[Research advances of liposomes and exosomes in drug delivery and biomarker screening]
- PMID: 40331611
- PMCID: PMC12059997
- DOI: 10.3724/SP.J.1123.2024.08012
[Research advances of liposomes and exosomes in drug delivery and biomarker screening]
Abstract
Vesicles, are categorized as artificial (i.e., liposomes) or natural (i.e., extracellular vesicles (EVs)) and play significant roles in drug-delivery and biomarker-screening applications. Liposomes, as a representative form of artificial vesicle, are spherical lipid structures composed of one or more artificially synthesized phospholipid bilayers. Liposomes are highly biocompatible and bioavailable, very stable, and easily synthesized; hence, they are among the most commonly used and frequently applied nanocarriers in targeted drug-delivery systems (DDS). EVs are natural small membrane-bound vesicles actively secreted by cells and contain a variety of components, including nucleic acids, proteins, and lipids. They also serve as important mediators of intercellular communication. As the smallest EV subtype, with diameters of only 30-100 nm, exosomes contain unique biomolecules that are considered to be the fingerprints of the parent cells. In the pathological state, the content of exosomes will change; consequently, exosomes are potential disease-diagnosis biomarkers. Recent clinical trials have shown that exosomes are ideal nanocarriers in targeted drug-delivery therapies for a variety of diseases. Compared with traditional artificial liposomal carriers, exosomes display unique advantages and provide the DDS field with new possibilities. Liposomes and exosomes are receiving increasing levels of attention in the drug-delivery and biomarker-screening fields. This article introduces techniques for the preparation of liposomes, and the enrichment and separation of exosomes, and delves into research progress on their use in drug-delivery and biomarker-screening applications. Finally, challenges facing the use of liposomes and exosomes in clinical applications are discussed.
囊泡分为人工囊泡和天然囊泡。其中,人工囊泡的一种代表性形式是脂质体,它们是由人工合成的,由一个或多个磷脂双分子层构成的球形脂质结构。脂质体的生物相容性和生物利用度较高,稳定性好且易于合成,是靶向药物递送系统(DDS)中常用的纳米载体之一,使用频率较高。作为一种天然囊泡,细胞外囊泡(EVs)是由细胞主动分泌的一种具有膜结构的微小囊泡,内含核酸、蛋白质及脂类等多种成分,是细胞间通信的重要媒介。外泌体是EVs中的最小亚型,直径为30~100 nm,内含独特的生物分子,这些分子可被视为亲代细胞的“指纹”。在病理状态下,外泌体的含量会发生变化,因此被视为诊断疾病的潜在生物标志物。近年来,脂质体与外泌体在药物递送和生物标志物筛选领域日益受到关注。本文介绍了脂质体的制备技术及外泌体的富集分离技术,并深入探讨了它们在药物递送及生物标志物筛选方面的研究进展。最后,文章提出了脂质体与外泌体在临床应用中所面临的挑战。
Keywords: biomarker screening; drug delivery; enrichment and separation; exosomes; liposomes; review; vesicles.
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