution, possess a very high quantum yield (QY, 74.15%) and good photostability. The fluorescence of S,N-CDs can be specifically quenched by doxycycline, providing a convenient turn-off assay of doxycycline. This assay shows a wide linear detection range from 0.08 to 60 μM with a low detection limit of 20 nM. The present method also displays a good selectivity. More importantly, the S,N-CDs have an excellent biocompatibility and low cytotoxicity, allowing the multicolor cell imaging and doxycycline detection in living cells. Consequently, the developed doxycycline methods is facile, low-cost, biocompatible, sensitive and selective, which may hold the potential applications in the fields of food safety and environmental monitoring, as well as cancer therapy and related mechanism research.

摘要

通过对柠檬酸(CA)和硫氰酸铵进行水热一步法合成了一种新型硫氮共掺杂碳点(S,N-CDs),并开发了其生物医学应用程序,包括在活细胞中探测多西环素和进行多色细胞成像。所制备的S,N-CDs在水溶液中稳定,具有很高的量子产率(QY,74.15%)和良好的光稳定性。S,N-CDs的荧光可被多西环素特异性猝灭,为多西环素提供了一种便捷的关闭型检测方法。该检测方法的线性检测范围宽,为0.08至60 μM,检测限低至20 nM。本方法还具有良好的选择性。更重要的是,S,N-CDs具有优异的生物相容性和低细胞毒性,可用于活细胞中的多色细胞成像和多西环素检测。因此,所开发的多西环素检测方法简便、低成本、生物相容性好、灵敏且具有选择性,在食品安全、环境监测以及癌症治疗和相关机制研究等领域可能具有潜在应用。

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