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.
中科院分区:
文献类型:
--
作者:
Shazly, Tarek M.;Baker, Aaron B.;Naber, John R.;Bon, Adriana;Van Vliet, Krystyn J.;Edelman, Elazer R.
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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DOI:
10.1163/156856208786140337
发表时间:
2008-01-01
影响因子:
3.6
作者:
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影响因子:
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通讯作者:
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影响因子:
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