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Effectiveness of deferiprone-loaded nanocarrier in experimentally induced rhabdomyolysis: A dose-comparison study.
Rashed, Rasha Refaat; Deghiedy, Noha Mohammed; El-Hazek, Rania M; El-Sabbagh, Walaa A; Rashed, Engy Refaat; El-Ghazaly, Mona A.
Afiliação
  • Rashed RR; Drug Radiation Research Department, National Centre for Radiation Research and Technology, Atomic Energy Authority, Egypt.
  • Deghiedy NM; Department of Polymers Chemistry, National Centre for Radiation Research and Technology, Atomic Energy Authority, Egypt.
  • El-Hazek RM; Drug Radiation Research Department, National Centre for Radiation Research and Technology, Atomic Energy Authority, Egypt.
  • El-Sabbagh WA; Drug Radiation Research Department, National Centre for Radiation Research and Technology, Atomic Energy Authority, Egypt.
  • Rashed ER; Drug Radiation Research Department, National Centre for Radiation Research and Technology, Atomic Energy Authority, Egypt. Electronic address: engyrefaat@yahoo.com.
  • El-Ghazaly MA; Drug Radiation Research Department, National Centre for Radiation Research and Technology, Atomic Energy Authority, Egypt.
Bioorg Chem ; 100: 103913, 2020 07.
Article em En | MEDLINE | ID: mdl-32413633
ABSTRACT
Herein, the efficacy of free deferiprone (DFP) and DFP-loaded starch/polyethylene glycol/polyacrylic acid (St/PEG/PAAc) nanogel [Nano-DFP] in modulating the biochemical changes induced by glycerol model of rhabdomyolysis (RBD) in male rats was investigated. In this respect, gamma radiation-induced crosslinking was used to produce St/PEG/PAAc nanogel particles, and then, it was used as a nanocarrier for DFP as an attempt to overcome the poor bioavailability and short half-life of DFP. St/PEG/PAAc nanogel was characterized by Fourier transform infrared, dynamic light scattering and Transmission electron microscopy. Free DFP was administered to rats in two doses; 25 and 50 mg following RBD induction, while the loaded nanogel was administered at a dose of 25 mg. The liver and kidney functions were then fully assessed in association with the histological tissue examination of both organs and the femur muscle. Both doses of DFP significantly antagonized the RBD-induced changes in most of the assessed organs functions. The higher dose of DFP, however, showed a statistically more pronounced modulation of RBD effects on each of kidney, liver and skeletal muscles. Nano-DFP; at 25 mg dose, resulted in a statistically significant correction of most of the RBD-related biomarkers with a comparable magnitude to the higher DFP dose rather than the corresponding lower one.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Rabdomiólise / Portadores de Fármacos / Quelantes de Ferro / Deferiprona / Nanogéis Limite: Animals Idioma: En Revista: Bioorg Chem Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Egito

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Rabdomiólise / Portadores de Fármacos / Quelantes de Ferro / Deferiprona / Nanogéis Limite: Animals Idioma: En Revista: Bioorg Chem Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Egito