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2000
Volume 17, Issue 1
  • ISSN: 1872-2105
  • E-ISSN: 2212-4020

Abstract

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. Objective: 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 patent composition, VDDSs are classified into lipid-based and nonlipid- 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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/content/journals/nanotec/10.2174/1872210516666220228150624
2023-03-01
2025-10-06
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/content/journals/nanotec/10.2174/1872210516666220228150624
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  • Article Type:
    Review Article
Keyword(s): bioavailability; colloidal dispersion; Drug delivery; drug targeting; liposomes; niosomes
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