Novel injectable porous poly(γ-benzyl-L-glutamate) microspheres for cartilage tissue engineering: preparation and evaluation

被引:39
作者
Fang, Jianjun [1 ]
Yong, Qi [2 ]
Zhang, Kunxi [1 ]
Sun, Wentao [2 ]
Yan, Shifeng [1 ]
Cui, Lei [2 ]
Yin, Jingbo [1 ]
机构
[1] Shanghai Univ, Dept Polymer Mat, Shanghai 200444, Peoples R China
[2] Capital Med Univ, Beijing Shijitan Hosp, Med Sci & Res Ctr, Beijing 100038, Peoples R China
基金
中国国家自然科学基金; 上海市自然科学基金;
关键词
HUMAN NASAL CHONDROCYTES; MICROCARRIERS ENHANCES REDIFFERENTIATION; RING-OPENING POLYMERIZATION; DRUG-DELIVERY; PROTEIN ADSORPTION; CELL MICROCARRIERS; SPINNER CULTURE; BIODEGRADATION; ATTACHMENT; SCAFFOLD;
D O I
10.1039/c4tb01333f
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
In search of an injectable cellular delivery vehicle for tissue regeneration, porous microspheres fabricated from the synthetic polypeptide of poly(gamma-benzyl-L-glutamate) (PBLG) were developed. The structural and morphological characteristics of the microspheres could be adjusted by changing the amounts of the gelatin porogen. PBLG microspheres fabricated from 6.5% gelatin content exhibited an average pore diameter of 50.9 +/- 10.3 mu m and a porosity of 86.58 +/- 2.37%. Degradation in vitro of the microspheres could be well controlled by adjusting the molecular weight of PBLG, and the degradability in vivo showed a satisfactory degradation time range from 8 to 12 weeks. Articular chondrocytes, which were seeded within the PBLG porous microspheres, exhibited progressive proliferation and deposition of the cartilaginous extracellular matrix. After cultivation for 2 days in vitro, the PBLG porous microspheres loaded with chondrocytes were injected subcutaneously into nude mice. At 4, 8 and 12 weeks postinjection, neo-generated tissue was harvested for histological observations, which showed a typical cartilage structure and cartilaginous matrix accumulation. A gradual increase of GAG and COL II content in neo-generated tissue was detected by biochemical analysis. These results indicate that the fabricated porous microspheres showing controllable degradation properties, good biocompatibility and cytocompatibility are potentially useful as an injectable vehicle for cartilage tissue engineering.
引用
收藏
页码:1020 / 1031
页数:12
相关论文
共 49 条
[1]   Biological responses to materials [J].
Anderson, JM .
ANNUAL REVIEW OF MATERIALS RESEARCH, 2001, 31 :81-110
[2]  
Bergsma E. J., 1995, BIOMATERIALS, V16, P25
[3]   FOREIGN-BODY REACTIONS TO RESORBABLE POLY(L-LACTIDE) BONE PLATES AND SCREWS USED FOR THE FIXATION OF UNSTABLE ZYGOMATIC FRACTURES [J].
BERGSMA, EJ ;
ROZEMA, FR ;
BOS, RRM ;
DEBRUIJN, WC .
JOURNAL OF ORAL AND MAXILLOFACIAL SURGERY, 1993, 51 (06) :666-670
[4]   The influence of microscale topography on fibroblast attachment and motility [J].
Berry, CC ;
Campbell, G ;
Spadiccino, A ;
Robertson, M ;
Curtis, ASG .
BIOMATERIALS, 2004, 25 (26) :5781-5788
[5]  
Bouchet BY, 2000, J BIOMED MATER RES, V52, P716, DOI 10.1002/1097-4636(20001215)52:4<716::AID-JBM17>3.0.CO
[6]  
2-T
[7]   The effects of scaffold thickness on tissue engineered cartilage in photocrosslinked poly(ethylene oxide) hydrogels [J].
Bryant, SJ ;
Anseth, KS .
BIOMATERIALS, 2001, 22 (06) :619-626
[8]   Porous Scaffolds Based on Cross-Linking of Poly(L-glutamic acid) [J].
Cao, Bin ;
Yin, Jingbo ;
Yan, Shifeng ;
Cui, Lei ;
Chen, Xuesi ;
Xie, Yongtao .
MACROMOLECULAR BIOSCIENCE, 2011, 11 (03) :427-434
[9]  
CHO CS, 1988, J CONTROL RELEASE, V7, P283
[10]   Highly open porous biodegradable microcarriers:: In vitro cultivation of chondrocytes for injectable delivery [J].
Chung, Hyun Jung ;
Kim, In Kyoung ;
Kim, Taek Gyoung ;
Park, Tae Gwan .
TISSUE ENGINEERING PART A, 2008, 14 (05) :607-615