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Purification and characterization of saxitoxin from Mytilus chilensis of southern Chile.
Rubio, D P; Roa, L G; Soto, D A; Velasquez, F J; Gregorcic, N A; Soto, J A; Martinez, M C; Kalergis, A M; Vasquez, A E.
Affiliation
  • Rubio DP; Sección de Biotecnología, Departamento de Salud Ambiental, Instituto de Salud Púbica de Chile, Chile.
  • Roa LG; Sección de Química y Alimentos, Departamento de Salud Ambiental, Instituto de Salud Púbica de Chile, Chile.
  • Soto DA; Sección de Biotecnología, Departamento de Salud Ambiental, Instituto de Salud Púbica de Chile, Chile.
  • Velasquez FJ; Sección de Biotecnología, Departamento de Salud Ambiental, Instituto de Salud Púbica de Chile, Chile.
  • Gregorcic NA; Sección de Biotecnología, Departamento de Salud Ambiental, Instituto de Salud Púbica de Chile, Chile.
  • Soto JA; Sección de Biotecnología, Departamento de Salud Ambiental, Instituto de Salud Púbica de Chile, Chile; Millennium Institute on Immunology and Immunotherapy, Chile; Departamento de Genética Molecular y Microbiología, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Chile.
  • Martinez MC; Sección Microbiología de Alimentos, Departamento de Salud Ambiental, Instituto de Salud Púbica de Chile, Chile.
  • Kalergis AM; Millennium Institute on Immunology and Immunotherapy, Chile; Departamento de Genética Molecular y Microbiología, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Chile.
  • Vasquez AE; Sección de Biotecnología, Departamento de Salud Ambiental, Instituto de Salud Púbica de Chile, Chile; Millennium Institute on Immunology and Immunotherapy, Chile. Electronic address: avasquez@ispch.cl.
Toxicon ; 108: 147-53, 2015 Dec 15.
Article in En | MEDLINE | ID: mdl-26435338
In the current communication we describe an innovative method to purify saxitoxin (STX), a toxin presents in contaminated muscle of Mylitus chilensis extracted in the southern part of Chile, using a liquid chromatographic methodology based on ionic pairs. The STX was extracted using HCl and treated with ammonium sulfate following a treatment with trichloroacetic acid and hexane/diethyl ether (97/3). The samples were analyzed by a semi-preparative HPLC in order to collect pure fractions of STX and these fractions were eluted in solid-phase cationic interchange SCX extraction columns. The purified STX was stable and homogeneous and its identity was confirmed by LC-MS-MS, which demonstrated a high quality purification of STX, without presence of analogs such as neosaxitoxin (Neo) and decarbamoyl saxitoxin (dcSTX). The STX biological activity was analyzed in a bioassay in mice model and compared to the standard STX produced by the FDA and no significant differences were observed.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Saxitoxin / Chromatography, High Pressure Liquid / Mytilus Limits: Animals Country/Region as subject: America do sul / Chile Language: En Journal: Toxicon Year: 2015 Document type: Article Affiliation country: Chile Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Saxitoxin / Chromatography, High Pressure Liquid / Mytilus Limits: Animals Country/Region as subject: America do sul / Chile Language: En Journal: Toxicon Year: 2015 Document type: Article Affiliation country: Chile Country of publication: United kingdom