IF 2.6 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Kimiya Pourdehghan, Faraz Najafi, Fatemeh Majdi, Nooshafarin Amani, Nasrin Samadi, Hamid Akbari Javar
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引用次数: 0

摘要

伤口是由内部或外部病理过程引起的皮肤或粘膜上皮完整性的破坏。本研究采用电纺丝技术制备了含有度洛西汀的纳米纤维伤口敷料。含 20% 和 40% 度洛西汀的纳米纤维直径分别约为 236 nm 和 272 nm。拉伸测试结果表明,断裂伸长率从无药纳米纤维的 11.5%飙升至含 40% 度洛西汀纳米纤维的 40.01%。所有纳米纤维都具有均匀的无珠结构。含药和不含药纳米纤维的接触角分别为 84.3° 和 99.3°。药物释放曲线显示,在前 8 小时的爆发性释放之后,药物释放曲线出现了较长时间的缓慢持续释放。纳米纤维对革兰氏阳性菌和革兰氏阴性菌具有抗菌活性,含有 40% 度洛西汀的交联纳米纤维对金黄色葡萄球菌的抑制区直径最大,约为 43 毫米,对大肠杆菌的抑制区直径最大,约为 40 毫米,对绿脓杆菌的抑制区直径最大,约为 30 毫米。临床研究表明,含 40% 度洛西汀的纳米纤维的伤口面积缩小率约为 96.41%,高于含苯妥英的阳性对照组(约 92.24%)和含 20% 度洛西汀的另一组(81.68%)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Preparation and characterization of Duloxetine-loaded nanofiber scaffold composed of polyvinyl alcohol and chitosan as wound healing agent, fabricated by electrospinning method.

Wound is a disruption in the epithelial integrity of the skin or mucosa, which is caused by internal or external pathological processes. In this study, a nanofiber as wound dressing loaded with Duloxetine was produced by electrospinning technique. The diameter of nanofibers containing 20% and 40% Duloxetine was around 236 nm and 272 nm, respectively. Tensile testing results showed that elongation at break percentage soared from 11.5% for drug-free nanofibers to 40.01% for nanofibers containing 40% Duloxetine. All nanofibers had uniform bead-free structure. Contact angle of nanofibers with and without drug was 84.3° and 99.3°, respectively. The drug release profile revealed that after the burst release over the first 8 hours, the curve witnessed a slow sustained release for a longer period. The nanofibers had antibacterial activity against gram-positive and gram-negative bacteria and the crosslinked nanofibers with 40% duloxetine had the largest diameter of inhibition zone at roughly 43 mm for Staphylococcus aureus, 40 mm for Escherichia coli, and 30 mm for Pseudomonas aeruginosa. Clinical studies showed that the percentage of wound area reduction was approximately 96.41% for nanofibers containing 40% duloxetine which was higher than positive control containing phenytoin at around 92.24% and also the other group with 20% duloxetine at 81.68%.

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来源期刊
CiteScore
5.90
自引率
2.90%
发文量
82
审稿时长
1 months
期刊介绍: Pharmaceutical Development & Technology publishes research on the design, development, manufacture, and evaluation of conventional and novel drug delivery systems, emphasizing practical solutions and applications to theoretical and research-based problems. The journal aims to publish significant, innovative and original research to advance the frontiers of pharmaceutical development and technology. Through original articles, reviews (where prior discussion with the EIC is encouraged), short reports, book reviews and technical notes, Pharmaceutical Development & Technology covers aspects such as: -Preformulation and pharmaceutical formulation studies -Pharmaceutical materials selection and characterization -Pharmaceutical process development, engineering, scale-up and industrialisation, and process validation -QbD in the form a risk assessment and DoE driven approaches -Design of dosage forms and drug delivery systems -Emerging pharmaceutical formulation and drug delivery technologies with a focus on personalised therapies -Drug delivery systems research and quality improvement -Pharmaceutical regulatory affairs This journal will not consider for publication manuscripts focusing purely on clinical evaluations, botanicals, or animal models.
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