Related Experiment Video
Updated: Jul 20, 2026

2-Methacryloyloxyethyl Phosphorylcholine Polymer Treatment of Complete Dentures to Inhibit Denture Plaque Deposition
Published on: December 26, 2016
Microperoxidase primer promotes adhesion of butylborane-polymerized resin to dentin
Yohsuke Taira1, Kohyoh Soeno, Mitsuru Atsuta
1Division of Fixed Prosthodontics and Oral Rehabilitation, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan. yohsuke@net.nagasaki-u.ac.jp
Abstract:
The purpose of this study was to investigate the effect of dentin primers containing microperoxidase (MP-11) with 2-hydroxyethyl methacrylate (HEMA) on the bond strength between a tri-n-butylborane-initiated self-polymerizing resin and dentin. Bovine dentin surfaces were etched with 10 wt % phosphoric acid, primed, and then bonded with stainless steel rods. Tensile bond strength after 24 h of storage in water was significantly influenced by both MP-11 and HEMA. Groups with no MP-11 showed the lowest values. Without HEMA, the bond strengths of groups using 0.01, 0.1, and 1.0 micromol/g MP-11 were statistically identical, and also greater than that of the no MP-11 control. In the presence of HEMA, the bond strength was significantly enhanced with an increasing concentration of MP-11. The highest bond strength of 29.0 MPa was obtained with aqueous HEMA primer, containing 1.0 micromol/g MP-11. Microscopic observation showed the formation of a hybrid layer at the bonded interface. Polymerization of the resin was significantly accelerated with the MP-11 primer. In conclusion, MP-11 has a potential for adhesive bonding promoter between the resin and the demineralized dentin surface.
Related Concept Videos
Hydroboration-Oxidation of Alkenes
Electrophilic 1,2- and 1,4-Addition of HX to 1,3-Butadiene
Cationic Chain-Growth Polymerization: Mechanism
Electrophilic 1,2- and 1,4-Addition of X2 to 1,3-Butadiene
Olefin Metathesis Polymerization: Acyclic Diene Metathesis (ADMET)
Similar to cross-metathesis, ADMET also involves the formation of metallacyclobutane intermediate by [2+2] cycloaddition of one of the double bonds of a terminal diene with...
Preparation of Alcohols via Addition Reactions
The acid-catalyzed addition of water to the double bond of alkenes is a large-scale industrial method used to synthesize low-molecular-weight alcohols. An acidic atmosphere is required to allow the hydrogen in the water molecule to act as an electrophile and attack the double bond in an alkene. The addition of a proton to the double bond creates a carbocation intermediate. The proton preferentially bonds to the less substituted end of the double bond to create a more stable carbocation...