In vitro/in vivo assessment of flurbiprofen-matrix type transdermal delivery system

In this study, matrix type patch formulations of flurbiprofen using certain skin permeation enhancers [isopropyl myristate (IPM), isopropyl palmitate (IPP) and Tween 80] were formulated, evaluated and compared. The cumulative amounts permeated and the permeation rates were higher for the prepared...

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Autores principales: Aamir, Muhammad F., Ahmad, Mahmood, Murtaza, Ghulam, Khan, Shujaat A.
Formato: Articulo
Lenguaje:Inglés
Publicado: 2011
Materias:
Acceso en línea:http://sedici.unlp.edu.ar/handle/10915/8139
http://www.latamjpharm.org/resumenes/30/2/LAJOP_30_2_1_15.pdf
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id I19-R120-10915-8139
record_format dspace
institution Universidad Nacional de La Plata
institution_str I-19
repository_str R-120
collection SEDICI (UNLP)
language Inglés
topic Farmacia
flurbiprofen; permeation enhancer; permeation studies; pharmacokinetics
Fenómenos Farmacológicos
Agentes Antiinflamatorios no Esteroides
spellingShingle Farmacia
flurbiprofen; permeation enhancer; permeation studies; pharmacokinetics
Fenómenos Farmacológicos
Agentes Antiinflamatorios no Esteroides
Aamir, Muhammad F.
Ahmad, Mahmood
Murtaza, Ghulam
Khan, Shujaat A.
In vitro/in vivo assessment of flurbiprofen-matrix type transdermal delivery system
topic_facet Farmacia
flurbiprofen; permeation enhancer; permeation studies; pharmacokinetics
Fenómenos Farmacológicos
Agentes Antiinflamatorios no Esteroides
description In this study, matrix type patch formulations of flurbiprofen using certain skin permeation enhancers [isopropyl myristate (IPM), isopropyl palmitate (IPP) and Tween 80] were formulated, evaluated and compared. The cumulative amounts permeated and the permeation rates were higher for the prepared formulations as compared to the controls (without enhancers). The results also revealed better skin permeation characteristics of flurbiprofen using IPM than other enhancers. The pharmacokinetic parameters of the optimized formulation (F7), calculated from the blood levels of the drug, revealed a profile with the ability to maintain adequate plasma levels for 24 h (i.e. up to the next application): AUC<sub>(0-24)</sub> 10.406 ± 1.34ng.h/ml, T<sub>max</sub> 1.5 ± 0.91 and C<sub>max</sub> 1.3049 ± 0.21 µg.ml<sup>-1</sup>-. The amount of drug bioavailable for targeting the site of action is comparable to that of market control. Based on experimental results, preparation of 10 % flurbiprofen matrix type patch formulation containing IPM is promising
format Articulo
Articulo
author Aamir, Muhammad F.
Ahmad, Mahmood
Murtaza, Ghulam
Khan, Shujaat A.
author_facet Aamir, Muhammad F.
Ahmad, Mahmood
Murtaza, Ghulam
Khan, Shujaat A.
author_sort Aamir, Muhammad F.
title In vitro/in vivo assessment of flurbiprofen-matrix type transdermal delivery system
title_short In vitro/in vivo assessment of flurbiprofen-matrix type transdermal delivery system
title_full In vitro/in vivo assessment of flurbiprofen-matrix type transdermal delivery system
title_fullStr In vitro/in vivo assessment of flurbiprofen-matrix type transdermal delivery system
title_full_unstemmed In vitro/in vivo assessment of flurbiprofen-matrix type transdermal delivery system
title_sort in vitro/in vivo assessment of flurbiprofen-matrix type transdermal delivery system
publishDate 2011
url http://sedici.unlp.edu.ar/handle/10915/8139
http://www.latamjpharm.org/resumenes/30/2/LAJOP_30_2_1_15.pdf
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