Poly(BETA-AMINO) ester based electrospun membranes with modulated degradation and release kinetics for potential wound dressing applications

IF 5.2 2区 医学 Q1 PHARMACOLOGY & PHARMACY International Journal of Pharmaceutics Pub Date : 2025-03-15 DOI:10.1016/j.ijpharm.2025.125476
Liam Ayaden , Mickael Maton , Feng Chai , Nicolas Blanchemain , Stéphanie Degoutin
{"title":"Poly(BETA-AMINO) ester based electrospun membranes with modulated degradation and release kinetics for potential wound dressing applications","authors":"Liam Ayaden ,&nbsp;Mickael Maton ,&nbsp;Feng Chai ,&nbsp;Nicolas Blanchemain ,&nbsp;Stéphanie Degoutin","doi":"10.1016/j.ijpharm.2025.125476","DOIUrl":null,"url":null,"abstract":"<div><div>Chronic wounds show no healing tendency over a period of up to 4 to 6 weeks despite any local treatment. These wounds present the persistence of the inflammatory stimulus and a high sensitivity to bacterial infection. Engineering innovative wound dressings is key to facilitating the wound treatment, reducing healing time, and preventing recurrent infections. In this context, this project focused on the design of electrospun bioactive membrane based on Poly(Beta-amino)ester polymers (PBAEs) loaded with antibiotics (ciprofloxacin, CFX) for potential wound dressing applications. First, two PBAE macromers of different lengths were synthesized from the reaction of isobutylamine with two polyethylene glycol diacrylates (PEGDA). Both synthesized macromers exhibited opposite properties in terms of hydrophobicity (one is hydrophobic whereas the other one is hydrophilic) and crystallinity (amorphous or semi-crystalline). Then, both compounds were successfully electrospun with polyethylene oxide (PEO) and subjected to UV-curing to induce crosslinking of PBAE macromer. The membrane properties were similar in terms of hydrophilicity and crystallinity to the respective PBAE compounds, and these properties influenced degradation rates and drug release profiles. Finally, the antibacterial activity of the released drug was assessed to validate the bioactive profile of the membrane regarding bacterial infection.</div></div>","PeriodicalId":14187,"journal":{"name":"International Journal of Pharmaceutics","volume":"674 ","pages":"Article 125476"},"PeriodicalIF":5.2000,"publicationDate":"2025-03-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Pharmaceutics","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0378517325003126","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
引用次数: 0

Abstract

Chronic wounds show no healing tendency over a period of up to 4 to 6 weeks despite any local treatment. These wounds present the persistence of the inflammatory stimulus and a high sensitivity to bacterial infection. Engineering innovative wound dressings is key to facilitating the wound treatment, reducing healing time, and preventing recurrent infections. In this context, this project focused on the design of electrospun bioactive membrane based on Poly(Beta-amino)ester polymers (PBAEs) loaded with antibiotics (ciprofloxacin, CFX) for potential wound dressing applications. First, two PBAE macromers of different lengths were synthesized from the reaction of isobutylamine with two polyethylene glycol diacrylates (PEGDA). Both synthesized macromers exhibited opposite properties in terms of hydrophobicity (one is hydrophobic whereas the other one is hydrophilic) and crystallinity (amorphous or semi-crystalline). Then, both compounds were successfully electrospun with polyethylene oxide (PEO) and subjected to UV-curing to induce crosslinking of PBAE macromer. The membrane properties were similar in terms of hydrophilicity and crystallinity to the respective PBAE compounds, and these properties influenced degradation rates and drug release profiles. Finally, the antibacterial activity of the released drug was assessed to validate the bioactive profile of the membrane regarding bacterial infection.

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
聚(β -氨基)酯基电纺丝膜与调节降解和释放动力学的潜在伤口敷料应用
尽管进行了任何局部治疗,慢性伤口在长达4至6周的时间内没有愈合趋势。这些伤口表现出持续的炎症刺激和对细菌感染的高度敏感性。工程创新创面敷料是促进创面治疗、缩短愈合时间和防止复发感染的关键。在此背景下,本项目侧重于设计基于聚(β -氨基)酯聚合物(PBAEs)负载抗生素(环丙沙星,CFX)的电纺丝生物活性膜,用于潜在的伤口敷料应用。首先,由异丁胺与两种聚乙二醇二丙烯酸酯(PEGDA)反应合成了两个不同长度的PBAE大分子。两种合成的大分子在疏水性(一种是疏水性,另一种是亲水性)和结晶度(无定形或半结晶)方面表现出相反的性质。然后,将两种化合物与聚氧聚乙烯(PEO)进行静电纺丝,并进行紫外光固化以诱导PBAE大分子交联。在亲水性和结晶度方面,膜的性质与各自的PBAE化合物相似,这些性质影响降解率和药物释放谱。最后,对释放药物的抗菌活性进行了评估,以验证膜对细菌感染的生物活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
CiteScore
10.70
自引率
8.60%
发文量
951
审稿时长
72 days
期刊介绍: The International Journal of Pharmaceutics is the third most cited journal in the "Pharmacy & Pharmacology" category out of 366 journals, being the true home for pharmaceutical scientists concerned with the physical, chemical and biological properties of devices and delivery systems for drugs, vaccines and biologicals, including their design, manufacture and evaluation. This includes evaluation of the properties of drugs, excipients such as surfactants and polymers and novel materials. The journal has special sections on pharmaceutical nanotechnology and personalized medicines, and publishes research papers, reviews, commentaries and letters to the editor as well as special issues.
期刊最新文献
"Hot spring"-mimetic microneedle patches delivering probiotics to accelerate infected wound healing via antibacterial, anti-inflammatory, and angiogenesis. Polysaccharides from Adansonia digitata combined with whey protein and alginate enhance the viscosity, swelling, controlled release, and mucoadhesion properties of hydrogels for oral drug delivery. Narrow-width surface acoustic wave device-driven olfactory epithelium-targeted intranasal atomization. Unlocking the potential of lipid-based nanoparticles for intranasal drug delivery in Parkinson's disease. An integrated framework streamlining the manufacturing of high drug loading pharmaceutical tablets.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1