Properties of AgNPs stabilized with polyvinylpyrrolidone relevant to antidiabetic agents.

Journal: Nanoscale
Published Date:

Abstract

Type 2 diabetes mellitus (DM2) is a chronic metabolic disease. Silver nanoparticles (AgNPs) show promise in their treatment. This study assessed the potential of AgNPs as DM2 treatment agent using in vitro, in vivo, and machine learning approaches. Male Wistar rats were used to study antihyperglycemic effects, while male mice evaluated hypoglycemic effects. In vivo studies showed that AgNPs inhibited α-amylase, α-glucosidase, and dipeptidyl peptidase-4, up to 3.51, 3827.76, and 11 times more effective than acarbose and sitagliptin, respectively. Advanced glycation end products inhibition by AgNPs was up to 61.4 times higher than metformin. In vivo experiments revealed that AgNPs antihyperglycemic activities were close to acarbose, while the same hypoglycemic effect was achieved with AgNP doses up to 167 times lower than that of glibenclamide. The results show the possibility to decrease the glibenclamide dose by two orders, that indicates high AgNP perspective to reduce drug toxicity and side effects.

Authors

  • Victoria Vera Pineda
    Faculty of Chemical Engineering, Autonomous University of Yucatan (UADY), Merida 97300, Yucatan, Mexico. [email protected].
  • Antonio Alvarez de la Paz
    Materials Research Institute, National Autonomous University of Mexico (UNAM), Mexico City 04510, Mexico. [email protected].
  • Nina Bogdanchikova
    Center for Nanoscience and Nanotechnology (CNyN), Campus Ensenada, National Autonomous University of Mexico (UNAM), Mexico City 04510, Mexico. [email protected].
  • Alexey Pestrykov
    Research School of Chemistry & Applied Biomedical Sciences, Tomsk Polytechnic University, Tomsk 634050, Russia. [email protected].
  • Juan José Acevedo Fernández
    Faculty of Medicine, Autonomous University of the State of Morelos (UAEM), Cuernavaca 62350, Morelos, Mexico. [email protected].
  • Maira Rubi Segura Campos
    Faculty of Chemical Engineering, Autonomous University of Yucatan (UADY), Merida 97300, Yucatan, Mexico. [email protected].