A systematic review of liposomal nanofibrous scaffolds as a drug delivery system: a decade of progress in controlled release and therapeutic efficacy.

IF 6.5 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Drug Delivery Pub Date : 2025-12-01 Epub Date: 2024-12-27 DOI:10.1080/10717544.2024.2445259
Houssam Aaref Abboud, Romána Zelkó, Adrienn Kazsoki
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引用次数: 0

Abstract

Drug-loaded liposomes incorporated in nanofibrous scaffolds is a promising approach as a multi-unit nanoscale system, which combines the merits of both liposomes and nanofibers (NFs), eliminating the drawback of liposomes' poor stability on the one hand and offering a higher potential of controlled drug release and enhanced therapeutic efficacy on the other hand. The current systematic review, which underwent a rigorous search process in PubMed, Web of Science, Scopus, Embase, and Central (Cochrane) employing (Liposome AND nanofib* AND electrosp*) as search keywords, aims to present the recent studies on using this synergic system for different therapeutic applications. The search was restricted to original, peer-reviewed studies published in English between 2014 and 2024. Of the 309 identified records, only 29 studies met the inclusion criteria. According to the literature, three different methods were identified to fabricate those nanofibrous liposomal scaffolds. The results consistently demonstrated the superiority of this dual system for numerous therapeutic applications in improving the therapy efficacy, enhancing both liposomes and drug stability, and releasing the encapsulated drug in a proper sustained release without significant initial burst release. Merging drug-loaded liposomes with NFs as liposomal nanofibrous scaffolds are a safe and efficient approach to deliver drug molecules and other substances for various pharmaceutical applications, particularly for wound dressing, tissue engineering, cancer therapy, and drug administration via the buccal and sublingual routes. However, further research is warranted to explore the potential of this system in other therapeutic applications.

脂质体纳米纤维支架作为药物递送系统的系统综述:十年来在控释和治疗效果方面的进展。
将载药脂质体掺入纳米纤维支架是一种很有前途的多单元纳米体系,它结合了脂质体和纳米纤维的优点,一方面消除了脂质体稳定性差的缺点,另一方面提供了更高的药物控释潜力和增强的治疗效果。本系统综述采用Liposome and nanofib* and electrosp*作为搜索关键词,在PubMed、Web of Science、Scopus、Embase和Central (Cochrane)中进行了严格的检索,旨在介绍该协同系统用于不同治疗应用的最新研究。该研究仅限于2014年至2024年间发表的英文原创同行评议研究。在309份确定的记录中,只有29项研究符合纳入标准。根据文献,确定了三种不同的方法来制备这些纳米纤维脂质体支架。结果一致地证明了这种双重系统在许多治疗应用中的优越性:提高治疗疗效,增强脂质体和药物稳定性,并以适当的缓释方式释放被封装的药物,而不会出现明显的初始爆发释放。将载药脂质体与NFs合并作为脂质体纳米纤维支架是一种安全有效的方法,可用于各种药物应用,特别是伤口敷料、组织工程、癌症治疗以及通过口腔和舌下途径给药。然而,需要进一步的研究来探索该系统在其他治疗应用中的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Drug Delivery
Drug Delivery 医学-药学
CiteScore
11.80
自引率
5.00%
发文量
250
审稿时长
3.3 months
期刊介绍: Drug Delivery is an open access journal serving the academic and industrial communities with peer reviewed coverage of basic research, development, and application principles of drug delivery and targeting at molecular, cellular, and higher levels. Topics covered include all delivery systems including oral, pulmonary, nasal, parenteral and transdermal, and modes of entry such as controlled release systems; microcapsules, liposomes, vesicles, and macromolecular conjugates; antibody targeting; protein/peptide delivery; DNA, oligonucleotide and siRNA delivery. Papers on drug dosage forms and their optimization will not be considered unless they directly relate to the original drug delivery issues. Published articles present original research and critical reviews.
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