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ACS Biomater Sci Eng ; 10(5): 3006-3016, 2024 May 13.
Artigo em Inglês | MEDLINE | ID: mdl-38640484

RESUMO

Soft implantable devices are crucial to optimizing form and function for many patients. However, periprosthetic capsule fibrosis is one of the major challenges limiting the use of implants. Currently, little is understood about how spatial and temporal factors influence capsule physiology and how the local capsule environment affects the implant structure. In this work, we analyzed breast implant capsule specimens with staining, immunohistochemistry, and real-time polymerase chain reaction to investigate spatiotemporal differences in inflammation and fibrosis. We demonstrated that in comparison to the anterior capsule against the convex surface of breast implants, the posterior capsule against the flat surface of the breast implant displays several features of a dysregulated foreign body reaction including increased capsule thickness, abnormal extracellular remodeling, and infiltration of macrophages. Furthermore, the expression of pro-inflammatory cytokines increased in the posterior capsule across the lifespan of the device, but not in the anterior capsule. We also analyzed the surface oxidation of breast explant samples with XPS analysis. No significant differences in surface oxidation were identified either spatially or temporally. Collectively, our results support spatiotemporal heterogeneity in inflammation and fibrosis within the breast implant capsule. These findings presented here provide a more detailed picture of the complexity of the foreign body reaction surrounding implants destined for human use and could lead to key research avenues and clinical applications to treat periprosthetic fibrosis and improve device longevity.


Assuntos
Implantes de Mama , Fibrose , Reação a Corpo Estranho , Propriedades de Superfície , Implantes de Mama/efeitos adversos , Humanos , Reação a Corpo Estranho/patologia , Reação a Corpo Estranho/metabolismo , Reação a Corpo Estranho/imunologia , Feminino , Silicones/química , Géis de Silicone/efeitos adversos , Citocinas/metabolismo , Inflamação/patologia , Inflamação/metabolismo , Macrófagos/metabolismo , Macrófagos/imunologia
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