Sustained release of vascular endothelial growth factor from mineralized poly(lactide-co-glycolide) scaffolds for tissue engineering

被引:327
作者
Murphy, WL
Peters, MC
Kohn, DH
Mooney, DJ
机构
[1] Univ Michigan, Dept Biomed Engn, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Biol & Mat Sci, Ann Arbor, MI 48109 USA
[3] Univ Michigan, Dept Chem Engn, Ann Arbor, MI 48109 USA
关键词
drug delivery; tissue engineering; VEGF; mineralization; bone; poly(lactide-co-glycolide);
D O I
10.1016/S0142-9612(00)00120-4
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Strategies to engineer bone tissue have focused on either: (1) the use of scaffolds for osteogenic cell transplantation or as conductive substrates for guided bone regeneration; or(2) release of inductive bioactive factors from these scaffold materials. This study describes an approach to add an inductive component to an osteoconductive scaffold for bone tissue engineering. We report the release of bioactive Vascular endothelial growth factor (VEGF) from a mineralized, porous, degradable polymer scaffold. Three dimensional, porous scaffolds of the copolymer 85:15 poly(lactide-co-glycolide) were fabricated by including the growth factor into a gas foaming/particulate leaching process. The scaffold was then mineralized via incubation in a simulated body fluid. Growth of a bone-like mineral film on the inner pore surfaces of the porous scaffold is confirmed by mass increase measurements and quantification of phosphate content within scaffolds. Release of I-125-labeled VEGF was tracked over a 15 day period to determine release kinetics from the mineralized scaffolds. Sustained release from the mineralized scaffolds was achieved, and growth of the mineral film had only a minor effect on the release kinetics from the scaffolds. The VEGF released from the mineralized and non-mineralized scaffolds was over 70% active for up to 12 days following mineralization treatment, and the growth of mineral had little effect on total scaffold porosity. (C) 2000 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:2521 / 2527
页数:7
相关论文
共 46 条
[1]  
ATHANASIOU KA, 1995, CLIN ORTHOP RELAT R, P272
[2]   CONTROLLED DELIVERY SYSTEMS FOR PROTEINS BASED ON POLY(LACTIC GLYCOLIC ACID) MICROSPHERES [J].
COHEN, S ;
YOSHIOKA, T ;
LUCARELLI, M ;
HWANG, LH ;
LANGER, R .
PHARMACEUTICAL RESEARCH, 1991, 8 (06) :713-720
[3]   IMPLANTABLE BIOHYBRID ARTIFICIAL ORGANS [J].
COLTON, CK .
CELL TRANSPLANTATION, 1995, 4 (04) :415-436
[4]   BONE TISSUE ENGINEERING [J].
CRANE, GM ;
ISHAUG, SL ;
MIKOS, AG .
NATURE MEDICINE, 1995, 1 (12) :1322-1324
[5]   Periodontal tissue engineering by growth factors [J].
Giannobile, WV .
BONE, 1996, 19 (01) :S23-S37
[6]  
GILDING DK, 1981, BIOCOMPATIBILITY CLI, P209
[7]  
Harris LD, 1998, J BIOMED MATER RES, V42, P396, DOI 10.1002/(SICI)1097-4636(19981205)42:3<396::AID-JBM7>3.3.CO
[8]  
2-P
[9]   BIOCERAMICS - FROM CONCEPT TO CLINIC [J].
HENCH, LL .
JOURNAL OF THE AMERICAN CERAMIC SOCIETY, 1991, 74 (07) :1487-1510
[10]   Three-dimensional culture of rat calvarial osteoblasts in porous biodegradable polymers [J].
Ishaug-Riley, SL ;
Crane-Kruger, GM ;
Yaszemski, MJ ;
Mikos, AG .
BIOMATERIALS, 1998, 19 (15) :1405-1412