Shin Heungsoo, Quinten Ruhé P, Mikos Antonios G, Jansen John A
Department of Bioengineering, Rice University, MS-142, P.O. Box 1892, Houston, TX 77251-1892, USA.
Biomaterials. 2003 Aug;24(19):3201-11. doi: 10.1016/s0142-9612(03)00168-6.
This study was designed to assess in vivo bone and soft tissue behavior of novel oligo(poly(ethylene glycol) fumarate) (OPF) hydrogels using a rabbit model. In vitro degradation of the OPF hydrogels was also investigated in order to compare with in vivo characteristics. Four groups of OPF hydrogel implants were synthesized by alternation of crosslinking density, poly(ethylene glycol) (PEG) block length of OPF, and cell-binding peptide content. The in vitro degradation rate of OPF hydrogels increased with decreasing crosslinking density of hydrogels, which was characterized by measuring weight loss and swelling ratio of hydrogels and medium pH change. Examination of histological sections of the subcutaneous and cranial implants showed that an uniform thin circumferential fibrous capsule was formed around the OPF hydrogel implants. Quantitative evaluation of the tissue response revealed that no statistical difference existed in capsule quality or thickness between implant groups, implantation sites or implantation times. At 4 weeks, there was a very limited number of inflammatory and multinuclear cells at the implant-fibrous capsule interface for all implants. However, at 12 weeks, OPF hydrogels with PEG block length of number average molecular weight 6090+/-90 showed extensive surface erosion and superficial fragmentation that was surrounded by a number of inflammatory cells, while OPF hydrogels with PEG block length of number average molecular weight 930+/-10 elicited minimal degradation. Constant fibrous capsule layers and number of inflammatory cells were observed regardless of the incorporation of cell-binding peptide and crosslinking density of OPF hydrogels with PEG block length of number average molecular weight 930+/-90. These results confirm that the degradation of implants can be controlled by tailoring the macromolecular structure of OPF hydrogels. Additionally, histological evaluation of implants proved that the OPF hydrogel is a promising material for biodegradable scaffolds in tissue engineering.
本研究旨在使用兔模型评估新型聚(乙二醇)富马酸酯(OPF)水凝胶在体内的骨和软组织行为。还对OPF水凝胶的体外降解进行了研究,以便与体内特性进行比较。通过改变交联密度、OPF的聚(乙二醇)(PEG)嵌段长度和细胞结合肽含量,合成了四组OPF水凝胶植入物。OPF水凝胶的体外降解速率随水凝胶交联密度的降低而增加,这通过测量水凝胶的重量损失、溶胀率和培养基pH变化来表征。对皮下和颅骨植入物的组织学切片检查表明,OPF水凝胶植入物周围形成了均匀的薄圆周纤维囊。对组织反应的定量评估显示,植入物组、植入部位或植入时间之间在囊的质量或厚度上没有统计学差异。在4周时,所有植入物在植入物-纤维囊界面处的炎性细胞和多核细胞数量非常有限。然而,在12周时,数均分子量为6090±90的PEG嵌段长度的OPF水凝胶出现广泛的表面侵蚀和表面破碎,并被大量炎性细胞包围,而数均分子量为930±10的PEG嵌段长度的OPF水凝胶引起的降解最小。无论是否掺入细胞结合肽以及数均分子量为930±90的PEG嵌段长度的OPF水凝胶的交联密度如何,均观察到恒定的纤维囊层和炎性细胞数量。这些结果证实,可以通过调整OPF水凝胶的大分子结构来控制植入物的降解。此外,植入物的组织学评估证明,OPF水凝胶是组织工程中用于可生物降解支架的有前途的材料。