Your browser doesn't support javascript.
loading
Pharmacokinetic characterization of mangosteen (Garcinia mangostana) fruit extract standardized to α-mangostin in C57BL/6 mice.
Petiwala, Sakina M; Li, Gongbo; Ramaiya, Atulkumar; Kumar, Anoop; Gill, Ravinder K; Saksena, Seema; Johnson, Jeremy J.
Afiliación
  • Petiwala SM; Department of Pharmacy Practice, College of Pharmacy, University of Illinois at Chicago, Chicago, IL.
  • Li G; Department of Pharmacy Practice, College of Pharmacy, University of Illinois at Chicago, Chicago, IL.
  • Ramaiya A; Department of Pharmacy Practice, College of Pharmacy, University of Illinois at Chicago, Chicago, IL.
  • Kumar A; Department of Medicine, Division of Gastroenterology and Hepatology, University of Illinois at Chicago, Chicago, IL.
  • Gill RK; Department of Medicine, Division of Gastroenterology and Hepatology, University of Illinois at Chicago, Chicago, IL.
  • Saksena S; Department of Medicine, Division of Gastroenterology and Hepatology, University of Illinois at Chicago, Chicago, IL.
  • Johnson JJ; Department of Pharmacy Practice, College of Pharmacy, University of Illinois at Chicago, Chicago, IL; University of Illinois Cancer Center, Chicago, IL. Electronic address: jjjohn@uic.edu.
Nutr Res ; 34(4): 336-45, 2014 Apr.
Article en En | MEDLINE | ID: mdl-24774070
ABSTRACT
Previously, we have reported the pharmacokinetic (PK) properties of α-mangostin in mice. For this study, we evaluated the PK profile of α-mangostin using a standardized mangosteen extract in C57BL/6 mice. The primary objective was to determine the PK properties of α-mangostin when administered as an extract. This experiment was designed to test our primary hypothesis that α-mangostin in an extract should achieve a desirable PK profile. This is especially relevant as dietary supplements of mangosteen fruit are regularly standardized to α-mangostin. Mice received 100 mg/kg of mangosteen fruit extract orally, equivalent to 36 mg/kg of α-mangostin, and plasma samples were analyzed over a 24-hour period. Concentrations of α-mangostin were determined by liquid chromatography-tandem mass spectrometry. In addition, we evaluated the stability in the presence of phase I and phase II enzymes in liver and gastrointestinal microsomes. Furthermore, we identified evidence of phase II metabolism of α-mangostin. Further research will be required to determine if less abundant xanthones present in the mangosteen may modulate the PK parameters of α-mangostin.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Extractos Vegetales / Garcinia mangostana / Xantonas / Frutas Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Nutr Res Año: 2014 Tipo del documento: Article País de afiliación: Israel

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Extractos Vegetales / Garcinia mangostana / Xantonas / Frutas Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Nutr Res Año: 2014 Tipo del documento: Article País de afiliación: Israel