Advancing burn wound treatment: exploring hydrogel as a transdermal drug delivery system.

IF 6.5 2区 医学 Q1 PHARMACOLOGY & PHARMACY Drug Delivery Pub Date : 2024-12-01 Epub Date: 2024-02-16 DOI:10.1080/10717544.2023.2300945
MeeiChyn Goh, Meng Du, Wang Rui Peng, Phei Er Saw, Zhiyi Chen
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Abstract

Burn injuries are prevalent and life-threatening forms that contribute significantly to mortality rates due to associated wound infections. The management of burn wounds presents substantial challenges. Hydrogel exhibits tremendous potential as an ideal alternative to traditional wound dressings such as gauze. This is primarily attributed to its three-dimensional (3D) crosslinked polymer network, which possesses a high water content, fostering a moist environment that supports effective burn wound healing. Additionally, hydrogel facilitates the penetration of loaded therapeutic agents throughout the wound surface, combating burn wound pathogens through the hydration effect and thereby enhancing the healing process. However, the presence of eschar formation on burn wounds obstructs the passive diffusion of therapeutics, impairing the efficacy of hydrogel as a wound dressing, particularly in cases of severe burns involving deeper tissue damage. This review focuses on exploring the potential of hydrogel as a carrier for transdermal drug delivery in burn wound treatment. Furthermore, strategies aimed at enhancing the transdermal delivery of therapeutic agents from hydrogel to optimize burn wound healing are also discussed.

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推进烧伤创面治疗:探索水凝胶作为透皮给药系统。
烧伤是一种常见的危及生命的创伤,由于相关的伤口感染而大大增加了死亡率。烧伤伤口的处理面临着巨大的挑战。作为纱布等传统伤口敷料的理想替代品,水凝胶显示出巨大的潜力。这主要归功于其三维(3D)交联聚合物网络,该网络具有高含水量,可营造湿润的环境,从而支持烧伤伤口的有效愈合。此外,水凝胶还能促进载入的治疗剂渗透到整个创面,通过水合作用对抗烧伤创面的病原体,从而促进愈合过程。然而,烧伤伤口上形成的焦痂会阻碍治疗剂的被动扩散,从而影响水凝胶作为伤口敷料的功效,尤其是在涉及深层组织损伤的严重烧伤情况下。本综述重点探讨了水凝胶作为载体在烧伤创面治疗中透皮给药的潜力。此外,还讨论了旨在加强水凝胶透皮给药的策略,以优化烧伤伤口愈合。
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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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