Liposome percutaneous penetration in vivo

Author:

Lymberopoulos A1,Demopoulou C2,Kyriazi M1,Katsarou MS1,Demertzis N1,Hatziandoniou S1,Maswadeh H1,Papaioanou G1,Demetzos C1,Maibach H3,Rallis M1

Affiliation:

1. Division of Pharmaceutical Technology, Department of Pharmacy, School of Health Sciences, National and Kapodistrian University of Athens, Panepistimiopolis, Athens, Greece

2. NCSR Demokritos, Institute of Radioisotopes and Radiodiagnostic Products, Agia Paraskevi, Athens, Greece

3. School of Medicine, University of California, San Francisco, CA, USA

Abstract

Objectives: Liposomes are reported as penetration enhancers for dermal and transdermal delivery. However, little is known about their percutaneous penetration and as to at which level they deliver encapsulated drugs. The penetration of multilamellar vesicles (MLVs) and small unilamellar vesicles (SUVs), in comparison to one of their lipid components, was investigated. Methods: Using the fluorescent lipid, Lissamine Rhodamine B-PE (R), as a constituent, MLV and SUV liposomes were prepared, tested, and R, MLV, or SUV were applied in vivo on the back of hairless mice. Absorption of each was evaluated at the levels of stratum corneum, living skin, and blood by fluorometry. Results: Penetration of the lipid R in stratum corneum in the nonliposomal form exceeded that in the liposomal form and only R penetrates the living skin in a statistically significant manner. No statistical significant absorption into blood was observed with either form. Conclusions: Liposomes size did not play an important role in penetration to stratum corneum. The lipid constituent in the nonliposomal form penetrated at higher rates into stratum corneum and living skin. Even though these liposomes entered stratum corneum, they were not significantly absorbed into viable skin or blood.

Publisher

SAGE Publications

Reference31 articles.

1. Aulton ME. Pharmaceutics: the design and manufacture of medicines. Edinburg Churchill Livingstone, 2007, p. 717.

2. Mezei M. Liposomes in drug delivery. Harwood Acedemic Publishers, 1993, pp. 124–135.

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