4.8 Article

A target-triggered and self-calibration aptasensor based on SERS for precise detection of a prostate cancer biomarker in human blood

期刊

NANOSCALE
卷 13, 期 16, 页码 7574-7582

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/d1nr00480h

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资金

  1. National Natural Science Foundation of China [11974077, 61975031, 82072986]
  2. Innovation Team Development Plan, Ministry of Education [IRT_15R10]
  3. Special Funds of the Central Government Guiding Local Science and Technology Development [2020L3008]
  4. United Fujian Provincial Health and Education Project for Tackling the Key Research [2019-WJ-03]
  5. program for Industry University Cooperation Project of Fujian Province [2020Y4006]

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The study developed a target-triggered and self-calibration aptasensor based on SERS technology for sensitive and reliable detection of PSA protein, with a promising potential for accurate screening of prostate cancer in human blood samples. The method showed comparable detection accuracy, a larger dynamic detection range, a lower detection limit, and lower sample requirement compared to the clinical commonly used method.
Sensitive and precise detection of prostate-specific antigen (PSA) is critical for prostate cancer screening and monitoring. Herein, a target-triggered and self-calibration aptasensor based on a core-satellite nanostructure using surface-enhanced Raman spectroscopy (SERS) technology was developed for the sensitive and reliable determination of PSA protein, with a limit of detection of 0.38 ag mL(-1) and a dynamic detection range of 10(-2) to 10(-15) mg mL(-1). Furthermore, the proposed approach for the detection of PSA in patient blood samples was performed, and results showed that it is capable of providing comparable detection accuracy associated with a larger dynamic detection range and a lower detection limit as well as less sample requirement (only 5 mu L) in comparison with the clinical commonly used method. Therefore, this SERS-based aptasensor for the detection of PSA in human blood samples has promising potential to be an alternative tool for clinical application in the accurate screening of prostate cancer.

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