Registro completo |
Provedor de dados: |
BJPS
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País: |
Brazil
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Título: |
Influence of ceramide 2 on in vitro skin permeation and retention of 5-ALA and its ester derivatives, for Photodynamic Therapy
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Autores: |
Pierre,Maria Bernadete Riemma
Lopez,Renata Fonseca Vianna
Bentley,Maria Vitória Lopes Badra
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Data: |
2009-03-01
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Ano: |
2009
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Palavras-chave: |
5-aminolevulinic acid
Ceramide 2
In vitro/Skin permeation
In vitro/Skin retention
Photodynamic therapy
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Resumo: |
Photodynamic therapy (PDT) based on topical 5-aminolevulinic acid (5-ALA), an endogenous precursor of protoporphyrin, is an interesting approach for the treatment of skin cancer. However, 5-ALA is a hydrophilic molecule and such a characteristic limits its appropriate cutaneous penetration and retention. In this way, more lipophilic molecules, such as esterified 5-ALA derivatives, have been under investigation in order to improve the skin penetration of this molecule. Drug formulation can also alter 5-ALA skin penetration. Therefore, the aim of this work was to study the influence of ceramide 2 - the main lipid of the SC- on the cutaneous delivery of 5-ALA and its ester derivatives in vitro, using Franz diffusion cell. The skin permeation of all studied drugs was decreased in the presence of ceramide, representing a desirable characteristic in order to avoid the risk of systemic side effects. Nevertheless, the SC and [epidermis + dermis] retention after 16 h has also been decreased in the presence of ceramide, as compared to control. In conclusion, ceramide was not a good adjuvant, meaning that research of other vehicles could be useful to improve cutaneous delivery of 5-ALA.
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Tipo: |
Info:eu-repo/semantics/article
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Idioma: |
Inglês
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Identificador: |
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1984-82502009000100013
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Editor: |
Universidade de São Paulo, Faculdade de Ciências Farmacêuticas
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Relação: |
10.1590/S1984-82502009000100013
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Formato: |
text/html
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Fonte: |
Brazilian Journal of Pharmaceutical Sciences v.45 n.1 2009
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Direitos: |
info:eu-repo/semantics/openAccess
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