4.6 Article

Ultrasensitive Detection of Hepatotoxic Microcystin Production from Cyanobacteria Using Surface-Enhanced Raman Scattering Immunosensor

期刊

ACS SENSORS
卷 4, 期 5, 页码 1203-1210

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acssensors.8b01453

关键词

surface-enhanced Raman scattering; microcystin-LR; toxins; biosensors; algal blooms

资金

  1. Johns Hopkins University (JHU) Water Institute Seed Grant
  2. JHU Whiting School of Engineering Seed Funds
  3. National Institute of Biomedical Imaging and Bioengineering [2-P41-EB015871-31]
  4. National Institute of General Medical Sciences [DP2GM128198]
  5. National Thousand Young Talents Program of China
  6. National Natural Science Foundation of China [51871246]
  7. Innovation -Driven Project of Central South Univ. [2018CX002]
  8. Hunan Provincial Science & Technology Program [2017XK2027]

向作者/读者索取更多资源

Microcystin-LR (MC-LR) is considered the most common hazardous toxin produced during harmful algal blooms. In addition to potential risk of long-term exposure to low concentrations in drinking water, acute toxicity due to MC-LR resulting from algal blooms could result in fatalities in rare cases. Although several methods are currently available to detect MC-LR, development of a low-cost, ultrasensitive measurement method would help limit exposure by enabling early detection and continuous monitoring of MC-LR Here, we develop a surface-enhanced Raman scattering (SERS) spectroscopic immunosensor for detection and quantification of the hepatotoxic MC-LR toxin in aquatic settings with excellent robustness, selectivity, and sensitivity. We demonstrate that the developed SERS sensor can reach a limit of detection (0.014 mu g/L) at least 1 order of magnitude lower and display a linear dynamic detection range (0.01 mu g/L to 100 mu g/L) 2 orders of magnitude wider in comparison to the commercial enzyme-linked immunosorbent assay test. The superior analytical performance of this SERS immunosensor enables monitoring of the dynamic production of MC-LR from a Microcystis aeruginosa culture. We believe that the present method could serve as a useful tool for detection of hepatotoxic microcystin toxins in various aquatic settings such as drinking water, lakes, and reservoirs. Further development of this technique could result in single-cell microcystin resolution or real-time monitoring to mitigate the associated toxicity and economic loss.

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