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Non-enzymatic electrochemical detection of H2O2 by assembly of CuO nanoparticles and black phosphorus nanosheets for early diagnosis of periodontitis

黑磷 牙周炎 生物传感器 过氧化氢 纳米技术 材料科学 化学 纳米颗粒 牙科 医学 生物化学 光电子学
作者
Kun Wang,Yue Sun,Wenzhou Xu,Wei Zhang,Fanrou Zhang,Qi Yu,Yuhong Zhang,Qingqing Zhou,Biao Dong,Chunyan Li,Lin Wang,Lin Xu
出处
期刊:Sensors and Actuators B-chemical [Elsevier BV]
卷期号:355: 131298-131298 被引量:60
标识
DOI:10.1016/j.snb.2021.131298
摘要

Periodontitis, as one of the most universal chronic inflammatory diseases worldwide, has raised numerous attentions since its tremendous destructive force against alveolar bone and soft tissue, ultimately leading to the tooth loss. Hydrogen peroxide (H2O2) is a major byproduct during the pathogenesis of periodontitis, which hints that direct and in-situ detection of H2O2 provides an effective way for early diagnosis of periodontitis. Herein, a non-enzymatic and highly electrocatalytic H2O2 biosensor was proposed by using a novel electrode composed of copper oxide nanoparticles (CuO NPs), black phosphorus nanosheets (BP NSs) and chitosan. Owing to the remarkable electrochemical redox capability of CuO NPs and marvelous conductivity of BP NSs, such heterostructure attained enhanced surface adsorption and efficient electron transfer, contributing to ultrasensitive determination of H2O2 in a real-time manner. The synergistic effects of CuO and BP demonstrated supreme electrocatalytic ability with a low practical detection limit (30 nM), excellent sensitivity (138.00 μA mM−1 cm−2), extraordinary selectivity, splendid reusability and long-term stability. In terms of biofluid level, this biosensor achieved feasible detection of H2O2 in saliva and gingival crevicular fluid samples and effectively differentiated patients of periodontitis from healthy people, which lay solid foundation for diagnosis of periodontitis. Referring to cellular scale, such device was successfully implemented to detect H2O2 released from macrophages and gingival fibroblasts, presenting favorable biosensing capability in living cells. Looking forward, this design of CuO/BP sensor could be extended to broader applications in monitoring physiological and dynamic in-clinic pathological processes in other inflammatory diseases.
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