纳米团簇
烯醇化酶
检出限
硫堇
纳米颗粒
电化学
化学
组合化学
材料科学
纳米技术
线性范围
色谱法
电极
医学
免疫组织化学
物理化学
内科学
作者
Yao Chen,Xin-Yue Ge,Shi-Yun Cen,Ai‐Jun Wang,Xiliang Luo,Jiu‐Ju Feng
标识
DOI:10.1016/j.snb.2020.127931
摘要
Abstract Neuron-specific enolase (NSE) is viewed as a tumor marker of small cell lung cancer (SCLC) with high diagnostic sensitivity and specificity, whose facile and sensitive detection is critical for clinical diagnosis. In this work, core-shell Au nanoparticles @Pd nanoclusters-poly(bismarck brown Y) (Au@Pd-P(BBY)) and hierarchically dendritic AuPt nanoassemblies (AuPt NAs) were synthesized independently by a one-pot aqueous method. A dual-signal ratiometric electrochemical aptasensor was developed for ultrasensitive determination of NSE based on ferrocene grafted Au@Pd-P(BBY) (Fc-g-Au@Pd-P(BBY)) and reduced graphene oxide/thionine decorated AuPt NAs (rGO/Thi/AuPt NAs). Under optimal conditions, the changes in the peak currents linearly correlate to the NSE concentrations in the wide range of 0.0001―50.0 ng mL–1 with ultralow detection limit (0.03 pg mL–1, S/N = 3). The aptasensor was explored in a diluted human serum sample with acceptable results, showing its great potential in clinical diagnosis and treatment.
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