Abstract
Purpose: Based on DNase I and reduced graphene oxide (rGO)-magnetic silicon microspheres (MNPS), a highly sensitive and selective fluorescent probe for the detection of PD-L1 was developed. Design/methodology/approach: Here °C we present a feasibility of biosensor to detection of PD-L1 in lung tumors plasma. In the absence of PD-L1°C the PD-L1 aptamer is absorbed on the surface of graphene oxide modified magnetic nanoparticles °8rGO-MNPS°9 and leading to effective fluorescence quenching. Upon adding PD-L1°C the aptamer sequences could be specifically recognized by PD-L1 and the aptamer/PD-L1 complex is formed°C resulting in the recovery of quenched fluorescence. Findings: This sensor can detect PD-L1 with a linear range from 100 pg mL−1 to 100 ng mL−1, and a detection limit of 10 pg•m−1 was achieved. Originality/value: This method provides an easy and sensitive method for the detection of PD-L1 and will be beneficial to the early diagnosis and prognosis of tumors.
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CITATION STYLE
He, X., Yang, G. Y., Yang, E., Zhang, M., Luo, D., Liu, J., … Ran, F. (2021). Utilizing DNase I and graphene oxide modified magnetic nanoparticles for sensing PD-L1 in human plasma. Sensor Review, 41(3), 229–234. https://doi.org/10.1108/SR-04-2020-0087
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