可见光诱导dlp打印的氧释放TPMS支架减轻骨缺损早期缺氧。

IF 9.6 2区 医学 Q1 ENGINEERING, BIOMEDICAL
Anastasia B Timoshenko, Ali Ghasemkhani, Chanul Kim, Domenic J Cordova, Maria Astudillo Potes, Valeria Aceves, Indranath Mitra, Justin E Bird, Ryan S Gray, Stephanie K Seidlits, Benjamin D Elder, Maryam Tilton
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引用次数: 0

摘要

在大的或血管化不良的骨缺损内缺氧仍然是成功再生的关键障碍,特别是在血管长入之前的早期植入后时期。本文报道了COSnPPOD (coo2 - silica NP平台for Osteogenic development)的开发,这是一种可见光数字光处理印刷水凝胶支架,将氧释放纳米颗粒(NPs)集成在原始型三周期最小表面结构中。该支架结合了明胶甲基丙烯酸酯-聚(乙二醇)二丙烯酸酯基质和过氧化钙(CaO2)负载的中空二氧化硅NPs,在保持结构保真度的同时,实现了局部、短期的氧气释放。COSnPPOD支架在体外表现出良好的降解动力学,可调节的刚度和增加的蛋白质吸附。在成骨前细胞模型中,COSnPPOD维持细胞活力并支持成骨基因表达,而没有细胞毒性作用。虽然总体基因表达与对照组相当,但磷酸化蛋白1 (Spp1)的表达增加了16倍,这表明支架驱动的基质重塑途径的激活。在体内,COSnPPOD支架增强了小鼠颅骨缺损模型的骨再生,与未处理的缺损和水凝胶对照相比,其骨形成和胶原沉积明显增加。此外,血管内皮生长因子免疫染色在缺损内增加,与促血管生成反应一致,未观察到全身毒性。这些发现表明COSnPPOD是一种很有前途的支架系统,它结合了持续氧合和仿生几何结构来支持局部骨再生。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Visible Light Induced DLP-Printed Oxygen-Releasing TPMS Scaffolds Mitigate Early Hypoxia in Bone Defects.

Oxygen deprivation within large or poorly vascularized bone defects remains a key barrier to successful regeneration, especially during the early postimplantation period before vascular ingrowth. Here, the development of COSnPPOD (CaO2-Silica NP Platform for Osteogenic Development) is reported, a visible light digital light processing-printed hydrogel scaffold that integrates oxygen-releasing nanoparticles (NPs) within a Primitive-type triply periodic minimal surface architecture. The scaffold combines a gelatin methacrylate-poly(ethylene glycol) diacrylate matrix with calcium peroxide (CaO2)-loaded hollow silica NPs, enabling localized, short-term oxygen release while preserving structural fidelity. COSnPPOD scaffolds demonstrate favorable degradation kinetics, tunable stiffness, and increased protein adsorption in vitro. In a preosteoblast model, COSnPPOD maintains cell viability and supports osteogenic gene expression without cytotoxic effects. While overall gene expression is comparable to controls, a 16-fold increased expression of phosphoprotein 1 (Spp1) suggests scaffold-driven activation of matrix remodeling pathways. In vivo, COSnPPOD scaffolds enhance bone regeneration in a murine calvarial defect model, with significantly greater bone formation and collagen deposition than untreated defects and hydrogel controls. Additionally, vascular endothelial growth factor immunostaining is increased within the defect, consistent with a proangiogenic response, and no systemic toxicity is observed. These findings establish COSnPPOD as a promising scaffold system that combines sustained oxygenation with biomimetic geometry to support localized bone regeneration.

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来源期刊
Advanced Healthcare Materials
Advanced Healthcare Materials 工程技术-生物材料
CiteScore
14.40
自引率
3.00%
发文量
600
审稿时长
1.8 months
期刊介绍: Advanced Healthcare Materials, a distinguished member of the esteemed Advanced portfolio, has been dedicated to disseminating cutting-edge research on materials, devices, and technologies for enhancing human well-being for over ten years. As a comprehensive journal, it encompasses a wide range of disciplines such as biomaterials, biointerfaces, nanomedicine and nanotechnology, tissue engineering, and regenerative medicine.
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