抗坏血酸
碱性磷酸酶
检出限
化学
配体(生物化学)
级联
发光
荧光
磷酸酶
水解
色谱法
核化学
酶
组合化学
生物化学
受体
材料科学
光电子学
量子力学
物理
食品科学
作者
Yingying Guo,Tianlu Zhao,Qiao‐Nan Guo,Mingji Ding,Xiangrong Chen,Lin Jianqing
标识
DOI:10.1016/j.microc.2023.109170
摘要
An upconversion signal readout platform for the detection of alkaline phosphatase (ALP) was constructed by combining the inner filter effect (IFE) and the cascade signal amplification strategy. First, 3, 3′, 5, 5′ -tetramethylbenzidine (TMB) is oxidized by Ag+ to the oxidative product (TMBox), which quenches the up-conversion luminescence (UCL) of the ligand-free up-conversion nanoparticles (UCNPs) through the IFE principle. However, when in the presence of ascorbic acid 2-phosphate (AAP) and ALP, AAP is catalytically hydrolyzed by ALP to produce ascorbic acid (AA), which could not only decrease TMBox formation by reducing Ag+, but also reduce the TMBox generated to TMB, thereby resulting in fluorescence recovery of UCNP. Under optimal experimental conditions, ALP was linearly correlated in the range of 0.15∼8 U/L with a LOD of 0.032 U/L (S/N=3). In addition, the developed method was applied to the detection of ALP in actual serum samples, and the detection result was close to that of the traditional pNPP-based standard assay, which showed that the UCNP-TMB nanosystem has great potential to accurately detect ALP in the clinical bioassay.
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