Biocompatibility of resin-based sealers

  • Hidefumi MAEDA
    Department of Endodontics, Kyushu University Hospital
  • Atsushi TOMOKIYO
    Department of Endodontology and Operative Dentistry, Faculty of Dental Science, Kyushu University
  • Katsuaki KOORI
    Department of Endodontology and Operative Dentistry, Faculty of Dental Science, Kyushu University
  • Shinsuke FUJII
    Department of Endodontics, Kyushu University Hospital
  • Satoshi MONNOUCHI
    Department of Endodontology and Operative Dentistry, Faculty of Dental Science, Kyushu University
  • Naohisa WADA
    Department of Endodontics, Kyushu University Hospital
  • Kiyomi KONO
    Department of Endodontology and Operative Dentistry, Faculty of Dental Science, Kyushu University
  • Naohide YAMAMOTO
    Department of Endodontology and Operative Dentistry, Faculty of Dental Science, Kyushu University
  • Yoko TERAMATSU
    Department of Endodontology and Operative Dentistry, Faculty of Dental Science, Kyushu University
  • Akifumi AKAMINE
    Department of Endodontics, Kyushu University Hospital Department of Endodontology and Operative Dentistry, Faculty of Dental Science, Kyushu University

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Other Title
  • レジンシーラーの細胞親和性について
  • —スーパーボンド根充シーラーとAH Plusとの比較—
  • —Comparison of Superbond sealer with AH Plus—

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Abstract

<p>Abstract : Endodontic sealers require biocompatibility and insolubility as well as close sealing. In this study, we examined the biocompatibility of the resin-based sealers, Superbond sealer (SB) and AH Plus sealer (AP). Each sealer was set in disc molds. The specimens after setting for 24 hours were prepared as a fresh group, and the discs washed for 7 days after setting were used as a washed group. Proliferation and differentiation assays were performed using human periodontal ligament cells (HPDLC) cultured on these discs. HPDLC cultured on washed SB discs showed proliferation, while the growth of cells on fresh SB, washed AP, or fresh AP was almost completely inhibited. SEM observation revealed tight attachment of HPDLC on the surface of washed SB, but no cells on washed AP. The gene expression of osteocalcin in HPDLC cultured on washed SB in osteogenic differentiation medium (DM) was upregulated. These results suggested that both SB and AP inhibited the cell growth initially after setting, but 7 days of washing of SB allowed HPDLC to proliferate on it, while AP still continued to elute cytotoxic components even after washing. Furthermore, washed SB would enable HPDLC on it to differentiate into cementoblast/osteoblast-like cells when cultured in DM.</p>

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