J Korean Acad Periodontol.  2003 Sep;33(3):533-542. 10.5051/jkape.2003.33.3.533.

Histologic evaluation of Regenafil(TM) on defects of extraction socket

Affiliations
  • 1Department of Periodontics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Korea.

Abstract

The purpose of this study is to evaluate histologic result of bone substituting material on defects followed tooth extraction. We compare the histologic findings control, DFDBA, Bio-Oss(R), and Regenafil(TM), Briefly, mandibular premolar teeth were extracted available for bone filling. All alveolar sites were checked after extraction and thoroughly debrided with a dental curet to remove the periodontal ligament. Extraction sites were prepared dehiscence on buccal side 7mm height from alveolar crest. The graft materials were filled into the extraction socket and dehiscenc defects. The animals were sacrificed 12 weeks after implantation. Both treated and control mandibular sites were histologically evaluated with light microscopy. Histologic observation at 12 weeks revealed that control and experimental sites were healed uneventfully and directly apposed to new bone without any adverse tissue reaction. DFDBA and Bio-Oss(R) sites maintain width of alveolar crest but were not fully resorbed. Regenafil(TM) sites also maintain width and particles were resorbed more than other graft materials. From this results, it was suggested that Regenafil(TM) is promising boen substituting materials maintaining the width of alveolar crest and height follewed tooth extraction.

Keyword

descience defects; Regenafil(TM); DFDBA; Bio-Oss(R)

MeSH Terms

Animals
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