尼奥体
脂质体
药物输送
药品
生物利用度
纳米技术
两亲性
材料科学
药理学
化学
膜
小泡
医学
聚合物
生物化学
共聚物
复合材料
作者
Mona Qushawy,Asma Massad Alenzi,Sana Abdulaziz Albalawi,Shatha G. Alghamdi,Rawan F. Albalawi,Hadeel Albalawi
标识
DOI:10.2174/1872210516666220228150624
摘要
Background: Colloidal dispersions, also known as vesicular drug delivery systems (VDDSs), are highly ordered assemblies composed of one or more concentric bilayers formed by the self-assembly of amphiphilic building blocks in the presence of water. Objectives: VDDSs are important to target the entrapped drugs at specific sites inside the body, control the drug release, enhance the drug bioavailability, and reduce undesired side effects. Methods: There are different types of VDDSs suitable for the entrapment of both hydrophilic and lipophilic drugs. According to the composition, VDDSs are classified into lipid-based and non-lipid-based VDDSs. Results: There are different types of VDDSs which include liposomes, ethosomes, transferosomes, ufasomes, colloidosomes, cubosomes, niosomes, bilosomes, aquasomes, etc. Conclusion: This review article aims to address the different types of VDDSs, their advantages and disadvantages, and their therapeutic applications.
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