Nummelin Sami, Liljeström Ville, Saarikoski Eve, Ropponen Jarmo, Nykänen Antti, Linko Veikko, Seppälä Jukka, Hirvonen Jouni, Ikkala Olli, Bimbo Luis M, Kostiainen Mauri A
Department of Biotechnology and Chemical Technology, Aalto University School of Chemical Technology, 00076 Aalto (Finland) http://chemtech.aalto.fi/bihy.
Department of Applied Physics, Aalto University School of Science, 00076 Aalto (Finland).
Chemistry. 2015 Oct 5;21(41):14433-9. doi: 10.1002/chem.201501812. Epub 2015 Jul 1.
Compounds that can gelate aqueous solutions offer an intriguing toolbox to create functional hydrogel materials for biomedical applications. Amphiphilic Janus dendrimers with low molecular weights can readily form self-assembled fibers at very low mass proportion (0.2 wt %) to create supramolecular hydrogels (G'≫G'') with outstanding mechanical properties and storage modulus of G'>1000 Pa. The G' value and gel melting temperature can be tuned by modulating the position or number of hydrophobic alkyl chains in the dendrimer structure; thus enabling exquisite control over the mesoscale material properties in these molecular assemblies. The gels are formed within seconds by simple injection of ethanol-solvated dendrimers into an aqueous solution. Cryogenic TEM, small-angle X-ray scattering, and SEM were used to confirm the fibrous structure morphology of the gels. Furthermore, the gels can be efficiently loaded with different bioactive cargo, such as active enzymes, peptides, or small-molecule drugs, to be used for sustained release in drug delivery.
能够使水溶液凝胶化的化合物为制备用于生物医学应用的功能性水凝胶材料提供了一个引人关注的工具库。低分子量的两亲性Janus树枝状大分子在极低质量比例(0.2 wt %)下就能轻松形成自组装纤维,从而制备出具有出色机械性能且储能模量G'>1000 Pa的超分子水凝胶(G'≫G'')。通过调节树枝状大分子结构中疏水烷基链的位置或数量,可以调节G'值和凝胶熔化温度;从而能够精确控制这些分子组装体中的中尺度材料特性。通过将乙醇溶剂化的树枝状大分子简单注入水溶液中,几秒钟内即可形成凝胶。利用低温透射电子显微镜、小角X射线散射和扫描电子显微镜来确认凝胶的纤维结构形态。此外,这些凝胶可以有效地负载不同的生物活性物质,如活性酶、肽或小分子药物,用于药物递送中的持续释放。