Dey Jagannath, Tran Richard T, Shen Jinhui, Tang Liping, Yang Jian
Department of Bioengineering, The University of Texas at Arlington, Arlington, Texas 76019, USA.
Macromol Mater Eng. 2011 Dec 12;296(12):1149-1157. doi: 10.1002/mame.201100074.
We have recently reported upon the development of crosslinked urethane-doped polyester (CUPE) network elastomers, which was motivated by the desire to overcome the drawbacks presented by crosslinked network polyesters and biodegradable polyurethanes for soft tissue engineering applications. Although the effect of the isocyanate content and post-polymerization conditions on the material structure-property relationship was examined in detail, the ability of the diol component to modulate the material properties was only studied briefly. Herein, we present a detailed report on the development of CUPE polymers synthesized using diols 4, 6, 8, 10, or 12 methylene units in length in order to investigate what role the diol component plays on the resulting material's physical properties, and assess their long-term biological performance in vivo. An increase in the diol length was shown to affect the physical properties of the CUPE polymers primarily through lowered polymeric crosslinking densities and elevated material hydrophobicity. The use of longer chain diols resulted in CUPE polymers with increased molecular weights resulting in higher tensile strength and elasticity, while also increasing the material hydrophobicity to lower bulk swelling and prolong the polymer degradation rates. Although the number of methylene units largely affected the physical properties of CUPE, the choice of diol did not affect the overall polymer cell/tissue-compatibility both in vitro and in vivo. In conclusion, we have established the diol component as an important parameter in controlling the structure-property relationship of the polymer in addition to diisocyanate concentration and post-polymerization conditions. Expanding the family of CUPE polymers increases the choices of biodegradable elastomers for tissue engineering applications.
我们最近报道了交联聚氨酯掺杂聚酯(CUPE)网络弹性体的开发情况,其动机是希望克服交联网络聚酯和可生物降解聚氨酯在软组织工程应用中存在的缺点。尽管详细研究了异氰酸酯含量和后聚合条件对材料结构-性能关系的影响,但二醇组分对材料性能的调节能力仅进行了简要研究。在此,我们详细报告了使用长度为4、6、8、10或12个亚甲基单元的二醇合成的CUPE聚合物的开发情况,以研究二醇组分在所得材料物理性能中所起的作用,并评估其在体内的长期生物学性能。二醇长度的增加主要通过降低聚合物交联密度和提高材料疏水性来影响CUPE聚合物的物理性能。使用较长链二醇导致CUPE聚合物分子量增加,从而提高拉伸强度和弹性,同时也增加材料疏水性以降低整体膨胀并延长聚合物降解速率。尽管亚甲基单元的数量在很大程度上影响了CUPE的物理性能,但二醇的选择在体外和体内均未影响聚合物的整体细胞/组织相容性。总之,除了二异氰酸酯浓度和后聚合条件外,我们已确定二醇组分是控制聚合物结构-性能关系的重要参数。扩展CUPE聚合物家族增加了用于组织工程应用的可生物降解弹性体的选择。