Cargando…

Antimicrobial Monomers for Polymeric Dental Restoratives: Cytotoxicity and Physicochemical Properties

A trend for the next generation of polymeric dental restoratives is to incorporate multifunctional capabilities to regulate microbial growth and remineralize tooth surfaces. Polymerizable 2-(methacryloyloxy)-N-(2-(methacryloyloxy)ethyl)-N,N-dimethylethan-1-aminium bromide (IDMA1) and N,N′-([1,1′-bip...

Descripción completa

Detalles Bibliográficos
Autores principales: Bienek, Diane R., Frukhtbeyn, Stanislav A., Giuseppetti, Anthony A., Okeke, Ugochukwu C., Skrtic, Drago
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5872106/
https://www.ncbi.nlm.nih.gov/pubmed/29495522
http://dx.doi.org/10.3390/jfb9010020
_version_ 1783309765354455040
author Bienek, Diane R.
Frukhtbeyn, Stanislav A.
Giuseppetti, Anthony A.
Okeke, Ugochukwu C.
Skrtic, Drago
author_facet Bienek, Diane R.
Frukhtbeyn, Stanislav A.
Giuseppetti, Anthony A.
Okeke, Ugochukwu C.
Skrtic, Drago
author_sort Bienek, Diane R.
collection PubMed
description A trend for the next generation of polymeric dental restoratives is to incorporate multifunctional capabilities to regulate microbial growth and remineralize tooth surfaces. Polymerizable 2-(methacryloyloxy)-N-(2-(methacryloyloxy)ethyl)-N,N-dimethylethan-1-aminium bromide (IDMA1) and N,N′-([1,1′-biphenyl]-2,2′-diylbis(methylene))bis(2-(methacryloyloxy)-N,N-dimethylethan-1-aminium) bromide (IDMA2), intended for utilization in bi-functional antimicrobial and remineralizing composites, were synthesized, purified with an ethanol-diethyl ether-hexane solvent system, and validated by nuclear magnetic resonance ((1)H and (13)C NMR) spectroscopy, mass spectrometry, and Fourier-transform infrared spectroscopy. When incorporated into light-curable urethane dimethacrylate (UDMA)/polyethylene glycol-extended UDMA (PEG-U)/ethyl 2-(hydroxymethyl)acrylate (EHMA) (assigned UPE) resins, IDMAs did not affect the overall resins’ hydrophilicity/hydrophobicity balance (water contact angle: 60.8–65.5°). The attained degrees of vinyl conversion (DVC) were consistently higher in both IDMA-containing copolymers and their amorphous calcium phosphate (ACP) composites (up to 5% and 20%, respectively) reaching 92.5% in IDMA2 formulations. Notably, these high DVCs values were attained without an excessive increase in polymerization stress. The observed reduction in biaxial flexure strength of UPE-IDMA ACP composites should not prevent further evaluation of these materials as multifunctional Class V restoratives. In direct contact with human gingival fibroblasts, at biologically relevant concentrations, IDMAs did not adversely affect cell viability or their metabolic activity. Ion release from the composites was indicative of their strong remineralization potential. The above, early-phase biocompatibility and physicochemical tests justify further evaluation of these experimental materials to identify formulation(s) suitable for clinical testing. Successful completion is expected to yield a new class of restoratives with well-controlled bio-function, which will physicochemically, mechanically, and biologically outperform the conventional Class V restoratives.
format Online
Article
Text
id pubmed-5872106
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-58721062018-03-30 Antimicrobial Monomers for Polymeric Dental Restoratives: Cytotoxicity and Physicochemical Properties Bienek, Diane R. Frukhtbeyn, Stanislav A. Giuseppetti, Anthony A. Okeke, Ugochukwu C. Skrtic, Drago J Funct Biomater Article A trend for the next generation of polymeric dental restoratives is to incorporate multifunctional capabilities to regulate microbial growth and remineralize tooth surfaces. Polymerizable 2-(methacryloyloxy)-N-(2-(methacryloyloxy)ethyl)-N,N-dimethylethan-1-aminium bromide (IDMA1) and N,N′-([1,1′-biphenyl]-2,2′-diylbis(methylene))bis(2-(methacryloyloxy)-N,N-dimethylethan-1-aminium) bromide (IDMA2), intended for utilization in bi-functional antimicrobial and remineralizing composites, were synthesized, purified with an ethanol-diethyl ether-hexane solvent system, and validated by nuclear magnetic resonance ((1)H and (13)C NMR) spectroscopy, mass spectrometry, and Fourier-transform infrared spectroscopy. When incorporated into light-curable urethane dimethacrylate (UDMA)/polyethylene glycol-extended UDMA (PEG-U)/ethyl 2-(hydroxymethyl)acrylate (EHMA) (assigned UPE) resins, IDMAs did not affect the overall resins’ hydrophilicity/hydrophobicity balance (water contact angle: 60.8–65.5°). The attained degrees of vinyl conversion (DVC) were consistently higher in both IDMA-containing copolymers and their amorphous calcium phosphate (ACP) composites (up to 5% and 20%, respectively) reaching 92.5% in IDMA2 formulations. Notably, these high DVCs values were attained without an excessive increase in polymerization stress. The observed reduction in biaxial flexure strength of UPE-IDMA ACP composites should not prevent further evaluation of these materials as multifunctional Class V restoratives. In direct contact with human gingival fibroblasts, at biologically relevant concentrations, IDMAs did not adversely affect cell viability or their metabolic activity. Ion release from the composites was indicative of their strong remineralization potential. The above, early-phase biocompatibility and physicochemical tests justify further evaluation of these experimental materials to identify formulation(s) suitable for clinical testing. Successful completion is expected to yield a new class of restoratives with well-controlled bio-function, which will physicochemically, mechanically, and biologically outperform the conventional Class V restoratives. MDPI 2018-02-27 /pmc/articles/PMC5872106/ /pubmed/29495522 http://dx.doi.org/10.3390/jfb9010020 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Bienek, Diane R.
Frukhtbeyn, Stanislav A.
Giuseppetti, Anthony A.
Okeke, Ugochukwu C.
Skrtic, Drago
Antimicrobial Monomers for Polymeric Dental Restoratives: Cytotoxicity and Physicochemical Properties
title Antimicrobial Monomers for Polymeric Dental Restoratives: Cytotoxicity and Physicochemical Properties
title_full Antimicrobial Monomers for Polymeric Dental Restoratives: Cytotoxicity and Physicochemical Properties
title_fullStr Antimicrobial Monomers for Polymeric Dental Restoratives: Cytotoxicity and Physicochemical Properties
title_full_unstemmed Antimicrobial Monomers for Polymeric Dental Restoratives: Cytotoxicity and Physicochemical Properties
title_short Antimicrobial Monomers for Polymeric Dental Restoratives: Cytotoxicity and Physicochemical Properties
title_sort antimicrobial monomers for polymeric dental restoratives: cytotoxicity and physicochemical properties
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5872106/
https://www.ncbi.nlm.nih.gov/pubmed/29495522
http://dx.doi.org/10.3390/jfb9010020
work_keys_str_mv AT bienekdianer antimicrobialmonomersforpolymericdentalrestorativescytotoxicityandphysicochemicalproperties
AT frukhtbeynstanislava antimicrobialmonomersforpolymericdentalrestorativescytotoxicityandphysicochemicalproperties
AT giuseppettianthonya antimicrobialmonomersforpolymericdentalrestorativescytotoxicityandphysicochemicalproperties
AT okekeugochukwuc antimicrobialmonomersforpolymericdentalrestorativescytotoxicityandphysicochemicalproperties
AT skrticdrago antimicrobialmonomersforpolymericdentalrestorativescytotoxicityandphysicochemicalproperties