Etching Efficacy of Self-Etching Functional Monomers

J Dent Res. 2018 Aug;97(9):1010-1016. doi: 10.1177/0022034518763606. Epub 2018 Mar 19.

Abstract

Besides chemically interacting with hard tooth tissue, acidic functional monomers of self-etch adhesives should etch the prepared tooth surface to dissolve the smear layer and to provide surface micro-retention. Although the etching efficacy of functional monomers is commonly determined in terms of pH, the pH of adhesives cannot accurately be measured. Better is to measure the hydroxyapatite (HAp)-dissolving capacity, also considering that functional monomers may form monomer-Ca salts. Here, the etching efficacy of 6 functional monomers (GPDM, phenyl-P, MTEGP, 4-META, 6-MHP and 10-MDP) was investigated. Solutions containing 15 wt% monomer, 45 wt% ethanol, and 40 wt% water were prepared. Initially, we observed enamel surfaces exposed to monomer solution by scanning electron microscopy (SEM). X-ray diffraction (XRD) was employed to detect monomer-Ca salt formation. Phenyl-P exhibited a strong etching effect, while 10-MDP-treated enamel showed substance deposition, which was identified by XRD as 10-MDP-Ca salt. To confirm these SEM/XRD findings, we determined the etching efficacy of functional monomers by measuring both the concentration of Ca released from HAp using inductively coupled plasma-atomic emission spectroscopy (ICP-AES) and the amount of monomer-Ca salt formation using 31P magic-angle spinning (MAS) nuclear magnetic resonance (NMR). ICP-AES revealed that the highest Ca concentration was produced by phenyl-P and the lowest Ca concentration, almost equally, by 4-META and 10-MDP. Only 10-MDP formed 10-MDP-Ca salts, indicating that 10-MDP released more Ca from HAp than was measured by ICP-AES. Part of the released Ca was consumed to form 10-MDP-Ca salts. It is concluded that the repeatedly reported higher bonding effectiveness of 10-MDP-based adhesives must not only be attributed to the more intense chemical bonding of 10-MDP but also to its higher etching potential, a combination the other functional monomers investigated lack.

Keywords: X-ray crystallography; adhesives; enamel; hydroxyapatite; microscopy; nuclear magnetic resonance.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Dental Cements / chemistry*
  • Dental Etching / methods*
  • Glycerolphosphate Dehydrogenase / chemistry
  • Hydrogen-Ion Concentration
  • Magnetic Resonance Spectroscopy
  • Materials Testing
  • Methacrylates / chemistry*
  • Microscopy, Electron, Scanning
  • Organophosphorus Compounds / chemistry
  • Phosphonoacetic Acid / analogs & derivatives*
  • Phosphonoacetic Acid / chemistry
  • Spectrophotometry, Atomic
  • Surface Properties
  • X-Ray Diffraction

Substances

  • 6-methacryloyloxyhexyl phosphonoacetate
  • Dental Cements
  • Methacrylates
  • Organophosphorus Compounds
  • Phenyl-P adhesion promoting monomer
  • 4-methacryloxyethyltrimellitic acid anhydride
  • methacryloyloxydecyl dihydrogen phosphate
  • Glycerolphosphate Dehydrogenase
  • Phosphonoacetic Acid