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Application of amino acid derivative monomer on dentin adhesion and

Research Project

Project/Area Number 14571813
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Conservative dentistry
Research InstitutionOKAYAMA UNIVERSITY

Principal Investigator

TORII Yasuhiro  Okayama Univ., Graduate Sch. of Med. and Dent., Associate Professor, 大学院・医歯学総合研究科, 助教授 (10188831)

Co-Investigator(Kenkyū-buntansha) ITOTA Toshiyuki  Okayama Univ., Med. and Dent. Hospital, Assistant Professor, 医学部・歯学部附属病院, 講師 (60294419)
YOSHIYAMA Masahiro  Okayama Univ., Graduate School of Med. and Dent., Professor, 大学院・医歯学総合研究科, 教授 (10201071)
SUZUKI Kazuomi  Okayama Univ., Graduate School of Med. and Dent., Professor, 大学院・医歯学総合研究科, 教授 (30050058)
伊東 孝介  岡山大学, 大学院・医歯学総合研究科, 助手 (50294418)
Project Period (FY) 2002 – 2003
Project Status Completed (Fiscal Year 2003)
Budget Amount *help
¥3,500,000 (Direct Cost: ¥3,500,000)
Fiscal Year 2003: ¥1,700,000 (Direct Cost: ¥1,700,000)
Fiscal Year 2002: ¥1,800,000 (Direct Cost: ¥1,800,000)
KeywordsDentin / Adhesion / Composite resin / Amino acid derivative / Molecular structure
Research Abstract

In this study, several kinds of amino-acid monomers with different molecular structure were newly synthesized and their effect on the adhesion between resin and tooth was investigated to clarify the relation between the bonding effectiveness and molecular structure of adhesive monomer.
Firstly, N-acryloyl aspartic acid (N-AAsp) was synthesized by the reaction between acrylic chloride and DL-aspartic acid. N-AAsp can be dissolved in distilled water up to 25wt%. The maximum bond strength to enamel and dentin, 16 MPa, was obtained when 20wt% N-AAsp aqueous solution was used as a self-etching primer.
Secondly, the bonding efficacy of N-acryloy Glycine (N-AGly) having one carboxyl group to dentin was estimated, comparing with that of N-AAsp having two carboxyl groups. As a result, N-AAsp was more effective on dentin bonding.
In addition, N-acryloyl Glutamic acid (N-AGlu) was synthesized. N-AGlu has two carboxyl groups and same structure of the principal chain as N-AAsp, but the structure of side chain is different. The pKa values of the carboxyl group in the side chain of N-AGlu and N-AAsp were 4.53 and 4.19, respectively. The N-AGlu exhibited no bonding efficacy on the ground dentin surface, whereas N-AAsp present good efficacy. On the other hand, N-AGlu showed bonding effect equal with the N-AAsp when it was applied on the dentin after the smear layer was removed.
Our results indicate that the amino-acid monomers having two carboxyl groups have good potential value as a self-etching primer for bonding to tooth. The results also suggest that the pKa value of carboxyl group in monomer molecules is important factor in the appearance of dentine adhesive property.

Report

(3 results)
  • 2003 Annual Research Report   Final Research Report Summary
  • 2002 Annual Research Report
  • Research Products

    (2 results)

All Other

All Publications (2 results)

  • [Publications] Torii, Y., Itou, K., Nishitani, Y., Yoshiyama, M., Ishikawa, K., Suzuki, K.: "Effect of self-etching primers containing N-acryloyl aspartic acid on enamel adhesion."Dental Materials. 19. 253-258 (2003)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Torii, Y., Itou, K., Nishitani, Y., Yoshiyama, M., Ishikawa, K., Suzuki, K.: "Effect of self-etching primers containing N-acryloyl aspartic acid on enamel adhesion."Dental Materials. 19(4). 253-258 (2003)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2003 Final Research Report Summary

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Published: 2002-04-01   Modified: 2016-04-21  

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