自生物矿化原位注射富含CaSO4纳米棒的胶原-透明质酸复合水凝胶用于微创方式的仿生骨重建

Xingzhu Liu, Yajie Zhang, Zahid Hussain, Penghui Zheng, Mingsheng Xu, Hongbo Zhao, Yuanshan Liu, Yi Cao, Ismat Ullah, Akiyoshi Osaka, Renjun Pei
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摘要

可原位注射的天然聚合物基水凝胶可用于填充不规则缺陷和促进组织再生。然而,大多数水凝胶的自我生物矿化能力有限,不能引导新骨的形成。本文针对将材料推进到临床研究中所遇到的挑战,通过降冰片烯(Nb)和四嗪(Tz)的生物正交反应,开发了一种嵌入硫酸钙纳米棒(CSN)的可注射胶原-透明质酸(Col-HA)水凝胶。配制的复合水凝胶不仅具有增强细胞粘附和增殖的潜力,而且还可以作为控制Ca2+释放的系统。这种复合水凝胶表现出令人印象深刻的注射性,允许直接原位注射和随后的复合水凝胶适应不规则形状的骨缺陷。csn掺入的复合水凝胶促进自生物矿化,从而在水凝胶内快速形成骨样羟基磷灰石(HAp)。此外,复合水凝胶稳定持续地释放Ca2+,刺激成骨前细胞的分化,促进原位骨生长。我们的研究结果表明,复合水凝胶可以通过微创应用成功介导优化后的CSN降解,有效加速HAp的形成,促进原位骨发育。
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Self-biomineralized in situ injectable CaSO4 nanorods-enriched collagen-hyaluronic acid composite hydrogels for biomimetic bone reconstruction in a minimally invasive manner
In situ injectable natural polymer-based hydrogels can be utilized to fill irregular defects and promote tissue regeneration. However, most hydrogels showed limited ability for self-biomineralization and can not guide the formation of new bone. Herein, according to the challenges encountered in advancing materials to clinical research, an injectable collagen-hyaluronic acid (Col-HA) hydrogel embedded with calcium sulfate nanorods (CSN) was developed via a bio-orthogonal reaction between norbornene (Nb) and tetrazine (Tz). The formulated [email protected] composite hydrogels not only have the potential to enhance cell adhesion and proliferation, but also serve as the system to control Ca2+ release. This composite hydrogel displayed impressive injectability, allowing straightforward in situ injection and subsequent adaption of composite hydrogels to irregularly shaped bone defects. CSN-incorporated composite hydrogels facilitate self-biomineralization, thereby fast-forming bone-like hydroxyapatite (HAp) within the hydrogel. Furthermore, Ca2+ released in a steady and sustained way from the composite hydrogels stimulated the differentiation of preosteoblasts, and promoted in situ bone growth. Our findings suggested that [email protected] composite hydrogels can successfully mediate the optimized CSN degradation, effectively accelerate HAp formation, and boost in situ bone development via the minimally invasive application.
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