Tissue integration of growth factor-eluting layer-by-layer polyelectrolyte multilayer coated implants

被引:240
作者
Macdonald, Mara L. [1 ,2 ]
Samuel, Raymond E. [1 ]
Shah, Nisarg J. [1 ]
Padera, Robert F. [4 ]
Beben, Yvette M. [3 ]
Hammond, Paula T. [1 ]
机构
[1] MIT, Dept Chem Engn, Cambridge, MA 02139 USA
[2] MIT, Harvard Mit Div Hlth Sci & Technol, Cambridge, MA 02139 USA
[3] MIT, Dept Biol, Cambridge, MA 02139 USA
[4] Brigham & Womens Hosp, Dept Pathol, Boston, MA 02115 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
Bone morphogenetic protein 2 (BMP-2); Polyelectrolyte multilayer; Bone tissue engineering; Coating; Layer-by-Layer; Controlled drug release; FILMS; DELIVERY; RELEASE; PROTEIN;
D O I
10.1016/j.biomaterials.2010.10.052
中图分类号
R318 [生物医学工程];
学科分类号
100103 [病原生物学];
摘要
Drug eluting coatings that can direct the host tissue response to implanted medical devices have the potential to ameliorate both the medical and financial burden of complications from implantation. However, because many drugs useful in this arena are biologic in nature, a paucity of delivery strategies for biologics, including growth factors, currently limits the control that can be exerted on the implantation environment. Layer-by-Layer (LbL) polyelectrolyte multilayer films are highly attractive as ultrathin biologic reservoirs, due to the capability to conformally coat difficult geometries, the use of aqueous processing likely to preserve fragile protein function, and the tunability of incorporation and release profiles. Herein, we describe the first LbL films capable of microgram-scale release of the biologic Bone Morphogenetic Protein 2 (BMP-2), which is capable of directing the host tissue response to create bone from native progenitor cells. Ten micrograms of BMP-2 are released over a period of two weeks in vitro; less than 1% is released in the first 3 h (compared with commercial collagen matrices which can release up to 60% of BMP-2, too quickly to induce differentiation). BMP-2 released from LbL films retains its ability to induce bone differentiation in MC3T3 E1S4 pre-osteoblasts, as measured by induction of alkaline phosphatase and stains for calcium (via Alizarin Red) and calcium matrix (via Von Kossa). In vivo, BMP-2 film coated scaffolds were compared with film coated scaffolds lacking BMP-2. BMP-2 coatings implanted intramuscularly were able to initiate host progenitor cells to differentiate into bone, which matured and expanded from four to 9 weeks as measured by MicroCT and histology. Such LbL films represent new steps towards controlling and tuning host response to implanted medical devices, which may ultimately increase the success of implanted devices, provide alternative new approaches toward bone wound healing, and lay the foundation for development of a multi-therapeutic release coating. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1446 / 1453
页数:8
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