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Transient Biocompatible Polymeric Platforms for Long-Term Controlled Release of Therapeutic Proteins and Vaccines.
Acar, Handan; Banerjee, Saikat; Shi, Heliang; Jamshidi, Reihaneh; Hashemi, Nastaran; Cho, Michael W; Montazami, Reza.
Afiliação
  • Acar H; Department of Mechanical Engineering, Iowa State University, Ames, IA 50011, USA.
  • Banerjee S; Department of Biomedical Sciences, College of Veterinary Medicine, Iowa State University, Ames, IA 50011, USA.
  • Shi H; Center of Advanced Host Defenses Immunobiotics and Translational Medicine, Iowa State University, Ames, IA 50011, USA.
  • Jamshidi R; Department of Biomedical Sciences, College of Veterinary Medicine, Iowa State University, Ames, IA 50011, USA.
  • Hashemi N; Center of Advanced Host Defenses Immunobiotics and Translational Medicine, Iowa State University, Ames, IA 50011, USA.
  • Cho MW; Department of Mechanical Engineering, Iowa State University, Ames, IA 50011, USA.
  • Montazami R; Center of Advanced Host Defenses Immunobiotics and Translational Medicine, Iowa State University, Ames, IA 50011, USA.
Materials (Basel) ; 9(5)2016 May.
Article em En | MEDLINE | ID: mdl-28546855
ABSTRACT
Polymer-based interpenetrating networks (IPNs) with controllable and programmable degradation and release kinetics enable unique opportunities for physisorption and controlled release of therapeutic proteins or vaccines while their chemical and structural integrities are conserved. This paper presents materials, a simple preparation method, and release kinetics of a series of long-term programmable, biocompatible, and biodegradable polymer-based IPN controlled release platforms. Release kinetics of the gp41 protein was controlled over a 30-day period via tuning and altering the chemical structure of the IPN platforms. Post-release analysis confirmed structural conservation of the gp41 protein throughout the process. Cell viability assay confirmed biocompatibility and non-cytotoxicity of the IPNs.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2016 Tipo de documento: Article