<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>13(2)</volume><submitter>Wang L</submitter><pubmed_abstract>&lt;b>Background:&lt;/b> Synthetic hydrogels are commonly mechanically weak which limits the scope of their applications. &lt;b>Methods:&lt;/b> In this study, we synthesized an organic-inorganic hybrid hydrogel with ultrahigh strength, stiffness, and toughness via enzyme-induced mineralization of calcium phosphate in a double network of bacterial cellulose nanofibers and alginate-Ca&lt;sup>2+&lt;/sup>. &lt;b>Results:&lt;/b> Cellulose nanofibers formed the first rigid network via hydrogen binding and templated the deposition of calcium phosphate, while alginate-Ca&lt;sup>2+&lt;/sup> formed the second energy-dissipating network via ionic interaction. The two networks created a brick-mortar-like structure, in which the "tortuous fracture path" mechanism by breaking the interlaced calcium phosphate-coated bacterial cellulo</pubmed_abstract><journal>Theranostics</journal><pagination>673-684</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9830447</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Enzymatically-mineralized double-network hydrogels with ultrahigh mechanical strength, toughness, and stiffness.</pubmed_title><pmcid>PMC9830447</pmcid><pubmed_authors>Li W</pubmed_authors><pubmed_authors>Zhao W</pubmed_authors><pubmed_authors>Wang G</pubmed_authors><pubmed_authors>Zhao Y</pubmed_authors><pubmed_authors>Zhang Q</pubmed_authors><pubmed_authors>Wang L</pubmed_authors></additional><is_claimable>false</is_claimable><name>Enzymatically-mineralized double-network hydrogels with ultrahigh mechanical strength, toughness, and stiffness.</name><description>&lt;b>Background:&lt;/b> Synthetic hydrogels are commonly mechanically weak which limits the scope of their applications. &lt;b>Methods:&lt;/b> In this study, we synthesized an organic-inorganic hybrid hydrogel with ultrahigh strength, stiffness, and toughness via enzyme-induced mineralization of calcium phosphate in a double network of bacterial cellulose nanofibers and alginate-Ca&lt;sup>2+&lt;/sup>. &lt;b>Results:&lt;/b> Cellulose nanofibers formed the first rigid network via hydrogen binding and templated the deposition of calcium phosphate, while alginate-Ca&lt;sup>2+&lt;/sup> formed the second energy-dissipating network via ionic interaction. The two networks created a brick-mortar-like structure, in which the "tortuous fracture path" mechanism by breaking the interlaced calcium phosphate-coated bacterial cellulo</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023</publication><modification>2025-04-04T21:55:04.148Z</modification><creation>2025-02-18T23:37:05.913Z</creation></dates><accession>S-EPMC9830447</accession><cross_references><pubmed>36632214</pubmed><doi>10.7150/thno.77417</doi></cross_references></HashMap>