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Chinese Journal of Lung Diseases(Electronic Edition) ›› 2025, Vol. 18 ›› Issue (06): 860-865. doi: 10.3877/cma.j.issn.1674-6902.2025.06.002

• Original Article • Previous Articles    

Construction of a novel sensor based on platinum-palladium supported molybdenum disulfide and boron nitride for the detection of neuron-specific enolase

Xuemei Chen1,2, Yutong Guo3, Jingcheng Liu1, Hang Qian1, Bing Wang1, Zhi Xu1,()   

  1. 1Department of Respiratory Medicine, Second Affiliated Hospital of Army Medical University, Chongqing 400037, China
    2Department of Endocrinology and Metabolic Diseases, Western District Hospital, Chongqing 400039, China
    3Department of Laboratory Medicine, Second Affiliated Hospital of Army Medical University, Chongqing 400037, China
  • Received:2025-09-09 Online:2025-12-25 Published:2026-01-12
  • Contact: Zhi Xu

Abstract:

Objective

To develop a high-performance electrochemical immunosensor for detecting the lung cancer biomarker neuron specific enolase (NSE).

Methods

Two dimensional nano material boron nitride (BN) was used as the adsorption matrix to deposit nano gold (Au), effectively increasing the specific surface area; Using molybdenum disulfide supported platinum palladium (MoS2@PtPd) nano mimetic enzyme complex for electron transfer catalysis and catalytic amplification signal detection of NSE; Determine the optimal conditions by examining the key factors involved in constructing sensors, and conduct repeatability, stability, and specificity tests on the sensors; And conduct methodological validation on clinical specimens.

Results

It showes that the diameter range of BN was 200~500 nm, nm, the diameter range of MoS2 was 500~800 nm, and the MoS2 @ PtPd complex was about 50~120 nm. The current of BN binding on the electrode surface decreased by 40 μ A, and the current increased by 15 μ A after gold deposition. The blocking current of bovine serum albumin (BSA) decreased by 9 μ A, and the capture current of NSE decreased by 15 μ A; The optimal total concentration for catalyzing H2O2 is 3 μ M, and the optimal binding time for the secondary antibody to bind to the antigen is after 3 hours; When detecting NSE, the standard curve is: I=-5.13-0.40 LogCNSE, r=0.92, and the low of detection (LOD) is 0.86 pg/ml; The relative standard deviation (R.S.D.) between sensor batches was 2.91%, and after 21 days, the peak current remained at 98.14% of its initial current; Compared with other interfering proteins at a concentration of 1 ng/ml, NSE was (2.10±0.05)μA, alpha fetoprotein (AFP) was (0.12±0.03)μA, carcinoembryonic antigen (CEA) was (0.15±0.02)μA, albumin (ALB) was (0.21±0.02)μA, and ferritin (FER) was (0.19±0.03)μA (P<0.05); The relative deviation of four serum samples with severe applicability ranges from 1.70% to 4.11%, and the recovery rate ranges from 93.09% to 103.12%.

Conclusion

The novel immunosensor based on MoS2 @ PtPd catalytic combined with BN/Au membrane is simple to construct and has good performance for NSE detection. It provides an alternative method for early diagnosis of lung cancer, and has clinical significance.

Key words: Bronchopulmonary carcinoma, Neuron-specific enolase, Electrochemical immunosensor, Nanomaterial, Molybdenum disulfide

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