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一种利用蛋白质导向金纳米团簇检测环境空气中臭氧的“开启型”荧光传感器。

A "turn-on" fluorescent sensor for ozone detection in ambient air using protein-directed gold nanoclusters.

作者信息

Wu Di, Qi Wenjing, Liu Chun, Zhang Qing

机构信息

Chongqing Key Laboratory of Green Synthesis and Applications, College of Chemistry, Chongqing Normal University, Chongqing, 401331, China.

Qijiang Environmental Monitoring Station, LongJiao Road 2#, Chongqing, 401420, China.

出版信息

Anal Bioanal Chem. 2017 Apr;409(10):2539-2546. doi: 10.1007/s00216-017-0199-8. Epub 2017 Jan 26.

Abstract

A "turn-on" fluorescent sensor for ozone using bovine serum albumin-directed gold nanoclusters (BSA-Au NCs) via energy transfer was developed. The spectral overlap of fluorescent spectrum of BSA-Au NCs with absorption spectrum of indigo carmine (IDS) was utilized. Ozone cleaves C = C bond of IDS and suppresses energy transfer from BSA-Au NCs to IDS. Therefore, this proposed fluorescent sensor is a "turn-on" detection motif. It is the first application of fluorescent nanoclusters in sensitively detecting ozone from 0.2 to 12 μM with the limit of detection of 35 nM (the volume of 500 μL, 1.68 ppb). The proposed fluorescent sensor for ozone is more sensitive and faster (within 2 min) than most methods and is with good selectivity for ozone detection against other reactive oxygen species, reactive nitrogen, or metallic ions. Besides, the proposed method is also utlized in ozone detection in ambient air by monitoring 1 h (60 min) in Qijiang district in Chongqing city. The average of concentration of ozone in ambient air ranges from 44.97 to 52.85 μg/m. The results are compared with the automatic monitoring data provided by Qijiang Environmental Monitoring Station and the relative deviations range, respectively, from 2.1 to 5.6%, which suggests that it is a promising fluorescent sensor for ozone in ambient air. This study not only develops a new model of energy transfer motif using BSA-Au NCs as donor and IDS as acceptor but also expands the application of BSA-Au NCs in environmental science. Graphical abstract A "turn-on" fluorescent sensor for ozone detection using bovine serum albumin-directed gold nanoclusters (BSA-Au NCs) via energy transfer is developed. It is the first time to utilize spectral overlap of fluorescent spectrum of BSA-Au NCs with absorption spectrum of indigo carmine and to achieve fast, sensitive, and selective ozone detection with a limit of detection of down to 35 nM (the volume of 500 μL, 1.68 ppb).

摘要

通过能量转移开发了一种使用牛血清白蛋白导向的金纳米团簇(BSA-Au NCs)的“开启”型臭氧荧光传感器。利用了BSA-Au NCs荧光光谱与靛蓝胭脂红(IDS)吸收光谱的光谱重叠。臭氧会裂解IDS的C = C键,并抑制从BSA-Au NCs到IDS的能量转移。因此,这种提出的荧光传感器是一种“开启”检测模式。这是荧光纳米团簇首次用于灵敏检测0.2至12μM的臭氧,检测限为35 nM(500μL体积,1.68 ppb)。所提出的臭氧荧光传感器比大多数方法更灵敏、更快(2分钟内),并且对臭氧检测具有良好的选择性,可抵御其他活性氧、活性氮或金属离子。此外,通过在重庆市綦江区监测1小时(60分钟),该方法还用于环境空气中的臭氧检测。环境空气中臭氧浓度的平均值范围为44.97至52.85μg/m。将结果与綦江区环境监测站提供的自动监测数据进行比较,相对偏差范围分别为2.1%至5.6%,这表明它是一种用于环境空气中臭氧检测的有前景的荧光传感器。本研究不仅开发了一种以BSA-Au NCs为供体、IDS为受体的能量转移模式新模型,还扩展了BSA-Au NCs在环境科学中的应用。图形摘要:通过能量转移开发了一种使用牛血清白蛋白导向的金纳米团簇(BSA-Au NCs)的用于臭氧检测的“开启”型荧光传感器。首次利用BSA-Au NCs荧光光谱与靛蓝胭脂红吸收光谱的光谱重叠,实现了快速、灵敏和选择性的臭氧检测,检测限低至35 nM(500μL体积,1.68 ppb)。

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