Chemical Tuning of Fibers Drawn from Extensible Hyaluronic Acid Networks.

Chemical Tuning of Fibers Drawn from Extensible Hyaluronic Acid Networks.
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DOI:
10.1021/jacs.0c09691
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发表时间:
2020-11-18
影响因子:
15
通讯作者:
Anderson, Daniel G.
Anderson, Daniel G.
中科院分区:
化学1区
文献类型:
--
作者:
Chu, Crystal K.;Joseph, Alby J.;Limjoco, Matthew D.;Yang, Jiawei;Bose, Suman;Thapa, Lavanya S.;Langer, Robert;Anderson, Daniel G.

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Polymer fibers with specific chemical and mechanical properties are key components of many biomaterials used for regenerative medicine and drug delivery. Here we develop a bioinspired, low-energy process to produce mechanically tunable biopolymer fibers drawn from aqueous solutions. Hyaluronic acid (HA) forms dynamic crosslinks with branched polyethylene glycol polymers end-functionalized with boronic acids of varied structure to produce extensible polymer networks. This dynamic fiber precursor (DFP) is directly drawn by pultrusion into HA fibers that display high aspect ratios, ranging from 4–20 microns in diameter and up to ~10 meters in length. Dynamic rheology measurements of the DFP and tensile testing of the resulting fibers reveal design considerations to tune the propensity for fiber formation and fiber mechanical properties, including the effect of polymer structure and concentration on elastic modulus, tensile strength, and ultimate strain. The materials’ humidity-responsive contractile behavior, a unique property of spider silks rarely observed in synthetic materials, highlights possibilities for further biomimetic and stimulus-responsive fiber applications. This work demonstrates that chemical modification of dynamic interactions can be used to tune the mechanical properties of pultrusion-based fibers and their precursors.
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