Yali Miao , Teliang Lu , Shangbin Cui , Ziyang Xu , Xiao Liu , Yu Zhang
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引用次数: 0
Abstract
Background
Injectable hydrogels are widely used in drug delivery and the repair of irregular tissue defects due to their advantages such as convenient and minimally invasive operation. Although the existing injectable hydrogels have excellent biocompatibility and osteoconduction, they still face clinical challenges such as low osteogenic activity. The key requirements for improved injectable hydrogels as repair materials for non-load bearing bone defects are optimal handling properties, the ability to fill irregular defects and provide osteoinductive stimulation.
Methods
We developed an approach to construct injectable hydrogels through a two-step gelation process. In the first step of gelation, the denaturation and rehybridization mechanism of natural biopolymer DNA was utilized to form interconnected structure through hydrogen bonding between complementary base pairs between the DNA strands. In the second step of gelation, the introduction of halloysite nanotubes (HNTs) loaded with osteogenic model drug dexamethasone (Dex) provided additional crosslinking sites through non-covalent interactions with the DNA backbone, including electrostatic interaction and hydrogen bonding interaction.
Results
The DNA-based nanocomposite hydrogel material developed in our work can be used as an injectable filling material for the repair of non-load bearing bone defect and can be loaded with osteogenic model drug dexamethasone (Dex) for improved osteoinductivity, promoting new bone regeneration in vivo.
Translational potential of this article
This article highlights the potential of using nanocomposite hydrogels to repair non-load bearing bone defects, which are common injuries in the clinic. This study provides a deeper understanding of how to optimize the properties of hydrogels to regulate cell differentiation and tissue formation.
背景可注射水凝胶因其操作方便、微创等优点被广泛应用于药物输送和不规则组织缺损的修复。虽然现有的可注射水凝胶具有良好的生物相容性和骨传导性,但它们仍然面临着成骨活性低等临床挑战。改良可注射水凝胶作为非承重骨缺损修复材料的关键要求是具有最佳的操作性能、填充不规则缺损的能力以及提供骨诱导刺激。在凝胶化的第一步,利用天然生物聚合物 DNA 的变性和再杂化机制,通过 DNA 链之间互补碱基对的氢键作用形成相互连接的结构。在凝胶化的第二步,加入了成骨模型药物地塞米松(Dex)的海泡石纳米管(HNTs)通过与 DNA 主干的非共价相互作用(包括静电作用和氢键作用)提供了额外的交联位点。结果我们工作中开发的基于DNA的纳米复合水凝胶材料可用作修复非承重骨缺损的注射填充材料,并可负载成骨模型药物地塞米松(Dex)以改善骨诱导性,促进体内新骨再生。这项研究加深了人们对如何优化水凝胶特性以调节细胞分化和组织形成的理解。
期刊介绍:
The Journal of Orthopaedic Translation (JOT) is the official peer-reviewed, open access journal of the Chinese Speaking Orthopaedic Society (CSOS) and the International Chinese Musculoskeletal Research Society (ICMRS). It is published quarterly, in January, April, July and October, by Elsevier.