全面分析用于治疗皮肤和软组织感染的脂质体纳米载体

Dyala M Khasawneh, Rami J Oweis, Mo'tasem Alsmadi
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摘要

细菌性皮肤和软组织感染(SSTI)是皮肤和深层组织的广泛微生物入侵。局部给药系统是治疗 SSTI 最受欢迎的给药途径。这是因为外用给药系统诱发全身性不良反应的风险极低,可减少细菌耐药性的产生,而且易于使用。然而,它们也有一些缺点,包括对药物释放曲线缺乏控制、皮肤刺激以及某些化合物在皮肤中的渗透性有限。为了解决这些局限性,人们开发了几种纳米载体系统,其中纳米脂质体是用于局部治疗 SSTI 的主要给药系统。尽管在过去十年中对脂质体进行了大量研究,但在设计这些专门用于 SSTI 的载体的详细知识方面仍然存在差距。因此,我们迫切需要开展全面的研究,重点关注纳米脂质体在治疗 SSTI 方面的应用,并广泛了解 SSTI 和脂质体制剂。本综述探讨了细菌性 SSTI,涵盖其流行病学、分类、微生物学和管理。它强调了基于脂质体的纳米颗粒在加强局部给药抗生素和天然抗菌化合物以治疗 SSTI 方面的贡献。报告还深入探讨了脂质体配方变化对疾病治疗效果的影响。此外,它还提供了将脂质体的特性与感染类型、深度、性质和致病因子相匹配的指南。这标志着药物设计、开发和递送领域的重大飞跃。
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A Comprehensive Analysis of Liposomal-Based Nanocarriers for Treating Skin and Soft Tissue Infection.

Bacterial skin and soft tissue infections (SSTIs) are widespread microbic invasions of the skin and deeper tissues. Topical drug delivery systems are the most favored administration pathway when treating SSTIs. This is down to their minimal risk of inducing systemic adverse events, reduced development of bacterial resistance, and ease of application. However, they have several drawbacks, including the lack of control over the drug release profile, skin irritations, and the limited permeability of certain compounds through the skin. To address these limitations, several nanocarrier systems were developed, with nanoliposomes standing out as the leading delivery system for the topical management of SSTIs. Despite considerable research into liposomes over the past decade, there remains a gap in detailed knowledge about designing these carriers specifically for SSTIs. Consequently, there is a pressing need for comprehensive research that focuses on the use of nanoliposomes for SSTIs and offers an extensive understanding of both SSTIs and liposomal formulations. This review explores bacterial SSTIs, covering their epidemiology, classification, microbiology, and management. It emphasizes the contribution of liposome-based nanovesicles in enhancing the local administration of antibiotics and natural antibacterial compounds for SSTI management. It also delves into the effects of liposomal formulation changes on the disease therapeutic outcomes. Additionally, it provides a guide for aligning the characteristics of the liposomes with the infection types, depths, properties, and causative agents. This signifies a substantial leap forward in the domains of drug design, development, and delivery.

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