Enhanced drug release control in coaxial electrospun fibers via heat pressing: Reducing burst release and achieving dual-phase delivery

IF 6 2区 医学 Q1 PHARMACOLOGY & PHARMACY International Journal of Pharmaceutics Pub Date : 2025-04-15 Epub Date: 2025-03-22 DOI:10.1016/j.ijpharm.2025.125501
Ji-Feng Wang, Jin-Jia Hu
{"title":"Enhanced drug release control in coaxial electrospun fibers via heat pressing: Reducing burst release and achieving dual-phase delivery","authors":"Ji-Feng Wang,&nbsp;Jin-Jia Hu","doi":"10.1016/j.ijpharm.2025.125501","DOIUrl":null,"url":null,"abstract":"<div><div>Burst release is a common challenge in drug delivery systems (DDS), potentially leading to subtherapeutic or toxic drug concentrations. Coaxial electrospinning has emerged as a promising technique to address this issue by encapsulating drugs within core-sheath fiber structures, thereby preventing direct exposure of the drug to the environment and ensuring a gradual release profile. However, secondary processing of coaxial electrospun membranes, such as cutting or slicing, can damage the core-sheath structure of fibers, exposing the drug-loaded core and exacerbating burst release. In this study, we applied heat pressing along the intended cutting line prior to cutting, aiming to thermally seal the core-sheath structure of fibers and prevent drug leakage from the core at cut edges. As a result, the heat-pressed group exhibited a significantly reduced initial burst release followed by a more sustained release compared to the control group, which involved no heat pressing before cutting. The release profiles of both groups were well described by the Korsmeyer-Peppas model with n = 0.32 (R<sup>2</sup> = 0.95) for the control group and n = 0.49 (R<sup>2</sup> = 0.99) for the heat-pressed group. Notably, the release behavior of the heat-pressed group exhibited a closer approximation (R<sup>2</sup> = 0.96) to a first-order model compared to the control group (R<sup>2</sup> = 0.59). Furthermore, we successfully developed a dual-phase DDS by manipulating the ratio of unsealed (fast release) and sealed (slow release) portions of an electrospun membrane. In conclusion, heat pressing presents a simple yet effective strategy for enhancing the performance and reliability of coaxial electrospun DDS, offering potential for broader applications in controlled drug delivery.</div></div>","PeriodicalId":14187,"journal":{"name":"International Journal of Pharmaceutics","volume":"674 ","pages":"Article 125501"},"PeriodicalIF":6.0000,"publicationDate":"2025-04-15","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/S0378517325003382","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/3/22 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
引用次数: 0

Abstract

Burst release is a common challenge in drug delivery systems (DDS), potentially leading to subtherapeutic or toxic drug concentrations. Coaxial electrospinning has emerged as a promising technique to address this issue by encapsulating drugs within core-sheath fiber structures, thereby preventing direct exposure of the drug to the environment and ensuring a gradual release profile. However, secondary processing of coaxial electrospun membranes, such as cutting or slicing, can damage the core-sheath structure of fibers, exposing the drug-loaded core and exacerbating burst release. In this study, we applied heat pressing along the intended cutting line prior to cutting, aiming to thermally seal the core-sheath structure of fibers and prevent drug leakage from the core at cut edges. As a result, the heat-pressed group exhibited a significantly reduced initial burst release followed by a more sustained release compared to the control group, which involved no heat pressing before cutting. The release profiles of both groups were well described by the Korsmeyer-Peppas model with n = 0.32 (R2 = 0.95) for the control group and n = 0.49 (R2 = 0.99) for the heat-pressed group. Notably, the release behavior of the heat-pressed group exhibited a closer approximation (R2 = 0.96) to a first-order model compared to the control group (R2 = 0.59). Furthermore, we successfully developed a dual-phase DDS by manipulating the ratio of unsealed (fast release) and sealed (slow release) portions of an electrospun membrane. In conclusion, heat pressing presents a simple yet effective strategy for enhancing the performance and reliability of coaxial electrospun DDS, offering potential for broader applications in controlled drug delivery.

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
通过热压增强同轴静电纺丝纤维的药物释放控制:减少爆发释放和实现双相递送。
突发释放是药物传递系统(DDS)中常见的挑战,可能导致亚治疗或毒性药物浓度。同轴静电纺丝已成为解决这一问题的一种很有前途的技术,它将药物封装在芯鞘纤维结构中,从而防止药物直接暴露于环境中,并确保逐渐释放。然而,同轴静电纺丝膜的二次加工,如切割或切片,会破坏纤维的芯鞘结构,使载药的芯暴露出来,加剧爆裂释放。在本研究中,我们在切割前沿着预定的切割线进行热压,旨在热密封纤维的芯-鞘结构,防止药物从切割边缘的芯泄漏。结果,与切割前不进行热压的对照组相比,热压组表现出明显减少的初始爆裂释放,随后更持久的释放。两组释药曲线均符合korsmemeyer - peppas模型,对照组n = 0.32 (R2 = 0.95),热压组n = 0.49 (R2 = 0.99)。值得注意的是,与对照组(R2 = 0.59)相比,热压组的释放行为更接近于一阶模型(R2 = 0.96)。此外,我们通过控制电纺丝膜的非密封(快速释放)和密封(缓慢释放)部分的比例,成功地开发了双相DDS。综上所述,热压是一种简单而有效的方法,可以提高同轴静电纺丝DDS的性能和可靠性,在控制药物输送方面具有更广泛的应用潜力。
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
Predictive population balance modeling of pharmaceutical tablet disintegration and dissolution behavior A hybrid modelling framework for the description of friction forces in autoinjector devices Development of rutin-loaded cerosomes for topical photoprotection and skin barrier modulation Formulation and optimization of hydralazine hydrochloride-loaded mucoadhesive niosomes for sublingual hypertension management; in vitro characterization and in vivo pharmacodynamic evaluation Perspectives on chikungunya vaccinology: from traditional platforms to epitope-driven rational design
×
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