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 10.2μg/L and 3.3μg/L, respectively, which are both lower than the conventional cell-based assay (21.2μg/L of HeLa cells and 9.8μg/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±4.3μg/L) are both lower than Cell Counting Kit-8 assay (CCK8) (62.7±7.1 and 45.8±6.7μg/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.

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