Title Vascularisation of composite bone scaffolds in rodents with "microfil" perfusion. systematic review /
Translation of Title Vascularisation of Composite Bone Scaffolds in Rodents with "Microfil" Perfusion. Systematic Review.
Authors Tesing, Melanie
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Pages 43
Keywords [eng] Composite scaffolds, Vascularisation, Microfil, Micro-CT, Growth factors, Bone tissue engineering
Abstract [eng] Introduction: Extensive research in oral and maxillofacial surgery aims to find an ideal alternative to autogenous bone for critical-size bony reconstructions. However, no such material has been found. Despite ongoing challenges, three-dimensional (3D) composite scaffolds show promise in improving vascularisation and bone regeneration by closely mimicking natural bone. A new investigation technique combining “Microfil” perfusion and micro-computed tomography (CT) allows efficient analysis of neovascularisation, bone regeneration, scaffold integration, and quantitative comparison between studies. Purpose: This systematic review aims to investigate the effect of 3D composite scaffolds on new bone formation and vascularisation in critical-sized calvarial defects in rodents using “Microfil” perfusion and micro-CT. Method: A comprehensive electronic search was conducted according to the PRISMA guidelines in PubMed and Medline from January 2013 to October 2023 limited to English language publications with available full texts. In vivo studies about “vascularisation bone scaffolds” using scaffolds made from a combination of inorganic and organic synthetic materials and analysing the neovascularisation and bone regeneration with “Microfil” and micro-CT techniques were investigated. Results: The full text of 48 studies was assessed for eligibility, with 8 studies meeting the inclusion criteria. Among these, scaffolds with larger pore sizes (&#8805;400 &#956;m) exhibited a trend towards improved vascularisation and bone regeneration outcomes (p<0.05 for bone volume fraction (BV/TV), p=0.053 for vascularised area (VA)). Additionally, composite scaffolds showed significantly higher new bone area (NBA) than non-composite scaffolds (p<0.05). Moreover, modified scaffolds incorporating angiogenic and/or osteogenic factors excelled pure scaffolds in vascularisation and bone regeneration (p<0.01 for NBA, p<0.05 for VA and BV/TV, p=0.051 for vessel number (VN)). Combining two modifying factors generated even better results (p<0.01 for VN and NBA, p<0.05 for BV/TV, p=0.071 for VA). Nevertheless, three included studies showed a high risk of bias in at least one category, and all included studies presented missing information in half of the assessed items. Conclusion: Enhancing vascularisation and bone regeneration in critical-sized calvarial defects using 3D composite scaffolds may benefit from modifications with angiogenic and/or osteogenic factors, especially when delivered together and with larger pore sizes. A properly designed scaffold structure could potentially erase the need for adding angiogenic and/or osteogenic factors. Future studies with larger sample sizes and similar study designs should investigate the optimal morphology as well as osseo- and angioinductive properties of these scaffolds.
Dissertation Institution Vilniaus universitetas.
Type Master thesis
Language English
Publication date 2024