Assessing the Biocompatibility and Regeneration of Electrospun‐Nanofiber Composite Tracheal Grafts

生物相容性 再生(生物学) 纳米纤维 静电纺丝 复合数 材料科学 生物医学工程 复合材料 医学 聚合物 细胞生物学 生物 冶金
作者
Lily Kreber,Lumei Liu,Sayali Dharmadhikari,Zheng Hong Tan,Coreena Chan,Joey Huddle,Zainab Hussein,Kimberly M. Shontz,Christopher K. Breuer,Jed Johnson,Tendy Chiang
出处
期刊:Laryngoscope [Wiley]
卷期号:134 (3): 1155-1162
标识
DOI:10.1002/lary.30955
摘要

Composite tracheal grafts (CTG) combining decellularized scaffolds with external biomaterial support have been shown to support host-derived neotissue formation. In this study, we examine the biocompatibility, graft epithelialization, vascularization, and patency of three prototype CTG using a mouse microsurgical model.Tracheal replacement, regenerative medicine, biocompatible airway splints, animal model.CTG electrospun splints made by combining partially decellularized tracheal grafts (PDTG) with polyglycolic acid (PGA), poly(lactide-co-ε-caprolactone) (PLCL), or PLCL/PGA were orthotopically implanted in mice (N = 10/group). Tracheas were explanted two weeks post-implantation. Micro-Computed Tomography was conducted to assess for graft patency, and histological analysis was used to assess for epithelialization and neovascularization.Most animals (greater than 80%) survived until the planned endpoint and did not exhibit respiratory symptoms. MicroCT confirmed the preservation of graft patency. Grossly, the PDTG component of CTG remained intact. Examining the electrospun component of CTG, PGA degraded significantly, while PLCL+PDTG and PLCL/PGA + PDTG maintained their structure. Microvasculature was observed across the surface of CTG and infiltrating the pores. There were no signs of excessive cellular infiltration or encapsulation. Graft microvasculature and epithelium appear similar in all groups, suggesting that CTG did not hinder endothelialization and epithelialization.We found that all electrospun nanofiber CTGs are biocompatible and did not affect graft patency, endothelialization and epithelialization. Future directions will explore methods to accelerate graft regeneration of CTG.N/A Laryngoscope, 134:1155-1162, 2024.
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