Guo Liang, Liu Xuezhe, Wang Yao, Yi Jiaoyu, Li Juanjuan, Xu Yong, Cai Kaiyong, Dai Wufei, Feng Qian, Tao Bo
Department of Thoracic Surgery, Shanghai Pulmonary Hospital, Tongji University School of Medicine, Shanghai, China.
Key Laboratory of Biorheological Science and Technology, Ministry of Education, College of Bioengineering, Chongqing University, Chongqing, China.
Mater Today Bio. 2024 Aug 30;28:101208. doi: 10.1016/j.mtbio.2024.101208. eCollection 2024 Oct.
Artificial tracheal substitutes encounter significant challenges during long-segmental tracheal defects (LSTD) reconstruction, notably early postoperative anastomotic stenosis and tracheal chondromalacia. Mitigating early anastomotic stenosis by creating a compliant sutureless substitute is pivotal. Enhancing its chondrogenic capacity is equally critical for sustained healthy tracheal cartilage regeneration. This study proposes a self-healing hydrogel for sutureless tracheal anastomosis to mitigate anastomotic stenosis, enriched with kartogenin (KGN) and transforming growth factor-β1 (TGFβ1) to bolster chondrogenic properties. Initially, two precursor solutions were prepared: 1) aldehyde-modified hyaluronic acid with sulfonation and β-cyclodextrin-CHO loaded with KGN; 2) hydrazide-grafted gelatin loaded with TGFβ1. Coextrusion of these solutions resulted in a gelated G + TGFβ1/sH-CD + KGN hydrogel, characterized by a robust covalent bonding network of acylhydrazones between hydrazide and aldehyde groups, imparting excellent self-healing properties. The G + TGFβ1/sH-CD + KGN hydrogels, showcasing favorable cytocompatibility, excellent injectability, and rapid gelation, were loaded with bone marrow stem cells. These were customized into O-shaped rings and assembled into a malleable tracheal substitute using our established ring-to-tube method. This resultant compliant substitute facilitated sutureless anastomosis of LSTD in a rabbit model, attributed to the Schiff base reaction between the hydrogel's carbonyl group and the tissue's amino group. Notably, the tracheal substitute reduced early postoperative anastomotic stenosis, maintained tracheal patency, alleviated sputum blockage, promoted reepithelization, and increased the survival rate of the experimental rabbits. The sustained release of chondrocytokines resulted in excellent tracheal cartilage regeneration. Employing chondrocytokines-loaded hydrogels with self-healing properties represents a significant advancement in sutureless tracheal anastomosis and tracheal cartilage regeneration, holding promising potential in inhibiting early postoperative anastomotic stenosis and tracheal chondromalacia when treating LSTD.
人工气管替代物在长节段气管缺损(LSTD)重建过程中面临重大挑战,尤其是术后早期吻合口狭窄和气管软骨软化。通过制造一种柔顺的无缝合替代物来减轻早期吻合口狭窄至关重要。增强其软骨生成能力对于持续健康的气管软骨再生同样关键。本研究提出一种用于无缝合气管吻合的自愈合水凝胶,以减轻吻合口狭窄,该水凝胶富含卡托金(KGN)和转化生长因子-β1(TGFβ1)以增强软骨生成特性。首先,制备两种前驱体溶液:1)经磺化的醛修饰透明质酸和负载KGN的β-环糊精-CHO;2)负载TGFβ1的酰肼接枝明胶。这些溶液的共挤出产生了凝胶化的G + TGFβ1/sH-CD + KGN水凝胶,其特征在于酰肼和醛基之间形成了强大的酰腙共价键网络,赋予了优异的自愈合性能。G + TGFβ1/sH-CD + KGN水凝胶具有良好的细胞相容性、出色的可注射性和快速凝胶化特性,并负载了骨髓干细胞。将这些定制成O形环,并使用我们建立的环到管方法组装成可塑的气管替代物。这种所得的柔顺替代物在兔模型中促进了LSTD的无缝合吻合,这归因于水凝胶的羰基与组织的氨基之间的席夫碱反应。值得注意的是,气管替代物减少了术后早期吻合口狭窄,维持了气管通畅,减轻了痰液阻塞,促进了上皮再形成,并提高了实验兔的存活率。软骨细胞因子的持续释放导致了优异的气管软骨再生。采用具有自愈合特性的负载软骨细胞因子的水凝胶代表了无缝合气管吻合和气管软骨再生方面的重大进展,在治疗LSTD时抑制术后早期吻合口狭窄和气管软骨软化方面具有广阔的前景。