Background: collagenous and noncollagenous membranes have been investigated in many animal systems but their effects in the macaque model are unknown.
Objective: to determine subcutaneous cellular reactions and degradation characteristics following implantation of collagenous and noncollagenous membranes in a macaque model.
Methods: six adult male Macaca fascicularis, aged above 7 years, were used. Six commercially available collagenous (Bio-Gide [BG], Tissue Fleece [TFL] TissueFoil E forte [TFO], Lycoll [LC], Surgicoll [SG] and Tutodent [TU]) and two noncollagenous (Tabotamp [TA] and Gelita-Tampon [GT]) membranes (size 2 × 2 cm each) were implanted in unconnected subcutaneous pouches in the monkey's back and wounds were allowed to heal by primary intention. The total sample size for each membrane was six. Two monkeys were sacrificed for each experimental period of 4, 14 and 28 days. Explanted specimens were prepared for histologic and histomorphometric analysis. Digitized images of implant sites were systematically sampled using an Image Analyzer with a grid containing 35 intersection points. Four parameters were quantified: membrane degradation, foreign body reaction, tissue organization and vascularization.
Results: biodegradation rate and vascularization scored higher in collagenous than in noncollagenous membranes. Except for TFL and TU, the remaining six membranes showed a moderately intense foreign body reaction at week 2. Tissue organization was initiated early in four out of six collagenous (TFL>LC>SG>TFO>BG>TU) compared with one of two noncollagenous (TA>GT) membranes.
Conclusions: the results suggest that differences in membrane structure and composition underlie their different cellular reactions and degradation characteristics.
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http://dx.doi.org/10.1111/j.1600-0501.2010.01970.x | DOI Listing |
Tissue Eng Part A
January 2025
Department of Biomedical Engineering, Washington University in St. Louis, St. Louis, Missouri, USA.
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View Article and Find Full Text PDFBiomater Sci
January 2025
Hospital of Stomatology, Sun Yat-sen University, Guangzhou, China.
: To explore the relationship between the stability of poly(gamma-glutamic acid) (γ-PGA) dispersion systems with γ-PGA of different molecular weights (MWs) and concentrations and type I collagen mineralization. : γ-PGA was used as a noncollagenous protein (NCP) analogue to regulate the stability of supersaturated γ-PGA-stabilized amorphous calcium phosphate (PGA-ACP) solutions by changing the γ-PGA MW (2, 10, 100, 200 and 500 kDa) and concentration (400, 500 and 600 μg mL). Then, the optical density (OD) at 72 h was measured to determine the PGA-ACP solution stability.
View Article and Find Full Text PDFBone Res
January 2025
Department of Biochemistry and Structural Biology, University of Texas Health Science Center, San Antonio, TX, USA.
Int J Mol Sci
November 2024
Department of Preclinical Discipline, Faculty of Medicine and Pharmacy, University of Oradea, 10, 1 December Square, 410073 Oradea, Romania.
Bone regeneration is a highly dynamic and complex process that involves hematopoietic stem cells and mesenchymal cells, collagen fibers, non-collagenous proteins and biomolecules from extracellular matrices, and different cytokines and immune cells, as well as growth factors and hormones. Some phytochemicals due to antioxidant and anti-inflammatory effects can modulate the bone signaling pathways and improve bone healing and thus can be a good candidate for osteoregeneration. The aim of this study was to analyze the impact of L.
View Article and Find Full Text PDFOdontology
December 2024
Department of Medical Genetics, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey.
Osteogenesis imperfecta, a common genetic connective tissue disorder affecting bone with multisystemic implications, is caused by genomic alterations at various levels that disrupt the biosynthesis stages of collagen Type I. This study evaluated the intraoral and clinical findings of 43 OI cases in relation to genetic variants, aiming to contribute new insights into the roles of collagen and non-collagen genes in the oral-dental pathology of OI. Significant associations were found between OI variants and dental anomalies such as dentinogenesis imperfecta, enamel hypoplasia, taurodontism, and hypodontia.
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