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Gelatin/chitosan/hyaluronan scaffold integrated with PLGA microspheres for cartilage tissue engineering
被引:149
作者:
Tan, Huaping
Wu, Jindan
Lao, Lihong
Gao, Changyou
[1
]
机构:
[1] Zhejiang Univ, Key Lab Macromol Synth & Functionalizat, Minist Educ, Hangzhou 310027, Zhejiang, Peoples R China
关键词:
Microspheres;
PLGA;
Scaffolds;
Compressive properties;
Chondrocytes;
POLY(L-LACTIC ACID) SCAFFOLDS;
CHITOSAN-GELATIN SCAFFOLDS;
IN-VITRO CHARACTERIZATION;
ENDOTHELIAL GROWTH-FACTOR;
PARTICLE LEACHING METHOD;
TRI-COPOLYMER SCAFFOLD;
CONTROLLED-RELEASE;
SUSTAINED-RELEASE;
DRUG-DELIVERY;
CHONDROCYTES;
D O I:
10.1016/j.actbio.2008.07.030
中图分类号:
R318 [生物医学工程];
学科分类号:
0831 ;
摘要:
Poly(lactide-co-glycotide) (PLGA) microspheres integrated into gelatin/chitosan/hyaluronan scaffolds were fabricated by freeze-drying and crosslinking with 1-ethyl-3-(3-dimethyl aminopropyl)carbodiimide. The effects of the microspheres on porosity, density, compressive modulus, phosphate-buffered saline uptake ratio and weight loss of the scaffolds were evaluated. Generally, a scaffold with a higher PLGA content had a lower porosity and weight loss, and a medium uptake ratio, but a larger apparent density and compressive modulus. When the PLGA content was lower than 50%, the PLGA-integrated scaffolds had a similar pore size (similar to 200 mu m) as that of the control, and as much as 90% of their porosity could be preserved. In vitro chondrocyte culture in the 50% PLGA-integrated scaffold demonstrated that the cells could proliferate and secrete extracellular matrix at the same level as in the control gelatin/chitosan/hyaluronan scaffold. (C) 2008 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
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页码:328 / 337
页数:10
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