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Evaluation of Hydrophobic Nanoparticulate Delivery System for Insulin

Insulin loaded hydrophobic nanoparticles were prepared by solvent diffusion followed by lyophilization. Nanoparticles were characterized for mean size by dynamic laser scattering and for shape by scanning electron microscopy. Insulin encapsulation efficiency, in vitro stability of nanoparticles in p...

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Detalles Bibliográficos
Autores principales: Singnurkar, P. S., Gidwani, S. K.
Formato: Texto
Lenguaje:English
Publicado: Medknow Publications 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3040864/
https://www.ncbi.nlm.nih.gov/pubmed/21369431
http://dx.doi.org/10.4103/0250-474X.49091
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author Singnurkar, P. S.
Gidwani, S. K.
author_facet Singnurkar, P. S.
Gidwani, S. K.
author_sort Singnurkar, P. S.
collection PubMed
description Insulin loaded hydrophobic nanoparticles were prepared by solvent diffusion followed by lyophilization. Nanoparticles were characterized for mean size by dynamic laser scattering and for shape by scanning electron microscopy. Insulin encapsulation efficiency, in vitro stability of nanoparticles in presence of proteolytic enzymes and in vitro release were determined by high pressure liquid chromatography analysis. The biological activity insulin from the nanopraticles was estimated by enzyme-linked immunosorbant assay and in vivo using Wister diabetic rats. Nanoparticles ranged 0.526±0.071 μm in diameter. Insulin encapsulation efficiency was 95.7±1.2%. Insulin hydrophobic nanoparticles suppressed insulin release promoted sustained release in pH 7.4 phosphate buffer and shown to protect insulin from enzymatic degradation in vitro in presence of chymotripsin. Nanoencapsulated insulin was bioactive, demonstrated through both in vivo and in vitro.
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spelling pubmed-30408642011-03-02 Evaluation of Hydrophobic Nanoparticulate Delivery System for Insulin Singnurkar, P. S. Gidwani, S. K. Indian J Pharm Sci Research Paper Insulin loaded hydrophobic nanoparticles were prepared by solvent diffusion followed by lyophilization. Nanoparticles were characterized for mean size by dynamic laser scattering and for shape by scanning electron microscopy. Insulin encapsulation efficiency, in vitro stability of nanoparticles in presence of proteolytic enzymes and in vitro release were determined by high pressure liquid chromatography analysis. The biological activity insulin from the nanopraticles was estimated by enzyme-linked immunosorbant assay and in vivo using Wister diabetic rats. Nanoparticles ranged 0.526±0.071 μm in diameter. Insulin encapsulation efficiency was 95.7±1.2%. Insulin hydrophobic nanoparticles suppressed insulin release promoted sustained release in pH 7.4 phosphate buffer and shown to protect insulin from enzymatic degradation in vitro in presence of chymotripsin. Nanoencapsulated insulin was bioactive, demonstrated through both in vivo and in vitro. Medknow Publications 2008 /pmc/articles/PMC3040864/ /pubmed/21369431 http://dx.doi.org/10.4103/0250-474X.49091 Text en © Indian Journal of Pharmaceutical Sciences http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Paper
Singnurkar, P. S.
Gidwani, S. K.
Evaluation of Hydrophobic Nanoparticulate Delivery System for Insulin
title Evaluation of Hydrophobic Nanoparticulate Delivery System for Insulin
title_full Evaluation of Hydrophobic Nanoparticulate Delivery System for Insulin
title_fullStr Evaluation of Hydrophobic Nanoparticulate Delivery System for Insulin
title_full_unstemmed Evaluation of Hydrophobic Nanoparticulate Delivery System for Insulin
title_short Evaluation of Hydrophobic Nanoparticulate Delivery System for Insulin
title_sort evaluation of hydrophobic nanoparticulate delivery system for insulin
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3040864/
https://www.ncbi.nlm.nih.gov/pubmed/21369431
http://dx.doi.org/10.4103/0250-474X.49091
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