College of Chemistry, Sichuan University, 29 Wangjiang Road, Chengdu 610064, China.
Nanoscale. 2017 Oct 19;9(40):15606-15611. doi: 10.1039/c7nr03673f.
The inner filter effect (IFE) is an effective way for fluorescence modulation and thus has been extensively explored for the development of fluorescence assays. Theoretically, the key to maximize the sensitivity of IFE-based fluorescence assays is to enlarge the overlap between the absorption of the absorber and the excitation/emission of the fluorophore. Therefore, in this work, the tunable excitation of quantum dots (QDs) was explored for screening of the IFE pair having the best IFE-based assay sensitivity. A series of QDs, including CdTe QDs with different sizes, carbon dots, Cu-doped CdS QDs, and Mn-doped ZnS QDs, were investigated. PNPP (p-nitrophenylphosphate) was chosen as the absorber since its absorption overlapped with the above QDs. Besides, it can be catalytically converted to p-nitrophenol (PNP) by alkaline phosphatase (ALP) together with an absorption spectrum change (red-shift). Interestingly, it was found that the IFE efficiency of different PNPP-QD pairs increased almost linearly with the corresponding spectral overlap, and Mn-doped ZnS QDs were eventually chosen for the IFE assay of ALP because of the maximum spectral overlap and thus the best sensitivity. A simple and sensitive turn-on phosphorescence ALP assay was developed, with a detection limit of 4 × 10 U L. Because of the high sensitivity, we also found that ALP of different origins possessed different enzymatic activities. The developed ALP phosphorescence assay was successfully employed for the analysis of ALP in serum samples.
内滤效应(IFE)是一种有效的荧光调制方法,因此被广泛用于开发荧光分析方法。从理论上讲,最大限度地提高基于 IFE 的荧光分析方法灵敏度的关键是扩大吸收体的吸收与荧光团的激发/发射之间的重叠。因此,在这项工作中,探索了可调谐的量子点(QD)激发,以筛选具有最佳 IFE 基分析灵敏度的 IFE 对。研究了一系列 QD,包括具有不同尺寸的 CdTe QD、碳点、Cu 掺杂的 CdS QD 和 Mn 掺杂的 ZnS QD。选择 PNPP(对硝基苯磷酸酯)作为吸收体,因为它的吸收与上述 QD 重叠。此外,它可以与碱性磷酸酶(ALP)一起被催化转化为对硝基苯酚(PNP),同时伴随着吸收光谱的变化(红移)。有趣的是,发现不同的 PNPP-QD 对的 IFE 效率几乎与相应的光谱重叠呈线性增加,最终选择 Mn 掺杂的 ZnS QD 用于 ALP 的 IFE 分析,因为它们具有最大的光谱重叠,因此具有最佳的灵敏度。开发了一种简单灵敏的磷光 ALP 测定法,检测限为 4×10 U L。由于灵敏度高,我们还发现不同来源的 ALP 具有不同的酶活性。该开发的 ALP 磷光分析已成功用于血清样品中 ALP 的分析。