Please use this identifier to cite or link to this item: https://doi.org/10.1021/bm2015812
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dc.titleEarly stiffening and softening of collagen: Interplay of deformation mechanisms in biopolymer networks
dc.contributor.authorKurniawan, N.A.
dc.contributor.authorWong, L.H.
dc.contributor.authorRajagopalan, R.
dc.date.accessioned2014-06-17T07:39:12Z
dc.date.available2014-06-17T07:39:12Z
dc.date.issued2012-03-12
dc.identifier.citationKurniawan, N.A., Wong, L.H., Rajagopalan, R. (2012-03-12). Early stiffening and softening of collagen: Interplay of deformation mechanisms in biopolymer networks. Biomacromolecules 13 (3) : 691-698. ScholarBank@NUS Repository. https://doi.org/10.1021/bm2015812
dc.identifier.issn15257797
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/63761
dc.description.abstractCollagen networks, the main structural/mechanical elements in biological tissues, increasingly serve as biomimetic scaffolds for cell behavioral studies, assays, and tissue engineering, and yet their full spectrum of nonlinear behavior remains unclear. Here, with self-assembled type-I collagen as model, we use metrics beyond those in standard single-harmonic analysis of rheological measurements to reveal strain-softening and strain-stiffening of collagen networks both in instantaneous responses and at steady state. The results show how different deformation mechanisms, such as deformation-induced increase in the elastically active fibrils, nonlinear extension of individual fibrils, and slips in the physical cross-links in the network, can lead to the observed complex nonlinearity. We demonstrate how comprehensive rheological analyses can uncover the rich mechanical properties of biopolymer networks, including the above-mentioned softening as well as an early strain-stiffening, which are important for understanding physiological response of biological materials to mechanical loading. © 2012 American Chemical Society.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1021/bm2015812
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMICAL & BIOMOLECULAR ENGINEERING
dc.description.doi10.1021/bm2015812
dc.description.sourcetitleBiomacromolecules
dc.description.volume13
dc.description.issue3
dc.description.page691-698
dc.description.codenBOMAF
dc.identifier.isiut000301318100014
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