Effect of UVA-activated Riboflavin on Dentin Bonding

Author:

Cova A.1,Breschi L.23,Nato F.14,Ruggeri A.1,Carrilho M.5,Tjäderhane L.6,Prati C.7,Di Lenarda R.2,Tay F.R.8,Pashley D.H.9,Mazzoni A.110

Affiliation:

1. Department of SAU&FAL, University of Bologna, Via Irnerio, 48, 40100 Bologna, Italy

2. Department of Medical Sciences, Unit of Dental Sciences and Biomaterials, University of Trieste, Trieste, Italy

3. IGM, Unit of Bologna, C.N.R.-IOR, Bologna, Italy

4. Department of STeVA, University “Carlo Bo”, Urbino, Italy

5. Biomaterials Research Group, Bandeirante University of São Paulo – UNIBAN, Brazil

6. Institute of Dentistry, University of Oulu, Oulu University Hospital, Oulu, Finland

7. Department of Dental Sciences, University of Bologna, Bologna, Italy

8. Department of Endodontics, College of Dental Medicine, Georgia Health Sciences University, Augusta, GA, USA

9. Department of Oral Biology, College of Dental Medicine, Georgia Health Sciences University, Augusta, GA, USA

10. Laboratory of Cell Biology & Laboratory of Immunorheumatology and Tissue Regeneration–Ramses Laboratory, c/o Rizzoli Orthopedic Institute, Bologna, Italy

Abstract

Recent studies have reported collagen cross-linking after exposure to riboflavin followed by ultraviolet-A (UVA) exposure. This study is the first to investigate the effect of a riboflavin-containing primer on adhesive interface stability and dentinal matrix metalloproteinase activity. Human dentin was etched with 35% phosphoric acid, treated with 0.1% riboflavin, exposed to UVA for 2 min, and bonded with a two-step etch-and-rinse adhesive. Adhesive was applied to control specimens without riboflavin/UVA. Specimens were subjected to microtensile bond strength tests and pulled to failure after storage for 24 hrs, 6 mos, or 1 yr. Interfacial nanoleakage was evaluated by light and transmission electron microscopy. To investigate dentinal matrix metalloproteinase activity, we performed correlative zymographic assays on protein extracts obtained from phosphoric-acid-etched dentin powder with or without riboflavin/UVA treatment and XP Bond. Ultraviolet-activated riboflavin treatment increased the immediate bond strength to dentin at all aging intervals (p < 0.05 vs. control) and decreased interfacial nanoleakage in aged specimens (1 yr; p < 0.05). Zymograms revealed that riboflavin/UVA pre-treatment inhibited dentinal matrix metalloproteinase activity (especially MMP-9). In conclusion, dentinal collagen cross-linking induced by riboflavin/UVA increased immediate bond strength, stabilized the adhesive interface, and inhibited dentin matrix metalloproteinases, thereby increasing the durability of resin-dentin bonds.

Publisher

SAGE Publications

Subject

General Dentistry

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