Evaluation of Microemulsion and Lamellar Liquid Crystalline Systems for Transdermal Zidovudine Delivery

This study proposed to investigate and to compare colloidal carrier systems containing Zidovudine (3′-azido-3′-deoxythymidine) (AZT) for transdermal administration and optimization of antiretroviral therapy. Microemulsion (ME) and lamellar phase (LP) liquid crystal were obtained and selected from ps...

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Veröffentlicht in:Journal of pharmaceutical sciences 2016-07, Vol.105 (7), p.2188-2193
Hauptverfasser: Carvalho, André Luis Menezes, Silva, José Alexsandro da, Lira, Ana Amélia Moreira, Conceição, Tamara Matos Freire, Nunes, Rogéria de Souza, de Albuquerque Junior, Ricardo Luiz Cavalcanti, Sarmento, Victor Hugo Vitorino, Leal, Leila Bastos, de Santana, Davi Pereira
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Sprache:eng
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Zusammenfassung:This study proposed to investigate and to compare colloidal carrier systems containing Zidovudine (3′-azido-3′-deoxythymidine) (AZT) for transdermal administration and optimization of antiretroviral therapy. Microemulsion (ME) and lamellar phase (LP) liquid crystal were obtained and selected from pseudoternary diagrams previously developed. Small-angle X-ray scattering and rheology analysis confirmed the presence of typical ME and liquid crystalline structures with lamellar arrangement, respectively. Both colloidal carrier systems, ME, and LP remained stable, homogeneous, and isotropic after AZT addition. In vitro permeation study (using pig ear skin) showed that the amount of permeated drug was higher for ME compared to the control and LP, obtaining a permeation enhancing effect on the order of approximately 2-fold (p < 0.05). Microscopic examination after in vivo skin irritation studies using mice suggested few histological changes in the skin of animals treated with the ME compared to the control group (hydrogel). Thus, ME proved to be adequate and have promising effects, being able to promote the drug permeation without causing apparent skin irritation. On the order hand, LP functioned as a drug reservoir reducing AZT partitioning into the skin.
ISSN:0022-3549
1520-6017
DOI:10.1016/j.xphs.2016.04.013