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1.
J Dent Res ; 99(2): 175-181, 2020 02.
Artigo em Inglês | MEDLINE | ID: mdl-31826696

RESUMO

A dentin biomodification strategy with selective proanthocyanidin (PAC)-enriched extracts reinforces dentin and dentin-resin interfaces. Enrichment of the extracts according to the degree of polymerization allows exploration of bioactive principles of PACs and structure-activity relationships. This study investigated the sustained dentin matrix biomodification and dentin-resin bioadhesion of 2 fractions consisting exclusively of B-type PAC dimers with or without a single galloyl motif (specifically, DIMERG and DIMERNG) and their precursor material, enriched grape seed extract (e-GSE; Vitis vinifera). The biomodification potential was determined by long-term evaluation of the apparent modulus of elasticity and collagen solubility (hydroxyproline release). Chemical characterization of the dentin matrix was performed by attenuated total reflectance-Fourier-transform infrared spectroscopy. The bioadhesive properties were assessed by a microtensile bond strength test at different time points, and macro-hybrid layers were produced to verify the degree of conversion of the adhesive resin. Fractions consisting of DIMERG, DIMERNG, and their precursor, e-GSE, increased the modulus of elasticity at all time points and reduced collagen degradation. Specimens treated with DIMERNG remained stable throughout 12 mo of storage, whereas a significant drop in the modulus of elasticity was observed for the DIMERG and e-GSE groups at 6 mo. The fractions and precursor did not affect the degree of resin conversion at the hybrid layer. Changes in infrared resonances corresponding to collagen cross-links in the dentin matrix occurred for all treatments. Higher bond strength was observed for dentin treated with e-GSE as compared with DIMERG and DIMERNG; all biointerfaces remained stable after 12 mo. Nongalloylated PACs mediate stable dentin biomodification, which includes protective activity against collagen degradation and reinforcement of the anchoring dentin matrix. Collectively, PACs with a higher degree of oligomerization offer a robust bioadhesion between the hydrophilic dentin matrix and the hydrophobic adhesive.


Assuntos
Colagem Dentária , Dentina , Extrato de Sementes de Uva , Proantocianidinas , Colágeno , Cimentos Dentários , Adesivos Dentinários , Teste de Materiais , Proantocianidinas/farmacologia , Resistência à Tração
2.
J Dent Res ; 96(4): 406-412, 2017 04.
Artigo em Inglês | MEDLINE | ID: mdl-27927886

RESUMO

Oligomeric proanthocyanidins (OPACs) are potent and renewable natural bioactives possible to be refined into chemically standardized mixtures for biological applications. Herein, we found that multiscale interactions of OPACs with the dentin matrix create tight biointerfaces with hydrophobic methacrylate adhesives on wet surfaces. An enriched mixture of OPACs, with a known phytochemical profile, was produced from grape seed crude extract ( Vitis vinifera; enriched grape seed extract [e-GSE]) and applied to dentin matrices to determine changes to the mechanical properties and biodegradability of the dentin matrix and favorable resin adhesion mechanisms. Methods included a 3-point flexural test, quantification of hydroxyproline (collagen solubilization), static and dynamic nanomechanical analyses, resin-dentin microtensile bond strength, and micropermeability at the adhesive interface. The e-GSE-modified dentin matrix exhibited remarkably low collagen solubilization and sustained the bulk elastic properties over 12 mo. Tan δ findings reveal a more elastic-like behavior of the e-GSE-modified dentin matrix, which was not affected by H-bond destabilization by urea. Dentin-methacrylate biointerfaces with robust and stable adhesion were created on e-GSE-primed dentin surfaces, leading to a dramatic decrease of the interfacial permeability. Standardized OPAC mixtures provide a new mechanism of adhesion to type I collagen-rich tissues that does not rely on hydrophilic monomers. The bioadhesion mechanism involves physicochemical modifications to the dentin matrix, reduced tissue biodegradation, and bridging to methacrylate resins.


Assuntos
Colágeno/química , Colagem Dentária/métodos , Adesivos Dentinários/química , Dentina/química , Extrato de Sementes de Uva/química , Proantocianidinas/química , Reagentes de Ligações Cruzadas/química , Elasticidade , Humanos , Teste de Materiais , Metacrilatos/química , Dente Molar , Propriedades de Superfície , Resistência à Tração , Vitis
3.
Oper Dent ; 42(2): 196-202, 2017.
Artigo em Inglês | MEDLINE | ID: mdl-27892838

RESUMO

Secondary caries at the tooth-resin interface is the primary reason for replacement of resin composite restorations. The tooth-resin interface is formed by the interlocking of resin material with hydroxyapatite crystals in enamel and collagen mesh structure in dentin. Efforts to strengthen the tooth-resin interface have identified chemical agents with dentin collagen cross-linking potential and antimicrobial activities. The purpose of the present study was to assess protective effects of bioactive primer against secondary caries development around enamel and dentin margins of class V restorations, using an in vitro bacterial caries model. Class V composite restorations were prepared on 60 bovine teeth (n=15) with pretreatment of the cavity walls with control buffer solution, an enriched fraction of grape seed extract (e-GSE), 1-ethyl-3-(3-dimethyl aminopropyl)-carbodiimide/N-hydroxysuccinimide, or chlorhexidine digluconate. After incubating specimens in a bacterial model with Streptococcus mutans for four days, dentin and enamel were assessed by fluorescence microscopy. Results revealed that only the naturally occurring product, e-GSE, significantly inhibited the development of secondary caries immediately adjacent to the dentin-resin interface, as indicated by the caries inhibition zone. No inhibitory effects were observed in enamel margins. The results suggest that the incorporation of e-GSE into components of the adhesive system may inhibit secondary caries and potentially contribute to the protection of highly vulnerable dentin-resin margins.


Assuntos
Carbodi-Imidas/farmacologia , Cariostáticos/farmacologia , Resinas Compostas/farmacologia , Cárie Dentária/microbiologia , Cárie Dentária/prevenção & controle , Extrato de Sementes de Uva/farmacologia , Succinimidas/farmacologia , Animais , Bovinos , Restauração Dentária Permanente/métodos , Técnicas In Vitro , Microscopia de Fluorescência , Streptococcus mutans
4.
J Dent Res ; 93(4): 417-22, 2014 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-24574140

RESUMO

Although proanthocyanidins (PACs) modify dentin, the effectiveness of different PAC sources and the correlation with their specific chemical composition are still unknown. This study describes the chemical profiling of natural PAC-rich extracts from 7 plants using ultra high pressure/performance liquid chromatography (UHPLC) to determine the overall composition of these extracts and, in parallel, comprehensively evaluate their effect on dentin properties. The total polyphenol content of the extracts was determined (as gallic acid equivalents) using Folin-Ciocalteau assays. Dentin biomodification was assessed by the modulus of elasticity, mass change, and resistance to enzymatic biodegradation. Extracts with a high polyphenol and PAC content from Vitis vinifera, Theobroma cacao, Camellia sinensis, and Pinus massoniana induced a significant increase in modulus of elasticity and mass. The UHPLC analysis showed the presence of multiple types of polyphenols, ranging from simple phenolic acids to oligomeric PACs and highly condensed tannins. Protective effect against enzymatic degradation was observed for all experimental groups; however, statistically significant differences were observed between plant extracts. The findings provide clear evidence that the dentin bioactivities of PACs are source dependent, resulting from a combination of concentration and specific chemical constitution of the complex PAC mixtures.


Assuntos
Dentina/efeitos dos fármacos , Extratos Vegetais/farmacologia , Proantocianidinas/farmacologia , Antioxidantes/farmacologia , Arecaceae/química , Cacau/química , Camellia sinensis/química , Cromatografia Líquida de Alta Pressão , Cinnamomum aromaticum/química , Cinnamomum zeylanicum/química , Colagenases/farmacologia , Dentina/anatomia & histologia , Módulo de Elasticidade , Ácido Gálico/análise , Extrato de Sementes de Uva/farmacologia , Humanos , Pinus/química , Casca de Planta/química , Extratos Vegetais/análise , Polifenóis/análise , Polifenóis/farmacologia , Proantocianidinas/análise , Substâncias Protetoras/farmacologia , Sementes/química , Chá/química , Vitis/química
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