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Suppression of the tert-butylhydroquinone toxicity by its grafting onto chitosan and further cross-linking to agavin toward a novel antioxidant and prebiotic material.
Hernández-Valdepeña, Miguel A; Pedraza-Chaverri, José; Gracia-Mora, Isabel; Hernández-Castro, Rigoberto; Sánchez-Bartez, Francisco; Nieto-Sotelo, Jorge; Montiel, Carmina; Shirai, Keiko; Gimeno, Miquel.
Afiliação
  • Hernández-Valdepeña MA; Facultad de Química, Departamento de Alimentos y Biotecnología, Universidad Nacional Autónoma de México, Ciudad Universitaria, México D.F. 04510, Mexico.
  • Pedraza-Chaverri J; Facultad de Química, Departamento de Biología, Universidad Nacional Autónoma de México, Ciudad Universitaria, México D.F. 04510, Mexico.
  • Gracia-Mora I; Unidad de Investigación Preclínica (UNIPREC), Universidad Nacional Autónoma de México, Ciudad Universitaria, México D.F. 04510, Mexico.
  • Hernández-Castro R; Departamento de Ecología de Agentes Patógenos, Hospital General "Dr. Manuel Gea González", Tlalpan, Mexico.
  • Sánchez-Bartez F; Unidad de Investigación Preclínica (UNIPREC), Universidad Nacional Autónoma de México, Ciudad Universitaria, México D.F. 04510, Mexico.
  • Nieto-Sotelo J; Instituto de Biología, Universidad Nacional Autónoma de México, Ciudad Universitaria, México D.F. 04510, Mexico.
  • Montiel C; Facultad de Química, Departamento de Alimentos y Biotecnología, Universidad Nacional Autónoma de México, Ciudad Universitaria, México D.F. 04510, Mexico.
  • Shirai K; Universidad Autónoma Metropolitana, Biotechnology Department, Laboratory of Biopolymers and Pilot Plant of Bioprocessing of Agro-Industrial and Food By-Products, 09340 Mexico City, Mexico.
  • Gimeno M; Facultad de Química, Departamento de Alimentos y Biotecnología, Universidad Nacional Autónoma de México, Ciudad Universitaria, México D.F. 04510, Mexico. Electronic address: mgimeno@unam.mx.
Food Chem ; 199: 485-91, 2016 May 15.
Article em En | MEDLINE | ID: mdl-26775999
ABSTRACT
The enzyme-mediated grafting of tert-butylhydroquinone (TBHQ) onto chitosan and further crosslinking to agave inulin (agavin) has been successfully achieved in a mild and non-toxic two-step route. The resulting products were characterized by nuclear magnetic resonance (NMR) and Infra-red spectroscopies to assess the molecular structure. The study of acute oral toxicity in mice revealed no adverse short-term effects of consumption in the synthesized materials with non-toxicity evidence until 2000 mg/kg through an oral acute administration. Importantly, this study proves that the compound maintains the radical scavenging capacity of the phenolic antioxidant upon ferric-reducing antioxidant power (FRAP) and oxygen radical absorbance capacity (ORAC) assays with a measured half-maximal inhibitory concentration (IC50) for the best case of 1.54 g/L based on inhibition of 2,2'-azino-bis(3-ethylbenzothiazoline)-6-sulfonic acid diammonium salt (ABTS). Additionally, the novel compound presented high prebiotic activities as ascertained in the presence of lactic acid bacteria (LAB).
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Quitosana / Prebióticos / Hidroquinonas / Inulina / Antioxidantes Idioma: En Ano de publicação: 2016 Tipo de documento: Article País de afiliação: México

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Quitosana / Prebióticos / Hidroquinonas / Inulina / Antioxidantes Idioma: En Ano de publicação: 2016 Tipo de documento: Article País de afiliação: México