Abstract Liposomes, spherical vesicles made of phospholipids and cholesterol, have captivated researchers for their encapsulation abilities, biocompatibility, and versatility. This review delves into the core aspects and benefits of liposomal technology for enhancing transdermal drug delivery in treating skin dermatosis. It offers an extensive overview of liposomes, emphasizing various preparation methods, classification, and encapsulation techniques. The encapsulation of therapeutic compounds by liposomes boosts their utility as a stable and efficient drug delivery vehicle. Transdermal delivery presents a non-invasive alternative to oral and parenteral routes, allowing for controlled and sustained release of drugs while bypassing hepatic first-pass metabolism and minimizing systemic side effects. However, the stratum corneum acts as a formidable barrier to drug permeation. Liposomes, owing to their lipid bilayer structure that mimics skin composition, enhance drug solubility and partitioning, facilitate deeper skin penetration, and improve therapeutic efficacy, making them ideal carriers for transdermal applications. Transdermal delivery, favoured for its active and passive approaches and advantages over topical delivery, has been extensively studied and employed for therapeutics. Liposomes as delivery vehicles have significantly improved drug delivery efficiency and stability in transdermal applications. This review comprehensively examines the utility and mechanistic applications of liposomes. It also addresses the limitations and challenges in liposomal formulation that must be overcome for successful clinical trials. Graphical abstract
Choudhury et al. (Thu,) studied this question.