Abstract

In this study, the bone regeneration efficacy of dehydrothermally (DHT) cross-linked collagen membrane with or without a bone graft (BG) material was evaluated in a critical-sized rat model. An 8-mm-diameter defect was created in the calvaria of 40 rats, which were randomized into four groups: (1) control; (2) DHT; (3) BG; and, (4) DHT + BG. Evaluations were made at 2 and 8 weeks after surgery using micro-computed tomographic (micro-CT), histological, and histomorphometric analyses. Micro-CT analysis showed an increase in the new bone volume (NBV) of the BG and DHT + BG groups at 2 weeks after surgery, representing a significant difference (p < 0.05). At 8 weeks after surgery, the NBV increased in all four groups. However, larger NBVs were observed in the BG and DHT + BG groups, and a significant difference was no longer observed between the two groups. Histologic analysis demonstrated that the graft materials sustained the center of the defect in the BG and DHT + BG groups, which was shown in histomorphometric analysis as well. These results suggest that DHT membrane is a safe biomaterial with adequate tissue integration, and has a positive effect on new bone formation. Moreover, the best effects were achieved when DHT was used in conjunction with BG materials.

Highlights

  • The presence of sufficient bone volume is a prerequisite for the predictable osseointegration of a dental implant

  • TV was significantly increased in both groups receiving bone graft (BG) when compared with that in the control group

  • Porcine skin-derived collagen membranes focused on onthese these aspects to develop barrier membranes

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Summary

Introduction

The presence of sufficient bone volume is a prerequisite for the predictable osseointegration of a dental implant. A bone graft (BG) is often required for the bone regeneration of osseous defects prior to, or simultaneously with implant placement. Guided bone regeneration (GBR) is a well-established and widely used technique that promotes new bone formation using a barrier membrane to exclude epithelial and connective tissue proliferation within the defect [3,4]. Various non-degradable and degradable membranes have been developed according to these requirements, and several non-degradable membranes, such as titanium mesh and expanded polytetrafluoroethylene, showed successful outcomes in clinical and animal studies [6,7,8,9] These membranes are currently considered gold-standard materials, they have a fatal disadvantage.

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