methylcellulose and Mandibular-Diseases

methylcellulose has been researched along with Mandibular-Diseases* in 2 studies

Other Studies

2 other study(ies) available for methylcellulose and Mandibular-Diseases

ArticleYear
Injectable simvastatin in periodontal defects and alveolar ridges: pilot studies.
    Journal of periodontology, 2008, Volume: 79, Issue:8

    Topical injection of simvastatin in methylcellulose gel was shown to stimulate bone growth and inflammation over mouse calvaria and in rat mandible models. The purpose of these pilot studies was to evaluate the potential of locally injected simvastatin in human-sized periodontal defects.. Chronic periodontal defects were created bilaterally in seven 1-year-old beagle dogs: 3-walled intrabony defects distal of the mandibular second premolar and mesial of the fourth premolar and Class II furcation defects at the buccal furcation of the mandibular first molars. The edentulous space distal to the mandibular canine was left undisturbed. After 16 weeks of healing, defect sites were treated with scaling and root planing, and mandible sides were randomly selected to receive three weekly injections of 0.5 mg simvastatin in 30 microl methylcellulose gel and contralateral gel alone (n=3) or 2.0 mg simvastatin/methylcellulose gel and contralateral gel alone (n=4). Two months following drug application, block sections, including teeth and surrounding tissues, and submandibular lymph nodes were obtained for histomorphometric analysis.. Two trends were noted in this pilot study: buccal edentulous ridge thickness was 29% greater with simvastatin, 0.5 mg, compared to gel alone (P=0.0845), and the simvastatin groups had bone-height loss in interproximal intrabony and furcation defects, but the length of new cementum in the interproximal intrabony defects was greater with simvastatin, 0.5 mg (0.35+/-0.14 mm), compared to gel alone (0.06+/-0.15 mm; P=0.069). No new cementum was found in furcations.. Multiple injections of simvastatin are not appropriate for the treatment of intrabony or furcation defects. However, this approach shows potential to augment bone thickness in closed alveolar environments.

    Topics: Alveolar Bone Loss; Alveolar Process; Animals; Bicuspid; Bone Regeneration; Dental Cementum; Dogs; Drug Carriers; Female; Furcation Defects; Gels; Hydroxymethylglutaryl-CoA Reductase Inhibitors; Injections; Jaw, Edentulous, Partially; Male; Mandibular Diseases; Methylcellulose; Molar; Osteogenesis; Pilot Projects; Random Allocation; Simvastatin; Time Factors

2008
The effect of calcitonin on osseous healing in guinea pig mandible.
    Journal of endodontics, 2001, Volume: 27, Issue:3

    Calcitonin (CT) is reported to be an effective medication for the treatment of inflammatory root resorption and to be capable of stimulating osteoblast proliferation in cell culture studies. In this study the effect of CT on the healing of osseous defects was evaluated in the mandibles of guinea pigs. After raising tissue flaps two experimental cavities were created on both sides of the corpus mandible of 33 guinea pigs. CT was applied into cavities either in hydroxypropyl methycellulose (HPMC) gel or gelatin as carrier. HPMC and gelatin alone and an empty cavity were also examined as control groups. Histopathological examinations under light microscopy were performed on weeks 1, 3, and 6. At week 1 in CT+gelatin and CT+HPMC groups, prominent osteoblastic activity was observed when compared with control groups. At week 3 the presence of woven bone in the experimental cavity areas reflected the increased osteoblastic activity in all groups. At the end of week 6 woven bone was gradually replaced by osteogenic tissue undergoing remodelization with Haversian systems in all groups. It is suggested that the osseous healing of the experimental cavity was enhanced by CT application in early stages (i.e. at week 1). However there was no significant difference of osteogenic activity between the control and CT-treated groups at the end of weeks 3 and 6.

    Topics: Animals; Bone Remodeling; Calcitonin; Coloring Agents; Drug Carriers; Fluorescent Dyes; Follow-Up Studies; Gelatin; Gels; Granulation Tissue; Guinea Pigs; Haversian System; Hypromellose Derivatives; Mandible; Mandibular Diseases; Methylcellulose; Osteoblasts; Osteogenesis; Periosteum; Wound Healing

2001