Light-Cured Self-Etch Adhesives Undergo Hydroxyapatite-Triggered Self-Cure

J Dent Res. 2016 Mar;95(3):334-41. doi: 10.1177/0022034515618959. Epub 2015 Dec 3.

Abstract

Light cure is a popular mode of curing for dental adhesives. However, it suffers from inadequate light delivery when the restoration site is less accessible, in which case a self-cure mechanism is desirable to salvage any compromised polymerization. We previously reported a novel self-cure system mediated by ethyl 4-(dimethylamino)-benzoate (4E) and hydroxyapatite (HAp). The present work aims to investigate if such self-cure phenomenon takes place in adhesives that underwent prior inadequate light cure and to elucidate if HAp released from the dental etching process is sufficient to trigger it. Model self-etch adhesives were formulated with various components, including bis[2-methacryloyloxy)ethyl]-phosphate (2MP) as acidic monomer and trimethylbenzoyl-diphenylphosphine oxide (TPO) as photoinitiator. In vitro evolution of degree of conversion (DC) of HAp-incorporated adhesives was monitored by infrared spectroscopy during light irradiation and dark storage. Selected adhesives were allowed to etch and extract HAp from enamel, light-cured in situ, and stored in the dark, after which Raman line mapping was used to obtain spatially resolved DC across the enamel-resin interface. Results showed that TPO+4E adhesives reached DC similar to TPO-only counterparts upon completion of light irradiation but underwent another round of initiation that boosted DC to ~100% regardless of HAp level or prior light exposure. When applied to enamel, TPO-only adhesives had ~80% DC in resin, which gradually descended to ~50% in enamel, whereas TPO+4E adhesives consistently scored ~80% DC across the enamel-resin interface. These observations suggest that polymerization of adhesives that underwent insufficient light cure is salvaged by the novel self-cure mechanism, and such salvaging effect can be triggered by HAp released from dental substrate during the etching process.

Keywords: (2,4,6-trimethylbenzoyl) diphenylphosphine oxide; Fourier transform infrared spectroscopy; Raman spectroscopy; chemical-curing of dental adhesives; ethyl 4-dimethylaminobenzoate; light-curing of dental adhesives.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Darkness
  • Dental Enamel / chemistry
  • Dental Etching / methods*
  • Durapatite / chemistry*
  • Elastic Modulus
  • Humans
  • Light
  • Light-Curing of Dental Adhesives / methods*
  • Materials Testing
  • Methacrylates / chemistry
  • Methacrylates / radiation effects
  • Organophosphates / chemistry
  • Organophosphates / radiation effects
  • Phosphines / chemistry
  • Phosphines / radiation effects
  • Photoinitiators, Dental / chemistry
  • Photoinitiators, Dental / radiation effects
  • Pliability
  • Polymerization
  • Resin Cements / chemistry*
  • Resin Cements / radiation effects
  • Self-Curing of Dental Resins / methods*
  • Spectrophotometry, Infrared
  • Spectrum Analysis, Raman
  • Young Adult
  • para-Aminobenzoates / chemistry
  • para-Aminobenzoates / radiation effects

Substances

  • (2,4,6-trimethylbenzoyl) diphenylphosphine oxide
  • 2-methacryloyloxyethyl dihydrogen phosphate
  • Methacrylates
  • Organophosphates
  • Phosphines
  • Photoinitiators, Dental
  • Resin Cements
  • para-Aminobenzoates
  • ethyl 4-dimethylaminobenzoate
  • Durapatite