| Literature DB >> 35884986 |
Andrea Baldi1, Massimo Carossa1, Allegra Comba1, Mario Alovisi1, Felice Femiano2, Damiano Pasqualini1, Elio Berutti1, Nicola Scotti1.
Abstract
The present study aimed to evaluate the wear rate of polymer-infiltrated network composites and ceramics against enamel in a bruxism-simulated scenario. Ninety-six (n = 96) molars were divided into six groups (n = 16) according to their occlusal material: group 1-a polymer-infiltrated network ceramic (PINC); group 2-a second polymer-infiltrated network ceramic (PINC2); group 3-nanohybrid resin-based composite (CO); group 4-cubic zirconia (ZR); group 5-lithium disilicate (LS); and group 6-sound enamel (EN). A laser scanner was used to digitalize all of the occlusal surfaces before and after a fatigue test, which was conducted with a chewing simulator set at 80 N and semicircular movement in order to simulate bruxist movement and loads. Statistical analysis of volume loss was performed with a one-way ANOVA and post hoc Bonferroni test. ZR had significantly inferior wear to PINC (p ≤ 0.01) and CO (p = 0.04). LS wore the antagonist enamel significantly more than PINC, CO, PINC2 and EN (p ≤ 0.01). On the other hand, ZR wore the antagonist enamel significantly more than CO (p ≤ 0.01) and PINC2 (p = 0.05). In conclusion, PINCs better preserved antagonist enamel at the expense of a higher wear of their own. LS causes significantly higher enamel wear compared with PINCs. ZR caused significantly higher enamel wear compared with CO and PINC2, but it was wear-resistant.Entities:
Keywords: bruxism; polymer-infiltrated network ceramics; wear; zirconia
Year: 2022 PMID: 35884986 PMCID: PMC9313215 DOI: 10.3390/biomedicines10071682
Source DB: PubMed Journal: Biomedicines ISSN: 2227-9059
Figure 1An example of a prepared lower molar specimen. Standardized occlusal reduction of 1.5 mm was performed following occlusal anatomy; buccal and oral finish lines with a 2 mm-long bevel were created all around the tooth.
General description of the main materials used in the present study, along with their commercial name, manufacturer and composition.
| General Description | Commercial Name | Manufacturer | Composition |
|---|---|---|---|
| Polymer-infiltrated network ceramic (PINC) | Grandio Blocks | VOCO | 86 wt% nanohybrid filler in a polymeric matrix UDMA + DMA |
| Polymer-infiltrated network ceramic (PINC2) | Cerasmart | GC | 71 wt% silica and barium glass nanoparticles, Bis-MEPP, UDMA, DMA |
| Direct nano-hybrid resin-based composite (CO) | Venus Pearl | Kultzer | 59 wt% TCD-DI-HEA, 58% UDMA, 2% barium, 1% fluoride aluminium |
| Cubic ZrO2 (ZR) | Katana STML Zirconia | Kurakay | 88 wt% zinc oxide, 9% yttrium oxide, 3% hafnium dioxide, 0.5% aluminium oxide |
| CAD/CAM lithium disilicate (LS) | E-max CAD | Ivoclar | Silicon dioxide, lithium oxide, potassium oxide, phosphorus pentoxide, zinc oxide |
Figure 2CAD design of tabletop restorations, controlling standardized anatomy and thickness.
Detailed adhesive procedures performed on the substrate and the various tested materials.
| Substrate | Adhesive Procedure Performed |
|---|---|
| Tooth | Enamel etching for 30 s, dentin etching for 15 s with 37.5% phosphoric acid (K-etchant, Kuraray Noritake, Tokyo, Japan), 30 s rinsing, 30 s air-drying, primer application (Optibond FL Primer, Ker, Orange, CA, USA) over the surfaces with a light scrubbing motion 15 s, then gentle air drying and bonding application (Optibond FL Bond, Kerr, Orange, CA, USA) |
| PINC | Sandblasting with aluminium oxide (50 μm) at 1.5–2 bar, cleaning with an ultrasonic bath, heated silane 60 s (Ceramic Primer PLUS, Kuraray Noritake, Tokyo, Japan), drying 10 s with air and applying bonding (Optibond FL Bond, Kerr, Orange, CA, USA). A flowable RBC was then applied (Clearfil Majesty ES, Kuraray Noritake, Tokyo, Japan) and light-cured for 2 min at 1000 mW/cm2 (Cefalux 2, Voco, Cuxhaven, Germany) |
| PINC2 | Hydrofluoric acid at 5% (IPS Ceramic etching gel, Ivoclar, Shaan, Lichtenstein) 60 s, rinsing 60 s, cleaning with an ultrasonic bath, drying, applying silane, bonding and flowable RBC as described for PINC |
| CO | Same procedure as that performed for PINC |
| ZR | Sandblasting with aluminium oxide (25 µm) at 1.5–2 bar, cleaning with ultrasonic bath, primer application (Ceramic Primer PLUS, Kuraray Noritake, Tokyo, Japan), drying 20 s. Bonding and flowable RBC as described for PINC |
| LS | Hydrofluoric acid at 5% (IPS Ceramic etching gel, Ivoclar, Shaan, Lichtenstein) 30 s, followed by the same procedure as that performed for PINC2 |
Mean ± standard deviation, expressed in mm3, for both tested materials and their antagonists.
| Tested Material Wear (Lower Molar Wear) | Antagonist Wear | |
|---|---|---|
| Polymer-infiltrated network ceramic (PINC) | 0.0259 ± 0.008 | 0.0171 ± 0.005 |
| Second polymer-infiltrated network ceramic (PINC2) | 0.0154 ± 0.008 | 0.0128 ± 0.007 |
| Nano-hybrid resin-based composite (CO) | 0.0216 ± 0.006 | 0.009 ± 0.004 |
| Cubic zirconia (ZR) | 0.0098 ± 0.004 | 0.0314 ± 0.008 |
| Lithium disilicate (LS) | 0.0204 ± 0.007 | 0.0439 ± 0.009 |
| Enamel (EN) | 0.0205 ± 0.006 | 0.0211 ± 0.007 |
Figure 3SEM analysis showed different surface characteristics of the tested materials: PINC (on the left) showed uniform wear with a low visual roughness, even if an initial enucleation of some filler particles and some signs of subsuperfical cracks could be observed. LS (in the centre) showed mineral particles on the surface, which could enhance the roughness and, therefore, the abrasive effect towards the antagonist enamel. The cubic zirconia (on the right) showed a superficial delamination, which made this material less rough and, consequently, less aggressive towards the enamel.