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Nanoscale ; 16(18): 8950-8959, 2024 May 09.
Artigo em Inglês | MEDLINE | ID: mdl-38630023

RESUMO

Exosomal programmed death ligand-1 (ExoPD-L1) is a vital marker of immune activation in the early stages of tumor therapy and it can inhibit anti-tumor immune responses. However, due to the low expression of ExoPD-L1 in cancer cells, it is difficult to perform highly sensitive assays and accurately differentiate cancer sources. Therefore, we constructed a coaxial dual-path electrochemical biosensor for highly accurate identification and detection of ExoPD-L1 from lung cancer based on chemical-biological coaxial nanomaterials and nucleic acid molecular signal amplification strategies. The measurements showed that the detected ExoPD-L1 concentrations ranged from 6 × 102 particles per mL to 6 × 108 particles per mL, and the detection limit was 310 particles per mL. Compared to other sensors, the electrochemical biosensor designed in this study has a lower detection limit and a wider detection range. Furthermore, we also successfully identified lung cancer-derived ExoPD-L1 by analyzing multiple protein biomarkers expressed on exosomes through the "AND" logic strategy. This sensor platform is expected to realize highly sensitive detection and accurate analysis of multiple sources of ExoPD-L1 and provide ideas for the clinical detection of ExoPD-L1.


Assuntos
Antígeno B7-H1 , Técnicas Biossensoriais , Técnicas Eletroquímicas , Exossomos , Neoplasias Pulmonares , Técnicas Biossensoriais/métodos , Neoplasias Pulmonares/diagnóstico , Neoplasias Pulmonares/metabolismo , Humanos , Antígeno B7-H1/análise , Antígeno B7-H1/metabolismo , Exossomos/química , Exossomos/metabolismo , Limite de Detecção , Biomarcadores Tumorais/análise , Linhagem Celular Tumoral
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