Insulin-loaded nanoparticles are prepared by alginate ionotropic pre-gelation followed by chitosan polyelectrolyte complexation

• Tipo: Artigo em Revista Científica Internacional
• Data: 2007

Autores

Sarmento, B (Autor) Outra; Ribeiro, AJ (Autor) Outra; Veiga, F (Autor) Outra; Ferreira, DC (Autor) FFUP; Neufeld, RJ (Autor) Outra

Revista

Título: Journal of Nanoscience and Nanotechnology

Vol. 7

Páginas: 2833-2841

ISSN: 1533-4880

Editora: American Scientific Publishers

Indexação

ISI Web of Knowledge - 115 Citações

Scopus - 153 Citações

Classificação Científica

FOS: Ciências da engenharia e tecnologias > Engenharia dos materiais

Outras Informações

ID Authenticus: P-004-8HX

DOI: 10.1166/jnn.2007.609

Abstract (EN): Alginate nanoparticles were prepared from dilute alginate sol by inducing a pre-gel with calcium counter ions, followed by polyelectrolyte complex coating with chitosan. Particles in the nanometer size range were obtained with 0.05% alginate and 0.9 mM Ca2+. The mean particle size was influenced by time and stirring speed of nanoparticle preparation, by alginate guluronic acid content and chitosan molecular weight and by the initial alginate:chitosan mass ratio. The association efficiency of insulin into alginate nanoparticles, as well as loading capacity were mainly influenced by the alginate:chitosan mass ratio. Under optimized size conditions, the association efficiency and loading capacities were as high as 92% and 14.3%, respectively. Approximately 50% of the protein was partially retained by the nanoparticles in gastric pH environment up to 24 hours while a more extensive release close to 75% was observed under intestinal pH conditions. Mild formulation conditions, optimum particle size range obtained, high insulin entrapment efficiency, and resistance to gastrointestinal release seem to be synergic and promising factors toward development of an oral insulin delivery form.

Idioma: Inglês

Tipo (Avaliação Docente): Científica

Nº de páginas: 9