Localized Delivery of Dexamethasone from Electrospun Fibers Reduces the Foreign Body Response
Author(s) -
Nathaniel M. Vacanti,
Hao Cheng,
Paulina S. Hill,
João D. T. Guerreiro,
Tram T. Dang,
Minglin Ma,
Shanée Watson,
Nathaniel S. Hwang,
Robert Langer,
Daniel G. Anderson
Publication year - 2012
Publication title -
biomacromolecules
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.689
H-Index - 220
eISSN - 1526-4602
pISSN - 1525-7797
DOI - 10.1021/bm300520u
Subject(s) - dexamethasone , tissue engineering , regeneration (biology) , scaffold , regenerative medicine , mesenchymal stem cell , hyaluronic acid , chemistry , in vitro , drug delivery , in vivo , biomedical engineering , microbiology and biotechnology , anatomy , medicine , biochemistry , biology , cell , organic chemistry
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.
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