Formulation and evaluation of diclofenac emulgel using natural permeation enhancers

Background: This study aimed to formulate a stable diclofenac emulgel and determine the penetration rate using different natural penetration enhancers. Methodology: Carbopol (934) and Hydroxypropyl methyl cellulose (HPMC) were utilized as gelling agents due to their favorable viscosity characteristi...

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Main Authors: Chandra Sekhar Naik D, Shaik Noor Mahammed, Mudigedu Samreen, S. Vamsi, P. Hemalatha
Format: Article
Language:English
Published: Creative Pharma Assent 2025-04-01
Series:Journal of Applied Pharmaceutical Research
Subjects:
Online Access:https://japtronline.com/index.php/joapr/article/view/907
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author Chandra Sekhar Naik D
Shaik Noor Mahammed
Mudigedu Samreen
S. Vamsi
P. Hemalatha
author_facet Chandra Sekhar Naik D
Shaik Noor Mahammed
Mudigedu Samreen
S. Vamsi
P. Hemalatha
author_sort Chandra Sekhar Naik D
collection DOAJ
description Background: This study aimed to formulate a stable diclofenac emulgel and determine the penetration rate using different natural penetration enhancers. Methodology: Carbopol (934) and Hydroxypropyl methyl cellulose (HPMC) were utilized as gelling agents due to their favorable viscosity characteristics, which render them widely used for regulating the flow properties of topically administered dosage forms. In the research, diclofenac served as the active ingredient, while Carbopol (934) & HPMC (0.5%) acted as gelling forms to form a proper gel base. Emulsion contains Tween-20 (0.05%), PEG (0.6%), liquid paraffin (0.75%), span-20 (0.1%), along with natural penetration enhancers (0.3%) initially prepared gel base & the emulsion with natural penetration enhancers combine conjointly to shape an appropriate diclofenac emulgel. Results and discussion: According to the study, the improved batch exhibits a 95.08% release in 48 hours and remains stable for about three. The optimized batch exhibits 46.6% suppression in the microbiological assay, whereas the marketed treatment only demonstrates 32.3% inhibition. However, the skin irritation test results have no erythema or edema. The rabbits' skin showed no signs of discomfort. According to stability experiments, the synthesized emulgel's antifungal activity, rheological analysis, in vitro drug release, and physical appearance did not alter after three months of storage. Conclusion: Overall, it was recommended that, in contrast to cream, the emulgel formulation come after the drug release for controlled, long-term drug delivery.
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spelling doaj-art-cc38d4aa54294b989bbac01ceb8fbd122025-08-20T01:50:18ZengCreative Pharma AssentJournal of Applied Pharmaceutical Research2348-03352025-04-0113210811410.69857/joapr.v13i2.907908Formulation and evaluation of diclofenac emulgel using natural permeation enhancersChandra Sekhar Naik D0Shaik Noor Mahammed1Mudigedu Samreen2S. Vamsi3P. Hemalatha4Department of Pharmaceutics, Nimra College of Pharmacy, Ibrahimpatnam, Vijayawada, Andhra Pradesh, IndiaDepartment of Pharmaceutics, Nimra College of Pharmacy, Ibrahimpatnam, Vijayawada, Andhra Pradesh, IndiaDepartment of Pharmaceutics, Nimra College of Pharmacy, Ibrahimpatnam, Vijayawada, Andhra Pradesh, IndiaDepartment of Pharmaceutics, Nimra College of Pharmacy, Ibrahimpatnam, Vijayawada, Andhra Pradesh, IndiaDepartment of Pharmaceutics, Nimra College of Pharmacy, Ibrahimpatnam, Vijayawada, Andhra Pradesh, IndiaBackground: This study aimed to formulate a stable diclofenac emulgel and determine the penetration rate using different natural penetration enhancers. Methodology: Carbopol (934) and Hydroxypropyl methyl cellulose (HPMC) were utilized as gelling agents due to their favorable viscosity characteristics, which render them widely used for regulating the flow properties of topically administered dosage forms. In the research, diclofenac served as the active ingredient, while Carbopol (934) & HPMC (0.5%) acted as gelling forms to form a proper gel base. Emulsion contains Tween-20 (0.05%), PEG (0.6%), liquid paraffin (0.75%), span-20 (0.1%), along with natural penetration enhancers (0.3%) initially prepared gel base & the emulsion with natural penetration enhancers combine conjointly to shape an appropriate diclofenac emulgel. Results and discussion: According to the study, the improved batch exhibits a 95.08% release in 48 hours and remains stable for about three. The optimized batch exhibits 46.6% suppression in the microbiological assay, whereas the marketed treatment only demonstrates 32.3% inhibition. However, the skin irritation test results have no erythema or edema. The rabbits' skin showed no signs of discomfort. According to stability experiments, the synthesized emulgel's antifungal activity, rheological analysis, in vitro drug release, and physical appearance did not alter after three months of storage. Conclusion: Overall, it was recommended that, in contrast to cream, the emulgel formulation come after the drug release for controlled, long-term drug delivery.https://japtronline.com/index.php/joapr/article/view/907emulgeldiclofenacfactorial designcounter plots3d surface plots
spellingShingle Chandra Sekhar Naik D
Shaik Noor Mahammed
Mudigedu Samreen
S. Vamsi
P. Hemalatha
Formulation and evaluation of diclofenac emulgel using natural permeation enhancers
Journal of Applied Pharmaceutical Research
emulgel
diclofenac
factorial design
counter plots
3d surface plots
title Formulation and evaluation of diclofenac emulgel using natural permeation enhancers
title_full Formulation and evaluation of diclofenac emulgel using natural permeation enhancers
title_fullStr Formulation and evaluation of diclofenac emulgel using natural permeation enhancers
title_full_unstemmed Formulation and evaluation of diclofenac emulgel using natural permeation enhancers
title_short Formulation and evaluation of diclofenac emulgel using natural permeation enhancers
title_sort formulation and evaluation of diclofenac emulgel using natural permeation enhancers
topic emulgel
diclofenac
factorial design
counter plots
3d surface plots
url https://japtronline.com/index.php/joapr/article/view/907
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AT mudigedusamreen formulationandevaluationofdiclofenacemulgelusingnaturalpermeationenhancers
AT svamsi formulationandevaluationofdiclofenacemulgelusingnaturalpermeationenhancers
AT phemalatha formulationandevaluationofdiclofenacemulgelusingnaturalpermeationenhancers