| Literature DB >> 31566289 |
Jie Zou1, Shuangquan Wu2, Jie Chen3, Xiaojuan Lei4, Qihua Li1, Hui Yu1, Shan Tang3, Dongdong Ye1.
Abstract
Wrinkled hydrogels from biomass sources are potential structural biomaterials. However, for biorelated applications, engineering scalable, structure-customized, robust, and biocompatible wrinkled hydrogels with highly oriented nanostructures and controllable intervals is still a challenge. A scalable biomass material, namely cellulose, is reported for customizing anisotropic, all-cellulose, wrinkle-patterned hydrogels (AWHs) through an ultrafast, auxiliary force, acid-induced gradient dual-crosslinking strategy. Direct immersion of a prestretched cellulose alkaline gel in acid and relaxation within seconds allow quick buildup of a consecutive through-thickness modulus gradient with acid-penetration-directed dual-crosslinking, confirmed by visual 3D Raman microscopy imaging, which drives the formation of self-wrinkling structures. Moreover, guided by quantitative mechanics simulations, the structure of AWHs is found to exhibit programmable intervals and aligned nanostructures that differ between ridge and valley regions and can be controlled by tuning the prestretching strain and acid treatment time, and these AWHs successfully induce cell alignment. Thus, a new avenue is opened to fabricate polysaccharide-derived, programmable, anisotropic, wrinkled hydrogels for use as biomedical materials via a bottom-up method.Keywords: cellulose hydrogels; gradient crosslinking; mechanics simulations; wrinkled patterns
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Year: 2019 PMID: 31566289 DOI: 10.1002/adma.201904762
Source DB: PubMed Journal: Adv Mater ISSN: 0935-9648 Impact factor: 30.849