Papers

Nov, 2012

HEMA Inhibits Interfacial Nano-layering of the Functional Monomer MDP

JOURNAL OF DENTAL RESEARCH
  • Y. Yoshida
  • ,
  • K. Yoshihara
  • ,
  • S. Hayakawa
  • ,
  • N. Nagaoka
  • ,
  • T. Okihara
  • ,
  • T. Matsumoto
  • ,
  • S. Minagi
  • ,
  • A. Osaka
  • ,
  • K. Van Landuyt
  • ,
  • B. Van Meerbeek

Volume
91
Number
11
First page
1060
Last page
1065
Language
English
Publishing type
Research paper (scientific journal)
DOI
10.1177/0022034512460396
Publisher
SAGE PUBLICATIONS INC

Previous research showed that the functional monomer 10-methacryloxydecyl dihydrogen phosphate (MDP) ionically bonds to hydroxyapatite (HAp) and forms a nano-layered structure at the interface with HAp-based substrates. Such hydrophobic nano-layering is considered to contribute to the long-term durability of the bond to tooth tissue. However, dental adhesives are complex mixtures usually containing different monomers. This study investigated the effect of the monomer 2-hydroxyethylmethacrylate (HEMA) on the chemical interaction of MDP with HAp by x-ray diffraction (XRD), nuclear magnetic resonance (NMR), and quartz crystal microbalance (QCM). We examined the chemical interaction of 5 experimental MDP solutions with increasing concentrations of HEMA. XRD revealed that addition of HEMA inhibits nano-layering at the interface, while NMR confirmed that MDP remained adsorbed onto the HAp surface. QCM confirmed this adsorption of MDP to HAp, as well as revealed that the demineralization rate of HAp by MDP was reduced by HEMA. It was concluded that even though the adsorption of MDP to HAp was not hindered, addition of HEMA inhibited interfacial nano-layering. Potential consequences with regard to bond durability necessitate further research.

Link information
DOI
https://doi.org/10.1177/0022034512460396
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000309932100011&DestApp=WOS_CPL
ID information
  • DOI : 10.1177/0022034512460396
  • ISSN : 0022-0345
  • Web of Science ID : WOS:000309932100011

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