Antibacterial resin composites with sustained chlorhexidine release

dc.contributor.authorGONCALVES, FLAVIA
dc.contributor.authorSILVA, LARISSA S.T.
dc.contributor.authorROSCHEL, JULIA N.
dc.contributor.authorSOUZA, GRECA de
dc.contributor.authorCAMPOS, LUIZA de P. M.
dc.contributor.authorVARCA, GUSTAVO H.
dc.contributor.authorPARRA, DUCLERC
dc.contributor.authorPEREZ, MIRKO A.
dc.contributor.authorGORDILHO, ANTONIO C.
dc.contributor.authorBRANDT, WILLIAM C.
dc.contributor.authorBOARO, LETICIA
dc.coverageInternacional
dc.date.accessioned2026-03-30T13:27:31Z
dc.date.available2026-03-30T13:27:31Z
dc.date.issued2025
dc.description.abstractBackground: The addition of chlorhexidine in dental restorative materials is a promising strategy to reduce the recurrence of tooth decay lesions. However, the main challenge is to develop materials with antimicrobial activity in the long term. Objective: This study analyses the effect of filler type and concentration of resin composites supplemented with chlorhexidine loaded in carrier montmorillonite particles (MMT/CHX) regarding their chemical, physical, and short- and long-term antimicrobial proprieties. Materials: Experimental composites were synthesized with 0, 30, or 60% filler in two ratios, 70/30 and 80/20, of barium glass/colloidal silica, respectively, and 5 wt% MMT/CHX. Conversion was measured using near Fourier-transform infrared spectrometry. Sorption and solubility were determined by specimen weight before and after drying and immersing in water. Flexural strength (FS) and elastic modulus (E) were determined by three bending tests using a universal test machine. Chlorhexidine release was monitored for 50 days. Streptococcus mutans UA159 was used in all microbiological assays. Inhibition halo assay was performed for 12 months and, also, biofilm growth for the specimens and colony-forming unit (CFU). Remineralization assay was used on restored teeth using measurements of microhardness Knoop and CFUs. Results: Conversion, sorption, and solubility were not affected by filler type and concentration. FS and E increase with the filler concentration, independent from filler type. Chlorhexidine was significantly released for 15 days for all experimental materials, and the increase in filler concentration decreased its release. Halo inhibition was observed for a longer time (12 months) in materials with 60 wt% filler at 70/30 proportion. Also, 60 wt% filler materials, independent from the filler ratio, reduced the CFU in relation to the control group from 8 to 12 months. In the remineralization assay, besides the absence of differences in hardness among the groups, after biofilm growth, the CFU was also significantly lower in materials with 60 wt% filler. Conclusions: Materials with 60% filler, preferentially with 70% barium glass and 30% silica, and 5% MMT/CHX particles demonstrated long-term antimicrobial activity, reaching 12 months of effectiveness. Also, this formulation was associated with higher mechanical properties and similar conversion, sorption, and solubility compared to the other materials.
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipIDFAPESP: 16/01319-9; 17/13367-0
dc.format.extent1-15
dc.identifier.doi10.3390/pharmaceutics17091144
dc.identifier.fasciculo9
dc.identifier.issn1999-4923
dc.identifier.orcidhttps://orcid.org/0000-0002-7626-880X
dc.identifier.percentilfi90.5
dc.identifier.percentilfiCiteScore88.00
dc.identifier.urihttps://repositorio.ipen.br/handle/123456789/49575
dc.identifier.vol17
dc.language.isoeng
dc.relation.ispartofPharmaceutics
dc.rightsopenAccess
dc.titleAntibacterial resin composites with sustained chlorhexidine release
dc.typeArtigo de periódico
dspace.entity.typePublication
ipen.autorLUIZA MELLO DE PAIVA CAMPOS
ipen.autorGUSTAVO HENRIQUE COSTA VARCA
ipen.autorDUCLERC FERNANDES PARRA
ipen.codigoautor7219
ipen.codigoautor9593
ipen.codigoautor562
ipen.contributor.ipenauthorLUIZA MELLO DE PAIVA CAMPOS
ipen.contributor.ipenauthorGUSTAVO HENRIQUE COSTA VARCA
ipen.contributor.ipenauthorDUCLERC FERNANDES PARRA
ipen.identifier.fi5.5
ipen.identifier.fiCiteScore10.0
ipen.identifier.ipendoc31550
ipen.identifier.iwosWoS
ipen.subtituloone-year in vitro study
relation.isAuthorOfPublication36f6b8d9-59dd-4b20-a90b-22fed2c352f2
relation.isAuthorOfPublicationb9550043-2ea7-42f3-89f7-0b18e3b8b347
relation.isAuthorOfPublication67996d86-0a59-4ba2-8d38-facaa14e26c3
relation.isAuthorOfPublication.latestForDiscovery36f6b8d9-59dd-4b20-a90b-22fed2c352f2

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