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Localized delivery of dexamethasone from electrospun fibers reduces the foreign body response.
Vacanti, Nathaniel M; Cheng, Hao; Hill, Paulina S; Guerreiro, João D T; Dang, Tram T; Ma, Minglin; Watson, Shanée; Hwang, Nathaniel S; Langer, Robert; Anderson, Daniel G.
Afiliação
  • Vacanti NM; Department of Chemical Engineering, Massachusetts Institute of Technology , Cambridge, MA, USA.
Biomacromolecules ; 13(10): 3031-8, 2012 Oct 08.
Article em En | MEDLINE | ID: mdl-22920794
ABSTRACT
Synthetic scaffolds are crucial to applications in regenerative medicine; however, the foreign body response can impede regeneration and may lead to failure of the implant. Herein we report the development of a tissue engineering scaffold that allows attachment and proliferation of regenerating cells while reducing the foreign body response by localized delivery of an anti-inflammatory agent. Electrospun fibers composed of poly(l-lactic) acid (PLLA) and poly(ε-caprolactone) (PCL) were prepared with and without the steroid anti-inflammatory drug, dexamethasone. Analysis of subcutaneous implants demonstrated that the PLLA fibers encapsulating dexamethasone evoked a less severe inflammatory response than the other fibers examined. They also displayed a controlled release of dexamethasone over a period of time conducive to tissue regeneration and allowed human mesenchymal stem cells to adhere to and proliferate on them in vitro. These observations demonstrate their potential as a building block for tissue engineering scaffolds.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Materiais Biocompatíveis / Dexametasona / Reação a Corpo Estranho / Células-Tronco Mesenquimais / Anti-Inflamatórios Limite: Humans Idioma: En Revista: Biomacromolecules Ano de publicação: 2012 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Materiais Biocompatíveis / Dexametasona / Reação a Corpo Estranho / Células-Tronco Mesenquimais / Anti-Inflamatórios Limite: Humans Idioma: En Revista: Biomacromolecules Ano de publicação: 2012 Tipo de documento: Article