电化学发光
能量转移
对偶(语法数字)
降钙素原
化学
组合化学
材料科学
物理化学
电极
分子物理学
生物
文学类
艺术
免疫学
败血症
作者
Qiuling Deng,Ziyu Huang,Minjin Wu,Xiao‐Ping Wei,Jianping Li
标识
DOI:10.1021/acsabm.5c00315
摘要
A synergistic enhanced electrochemiluminescence (ECL) method was proposed. Synergistic enhancement was achieved by incorporating a coreactant accelerator through energy transfer between dual luminophores, g-C3N4 and Hf-MOF. In addition, a sandwich-type ECL immunosensor was developed for the ultrasensitive detection of procalcitonin (PCT), in which the primary antibody was labeled with the g-C3N4@Au nanoparticles that immobilized on an electrode surface and the secondary antibody was labeled with Hf-MOF. Apart from a luminophore, Hf-MOF also acted as a coreactant accelerator, catalyzing the generation of sulfate radical anions (SO4•-) by reactive oxygen and potassium persulfate. Furthermore, Hf-MOF acted as an acceptor of energy transfer of the luminophore intermediate g-C3N4, which greatly enhances the ECL signal. The ECL intensities of Hf-MOF/g-C3N4/S2O82- were 2.3 and 4.4 times higher than the ECL intensities of the Hf-MOF/S2O82- and g-C3N4/S2O82- systems, respectively. The response signal of the ECL immunosensor showed a good linear relationship with 10 fg/mL-100 ng/mL PCT, showing a detection limit of 3.3 fg/mL, which was much lower than of the reported method. The proposed method is feasible for the rapid identification and detection of systemic bacterial infections and for the prevention of abuse of antibiotics.
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