{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Yoo H"],"funding":["NIDCR NIH HHS"],"pagination":["106498"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC12359075"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["154"],"pubmed_abstract":["Chitosan (CS) and phloroglucinol (PhG), two extracts abundantly found in marine life, were investigated for their ability to biomodify demineralized dentin by enhancing collagen crosslinks and improving dentin extracellular matrix (ECM) mechanical and biochemical stability. Dentin obtained from non-carious extracted human molars were demineralized with phosphoric acid. Baseline Fourier-transform infrared (FTIR) spectra, apparent flexural elastic modulus (AE) and dry mass (DM) of each specimen were independently acquired. Specimens were randomly incubated for 5 min into either ultrapure water (no-treatment), 1% glutaraldehyde (GA), 1% CS or 1% PhG. Water and GA were used, respectively, as a negative and positive control for collagen crosslinks. Specimens' post-treatment FTIR spectra, AE, an"],"journal":["Journal of the mechanical behavior of biomedical materials"],"pubmed_title":["Use of marine occurrent extracts to enhance the stability of dentin extracellular matrix."],"pmcid":["PMC12359075"],"funding_grant_id":["R15 DE032836"],"pubmed_authors":["Alabsy M","Agostini-Walesch G","Mitchell JC","Carrilho MR","Yoo H","Gao F"],"additional_accession":[]},"is_claimable":false,"name":"Use of marine occurrent extracts to enhance the stability of dentin extracellular matrix.","description":"Chitosan (CS) and phloroglucinol (PhG), two extracts abundantly found in marine life, were investigated for their ability to biomodify demineralized dentin by enhancing collagen crosslinks and improving dentin extracellular matrix (ECM) mechanical and biochemical stability. Dentin obtained from non-carious extracted human molars were demineralized with phosphoric acid. Baseline Fourier-transform infrared (FTIR) spectra, apparent flexural elastic modulus (AE) and dry mass (DM) of each specimen were independently acquired. Specimens were randomly incubated for 5 min into either ultrapure water (no-treatment), 1% glutaraldehyde (GA), 1% CS or 1% PhG. Water and GA were used, respectively, as a negative and positive control for collagen crosslinks. Specimens' post-treatment FTIR spectra, AE, an","dates":{"release":"2024-01-01T00:00:00Z","publication":"2024 Jun","modification":"2026-05-01T22:56:52.854Z","creation":"2026-04-07T17:21:33.561Z"},"accession":"S-EPMC12359075","cross_references":{"pubmed":["38581962"],"doi":["10.1016/j.jmbbm.2024.106498"]}}