Liposomal delivery enhances cutaneous availability of ciclopirox olamine

The present study involves development and investigation of liposomal system for improving skin residence of ciclopirox olamine in cutaneous mycosis. Spherical unilamellar liposomes of ciclopirox olamine were prepared by ethanol injection method. The vesicle size and % entrapment efficiency were i...

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Detalles Bibliográficos
Autores principales: Shaikh, Karimunnisa S., Pawar, Atmaram P.
Formato: Articulo
Lenguaje:Inglés
Publicado: 2010
Materias:
Acceso en línea:http://sedici.unlp.edu.ar/handle/10915/7979
http://www.latamjpharm.org/resumenes/29/5/LAJOP_29_5_1_18.pdf
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id I19-R120-10915-7979
record_format dspace
institution Universidad Nacional de La Plata
institution_str I-19
repository_str R-120
collection SEDICI (UNLP)
language Inglés
topic Farmacia
antifungal; cholesterol; liposome; skin residence; topical; unilamellar
Farmacología
Monitoreo de drogas
Resistencia a drogas
Enfermedades de la piel
spellingShingle Farmacia
antifungal; cholesterol; liposome; skin residence; topical; unilamellar
Farmacología
Monitoreo de drogas
Resistencia a drogas
Enfermedades de la piel
Shaikh, Karimunnisa S.
Pawar, Atmaram P.
Liposomal delivery enhances cutaneous availability of ciclopirox olamine
topic_facet Farmacia
antifungal; cholesterol; liposome; skin residence; topical; unilamellar
Farmacología
Monitoreo de drogas
Resistencia a drogas
Enfermedades de la piel
description The present study involves development and investigation of liposomal system for improving skin residence of ciclopirox olamine in cutaneous mycosis. Spherical unilamellar liposomes of ciclopirox olamine were prepared by ethanol injection method. The vesicle size and % entrapment efficiency were in the range of 196 ± 1.73 to 1040.66 ± 7.02 nm and 34.28 ± 4.4 to 54.89 ± 1.9 respectively. The electrokinetic potential varied from -52.4 ± 2.0 to -71.7 ± 1.3 mV. A 32 factorial design was utilized to optimize the concentrations of cholesterol and Phospholipon® 90H. Cholesterol was found to be primarily responsible for the behaviour of the liposomes as compared to the phospholipid. FTIR study revealed that liposomal encapsulation preserved the principal characteristic group of ciclopirox olamine required for antifungal action. In-vitro artificial membrane and ex-vivo excised rat skin studies demonstrated reasonably higher cutaneous deposition of the drug. Liposomes proved interesting tool for maximizing the drug retention in skin, an important requisite in treatment of cutaneous fungal infections.
format Articulo
Articulo
author Shaikh, Karimunnisa S.
Pawar, Atmaram P.
author_facet Shaikh, Karimunnisa S.
Pawar, Atmaram P.
author_sort Shaikh, Karimunnisa S.
title Liposomal delivery enhances cutaneous availability of ciclopirox olamine
title_short Liposomal delivery enhances cutaneous availability of ciclopirox olamine
title_full Liposomal delivery enhances cutaneous availability of ciclopirox olamine
title_fullStr Liposomal delivery enhances cutaneous availability of ciclopirox olamine
title_full_unstemmed Liposomal delivery enhances cutaneous availability of ciclopirox olamine
title_sort liposomal delivery enhances cutaneous availability of ciclopirox olamine
publishDate 2010
url http://sedici.unlp.edu.ar/handle/10915/7979
http://www.latamjpharm.org/resumenes/29/5/LAJOP_29_5_1_18.pdf
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