Augmentation of postswelling surgical sealant potential of adhesive hydrogels.

Augmentation of postswelling surgical sealant potential of adhesive hydrogels.
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DOI:
10.1002/jbm.a.32942
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发表时间:
2010-12-15
影响因子:
4.9
通讯作者:
Edelman, Elazer R.
Edelman, Elazer R.
中科院分区:
工程技术3区
文献类型:
--
作者:
Shazly, Tarek M.;Baker, Aaron B.;Naber, John R.;Bon, Adriana;Van Vliet, Krystyn J.;Edelman, Elazer R.

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由星形聚乙二醇胺和线性葡聚糖醛聚合物(PEG:葡聚糖)形成的双组分水凝胶显示出作为组织特异性手术密封剂的前景。然而,PEG:葡聚糖溶胀后,软组织的粘附强度会显着降低,这可能会限制材料固定分离组织并防止手术部位渗漏的能力。我们将修饰的氨基酸 l-3,4-二羟基苯丙氨酸 (l-DOPA) 共价结合到 PEG: 葡聚糖中,以增强膨胀后密封剂的性能。 l-DOPA 是海洋动物粘合斑块的重要成分,已用于赋予合成材料湿粘合力。由于 PEG: 葡聚糖内聚力和粘附力都是由醛-胺相互作用介导的,因此 L-DOPA 侧基使其成为一种有效的网络调节剂,有可能影响多种材料特性。在水介质中浸泡一小时后,与纯水凝胶相比,掺杂有 3 mM l-DOPA/M 醛的 PEG: 葡聚糖平均溶胀减少 50.3%,刚度增加 287.4%,功能粘合强度增加 53.6%。将 l-DOPA 浓度增加至 11 mM l-DOPA/M 醛同样可以减少膨胀并减轻水合引起的性能损失,但会牺牲初始功能粘合强度、材料模量和生物相容性。总而言之,这些数据支持定制的左旋多巴缀合作为增强 PEG: 葡聚糖密封剂临床性能的有前途的方法。
Two-component hydrogels formed with star polyethylene glycol amine and linear dextran aldehyde polymers (PEG:dextran) show promise as tissue-specific surgical sealants. There is however a significant loss of adhesion strength to soft tissues following PEG:dextran swelling, which may limit material ability to appose disjoined tissues and prevent leakage from surgical sites. We covalently incorporated the modified amino acid l-3,4-dihydroxyphenylalanine (l-DOPA) into PEG:dextran to enhance post-swelling sealant performance. l-DOPA is an essential component of marine animal adhesive plaques and has been used to confer wet adhesion in synthetic materials. As both PEG:dextran cohesion and adhesion are mediated by aldehyde-amine interactions, l-DOPA side-groups make it a potent network modulator with potential to affect multiple material properties. Following one hour submersion in aqueous media, PEG:dextran doped with 3 mM l-DOPA/M aldehyde on average swelled 50.3% less, had 287.4% greater stiffness and had 53.6% greater functional adhesion strength compared to the neat hydrogel. Increased concentrations of l-DOPA up to 11 mM l-DOPA/M aldehyde similarly curtailed swelling and mitigated property loss with hydration, but sacrificed initial functional adhesion strength, material modulus and biocompatibility. Taken together, these data support tailored l-DOPA conjugation as a promising approach to enhance the clinical performance of PEG:dextran sealants.
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