Key Laboratory of Research and Utilization of Ethnomedicinal Plant Resources of Hunan Province, Hunan Provincial Higher Education Key Laboratory of Intensive Processing Research On Mountain Ecological Food, College of Biological and Food Engineering, Huaihua University, Huaihua, 418008, China.
Key Laboratory of Energy Catalysis and Conversion of Nanchang, College of Chemistry and Chemical Engineering, Jiangxi Normal University, Nanchang, 330022, China.
Mikrochim Acta. 2023 Jan 31;190(2):79. doi: 10.1007/s00604-023-05644-y.
The potential of coordination polymers (CPs) as a host of integrating multiple guest species to construct a fluorescence resonance energy transfer (FRET) nanoprobe was demonstrated. The ZnCPs built from zinc(II) and adenine was employed as a model of CPs to integrate carbon dot (CD) and phenol red (PR) for producing the FRET nanoprobe (CD/PR@ZnCPs). Benefiting from the confinement effect of ZnCPs, the integrated CD and PR can be brought in close proximity to favor the occurrence of FRET process from CD to PR, which leads to the quenching of CD fluorescence. However, the FRET process was disrupted upon the red-shift of PR absorption from 428 to 562 nm in alkaline medium, and consequently switches on the fluorescence of CD/PR@ZnCPs. Based on this finding, by utilizing urease to hydrolyze urea and mediate medium pH, a turn-on fluorescent method was established for the detection of urease activity. This fluorescent method has a linear response that covers 5 to 150 U/L urease with a detection limit of 0.74 U/L and exhibits an excellent selectivity over other enzymes. The successful determination of urease in saliva samples demonstrates the applicability of the fluorescent nanoprobe in complex biological matrix.
配位聚合物(CPs)作为一种整合多种客体物种的主体,具有构建荧光共振能量转移(FRET)纳米探针的潜力。本文选用腺嘌呤和锌(II)构建的 ZnCPs 作为 CPs 的模型,整合碳点(CD)和酚红(PR),制备 FRET 纳米探针(CD/PR@ZnCPs)。得益于 ZnCPs 的限域效应,整合的 CD 和 PR 可以紧密靠近,有利于从 CD 到 PR 的 FRET 过程的发生,从而导致 CD 荧光的猝灭。然而,当 PR 的吸收从 428nm 红移到 562nm 时,碱性介质中的吸收峰发生红移,FRET 过程被破坏,从而使 CD/PR@ZnCPs 的荧光恢复。基于这一发现,利用脲酶水解尿素并调节介质 pH 值,建立了一种用于检测脲酶活性的荧光开启方法。该荧光法的线性响应范围为 5 至 150 U/L 脲酶,检测限为 0.74 U/L,对其他酶具有优异的选择性。在唾液样本中成功测定了脲酶,证明了荧光纳米探针在复杂生物基质中的适用性。