Anti-proteolytic capacity and bonding durability of proanthocyanidin-biomodified demineralized dentin matrix.
- Author:
Rui-Rui LIU
1
;
Ming FANG
2
;
Ling ZHANG
2
;
Cheng-Fang TANG
2
;
Qi DOU
2
;
Ji-Hua CHEN
2
Author Information
- Publication Type:Journal Article
- MeSH: Chlorhexidine; chemistry; pharmacology; Collagenases; pharmacology; Dental Bonding; Dental Cements; chemistry; Dental Stress Analysis; instrumentation; Dentin; drug effects; ultrastructure; Dentin-Bonding Agents; chemistry; Gelatinases; pharmacology; Humans; Hydroxyproline; analysis; Matrix Metalloproteinase 8; pharmacology; Matrix Metalloproteinase Inhibitors; chemistry; pharmacology; Proanthocyanidins; chemistry; pharmacology; Stress, Mechanical; Surface Properties; Tensile Strength; Tooth Demineralization; pathology; physiopathology
- From: International Journal of Oral Science 2014;6(3):168-174
- CountryChina
- Language:English
- Abstract: Our previous studies showed that biomodification of demineralized dentin collagen with proanthocyanidin (PA) for a clinically practical duration improves the mechanical properties of the dentin matrix and the immediate resin-dentin bond strength. The present study sought to evaluate the ability of PA biomodification to reduce collagenase-induced biodegradation of demineralized dentin matrix and dentin/adhesive interfaces in a clinically relevant manner. The effects of collagenolytic and gelatinolytic activity on PA-biomodified demineralized dentin matrix were analysed by hydroxyproline assay and gelatin zymography. Then, resin-/dentin-bonded specimens were prepared and challenged with bacterial collagenases. Dentin treated with 2% chlorhexidine and untreated dentin were used as a positive and negative control, respectively. Collagen biodegradation, the microtensile bond strengths of bonded specimens and the micromorphologies of the fractured interfaces were assessed. The results revealed that both collagenolytic and gelatinolytic activity on demineralized dentin were notably inhibited in the PA-biomodified groups, irrespective of PA concentration and biomodification duration. When challenged with exogenous collagenases, PA-biomodified bonded specimens exhibited significantly less biodegradation and maintained higher bond strengths than the untreated control. These results suggest that PA biomodification was effective at inhibiting proteolytic activity on demineralized dentin matrix and at stabilizing the adhesive/dentin interface against enzymatic degradation, is a new concept that has the potential to improve bonding durability.
