Skin Permeation Enhancers and their Effects on Narcotic Transdermal Drug Delivery Systems through Response Surface Experimental Design

Drug delivery through skin is often obstructed by low permeability of skin towards most drugs; however, such problem would be solved by application of skin penetration enhancers in the formulations. In the present study, a drug in adhesive patch with buprenorphine as active ingredient was prepared....

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Main Authors: A. Moghimi, S.M. Taghizadeh
Format: Article
Language:fas
Published: Iran Polymer and Petrochemical Institute 2014-02-01
Series:علوم و تکنولوژی پلیمر
Subjects:
Online Access:http://jips.ippi.ac.ir/article_998_5ce213ca230d6d3c41d101aead323999.pdf
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author A. Moghimi
S.M. Taghizadeh
author_facet A. Moghimi
S.M. Taghizadeh
author_sort A. Moghimi
collection DOAJ
description Drug delivery through skin is often obstructed by low permeability of skin towards most drugs; however, such problem would be solved by application of skin penetration enhancers in the formulations. In the present study, a drug in adhesive patch with buprenorphine as active ingredient was prepared. Drug-in-adhesive transdermal drug delivery systems with different chemical penetration enhancers were designed. For this purpose a response-surface experimental design was used. Response surface methodology based on a three-level, three-variable Box–Behnken design was used to evaluate the interactive effects of dependent variables such as: the rate of skin permeation and adhesion properties including peel strength and tack value. The parameters such as drug release and adhesion were used as independent variables. Levulinic acid, lauryl alcohol and Tween 80 were used as penetration enhancers. In order to prepare samples, buprenorphine with constant concentration was incorporated into acrylic pressure sensitive adhesive with carboxylic functionality and this mixture was added to chemical penetration enhancer with different concentrations. The results show that the cumulative amount of drug release in presence of Tween 80 is 462.9 ± 0.006 μg so it is higher than cumulative amount of drug release in presence of levulinic acid (357.9 ± 0.005 μg) and lauryl alcohol (269.5 ± 0.001 μg). Results of adhesion properties such as peel strength and tack reveal that using levulinic acid and lauryl alcohol will increase peel strength while Tween 80 will decrease it. Besides, the results show that all these permeation enhancers have increased tack values.
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spelling doaj.art-297ffaef76a44682acd068aa206728992022-12-21T20:12:33ZfasIran Polymer and Petrochemical Instituteعلوم و تکنولوژی پلیمر1016-32552008-08832014-02-0126647345910.22063/jipst.2014.998998Skin Permeation Enhancers and their Effects on Narcotic Transdermal Drug Delivery Systems through Response Surface Experimental DesignA. Moghimi0S.M. Taghizadeh1Iran Polymer and Petrochemical Institute, P.O. Box: 14965-115, Tehran, IranIran Polymer and Petrochemical Institute, P.O. Box: 14965-115, Tehran, IranDrug delivery through skin is often obstructed by low permeability of skin towards most drugs; however, such problem would be solved by application of skin penetration enhancers in the formulations. In the present study, a drug in adhesive patch with buprenorphine as active ingredient was prepared. Drug-in-adhesive transdermal drug delivery systems with different chemical penetration enhancers were designed. For this purpose a response-surface experimental design was used. Response surface methodology based on a three-level, three-variable Box–Behnken design was used to evaluate the interactive effects of dependent variables such as: the rate of skin permeation and adhesion properties including peel strength and tack value. The parameters such as drug release and adhesion were used as independent variables. Levulinic acid, lauryl alcohol and Tween 80 were used as penetration enhancers. In order to prepare samples, buprenorphine with constant concentration was incorporated into acrylic pressure sensitive adhesive with carboxylic functionality and this mixture was added to chemical penetration enhancer with different concentrations. The results show that the cumulative amount of drug release in presence of Tween 80 is 462.9 ± 0.006 μg so it is higher than cumulative amount of drug release in presence of levulinic acid (357.9 ± 0.005 μg) and lauryl alcohol (269.5 ± 0.001 μg). Results of adhesion properties such as peel strength and tack reveal that using levulinic acid and lauryl alcohol will increase peel strength while Tween 80 will decrease it. Besides, the results show that all these permeation enhancers have increased tack values.http://jips.ippi.ac.ir/article_998_5ce213ca230d6d3c41d101aead323999.pdfbuprenorphineskin permeation enhancerexperimental designdrug releaseadhesion properties
spellingShingle A. Moghimi
S.M. Taghizadeh
Skin Permeation Enhancers and their Effects on Narcotic Transdermal Drug Delivery Systems through Response Surface Experimental Design
علوم و تکنولوژی پلیمر
buprenorphine
skin permeation enhancer
experimental design
drug release
adhesion properties
title Skin Permeation Enhancers and their Effects on Narcotic Transdermal Drug Delivery Systems through Response Surface Experimental Design
title_full Skin Permeation Enhancers and their Effects on Narcotic Transdermal Drug Delivery Systems through Response Surface Experimental Design
title_fullStr Skin Permeation Enhancers and their Effects on Narcotic Transdermal Drug Delivery Systems through Response Surface Experimental Design
title_full_unstemmed Skin Permeation Enhancers and their Effects on Narcotic Transdermal Drug Delivery Systems through Response Surface Experimental Design
title_short Skin Permeation Enhancers and their Effects on Narcotic Transdermal Drug Delivery Systems through Response Surface Experimental Design
title_sort skin permeation enhancers and their effects on narcotic transdermal drug delivery systems through response surface experimental design
topic buprenorphine
skin permeation enhancer
experimental design
drug release
adhesion properties
url http://jips.ippi.ac.ir/article_998_5ce213ca230d6d3c41d101aead323999.pdf
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