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通过程序内部应力控制带相反电荷水凝胶中的刚性聚电解质的上层建筑。

Control superstructure of rigid polyelectrolytes in oppositely charged hydrogels via programmed internal stress.

机构信息

1] Graduate School of Life Science, Hokkaido University, Sapporo 060-0810, Japan [2].

1] Faculty of Advanced Life Science, Hokkaido University, Sapporo 060-0810, Japan [2] [3].

出版信息

Nat Commun. 2014 Aug 8;5:4490. doi: 10.1038/ncomms5490.

Abstract

Biomacromolecules usually form complex superstructures in natural biotissues, such as different alignments of collagen fibres in articular cartilages, for multifunctionalities. Inspired by nature, there are efforts towards developing multiscale ordered structures in hydrogels (recognized as one of the best candidates of soft biotissues). However, creating complex superstructures in gels are hardly realized because of the absence of effective approaches to control the localized molecular orientation. Here we introduce a method to create various superstructures of rigid polyanions in polycationic hydrogels. The control of localized orientation of rigid molecules, which are sensitive to the internal stress field of the gel, is achieved by tuning the swelling mismatch between masked and unmasked regions of the photolithographic patterned gel. Furthermore, we develop a double network structure to toughen the hydrogels with programmed superstructures, which deform reversibly under large strain. This work presents a promising pathway to develop superstructures in hydrogels and should shed light on designing biomimetic materials with intricate molecular alignments.

摘要

生物大分子通常在天然生物组织中形成复杂的超结构,例如关节软骨中不同取向的胶原纤维,以实现多功能性。受自然启发,人们致力于在水凝胶中开发多尺度有序结构(被认为是软生物组织的最佳候选材料之一)。然而,由于缺乏控制局部分子取向的有效方法,很难在凝胶中形成复杂的超结构。在这里,我们介绍了一种在聚阳离子水凝胶中创建刚性聚阴离子各种超结构的方法。通过调节光刻图案化凝胶的掩蔽和未掩蔽区域之间的溶胀失配,可以控制对凝胶内部应力场敏感的刚性分子的局部取向。此外,我们开发了一种双重网络结构来增强具有编程超结构的水凝胶的韧性,这些超结构在大应变下可实现可逆变形。这项工作为在水凝胶中开发超结构提供了一种很有前途的途径,应该为设计具有复杂分子排列的仿生材料提供启示。

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