In Vitro Investigation of Novel Peptide Hydrogels for Enamel Remineralization

This study investigates the microstructure of dental enamel following demineralization and re-mineralization processes, using DIAGNOdent scores and images obtained via scanning electron microscopy (SEM), atomic force microscopy (AFM), and microhardness (Vickers). The research evaluates the effects o...

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Main Authors: Codruta Sarosi, Alexandrina Muntean, Stanca Cuc, Ioan Petean, Sonia Balint, Marioara Moldovan, Aurel George Mohan
Format: Article
Language:English
Published: MDPI AG 2024-12-01
Series:Gels
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Online Access:https://www.mdpi.com/2310-2861/11/1/11
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author Codruta Sarosi
Alexandrina Muntean
Stanca Cuc
Ioan Petean
Sonia Balint
Marioara Moldovan
Aurel George Mohan
author_facet Codruta Sarosi
Alexandrina Muntean
Stanca Cuc
Ioan Petean
Sonia Balint
Marioara Moldovan
Aurel George Mohan
author_sort Codruta Sarosi
collection DOAJ
description This study investigates the microstructure of dental enamel following demineralization and re-mineralization processes, using DIAGNOdent scores and images obtained via scanning electron microscopy (SEM), atomic force microscopy (AFM), and microhardness (Vickers). The research evaluates the effects of two experimental hydrogels, Anti-Amelogenin isoform X (ABT260, S1) and Anti-Kallikrein L1 (K3014, S2), applied to demineralized enamel surfaces over periods of 14 and 21 days. The study involved 60 extracted teeth, free from cavities or other lesions, divided into four groups: a positive group (+), a negative group (−) and groups S1 and S2. The last three groups underwent demineralization with 37% phosphoric acid for 20 min. The negative group (−) was without remineralization treatment. The DIAGNOdent scores indicate that the S1 group treated with Anti-Amelogenin is more effective in remineralizing the enamel surface compared to the S2 group treated with Anti-Kallikrein. These findings were corroborated by SEM and AFM images, which revealed elongated hydroxyapatite (HAP) nanoparticles integrated into the demineralized structures. Demineralization reduced enamel microhardness to about 1/3 of a healthy one. Both tested hydrogels restored enamel hardness, with S1 being more effective than S2. Both peptides facilitated the interaction between the newly added minerals and residual protein binders on the enamel surface, thereby contributing to effective enamel restoration.
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publishDate 2024-12-01
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spelling doaj-art-0e50b2c588f3444e8a8d83526acc360b2025-01-24T13:33:46ZengMDPI AGGels2310-28612024-12-011111110.3390/gels11010011In Vitro Investigation of Novel Peptide Hydrogels for Enamel RemineralizationCodruta Sarosi0Alexandrina Muntean1Stanca Cuc2Ioan Petean3Sonia Balint4Marioara Moldovan5Aurel George Mohan6Department of Polymer Composites, Institute of Chemistry Raluca Ripan, Babes Bolyai University, 30 Fantanele Street, 400294 Cluj-Napoca, RomaniaDepartment of Paediatric Dentistry, Faculty of Dental Medicine, Iuliu Hatieganu University of Medicine and Pharmacy, 31 A. Iancu Street, 400083 Cluj-Napoca, RomaniaDepartment of Polymer Composites, Institute of Chemistry Raluca Ripan, Babes Bolyai University, 30 Fantanele Street, 400294 Cluj-Napoca, RomaniaFaculty of Chemistry and Chemical Engineering, Babes-Bolyai University, 11 Arany Janos Street, 400028 Cluj-Napoca, RomaniaDepartment of Polymer Composites, Institute of Chemistry Raluca Ripan, Babes Bolyai University, 30 Fantanele Street, 400294 Cluj-Napoca, RomaniaDepartment of Polymer Composites, Institute of Chemistry Raluca Ripan, Babes Bolyai University, 30 Fantanele Street, 400294 Cluj-Napoca, RomaniaFaculty of Medicine and Pharmacy, University of Oradea, P-ta 1 Decembrie 10, 410087 Oradea, RomaniaThis study investigates the microstructure of dental enamel following demineralization and re-mineralization processes, using DIAGNOdent scores and images obtained via scanning electron microscopy (SEM), atomic force microscopy (AFM), and microhardness (Vickers). The research evaluates the effects of two experimental hydrogels, Anti-Amelogenin isoform X (ABT260, S1) and Anti-Kallikrein L1 (K3014, S2), applied to demineralized enamel surfaces over periods of 14 and 21 days. The study involved 60 extracted teeth, free from cavities or other lesions, divided into four groups: a positive group (+), a negative group (−) and groups S1 and S2. The last three groups underwent demineralization with 37% phosphoric acid for 20 min. The negative group (−) was without remineralization treatment. The DIAGNOdent scores indicate that the S1 group treated with Anti-Amelogenin is more effective in remineralizing the enamel surface compared to the S2 group treated with Anti-Kallikrein. These findings were corroborated by SEM and AFM images, which revealed elongated hydroxyapatite (HAP) nanoparticles integrated into the demineralized structures. Demineralization reduced enamel microhardness to about 1/3 of a healthy one. Both tested hydrogels restored enamel hardness, with S1 being more effective than S2. Both peptides facilitated the interaction between the newly added minerals and residual protein binders on the enamel surface, thereby contributing to effective enamel restoration.https://www.mdpi.com/2310-2861/11/1/11hydrogelpeptideAFMSEMremineralization
spellingShingle Codruta Sarosi
Alexandrina Muntean
Stanca Cuc
Ioan Petean
Sonia Balint
Marioara Moldovan
Aurel George Mohan
In Vitro Investigation of Novel Peptide Hydrogels for Enamel Remineralization
Gels
hydrogel
peptide
AFM
SEM
remineralization
title In Vitro Investigation of Novel Peptide Hydrogels for Enamel Remineralization
title_full In Vitro Investigation of Novel Peptide Hydrogels for Enamel Remineralization
title_fullStr In Vitro Investigation of Novel Peptide Hydrogels for Enamel Remineralization
title_full_unstemmed In Vitro Investigation of Novel Peptide Hydrogels for Enamel Remineralization
title_short In Vitro Investigation of Novel Peptide Hydrogels for Enamel Remineralization
title_sort in vitro investigation of novel peptide hydrogels for enamel remineralization
topic hydrogel
peptide
AFM
SEM
remineralization
url https://www.mdpi.com/2310-2861/11/1/11
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AT ioanpetean invitroinvestigationofnovelpeptidehydrogelsforenamelremineralization
AT soniabalint invitroinvestigationofnovelpeptidehydrogelsforenamelremineralization
AT marioaramoldovan invitroinvestigationofnovelpeptidehydrogelsforenamelremineralization
AT aurelgeorgemohan invitroinvestigationofnovelpeptidehydrogelsforenamelremineralization