用于皮肤鳞状细胞癌术后伤口愈合的电纺丝药物负载聚己内酯/聚己内酯-明胶多功能双层纳米纤维复合支架

Yongteng Song , Qingxi Hu , Suihong Liu , Guotai Yao , Haiguang Zhang
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引用次数: 0

摘要

皮肤鳞状细胞癌(cSCC)肿瘤切除手术因癌细胞切除不彻底而面临挑战,这增加了局部复发和微转移的风险,同时大面积的手术伤口容易造成严重感染。因此,我们制作了一种载药多功能双层纳米纤维皮肤支架,用于 cSCC 术后伤口护理。简而言之,抗菌药物恩诺沙星(ENR)通过电纺丝被负载到聚己内酯(PCL)纳米纤维中,形成抗菌纳米纤维膜(PCL-ENR)作为支架的外层。抗癌药物博莱霉素(BLM)通过电纺丝被负载到 PCL/明胶(Gelatin)纳米纤维中,形成抗癌纳米纤维膜(PG-BLM),作为支架的内层。ENR和BLM被成功载入支架。该支架具有优异的理化特性,外层具有疏水性和出色的抗菌活性,内层具有亲水性和出色的抗癌活性。支架的断裂伸长率和拉伸模量分别为 26.35 ± 1.61 % 和 15.25 ± 1.56 兆帕。体外和体内实验表明,该支架不仅具有良好的生物相容性,能促进伤口愈合,还能抑制A431细胞的增殖,在cSCC术后伤口护理方面具有很大的临床应用潜力。
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Electrospinning drug-loaded polycaprolactone/polycaprolactone-gelatin multi-functional bilayer nanofibers composite scaffold for postoperative wound healing of cutaneous squamous cell carcinoma
Cutaneous squamous cell carcinoma (cSCC) tumor resection surgery poses challenges due to incomplete cancer cell removal, which increases the risk of local recurrence and micrometastasis, while large-scale surgical wounds are susceptible to severe infections. Therefore, a drug-loaded multi-functional bilayer nanofibers skin scaffold was fabricated for postoperative wound care of cSCC. Briefly, the antibacterial drug enrofloxacin (ENR) was loaded into polycaprolactone (PCL) nanofibers using electrospinning to form an antibacterial nanofiber membrane (PCL-ENR) as the outer layer of scaffold. The anticancer drug bleomycin (BLM) was loaded into PCL/Gelatin (Gel) nanofibers via electrospinning to form an anticancer nanofiber membrane (PG-BLM) as the inner layer of scaffold. ENR and BLM were successfully loaded into the scaffold. The scaffold had excellent physicochemical properties, with the outer layer exhibiting hydrophobicity and excellent antibacterial activity, and the inner layer showing hydrophilicity and outstanding anticancer activity. The elongation at break and tensile modulus of the scaffold were 26.35 ​± ​1.61 ​% and 15.25 ​± ​1.56 ​MPa, respectively. In vitro and in vivo experiments suggested that the scaffold not only has good biocompatibility to promote wound healing but also could inhibit the proliferation of A431 ​cells, which has great potential clinical application in postoperative wound care of cSCC.
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