School of Chemical Sciences, University of Chinese Academy of Sciences, 19A YuQuan Road, Beijing, 100049, PR China.
(b)National Center for Nanoscience and Technology of China, Beijing, 100080, PR China.
Talanta. 2019 Nov 1;204:74-81. doi: 10.1016/j.talanta.2019.05.099. Epub 2019 May 27.
The abnormal expression level of alkaline phosphatase (ALP) will lead to serious diseases. Therefore, a sensitive and rapid assay for ALP activity monitoring is of vital importance. In this work, a fluorescence turn-off approach for the detection of ALP is designed on the basis of nitrogen doped carbon dots (N-CDs), which were synthesized by one-step hydrothermal method and applied as signal readout. p-Nitrophenylphosphate (PNPP) can be hydrolyzed into p-nitrophenol (PNP) by ALP and their absorption peaks are different under alkaline conditions, so it was chosen as the ALP substrate. The absorption spectrum of PNP has good overlap with the excitation and emission spectra of N-CDs, thus the fluorescence of N-CDs can be effectively quenched by PNP via the inner filter effect (IFE). Consequently, quantitative detection of ALP is realized because the relative fluorescence intensity is linearly with the ALP activity in a wide range from 0.05 to 40 U L. The detection limit is 0.02 U L (S/N = 3), which is much lower than the normal level of serum ALP in adults (about 40-190 U L). Moreover, the assay was successfully applied to evaluate ALP inhibitor efficiency and screen ALP inhibitors in drug discovery. It is also demonstrated that N-CDs possesses low cytotoxicity, excellent biocompatibility and photostability, and can be successfully applied in vivo fluorescence imaging, showing great potential in clinical applications.
碱性磷酸酶 (ALP) 异常表达水平会导致严重疾病。因此,灵敏、快速的 ALP 活性监测方法至关重要。在这项工作中,基于氮掺杂碳点 (N-CDs) 设计了一种用于检测 ALP 的荧光关闭方法,N-CDs 是通过一步水热法合成的,并用作信号读出。碱性条件下,对硝基苯磷酸酯 (PNPP) 可被 ALP 水解为对硝基苯酚 (PNP),且它们的吸收峰不同,因此选择其作为 ALP 底物。PNP 的吸收光谱与 N-CDs 的激发和发射光谱有很好的重叠,因此 PNP 可以通过内滤效应 (IFE) 有效猝灭 N-CDs 的荧光。因此,由于相对荧光强度与 ALP 活性在 0.05 至 40 U/L 的较宽范围内呈线性关系,实现了对 ALP 的定量检测。检测限为 0.02 U/L(S/N=3),远低于成年人血清 ALP 的正常水平(约 40-190 U/L)。此外,该测定法成功用于评估 ALP 抑制剂的效率和筛选药物发现中的 ALP 抑制剂。还证明 N-CDs 具有低细胞毒性、优异的生物相容性和光稳定性,并且可以成功应用于体内荧光成像,在临床应用中具有很大的潜力。