Formulation, Characterization and Evaluation of Minocycline Hydrochloride Loaded Polyurethane/Collagen Nanofibers via Electrospinning as Wound Dressings.

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
Tuğba Eren Böncü, Çiğdem Yücel, Ahmet Ceylan, Mehmet Çadir, Ertuğrul Şahmetlioğlu
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引用次数: 0

Abstract

Objective It was aimed to formulate minocyline.HCI loaded electrospun polyurethane/collagen (PU/Col) and polyurethane/collagen/polycaprolactone (PU/Col/PCL) nanofibers are intended for use as a wound dressing. Methods:The effect of polymer ratio and addition of PCL on the morphology, diameter, drug delivery, encapsulation efficiency, mechanical properties, antibacterial activity against Escherichia coli and Staphylococcus aureus, cytotoxicity, cell adhesion and proliferation were investigated. 3-(4,5-dimethyldiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay was used to test the cytotoxicity of the nanofibers on the human dermal fibroblast (HDF) cell line. Cell proliferation/adhesion was also determined by imaging HDF cells seeded on mats with scanning electron microscopy/fluorescence microscopy. Results:All nanofibers were bead-free and smooth in the diameter range of 866.7-882.4 nm. They had favorable encapsulation efficiency (≥79.3%), controlled drug release up to 24 hours and did not have cytotoxic effects. Although collagen was preferred for cell adhesion and proliferation, its spinnability and mechanical properties were poor. While PU improved the spinnability of collagen, its mechanical properties also enhanced with the addition of PCL. Nevertheles, all mats led to favorable cell adhesion and proliferation. All the nanofibers had antimicrobial activity against Escherichia coli and Staphylococcus aureus. Conclusion:In conclusion, PU/Col and PU/Col/PCL nanofiber mats, which had favorable encapsulation efficiency, controlled drug release and antibacterial activity at least 24 hours, cell viability, proliferation, adhesion, mechanical properties to be used as wound dressing, were successfully prepared.

通过电纺丝技术制备、表征和评估负载盐酸米诺环素的聚氨酯/胶原蛋白纳米纤维,并将其用作伤口敷料。
目的:制备负载 HCI 的电纺聚氨酯/胶原蛋白(PU/Col)和聚氨酯/胶原蛋白/聚己内酯(PU/Col/PCL)纳米纤维,以用作伤口敷料。方法:研究了聚合物比例和 PCL 添加量对纳米纤维的形态、直径、药物输送、封装效率、机械性能、对大肠杆菌和金黄色葡萄球菌的抗菌活性、细胞毒性、细胞粘附和增殖的影响。采用 3-(4,5-二甲基噻唑-2-基)-2,5-二苯基溴化四氮唑(MTT)试验检测纳米纤维对人真皮成纤维细胞(HDF)的细胞毒性。此外,还利用扫描电子显微镜/荧光显微镜对播种在垫子上的 HDF 细胞进行成像,以确定细胞的增殖/粘附情况。结果:所有纳米纤维都不含微珠,直径范围在 866.7-882.4 nm 之间,表面光滑。它们具有良好的封装效率(≥79.3%),药物释放可控达24小时,且无细胞毒性作用。虽然胶原蛋白是细胞粘附和增殖的首选,但其可纺性和机械性能较差。虽然聚氨酯改善了胶原蛋白的可纺性,但加入 PCL 后,其机械性能也有所提高。尽管如此,所有垫子都有利于细胞粘附和增殖。所有纳米纤维都对大肠杆菌和金黄色葡萄球菌具有抗菌活性。结论:总之,成功制备出的 PU/Col 和 PU/Col/PCL 纳米纤维毡具有良好的封装效率、药物释放可控性、至少 24 小时的抗菌活性、细胞活力、增殖、粘附性和机械性能,可用作伤口敷料。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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