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Objectives: The aim of this study was to evaluate the effect of M101 gel in bone and peri-implantitis healing and its safety of use.
Materials And Methods: M101 gel and solution (1 g/L) were evaluated in four different models: (i) human osteoblast culture; (ii) mouse calvarial defect; (iii) extraction model in dogs; (iv) peri-implantitis model in dogs. M101 cytocompatibility was evaluated in osteoblasts, and expression of ALP, Runx2, and BMP-2 was determined. Calvarial defect was induced in mice by bone drilling, and healing was evaluated after 5 weeks. In dogs, peri-implantitis was treated by non-surgical and surgical approaches with or without M101 gel application. Analyses were performed after 2 months. Socket healing was evaluated by micro-CT after tooth extraction. Local and systemic responses were evaluated after gel administration and intravenous injection.
Results: The cytocompatibility of M101 was confirmed in osteoblasts, and ALP, Runx2, and BMP-2 gene expression was increased after exposure (p < 0.05). In mice, calvarial bone defect healing was 1.6 folds more in the M101 gel treated group than in the untreated group (p < 0.001). In the extraction model, the local M101 gel application and systemic M101 administration did not induce an immunological response. In the peri-implantitis dog model, M101 gel as an adjuvant to non-surgical treatment led to improved PiPD reduction (p < 0.05) when compared to non-surgical treatment without M101 gel. No difference was observed when used as an adjunct to surgical treatment.
Conclusion: M101 may be a safe and interesting candidate as an adjuvant to improve bone healing and non-surgical treatment in peri-implantitis.
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http://dx.doi.org/10.1111/clr.70022 | DOI Listing |
Clin Oral Implants Res
August 2025
INSERM (French National Institute of Health and Medical Research), UMR 1260, Regenerative Nanomedicine, Fédération de Médecine Translationnelle de Strasbourg (FMTS), Strasbourg, France.
Objectives: The aim of this study was to evaluate the effect of M101 gel in bone and peri-implantitis healing and its safety of use.
Materials And Methods: M101 gel and solution (1 g/L) were evaluated in four different models: (i) human osteoblast culture; (ii) mouse calvarial defect; (iii) extraction model in dogs; (iv) peri-implantitis model in dogs. M101 cytocompatibility was evaluated in osteoblasts, and expression of ALP, Runx2, and BMP-2 was determined.
Int J Pharm
August 2021
INSERM (French National Institute of Health and Medical Research), UMR 1260, Regenerative Nanomedicine, Fédération de Médecine Translationnelle de Strasbourg (FMTS), Strasbourg, France; Université de Strasbourg, Faculté de Chirurgie-dentaire, 8 rue Sainte-Elisabeth, 67000 Strasbourg, France; PÃ
Periodontitis is an inflammatory disease associated with anaerobic bacteria leading to the destruction of tooth-supporting tissues. Porphyromonas gingivalis is a keystone anaerobic pathogen involved in the development of severe lesions. Periodontal treatment aims to suppress subgingival biofilms and to restore tissue homeostasis.
View Article and Find Full Text PDFBiosci Biotechnol Biochem
February 1997
Department of Applied Biological Chemistry, University of Tokyo, Japan.
The soluble and insoluble fractions obtained after sonication and centrifugation of Bifidobacterium adolescentis M101-4 cells were examined, and both of these fractions exhibited mitogenic activity in an assay of murine splenocytes and Peyer's patch cells in vitro. The soluble fraction was further treated by a 6-step procedure involving proteinase K-treatment, ultrafiltration with a 50-kDa cut-off molecular-sieving membrane, anion-exchange chromatography, dialysis, ultrafiltration through a 6-kDa cut-off membrane filter, and gel-filtration to yield a soluble high molecular weight fraction (SHF) which was effective for stimulating the proliferation of murine splenocytes. Almost three quarters of this fraction by weight was found to consist of carbohydrates containing glucose and galactose as major constituents, and the average molecular weight was estimated to be between 60,000 and 2,460,000, with the main peak at 1,550,000 Da, by the retention time of gel permeation chromatography.
View Article and Find Full Text PDFThe exopeptidase activities of five different strains of bifidobacteria occurring habitually in healthy human intestinal canal were measured on 61 synthetic substrates. The cluster analysis, based on the results, indicates that four strains, with the exception of Bifidobacterium adolescentis a M101-4, have similar exopeptidase profiles. All CFE from these five strains contained at least three kinds of aminopeptidases (aminopeptidase with broad substrate specificity, aminopeptidase hydrolyzing selectively X-Pro type and aminopeptidase hydrolyzing selectively Pro-X type) and carboxypeptidase.
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