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Preparation and in vitro characterization of chitosan nanoparticles containing Mesobuthus eupeus scorpion venom as an antigen delivery system
Mohammadpour Dounighi, N; Eskandari, R; Avadi, M. R; Zolfagharian, H; Mir Mohammad Sadeghi, A; Rezayat, M.
Affiliation
  • Mohammadpour Dounighi, N; Razi Vaccine and Serum Research Institute. Department of Human Vaccine and Serum. Karaj. IR
  • Eskandari, R; Islamic Azad University. Pharmaceutical Sciences Branch. Tehran. IR
  • Avadi, M. R; Islamic Azad University. Pharmaceutical Sciences Branch. Tehran. IR
  • Zolfagharian, H; Razi Vaccine and Serum Research Institute. Department of Human Vaccine and Serum. Karaj. IR
  • Mir Mohammad Sadeghi, A; Hakim Pharmaceutical Company. Department of Research and Development. Tehran. IR
  • Rezayat, M; Islamic Azad University. Pharmaceutical Sciences Branch. Tehran. IR
J. venom. anim. toxins incl. trop. dis ; J. venom. anim. toxins incl. trop. dis;18(1): 44-52, 2012. ilus, tab
Article de En | LILACS | ID: lil-618189
Bibliothèque responsable: BR33.1
ABSTRACT
Hydrophilic nanoparticles have been widely investigated in recent years as delivery systems for therapeutic macromolecules such as antigens. In the present study Mesobuthus eupeus venom-loaded chitosan nanoparticles were prepared via ionic gelation of tripolyphosphate (TPP) and chitosan. The optimum encapsulation efficiency (91.1 percent) and loading capacity (76.3 percent) were obtained by a chitosan concentration of 2 mg/mL, chitosan-to-TPP mass ratio of 2 and M. eupeus venom concentration of 500 µg/mL. The average nanoparticle size at optimum conditions was determined by Zetasizer (Malvern Instruments, UK). The nanoparticle size was about 370 nm (polydispersity index 0.429) while the zeta potential was positive. Transmission electron microscope (TEM) imaging showed a spherical, smooth and almost homogenous structure for nanoparticles. Fourier transform infrared (FTIR) spectroscopy confirmed tripolyphosphoric groups of TPP linked with ammonium groups of chitosan in the nanoparticles. The in vitro release of nanoparticles showed an initial burst release of approximately 60 percent in the first ten hours, followed by a slow and much reduced additional release for about 60 hours. It is suggested that the chitosan nanoparticles fabricated in our study may provide a suitable alternative to traditional adjuvant systems.(AU)
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Texte intégral: 1 Indice: LILACS Sujet Principal: Venins de scorpion / Sérums antivenimeux / Chitosane / Nanoparticules Limites du sujet: Animals langue: En Texte intégral: J. venom. anim. toxins incl. trop. dis Thème du journal: TOXICOLOGIA Année: 2012 Type: Article

Texte intégral: 1 Indice: LILACS Sujet Principal: Venins de scorpion / Sérums antivenimeux / Chitosane / Nanoparticules Limites du sujet: Animals langue: En Texte intégral: J. venom. anim. toxins incl. trop. dis Thème du journal: TOXICOLOGIA Année: 2012 Type: Article