Supermacroporous poly(vinyl alcohol)-carboxylmethyl chitosan-poly(ethylene glycol) scaffold: an in vitro and in vivo pre-assessments for cartilage tissue engineering

被引:16
作者
Lee, Si-Yuen [1 ]
Wee, Ai-Sze [1 ]
Lim, Chin-Keong [1 ,2 ]
Abbas, Azlina Amir [1 ]
Selvaratnam, Lakshmi [3 ]
Merican, Azhar Mahmood [1 ]
Ahmad, Tunku Sara [1 ]
Kamarul, Tunku [1 ]
机构
[1] Univ Malaya, Tissue Engn Grp, Natl Orthopaed Ctr Res & Learning NOCERAL, Dept Orthopaed Surg,Fac Med, Kuala Lumpur, Malaysia
[2] Univ Teknol MARA, Fac Dent, Ctr Studies Preclin Sci, Shah Alam 40450, Malaysia
[3] Monash Univ, Sch Med & Hlth Sci, Petaling Jaya, Malaysia
关键词
PHENOTYPE; MEMBRANE; HYDROGEL; BEHAVIOR; CULTURE;
D O I
10.1007/s10856-013-4907-4
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
This study aims to pre-assess the in vitro and in vivo biocompatibility of poly(vinyl alcohol)-carboxylmethyl-chitosan-poly(ethylene glycol) (PCP) scaffold. PCP was lyophilised to create supermacroporous structures. 3-(4, 5-dimethyl-thiazol-2yl)-2, 5-diphenyltetrazolium bromide (MTT) assay and immunohistochemistry (IHC) were used to evaluate the effectiveness of PCP scaffolds for chondrocytes attachment and proliferation. The ultrastructural was assessed using scanning electron microscopy (SEM) and transmission electron microscopy (TEM). Extracellular matrix (ECM) formation was evaluated using collagen type-II staining, glycosaminoglycan (GAG) and collagen assays. Histological analysis was conducted on 3-week implanted Sprague-Dawley rats. The MTT, IHC, SEM and TEM analyses confirm that PCP scaffolds promoted cell attachment and proliferation in vitro. The chondrocyte-PCP constructs secreted GAG and collagen type-II, both increased significantly from day-14 to day-28 (P < 0.05). PCP scaffolds did not elicit any adverse effects on the host tissue, but were partially degraded. These results suggest that supermacroporous PCP is a biocompatible scaffold for clinical applications.
引用
收藏
页码:1561 / 1570
页数:10
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