Synergistic effects of silver nanoparticles and cisplatin in combating inflammation and hyperplasia of airway stents

新生内膜增生 气道 静电纺丝 肉芽组织 支架 银纳米粒子 材料科学 化学 纳米技术 伤口愈合 纳米颗粒 医学 再狭窄 免疫学 外科 复合材料 聚合物
作者
Zhaonan Li,Chuan Tian,Dechao Jiao,Jing Li,Yahua Li,Xueliang Zhou,Huiping Zhao,Yanan Zhao,Xinwei Han
出处
期刊:Bioactive Materials [Elsevier BV]
卷期号:9: 266-280 被引量:37
标识
DOI:10.1016/j.bioactmat.2021.07.029
摘要

Anti-inflammatory and antihyperplasia activities are essential requirements for the successful use of airway stents. In this work, silver nanoparticles (AgNPs) and cisplatin (DDP) were combined in a synergistic modification strategy to improve the surface function of airway stents. Using polycaprolactone (PCL) as a drug carrier, a dual-functional PCL-AgNPs-DDP fiber film-coated airway stent was fabricated by electrospinning. The physicochemical and biological properties of the obtained fiber films were examined. The ATR-FTIR, XPS, SEM-EDS and TEM results suggested that AgNPs and DDP could be successfully immobilized onto the airway stent surface. The drug release and surface degradation results revealed that AgNPs and DDP can undergo sustained release from films for 30 d, and the weight loss was approximately 50% after 35 d. In addition, the dual-functional fiber film suppressed human embryonic lung fibroblast growth and exhibited excellent antibacterial activity against Staphylococcus aureus, Pseudomonas aeruginosa and Candida albicans. Furthermore, the effectiveness of the dual-functional fiber film-coated airway stent was evaluated by application to the trachea of New Zealand rabbits. The in vivo results indicated that PCL-AgNPs-DDP fiber film-coated airway stent can significantly inhibit granulation tissue formation and collagen deposition, reduced the expression of IL-8, TNF-α, IL-1α, PCNA, α-SMA and CD68, and ultimately achieved anti-inflammatory and antihyperplasia effects. Hence, this study provides a dual-functional surface-coated airway stent to address the clinical complications associated with respiratory tract inflammation and granulation tissue hyperplasia, thus inhibiting tracheal stenosis.

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