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  • Supracolloidal Assemblies as Sacrificial Templates for Porous Silk-Based Biomaterials

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Supracolloidal assemblies as sacrificial templates for porous silk-based biomaterials

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Supracolloidal assemblies as sacrificial templates for porous silk-based biomaterials. / Hardy, John; Ghezzi, Chiara; Saballos, Richard et al.
In: International Journal of Molecular Sciences, Vol. 16, No. 9, 28.08.2015, p. 20511-20522.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

Harvard

Hardy, J, Ghezzi, C, Saballos, R, Kaplan, DL & Schmidt, PCE 2015, 'Supracolloidal assemblies as sacrificial templates for porous silk-based biomaterials', International Journal of Molecular Sciences, vol. 16, no. 9, pp. 20511-20522. https://doi.org/10.3390/ijms160920511

APA

Hardy, J., Ghezzi, C., Saballos, R., Kaplan, D. L., & Schmidt, P. C. E. (2015). Supracolloidal assemblies as sacrificial templates for porous silk-based biomaterials. International Journal of Molecular Sciences, 16(9), 20511-20522. https://doi.org/10.3390/ijms160920511

Vancouver

Hardy J, Ghezzi C, Saballos R, Kaplan DL, Schmidt PCE. Supracolloidal assemblies as sacrificial templates for porous silk-based biomaterials. International Journal of Molecular Sciences. 2015 Aug 28;16(9):20511-20522. doi: 10.3390/ijms160920511

Author

Hardy, John ; Ghezzi, Chiara ; Saballos, Richard et al. / Supracolloidal assemblies as sacrificial templates for porous silk-based biomaterials. In: International Journal of Molecular Sciences. 2015 ; Vol. 16, No. 9. pp. 20511-20522.

Bibtex

@article{104bf4cfeada499e816ad6319286d86d,
title = "Supracolloidal assemblies as sacrificial templates for porous silk-based biomaterials",
abstract = "Tissues in the body are hierarchically structured composite materials with tissue-specific properties. Urea self-assembles via hydrogen bonding interactions into crystalline supracolloidal assemblies that can be used to impart macroscopic pores to polymer-based tissue scaffolds. In this communication, we explain the solvent interactions governing the solubility of urea and thereby the scope of compatible polymers. We also highlight the role of solvent interactions on the morphology of the resulting supracolloidal crystals. We elucidate the role of polymer-urea interactions on the morphology of the pores in the resulting biomaterials. Finally, we demonstrate that it is possible to use our urea templating methodology to prepare Bombyx mori silk protein-based biomaterials with pores that human dermal fibroblasts respond to by aligning with the long axis of the pores. This methodology has potential for application in a variety of different tissue engineering niches in which cell alignment is observed, including skin, bone, muscle and nerve. ",
keywords = "silk, urea, supramolecular, biomaterial, topographic influences",
author = "John Hardy and Chiara Ghezzi and Richard Saballos and Kaplan, {David L.} and Schmidt, {Prof. Christine E.}",
note = "This is an open access article distributed under the Creative Commons Attribution License (CC BY) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. ",
year = "2015",
month = aug,
day = "28",
doi = "10.3390/ijms160920511",
language = "English",
volume = "16",
pages = "20511--20522",
journal = "International Journal of Molecular Sciences",
issn = "1661-6596",
publisher = "MDPI AG",
number = "9",

}

RIS

TY - JOUR

T1 - Supracolloidal assemblies as sacrificial templates for porous silk-based biomaterials

AU - Hardy, John

AU - Ghezzi, Chiara

AU - Saballos, Richard

AU - Kaplan, David L.

AU - Schmidt, Prof. Christine E.

N1 - This is an open access article distributed under the Creative Commons Attribution License (CC BY) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

PY - 2015/8/28

Y1 - 2015/8/28

N2 - Tissues in the body are hierarchically structured composite materials with tissue-specific properties. Urea self-assembles via hydrogen bonding interactions into crystalline supracolloidal assemblies that can be used to impart macroscopic pores to polymer-based tissue scaffolds. In this communication, we explain the solvent interactions governing the solubility of urea and thereby the scope of compatible polymers. We also highlight the role of solvent interactions on the morphology of the resulting supracolloidal crystals. We elucidate the role of polymer-urea interactions on the morphology of the pores in the resulting biomaterials. Finally, we demonstrate that it is possible to use our urea templating methodology to prepare Bombyx mori silk protein-based biomaterials with pores that human dermal fibroblasts respond to by aligning with the long axis of the pores. This methodology has potential for application in a variety of different tissue engineering niches in which cell alignment is observed, including skin, bone, muscle and nerve.

AB - Tissues in the body are hierarchically structured composite materials with tissue-specific properties. Urea self-assembles via hydrogen bonding interactions into crystalline supracolloidal assemblies that can be used to impart macroscopic pores to polymer-based tissue scaffolds. In this communication, we explain the solvent interactions governing the solubility of urea and thereby the scope of compatible polymers. We also highlight the role of solvent interactions on the morphology of the resulting supracolloidal crystals. We elucidate the role of polymer-urea interactions on the morphology of the pores in the resulting biomaterials. Finally, we demonstrate that it is possible to use our urea templating methodology to prepare Bombyx mori silk protein-based biomaterials with pores that human dermal fibroblasts respond to by aligning with the long axis of the pores. This methodology has potential for application in a variety of different tissue engineering niches in which cell alignment is observed, including skin, bone, muscle and nerve.

KW - silk

KW - urea

KW - supramolecular

KW - biomaterial

KW - topographic influences

U2 - 10.3390/ijms160920511

DO - 10.3390/ijms160920511

M3 - Journal article

VL - 16

SP - 20511

EP - 20522

JO - International Journal of Molecular Sciences

JF - International Journal of Molecular Sciences

SN - 1661-6596

IS - 9

ER -