Statistical optimization of compression coated ketoprofen tablet using amylose/ethyl cellulose mixture for colonic delivery

In the present study the effect of two independent factors (amount of ethyl cellulose in coating layer and coating level) on ketoprofen release from compression coated tablet in order to optimize coated tablet for colonic delivery. 3 2 factorial design was used for designing coated formulation. Amou...

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Main Authors: Nirmala Devi, Manju Sharma
Format: Article
Language:English
Published: Creative Pharma Assent 2015-01-01
Series:Journal of Applied Pharmaceutical Research
Subjects:
Online Access:https://japtronline.com/index.php/joapr/article/view/41
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spelling doaj-cb7cc6646b5d4a61be4209ed72cc3a2a2021-09-11T15:17:00ZengCreative Pharma AssentJournal of Applied Pharmaceutical Research2348-03352015-01-0131101741Statistical optimization of compression coated ketoprofen tablet using amylose/ethyl cellulose mixture for colonic deliveryNirmala Devi0Manju Sharma1Shridhar University Pilani-Chirawa Road, Pilani-333 031 (Rajasthan)Faculty of Pharmacy, Hamdard University,New DelhiIn the present study the effect of two independent factors (amount of ethyl cellulose in coating layer and coating level) on ketoprofen release from compression coated tablet in order to optimize coated tablet for colonic delivery. 3 2 factorial design was used for designing coated formulation. Amount of ethyl cellulose (X1) and coating level (X2) were selected as independent variables. The studied responses were drug release at 5 hr (Y1) and drug release at 10 hr (Y2). The core tablets were compression coated with different ratio of amylose and ethylcellulose. In vitro drug release study was carried out in pH1.2 for 2 hr, pH 7.4 for 3 hr and goat caecal medium for 5 hr. Drug release revealed that amount of ethyl cellulose and coating level have antagonistic effect on drug release. Multiple regression analysis was used for generation of polynomial equation and optimization of formulation. The optimized formulation consisted of ethyl cellulose (14.33 %) and coating level (318 mg) provided a release profile that is closed to estimated values. The model is found to be accurate and robust for optimization of compression-coated tablet for colonic delivery of ketoprofenhttps://japtronline.com/index.php/joapr/article/view/41colon drug deliveryfactorial designindependent variablesmultiple linear regressionoptimization
collection DOAJ
language English
format Article
sources DOAJ
author Nirmala Devi
Manju Sharma
spellingShingle Nirmala Devi
Manju Sharma
Statistical optimization of compression coated ketoprofen tablet using amylose/ethyl cellulose mixture for colonic delivery
Journal of Applied Pharmaceutical Research
colon drug delivery
factorial design
independent variables
multiple linear regression
optimization
author_facet Nirmala Devi
Manju Sharma
author_sort Nirmala Devi
title Statistical optimization of compression coated ketoprofen tablet using amylose/ethyl cellulose mixture for colonic delivery
title_short Statistical optimization of compression coated ketoprofen tablet using amylose/ethyl cellulose mixture for colonic delivery
title_full Statistical optimization of compression coated ketoprofen tablet using amylose/ethyl cellulose mixture for colonic delivery
title_fullStr Statistical optimization of compression coated ketoprofen tablet using amylose/ethyl cellulose mixture for colonic delivery
title_full_unstemmed Statistical optimization of compression coated ketoprofen tablet using amylose/ethyl cellulose mixture for colonic delivery
title_sort statistical optimization of compression coated ketoprofen tablet using amylose/ethyl cellulose mixture for colonic delivery
publisher Creative Pharma Assent
series Journal of Applied Pharmaceutical Research
issn 2348-0335
publishDate 2015-01-01
description In the present study the effect of two independent factors (amount of ethyl cellulose in coating layer and coating level) on ketoprofen release from compression coated tablet in order to optimize coated tablet for colonic delivery. 3 2 factorial design was used for designing coated formulation. Amount of ethyl cellulose (X1) and coating level (X2) were selected as independent variables. The studied responses were drug release at 5 hr (Y1) and drug release at 10 hr (Y2). The core tablets were compression coated with different ratio of amylose and ethylcellulose. In vitro drug release study was carried out in pH1.2 for 2 hr, pH 7.4 for 3 hr and goat caecal medium for 5 hr. Drug release revealed that amount of ethyl cellulose and coating level have antagonistic effect on drug release. Multiple regression analysis was used for generation of polynomial equation and optimization of formulation. The optimized formulation consisted of ethyl cellulose (14.33 %) and coating level (318 mg) provided a release profile that is closed to estimated values. The model is found to be accurate and robust for optimization of compression-coated tablet for colonic delivery of ketoprofen
topic colon drug delivery
factorial design
independent variables
multiple linear regression
optimization
url https://japtronline.com/index.php/joapr/article/view/41
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