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Article: Bone-Inspired Mineralization with Highly Aligned Cellulose Nanofibers as Template

TitleBone-Inspired Mineralization with Highly Aligned Cellulose Nanofibers as Template
Authors
Keywordsalignment
bacterial nanocellulose
biomimetic mineralization
hardness
hydroxyapatite composite
Issue Date2019
Citation
ACS Applied Materials and Interfaces, 2019, v. 11, n. 45, p. 42486-42495 How to Cite?
AbstractBioinspired by the aligned structure and building blocks of bone, this work mineralized the aligned bacterial cellulose (BC) through in situ mineralization using CaCl2 and K2HPO4 solutions. The cellulose nanofibers were aligned by a scalable stretching process. The aligned and mineralized bacterial cellulose (AMBC) homogeneously incorporated hydroxyapatite (HAP) with a high mineral content and exhibited excellent mechanical strength. The ordered 3D structure allowed the AMBC composite to achieve a high elastic modulus and hardness and the development of a nanostructure inspired by natural bone. The AMBC composite exhibited an elastic modulus of 10.91 ± 3.26 GPa and hardness of 0.37 ± 0.18 GPa. Compared with the nonaligned mineralized bacterial cellulose (NMBC) composite with mineralized crystals of HAP randomly distributed into the BC scaffolds, the AMBC composite possessed a 210% higher elastic modulus and 95% higher hardness. The obtained AMBC composite had excellent mechanical properties by mimicking the natural structure of bone, which indicated that the organic BC aerogel with aligned nanofibers was a promising template for biomimetic mineralization.
Persistent Identifierhttp://hdl.handle.net/10722/318795
ISSN
2023 Impact Factor: 8.3
2023 SCImago Journal Rankings: 2.058
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorCheng, Zheng-
dc.contributor.authorYe, Zhou-
dc.contributor.authorNatan, Avi-
dc.contributor.authorMa, Yi-
dc.contributor.authorLi, Hongyan-
dc.contributor.authorChen, Yong-
dc.contributor.authorWan, Liqiang-
dc.contributor.authorAparicio, Conrado-
dc.contributor.authorZhu, Hongli-
dc.date.accessioned2022-10-11T12:24:35Z-
dc.date.available2022-10-11T12:24:35Z-
dc.date.issued2019-
dc.identifier.citationACS Applied Materials and Interfaces, 2019, v. 11, n. 45, p. 42486-42495-
dc.identifier.issn1944-8244-
dc.identifier.urihttp://hdl.handle.net/10722/318795-
dc.description.abstractBioinspired by the aligned structure and building blocks of bone, this work mineralized the aligned bacterial cellulose (BC) through in situ mineralization using CaCl2 and K2HPO4 solutions. The cellulose nanofibers were aligned by a scalable stretching process. The aligned and mineralized bacterial cellulose (AMBC) homogeneously incorporated hydroxyapatite (HAP) with a high mineral content and exhibited excellent mechanical strength. The ordered 3D structure allowed the AMBC composite to achieve a high elastic modulus and hardness and the development of a nanostructure inspired by natural bone. The AMBC composite exhibited an elastic modulus of 10.91 ± 3.26 GPa and hardness of 0.37 ± 0.18 GPa. Compared with the nonaligned mineralized bacterial cellulose (NMBC) composite with mineralized crystals of HAP randomly distributed into the BC scaffolds, the AMBC composite possessed a 210% higher elastic modulus and 95% higher hardness. The obtained AMBC composite had excellent mechanical properties by mimicking the natural structure of bone, which indicated that the organic BC aerogel with aligned nanofibers was a promising template for biomimetic mineralization.-
dc.languageeng-
dc.relation.ispartofACS Applied Materials and Interfaces-
dc.subjectalignment-
dc.subjectbacterial nanocellulose-
dc.subjectbiomimetic mineralization-
dc.subjecthardness-
dc.subjecthydroxyapatite composite-
dc.titleBone-Inspired Mineralization with Highly Aligned Cellulose Nanofibers as Template-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1021/acsami.9b15234-
dc.identifier.pmid31638768-
dc.identifier.scopuseid_2-s2.0-85074911523-
dc.identifier.volume11-
dc.identifier.issue45-
dc.identifier.spage42486-
dc.identifier.epage42495-
dc.identifier.eissn1944-8252-
dc.identifier.isiWOS:000497263600071-

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