Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
7145028 | Sensors and Actuators B: Chemical | 2016 | 8 Pages |
Abstract
Diarrhetic shellfish poisoning (DSP) toxin is a dangerous contamination in seafood worldwide that can threaten human health and fishing. A large number of animal bioassays and chemical analytical methods are employed for DSP toxin detection. However, these toxin detection methods are low-throughput and high-cost which hamper their wide applications. In this study, HeLa and HepG2 cell lines were selected as the sensitive elements to establish the CIBs for monitoring the cytotoxicity induced by a representative DSP toxin, okadaic acid (OA). The limit of detection (LOD) of HeLa- and HepG2-based biosensors are 10.2 μg/L and 3.3 μg/L, respectively, which are both lower than the conventional cell-based assay (21.2 μg/L of HeLa cells and 9.8 μg/L of HepG2 cells). The half maximal inhibitory concentration (IC50) values of OA in HeLa and HepG2 cells which were obtained from CIB (49.9 ± 4.9 and 39.2 ± 4.3 μg/L) are both lower than Cell Counting Kit-8 assay (CCK8) (62.7 ± 7.1 and 45.8 ± 6.7 μg/L). Besides, CIB measurement presents good correlation with mouse bioassay (MBA) and liquid chromatography-tandem mass spectrometry (LC-MS/MS). In summary, all the results indicate that the CIB technology had great potential to be an effective complement in DSP toxins detection.
Keywords
Related Topics
Physical Sciences and Engineering
Chemistry
Analytical Chemistry
Authors
Ling Zou, Qin Wang, Mengmeng Tong, Hongbo Li, Jun Wang, Ning Hu, Ping Wang,