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Toxicon. 2005 Jul;46(1):93-8.

A rapid detection method for paralytic shellfish poisoning toxins by cell bioassay.

Author information

1
Department of Toxicology, Aichi Prefectural Institute of Public Health, 7-6 Tsuji-machi, Nagare, Kita-ku, Nagoya, Aichi 462-8576, Japan. masanao_okumura@pref.aichi.lg.jp

Abstract

We report here a rapid detection method for paralytic shellfish poisoning (PSP) toxins using a cultured neuroblastoma cell line, modified from the bioassay system previously established by Manger et al. [Manger, R.L., Leja, L.S., Lee, S.Y., Hungerford, J.M., Kirkpatrick, M.A., Yasumoto, T., Wekell, M.M., 2003. Detection of paralytic shellfish poison by rapid cell bioassay: antagonism of voltage-gated sodium channel active toxins in vitro. J. AOAC Int. 86 (3), 540-543]. In the present study, we made two major modifications to the previous method. The first is the use of maitotoxin, a marine toxin of ciguatera fish poisoning, which enables the incubation period to be reduced to 6 h when applied to the microplate 15 min prior to the end of the incubation. The second is the use of WST-8, a dehydrogenase detecting water-soluble tetrazolium salt for determining the target cell viability, which permits the omission of a washing step and simplifies the counting process. In addition, we attempted to reduce the required materials as much as possible. Thus, our modified method should be useful for screening the PSP-toxins from shellfish.

PMID:
15922387
DOI:
10.1016/j.toxicon.2005.03.018
[Indexed for MEDLINE]

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