Enhancement of Skin Delivery of Drugs Using Proposome Depends on Drug Lipophilicity

The study aims to investigate the propylene glycol-based liposomes named 'proposomes' in enhancing skin permeation of drugs with different physicochemical properties. Ibuprofen, tofacitinib citrate, rhodamine B, and lidocaine were loaded into proposomes. These drug formulations were analyzed for particle size, zeta potential, polydispersity index, entrapment efficiency, and in vitro skin permeation. The confocal laser scanning microscopy was performed on skin treated with calcein and rhodamine B laden proposomes. The transdermal delivery relative to physicochemical properties of drugs such as logP, melting point, molecular weight, solubility, etc., were analyzed. We tested the safety of the proposomes using reconstructed human skin tissue equivalents, which were fabricated in-house. We also used human cadaver skin samples as a control. The proposomes had an average diameter of 128 to 148 nm. The drug's entrapment efficiencies were in the range of 42.9-52.7%, translating into the significant enhancement of drug permeation through the skin. The enhancement ratio was 1.4 to 4.0, and linearly correlated to logP, molecular weight, and melting point. Confocal imaging also showed higher skin permeation of calcein and rhodamine B in proposome than in solution. The proposome was found safe for skin application. The enhancement of skin delivery of drugs through proposomes was dependent on the lipophilicity of the drug. The entrapment efficiency was positively correlated with logP of the drug, which led to high drug absorption.

Automated summary

The study aimed to investigate the role of propylene glycol-based liposomes named 'proposomes' in enhancing skin permeation of drugs with different physicochemical properties. The results showed that proposomes significantly enhanced drug permeation through the skin, with enhancement ratio linearly correlated to drug's logP, molecular weight, and melting point. Confocal imaging demonstrated higher skin permeation of drugs in proposomes compared to solution, with proposomes found safe for skin application. The entrapment efficiency of drugs in proposomes was positively correlated with drug's logP, leading to high drug absorption.