Sequential growth factor delivery from complexed microspheres for bone tissue engineering

被引:152
作者
Basmanav, F. Buket [1 ]
Kose, Game T. [2 ]
Hasirci, Vasif [1 ]
机构
[1] Middle E Tech Univ, BIOMAT, Dept Biol Sci, Biotechnol Res Unit, TR-06531 Ankara, Turkey
[2] Yeditepe Univ, Fac Engn & Architecture, Dept Genet & Bioengn, Istanbul, Turkey
关键词
Bone tissue engineering; Complex microspheres; Bone morphogenetic proteins; Sequential delivery;
D O I
10.1016/j.biomaterials.2008.07.017
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Aim of the study was to design a 3D tissue-engineering scaffold capable of sequentially delivering two bone morphogenetic proteins (BMP). The novel delivery system consisted of microspheres of polyelectrolyte complexes of poly(4-vinyl pyridine) (P4VN) and alginic acid loaded with the growth factors BMP-2 and BMP-7 which themselves were loaded into the scaffolds constructed of PLGA. Microspheres carrying the growth factors were prepared using polyelectrolyte solutions with different concentrations (4-10%) to control the growth factor release rate. Release kinetics was studied using albumin as the model drug and the populations that release their contents very early and very late in the release study were selected to carry BMP-2 and BMP-7, respectively. Foam porosity changed when the microspheres were loaded. Bone marrow derived stem cells (BMSC) from rats were seeded into these foams. Alkaline phosphatase (ALP) activities were found to be lowest and cell proliferation was highest at all time points with foams carrying both the microsphere populations, regardless of BMP presence. With the present doses used neither BMP-2 nor BMP-7 delivery had any direct effect on proliferation, however, they enhanced osteogenic differentiation. Co-administration of BMP enhanced osteogenic differentiation to a higher degree than with their single administration. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4195 / 4204
页数:10
相关论文
共 52 条
[1]   Human mesenchymal stem cells modulate allogeneic immune cell responses [J].
Aggarwal, S ;
Pittenger, MF .
BLOOD, 2005, 105 (04) :1815-1822
[2]   Controlling of systemic absorption of gliclazide through incorporation into alginate beads [J].
Al-Kassas, Raida S. ;
Al-Gohary, Omaimah M. N. ;
Al-Faadhel, Monirah M. .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2007, 341 (1-2) :230-237
[3]   Cross-linked alginate-gelatine beads: a new matrix for controlled release of pindolol [J].
Almeida, PF ;
Almeida, AJ .
JOURNAL OF CONTROLLED RELEASE, 2004, 97 (03) :431-439
[4]   5-fluorouracil encapsulated alginate beads for the treatment of breast cancer [J].
Arica, B ;
Çalis, S ;
Kas, HS ;
Sargon, MF ;
Hincal, AA .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2002, 242 (1-2) :267-269
[5]   Bone morphogenetic proteins in tissue engineering: the road from laboratory to clinic, part II (BMP delivery) [J].
Bessa, P. C. ;
Casal, M. ;
Reis, R. L. .
JOURNAL OF TISSUE ENGINEERING AND REGENERATIVE MEDICINE, 2008, 2 (2-3) :81-96
[6]  
Bobis S, 2006, FOLIA HISTOCHEM CYTO, V44, P215
[7]  
Bruder SP., 2000, PRINCIPLES TISSUE EN, V2nd, P683
[8]   Effect of preparation conditions on the nutrient release properties of alginate-whey protein granular minicrospheres [J].
Chen, Lingyun ;
Subirade, Muriel .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2007, 65 (03) :354-362
[9]  
Croft A. P., 2004, CURR ANAESTH CRIT CA, V15, P410, DOI DOI 10.1016/J.CACC.2004.08.011
[10]   Pesticide and model drug release from carboxymethylceullose microspheres [J].
Darvari, R ;
Hasirci, V .
JOURNAL OF MICROENCAPSULATION, 1996, 13 (01) :9-24