Underestimated microbial infection of resorbable membranes on guided regeneration

再生(生物学) 体内 生物膜 抗菌剂 化学 生物 细胞生物学 微生物学 细菌 生物技术 生物化学 遗传学
作者
Victória L. Abdo,Lina J. Suárez,Lucca Gomes de Paula,Raphael Cavalcante Costa,Jamil Awad Shibli,Magda Feres,Valentim Adelino Ricardo Barão,Martinna Bertolini,João Gabriel Silva Souza
出处
期刊:Colloids and Surfaces B: Biointerfaces [Elsevier]
卷期号:226: 113318-113318 被引量:28
标识
DOI:10.1016/j.colsurfb.2023.113318
摘要

Barrier membranes are critical in creating tissuecompartmentalization for guided tissue (GTR) and bone regeneration (GBR) therapies. More recently, resorbable membranes have been widely used for tissue and bone regeneration due to their improved properties and the dispensable re-entry surgery for membrane removal. However, in cases with membrane exposure, this may lead to microbial contamination that will compromise the integrity of the membrane, surrounding tissue, and bone regeneration, resulting in treatment failure. Although the microbial infection can negatively influence the clinical outcomes of regenerative therapy, such as GBR and GTR, there is a lack of clinical investigations in this field, especially concerning the microbial colonization of different types of membranes. Importantly, a deeper understanding of the mechanisms of biofilm growth and composition and pathogenesis on exposed membranes is still missing, explaining the mechanisms by which bone regeneration is reduced during membrane exposure. This scoping review comprehensively screened and discussed the current in vivo evidence and possible new perspectives on the microbial contamination of resorbable membranes. Results from eligible in vivo studies suggested that different bacterial species colonized exposed membranes according to their composition (collagen, expanded polytetrafluoroethylene (non-resorbable), and polylactic acid), but in all cases, it negatively affected the attachment level and amount of bone gain. However, limited models and techniques have evaluated the newly developed materials, and evidence is scarce. Finally, new approaches to enhance the antimicrobial effect should consider changing the membrane surface or incorporating long-term released antimicrobials in an effort to achieve better clinical success.
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