Suppression of hydrolytic degradation in labile polymer networks via integrated styrenic nanogels

被引:3
作者
Rad, Ima Y. [1 ,3 ]
Lewis, Steven [1 ]
Barros, Matthew D. [1 ]
Kipper, Matt [2 ]
Stansbury, Jeffrey W. [1 ]
机构
[1] Univ Colorado Anschutz Med Campus, Craniofacial Biol Dept, Res Complex 1 North,13065 E 17th Ave, Aurora, CO 80045 USA
[2] Colorado State Univ, Chem & Biol Engn, Suzanne & Walter Scott Jr Bioengn, Suzanne & Walter Scott Jr Bioengn Bldg, Ft Collins, CO 80523 USA
[3] Sepanta Inc, 1027 Linden Gate Court, Ft Collins, CO 80524 USA
基金
美国国家卫生研究院;
关键词
Dental composite; Degradable linkage; Degradation; Hydrophobic network; Nanogel; Photopolymerization; Inert/Reactive additives; Dental adhesive resin; Styrenic copolymer; THERMOSETTING COMPOSITES; MECHANICAL-PROPERTIES; RESIN; DIVINYLBENZENE; COPOLYMERIZATION; POLYSTYRENE; FORMULATIONS; CONVERSION; PROPERTY; STRESS;
D O I
10.1016/j.dental.2021.05.001
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Objective. The objective of this study was to demonstrate an approach with potential to increase the life of dental restorative polymers in water, by maintaining their strength and toughness with varied content of inert or reactive styrenic pre-polymeric additives. It was hypothesized that addition of styrene-co-divinylbenzene nanogels to a conventional dimethacrylate resin (e.g. TEGDMA) would reduce its susceptibility towards hydrolytic degradation, while maintaining equivalent mechanical properties. Methods. Polymerization kinetics and functional group conversions were determined by Fourier transform infrared spectroscopy. Triple-detection gel permeation chromatography was used for nanogel particle characterization. A goniometer was used to measure water contact angle on experimental and control photocured polymers. Hydrolytic degradation and mass loss evaluation was performed after extended water storage of an intentionally hydrolytically degradable polymer. Resin viscosity was determined rheometrically and polymer mechanical properties were evaluated using three-point flexural testing with TEGDMA-nanogel formulations. Results. The polymer network with highest level of nanogel loading (50 wt%) and the highest level of internal nanogel crosslinking (50 mol%) had the lowest degree of equilibrium swelling ratio and mass loss. The flexural modulus and ultimate strength of polymerized TEGDMA and styrenic nanogel-modified TEGDMA were not statistically different (p > 0.05). Significance. Due to improved shielding throughout the bulk of methacrylate-based polymers, including an example with an intentionally hydrolytically labile network structure, and a dramatic decrease of water uptake while maintaining equivalent mechanical properties, styrenic nanogel additives especially in high loading levels provide an excellent alternative to eliminate the adverse effects of water and presumably salivary fluids. (C) 2021 The Academy of Dental Materials. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:1295 / 1306
页数:12
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