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一种具有成骨、抗菌和抗炎作用的纳米复合水凝胶平台,可加速骨重建。

An osteogenic, antibacterial, and anti-inflammatory nanocomposite hydrogel platform to accelerate bone reconstruction.

机构信息

CAS Key Laboratory of Nano-Bio Interface, Division of Nanobiomedicine, Suzhou Institute of Nano-Tech and Nano-Bionics (SINANO), Chinese Academy of Sciences, Suzhou, 215123, China.

School of Nano-Tech and Nano-Bionics, University of Science and Technology of China (USTC), Hefei, 230026, China.

出版信息

J Mater Chem B. 2023 Jun 28;11(25):5830-5845. doi: 10.1039/d3tb00641g.

Abstract

Fabricating an organic-inorganic nanocomposite hydrogel platform with antibacterial, anti-inflammatory, and osteoinductive properties that mimic bone extracellular matrix composition is decisive for guiding bone development in orthopedic practice. Despite significant progress in developing hydrogels for tissue repair, little attention has been paid to replicating the natural bone ECM microenvironments and addressing the importance of anti-inflammatory agents during osteogenesis. Herein, we developed ciprofloxacin and dexamethasone loaded strontium (Sr) and/or iron (Fe) substituted hydroxyapatite (HAp) nanomaterials precipitated in collagen (Col) to construct a multifunctional bioactive nanocomposite hydrogel platform to prevent inflammation and bacterial adhesion, leading to augmenting bone development in the defect site. The fabricated nanocomposite hydrogels (Sr:HAp-Col, Fe:HAp-Col, and Sr/Fe:HAp-Col) were physicochemically characterized and demonstrated high loading and prolonged drug release, and excellent antibacterial activity against Gram-positive and Gram-negative bacteria. In experiments, the Sr/Fe:HAp-Col sample exhibited enhanced bioactivity against the preosteoblast MC3T3-E1 cell line, with high alkaline phosphatase and bone-like inorganic calcium deposition, as well as increased gene expression of osteogenesis-related differentiation markers, including OPN, OCN, and RUNX2. Furthermore, experiments revealed that the Sr/Fe:HAp-Col matrix degraded over time by controlling the release of ions into the body, without causing acute inflammation at the implanted site or in the blood serum, or in the internal organs, including the heart, lungs, liver, and kidney of the Sprague-Dawley rat model. The micro-CT scan and histological examination showed high bone mineral density and more mature bone formation at the nanocomposite hydrogel implanted site associated with the ColMA hydrogel in the femur defect of the rat model. The strategy of applying collagen hydrogel supplemented with HAp to bone regeneration is promising due to its ability to mimic the natural bone ECM. Overall, the developed bioactive nanocomposite hydrogel may have great potential not only in bone regeneration but also in repairing nonunion-infected defects of other tissues.

摘要

制备具有抗菌、抗炎和成骨诱导特性的有机-无机纳米复合水凝胶平台,模拟骨细胞外基质的组成,对于指导骨科实践中的骨发育至关重要。尽管在开发用于组织修复的水凝胶方面取得了重大进展,但很少关注复制天然骨 ECM 微环境和解决成骨过程中抗炎剂的重要性。在这里,我们开发了载有环丙沙星和地塞米松的锶 (Sr) 和/或铁 (Fe) 取代的羟基磷灰石 (HAp) 纳米材料沉淀在胶原 (Col) 中,构建了一种多功能生物活性纳米复合水凝胶平台,以防止炎症和细菌黏附,从而增强缺陷部位的骨发育。所制备的纳米复合水凝胶(Sr:HAp-Col、Fe:HAp-Col 和 Sr/Fe:HAp-Col)进行了物理化学特性表征,并表现出高载药量和延长的药物释放,以及对革兰氏阳性和革兰氏阴性细菌的优异抗菌活性。实验中,Sr/Fe:HAp-Col 样品对前成骨细胞 MC3T3-E1 细胞系表现出增强的生物活性,具有高碱性磷酸酶和骨样无机钙沉积,以及成骨相关分化标志物(包括 OPN、OCN 和 RUNX2)的基因表达增加。此外,实验表明,Sr/Fe:HAp-Col 基质通过控制离子在体内的释放而随时间降解,不会在植入部位或血清中引起急性炎症,也不会在心脏、肺、肝脏和肾脏等内部器官中引起炎症。Sprague-Dawley 大鼠模型的微 CT 扫描和组织学检查显示,纳米复合水凝胶植入部位的骨矿物质密度较高,骨形成更成熟,与 ColMA 水凝胶联合应用于股骨缺损的大鼠模型。将胶原水凝胶与 HAp 联合应用于骨再生的策略具有广阔的前景,因为它能够模拟天然骨 ECM。总之,所开发的生物活性纳米复合水凝胶不仅在骨再生方面具有巨大潜力,而且在修复其他组织的非愈合感染性缺陷方面也具有巨大潜力。

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