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Investigation of the ex vivo and in vivo iontophoretic delivery of aceclofenac from topical gels in Albino rats

INTRODUCTION: Iontophoresis was used to enhance the delivery of aceclofenac (ACF) from topical gels formulated with various polymers for the purpose of relieving pain and inflammation. MATERIALS AND METHODS: Gels were formulated from hydroxypropyl methyl cellulose (HPMC), carbopol 934P, and sodium c...

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Autores principales: Bhatt, Bhavik, Koland, Marina, Shama, K Prasanna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3757900/
https://www.ncbi.nlm.nih.gov/pubmed/24015382
http://dx.doi.org/10.4103/2230-973X.114896
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author Bhatt, Bhavik
Koland, Marina
Shama, K Prasanna
author_facet Bhatt, Bhavik
Koland, Marina
Shama, K Prasanna
author_sort Bhatt, Bhavik
collection PubMed
description INTRODUCTION: Iontophoresis was used to enhance the delivery of aceclofenac (ACF) from topical gels formulated with various polymers for the purpose of relieving pain and inflammation. MATERIALS AND METHODS: Gels were formulated from hydroxypropyl methyl cellulose (HPMC), carbopol 934P, and sodium carboxymethyl cellulose (NaCMC). The formulations were evaluated for cathodal iontophoretic delivery of ACF through excised rat abdominal skin at three levels of current density of 0.5, 0.6 and 0.7 mA/cm(2). The in vivo effectiveness of the drug delivered passively as well as under the influence of iontophoresis at pH 7.4 at a current density of 0.5 mA/cm(2) was also investigated using male Albino rats with carrageenan induced paw edema. RESULTS AND DISCUSSION: In the ex vivo studies, though it was clear that iontophoresis significantly increased drug permeation through the excised skin from all formulations; the percentage drug permeated from HPMC gels was superior to that from carbopol 934P or NaCMC gels but increased with an increase in the current density only for the former. The steady state flux, permeability coefficient, enhancement factor were significantly greater from HPMC gels than from the gels of the ionic polymers due to the interference of competitive ions. With iontophoresis, the carrageenan induced paw edema was significantly reduced by 61.53% (P < 0.01) for HPMC gels as compared to the control although passive permeation without iontophoresis showed a 54.6% reduction (P < 0.05) at the end of 4 h. CONCLUSION: The results of the study indicate that ACF could be administered topically by using iontophoresis from a suitably formulated gel for effective control of pain and inflammation.
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spelling pubmed-37579002013-09-06 Investigation of the ex vivo and in vivo iontophoretic delivery of aceclofenac from topical gels in Albino rats Bhatt, Bhavik Koland, Marina Shama, K Prasanna Int J Pharm Investig Original Research Article INTRODUCTION: Iontophoresis was used to enhance the delivery of aceclofenac (ACF) from topical gels formulated with various polymers for the purpose of relieving pain and inflammation. MATERIALS AND METHODS: Gels were formulated from hydroxypropyl methyl cellulose (HPMC), carbopol 934P, and sodium carboxymethyl cellulose (NaCMC). The formulations were evaluated for cathodal iontophoretic delivery of ACF through excised rat abdominal skin at three levels of current density of 0.5, 0.6 and 0.7 mA/cm(2). The in vivo effectiveness of the drug delivered passively as well as under the influence of iontophoresis at pH 7.4 at a current density of 0.5 mA/cm(2) was also investigated using male Albino rats with carrageenan induced paw edema. RESULTS AND DISCUSSION: In the ex vivo studies, though it was clear that iontophoresis significantly increased drug permeation through the excised skin from all formulations; the percentage drug permeated from HPMC gels was superior to that from carbopol 934P or NaCMC gels but increased with an increase in the current density only for the former. The steady state flux, permeability coefficient, enhancement factor were significantly greater from HPMC gels than from the gels of the ionic polymers due to the interference of competitive ions. With iontophoresis, the carrageenan induced paw edema was significantly reduced by 61.53% (P < 0.01) for HPMC gels as compared to the control although passive permeation without iontophoresis showed a 54.6% reduction (P < 0.05) at the end of 4 h. CONCLUSION: The results of the study indicate that ACF could be administered topically by using iontophoresis from a suitably formulated gel for effective control of pain and inflammation. Medknow Publications & Media Pvt Ltd 2013 /pmc/articles/PMC3757900/ /pubmed/24015382 http://dx.doi.org/10.4103/2230-973X.114896 Text en Copyright: © International Journal of Pharmaceutical Investigation http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research Article
Bhatt, Bhavik
Koland, Marina
Shama, K Prasanna
Investigation of the ex vivo and in vivo iontophoretic delivery of aceclofenac from topical gels in Albino rats
title Investigation of the ex vivo and in vivo iontophoretic delivery of aceclofenac from topical gels in Albino rats
title_full Investigation of the ex vivo and in vivo iontophoretic delivery of aceclofenac from topical gels in Albino rats
title_fullStr Investigation of the ex vivo and in vivo iontophoretic delivery of aceclofenac from topical gels in Albino rats
title_full_unstemmed Investigation of the ex vivo and in vivo iontophoretic delivery of aceclofenac from topical gels in Albino rats
title_short Investigation of the ex vivo and in vivo iontophoretic delivery of aceclofenac from topical gels in Albino rats
title_sort investigation of the ex vivo and in vivo iontophoretic delivery of aceclofenac from topical gels in albino rats
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3757900/
https://www.ncbi.nlm.nih.gov/pubmed/24015382
http://dx.doi.org/10.4103/2230-973X.114896
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