Controlled drug release from a novel injectable biodegradable micro sphere/scaffold composite based on poly(propylene fumarate)

被引:76
|
作者
Kempen, DHR
Lu, LC
Kim, C
Zhu, X
Dhert, WJA
Currier, BL
Yaszemski, MJ
机构
[1] Mayo Clin & Mayo Fdn, Coll Med, Tissue Engn & Polymer Biomat Lab, Dept Orthopaed Surg, Rochester, MN 55905 USA
[2] Mayo Clin & Mayo Fdn, Coll Med, Dept Biomed Engn, Rochester, MN 55905 USA
[3] Univ Calif San Diego, Dept Orthoped Surg, La Jolla, CA 92161 USA
[4] Vet Adm Med Ctr, La Jolla, CA 92161 USA
[5] Univ Utrecht, Med Ctr, Dept Orthoped, NL-3508 GA Utrecht, Netherlands
关键词
poly(propylene fumarate); biodegradable microspheres; composite scaffold; injectable material; bone tissue engineering; drug delivery;
D O I
10.1002/jbm.a.30336
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The ideal biomaterial for the repair of bone defects is expected to have good mechanical properties, be fabricated easily into a desired shape, support cell attachment, allow controlled release of bioactive factors to induce bone formation, and biodegrade into nontoxic products to permit natural bone formation and remodeling. The synthetic polymer poly(propylene fumarate) (PPF) holds great promise as such a biomaterial. In previous work we developed poly(DL-lactic-co-glycolic acid) (PLGA) and PPF microspheres for the controlled delivery of bioactive molecules. This study presents an approach to incorporate these microspheres into an injectable, porous PPF scaffold. Model drug Texas red dextran (TRD) was encapsulated into biodegradable PLEA and PIT microspheres at 2 mu g/mg microsphere. Five porous composite formulations were fabricated via a gas foaming technique by combining the injectable PPF paste with the PLGA or PPF microspheres at 100 or 250 mg microsphere per composite formulation, or a control aqueous TRD solution (200 p,g per composite). All scaffolds had an interconnected pore network with an average porosity of 64.8 +/- 3.6%. The presence of microspheres in the composite scaffolds was confirmed by scanning electron microscopy and confocal microscopy. The composite scaffolds exhibited a sustained release of the model drug for at least 28 days and had minimal burst release during the initial phase of release, as compared to drug release from microspheres alone. The compressive moduli of the scaffolds were between 2.4 and 26.2 MPa after fabrication, and between 14.9 and 62.8 MPa after 28 days in PBS. The scaffolds containing PPF microspheres exhibited a significantly higher initial compressive modulus than those containing PLGA microspheres. Increasing the amount of microspheres in the composites was found to significantly decrease the initial compressive modulus. The novel injectable PPF-based microsphere/scaffold composites developed in this study are promising to serve as vehicles for controlled drug delivery for bone tissue engineering. (c) 2005 Wiley Periodicals, Inc.
引用
收藏
页码:103 / 111
页数:9
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