journal article·2018-12

Effect of adhesive-monomers and photoinitiator on C=C conversion and color stability of model self-adhesive flowable composites

Alessandra Amaral Monteiro, Vinícius Esteves Salgado, Rafael Pino Vitti, Marcus Vinícius Loureiro Bertolo, Larissa Maria Cavalcante, Luis Felipe J. Schneider

Publisher page

Abstract

Abstract The aim of this study was to determine the influence of the monomer type and photoinitiator systems on the degree of C=C conversion and color stability of model self-adhesive flowable composites (SAFCs). Three sets of flowable composites were formulated varying the monomer type: set 1 (control), with bisphenol-A glycidyl methacrylate and triethylene glycol dimethacrylate (BisGMA/TEGDMA) at 50/50 wt%; set 2, with BisGMA/TEGDMA/bis[2(methacryloyloxy)ethyl]phosphate (2MP) at 30/30/40 wt%; and set 3, with BisGMA/TEGDMA/4-ethyl-methacryloxy-trimetilato anhydride (4-META) at 30/30/40 wt%. For each set, different initiator systems were added: camphorquinone (CQ) + ethyl-4-dimethylamino benzoate (EDMAB); diphenyl(2,4,6-trimethylbenzoyl)-phosphine oxide (TPO); phenylbis(2,4,6-trimethylbenzoyl)phosphine oxide (BAPO); and the combinations CQ + EDMAB + TPO and CQ + EDMAB + BAPO. Degree of C=C conversion was determined by Fourier-transformed infrared spectroscopy with an attenuated total reflectance device (ATR-FTIR). The color stability was determined by CIE00 color difference formula (∆E*00), after water (T1) and coffee (T2) storages for 30 days. Data was submitted to two-way analysis of variance (ANOVA) followed by Student-Newman-Keuls test (α = 0.05). Degree of conversion and color stability were dependent on the resin matrix composition and the photoinitiator system. The 2MP-based set showed the highest DC, but also the poorest color stability. For the 4-META-base set, TPO and BAPO produced the highest degree of C=C conversion. The use of BAPO produced the best color stability for the acidic-monomer-based sets.
Source: openaire · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Dental materials and restorations · Photopolymerization techniques and applications · Additive Manufacturing and 3D Printing Technologies

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

References (42)

Show source-provided references
1. Composite resins in dentistry: the monomer systems10.1111/j.1600-0722.1997.tb00188.x ↗
2. Evaluation of a self-adhering flowable composite in terms of micro-shear bond strength and microleakage10.3109/00016357.2012.696697 ↗
3. Bonding and sealing ability of a new self-adhering flowable composite resin in class I restorations10.1007/s00784-012-0846-6 ↗
4. Composite resin – state of the art10.1016/j.dental.2010.10.020 ↗
5. State of the art of self-etch adhesives10.1016/j.dental.2010.10.023 ↗
6. Bonding effectiveness of self adhesive composites to dentin and enamel10.1016/j.dental.2012.10.001 ↗
7. Influence of phosphoric acid etching on microleakage of a self-etch adhesive and a self-adhering composite10.1111/j.1834-7819.2012.01689.x ↗
8. Diffusion and concurrent solubility of self-adhering and new resin-matrix composites during watersorption/desorption cycles10.1016/j.dental.2010.10.014 ↗
9. Curing dental resins and composites by photopolymerization10.1111/j.1708-8240.2000.tb00239.x ↗
10. Reduced glutathione prevents camphorquinone-induced apoptosis in human oral keratinocytes10.1016/j.dental.2013.11.008 ↗
11. Oxidative stress is responsible for genotoxicity of camphorquinone in primary human gingival fibroblastos10.1007/s00784-013-1178-x ↗
12. Color stability, conversion, water sorption and solubility of composite resins formulated with different photoinitiator systems10.1016/j.jdent.2012.11.020 ↗
13. Curing efficiency of dental composite resins formulated with camphorquinone or trimethylbenzoyl-diphenyl-phosphine oxide10.1016/j.dental.2011.11.014 ↗
14. Photo-polymerization efficiency of self-etch dental adhesives composed of camphorquinone or trimethylbenzoyl-diphenyl-phosphine oxide10.1016/j.ijadhadh.2013.04.002 ↗
15. Photopolymerization of phosphoric acid ester-based self-etch dental adhesives10.4012/dmj.2012-108 ↗
16. Relative photon absorption determination and the influence of photoinitiator system and water content on C=C conversion, water sorption/solubility of experimental self-etch adhesives10.1016/j.ijadhadh.2015.09.005 ↗
17. Molar extinction coefficients and the photon absorption efficiency of dental photoinitiators and light curing units10.1016/j.jdent.2004.11.013 ↗
18. Leprince JG.Photopolymerization of highly filled dimethacrylate-based composites using Type I or Type II photoinitiators and varying co-monomer ratios10.1016/j.dental.2015.11.032 ↗
19. The development of the CIE 2000 colour-difference formula: ciede200010.1002/col.1049 ↗
20. Study of the variation between CIELAB delta E* and CIEDE2000 color-differences of resin composites10.4012/dmj.26.21 ↗
21. Visual and instrumental shade matching using CIELAB and CIEDE2000 color difference formulas10.1016/j.dental.2015.10.015 ↗
22. The CIEDE2000 color-difference formula: implementation notes, supplementary test data, and mathematical observations10.1002/col.20070 ↗
23. Effect of monomer type on the CC degree of conversion, water sorption and solubility, and color stability of model dental composites10.1016/j.dental.2017.01.010 ↗
24. The effect of hydroxyapatite presence on the degree of conversion and polymerization rate in a model self-etching adhesive10.1016/j.dental.2011.10.003 ↗
25. Effect of initiator on photopolymerization of acidic, aqueous dental model adhesives10.1002/jbm.a.32185 ↗
26. 4-META use in dentistry: a literature review10.1067/mpr.2002.121584 ↗
27. The initiating radical yields and the efficiency of polymerization for various dental photoinitiators excited by different light curing units10.1016/j.dental.2005.06.006 ↗
28. BAPO as an alternative photoinitiator for the radical polymerization of dental resins10.1016/j.dental.2014.05.020 ↗
29. Hydrolytic stability of self-etching adhesive systems
30. A review of our development of dental adhesives — effects of radical polymerization initiators and adhesive monomers on adhesion10.4012/dmj.2009-057 ↗
31. Influence of photoinitiator system on physical-chemical properties of experimental self-adhesive composites10.1590/0103-6440201700841 ↗
32. Degree of conversion, depth of cure, and color stability of experimental dental composite formulated with camphorquinone and phenanthrenequinone photoinitiators10.1111/jerd.12131 ↗
33. Effect of photoinitiator combinations on hardness, depth of cure, and color of model resin composites10.1111/jerd.12146 ↗
34. Colour stability of composite resins after immersion in different drinks10.4012/dmj.25.371 ↗
35. Systematic review of the chemical composition of contemporary dental adhesives10.1016/j.biomaterials.2007.04.044 ↗
36. Adhesion/decalcification mechanisms of acid interactions with human hard tissues10.1002/jbm.1216 ↗
37. Relationship between bond-strength tests and clinical outcomes10.1016/j.dental.2009.11.148 ↗
38. Longevity of metal-ceramic crowns cemented with self-adhesive resin cement: a prospective clinical study
39. Shear bond strength of new self-adhesive flowable composite resins
40. Six-month clinical evaluation of a self-adhesive flowable composite in noncarious cervical lesions
41. Interference of functional monomers with polymerization efficiency of adhesives10.1111/eos.12245 ↗
42. Effects of functional monomers and photo-initiators on the degree of conversion of a dental adhesive10.1016/j.actbio.2012.01.013 ↗