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      Microencapsulated chitosan nanoparticles for pulmonary protein delivery: in vivo evaluation of insulin-loaded formulations.

      Journal of Controlled Release
      Animals, Blood Glucose, analysis, Chitosan, administration & dosage, chemistry, Drug Carriers, Drug Compounding, Hypoglycemic Agents, Insulin, Lung, metabolism, Male, Mannitol, Microscopy, Electron, Scanning, Microscopy, Electron, Transmission, Nanoparticles, ultrastructure, Powders, Rats, Rats, Sprague-Dawley

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          Abstract

          This work presents a new dry powder system consisting of microencapsulated protein-loaded chitosan nanoparticles (CS NPs). The developed system was evaluated in vivo in rats in order to investigate its potential to transport insulin (INS), a model protein, to the deep lung, where it is absorbed into systemic circulation. The INS-loaded CS NPs were prepared by ionotropic gelation and characterized for morphology, size, zeta potential, association efficiency and loading capacity. Afterwards, the NPs were co-spray dried with mannitol resulting in a dry powder with adequate aerodynamic properties for deposition in deep lungs. The assessment of the plasmatic glucose levels following intratracheal administration to rats revealed that the microencapsulated INS-loaded CS NPs induced a more pronounced and prolonged hypoglycemic effect compared to the controls. Accordingly, the developed system constitutes a promising alternative to systemically deliver therapeutic macromolecules to the lungs, but it can also be used to provide a local effect. Copyright © 2011 Elsevier B.V. All rights reserved.

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