Analysis of Dissolution of Salicylamide from Carrageenan Based Hard-Shell Capsules: A Study of the Drug-Matrix Interaction

In drug release kinetics, the drug-matrix interaction is one of the important mechanisms to be dictated. Unfortunately, there is still minimum information discussing the effect of interaction between a drug and its matrix to the release profile of the drug. Therefore, there is an urgent need to cond...

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Autores principales: Muhammad Al Rizqi Dharma Fauzi, Esti Hendradi, Pratiwi Pudjiastuti, Riyanto Teguh Widodo
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Lenguaje:EN
Publicado: Department of Chemistry, Universitas Gadjah Mada 2020
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Acceso en línea:https://doaj.org/article/87754166cc6946c1bb1e2e1724d2d20f
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spelling oai:doaj.org-article:87754166cc6946c1bb1e2e1724d2d20f2021-12-02T14:00:19ZAnalysis of Dissolution of Salicylamide from Carrageenan Based Hard-Shell Capsules: A Study of the Drug-Matrix Interaction1411-94202460-157810.22146/ijc.55047https://doaj.org/article/87754166cc6946c1bb1e2e1724d2d20f2020-11-01T00:00:00Zhttps://jurnal.ugm.ac.id/ijc/article/view/55047https://doaj.org/toc/1411-9420https://doaj.org/toc/2460-1578In drug release kinetics, the drug-matrix interaction is one of the important mechanisms to be dictated. Unfortunately, there is still minimum information discussing the effect of interaction between a drug and its matrix to the release profile of the drug. Therefore, there is an urgent need to conduct research related to the study of drug-matrix interaction. This paper reports the preparation of a drug delivery system (DDS) in the form of hard-shell capsules containing salicylamide (SCA) and analyses its drug-matrix interaction via dissolution test at different pH media and various release kinetics models. The matrix of hard-shell capsules was prepared from κ-carrageenan (CRG), crosslinked with maltodextrin (MD), and plasticized by sorbitol (SOR). The chemical properties of SCA were compared with paracetamol (PCT) using computational analysis to help to depict its drug-matrix interaction. The statistical analyses showed that SCA and PCT at pH 1.2, 4.5, and 6.8 had all different release profiles. Based on the goodness of fit evaluation, the diffusion mechanism of SCA at pH 1.2 and 4.5 could be best described by the Peppas-Sahlin model while the zeroth-order model fitted the dissolution profile at pH 6.8. In summary, it was proven that a different drug-matrix interaction produced a different dissolution profile.Muhammad Al Rizqi Dharma FauziEsti HendradiPratiwi PudjiastutiRiyanto Teguh WidodoDepartment of Chemistry, Universitas Gadjah Madaarticlepolymercarrageenandrug releaserelease kineticdissolutionChemistryQD1-999ENIndonesian Journal of Chemistry, Vol 21, Iss 1, Pp 148-156 (2020)
institution DOAJ
collection DOAJ
language EN
topic polymer
carrageenan
drug release
release kinetic
dissolution
Chemistry
QD1-999
spellingShingle polymer
carrageenan
drug release
release kinetic
dissolution
Chemistry
QD1-999
Muhammad Al Rizqi Dharma Fauzi
Esti Hendradi
Pratiwi Pudjiastuti
Riyanto Teguh Widodo
Analysis of Dissolution of Salicylamide from Carrageenan Based Hard-Shell Capsules: A Study of the Drug-Matrix Interaction
description In drug release kinetics, the drug-matrix interaction is one of the important mechanisms to be dictated. Unfortunately, there is still minimum information discussing the effect of interaction between a drug and its matrix to the release profile of the drug. Therefore, there is an urgent need to conduct research related to the study of drug-matrix interaction. This paper reports the preparation of a drug delivery system (DDS) in the form of hard-shell capsules containing salicylamide (SCA) and analyses its drug-matrix interaction via dissolution test at different pH media and various release kinetics models. The matrix of hard-shell capsules was prepared from κ-carrageenan (CRG), crosslinked with maltodextrin (MD), and plasticized by sorbitol (SOR). The chemical properties of SCA were compared with paracetamol (PCT) using computational analysis to help to depict its drug-matrix interaction. The statistical analyses showed that SCA and PCT at pH 1.2, 4.5, and 6.8 had all different release profiles. Based on the goodness of fit evaluation, the diffusion mechanism of SCA at pH 1.2 and 4.5 could be best described by the Peppas-Sahlin model while the zeroth-order model fitted the dissolution profile at pH 6.8. In summary, it was proven that a different drug-matrix interaction produced a different dissolution profile.
format article
author Muhammad Al Rizqi Dharma Fauzi
Esti Hendradi
Pratiwi Pudjiastuti
Riyanto Teguh Widodo
author_facet Muhammad Al Rizqi Dharma Fauzi
Esti Hendradi
Pratiwi Pudjiastuti
Riyanto Teguh Widodo
author_sort Muhammad Al Rizqi Dharma Fauzi
title Analysis of Dissolution of Salicylamide from Carrageenan Based Hard-Shell Capsules: A Study of the Drug-Matrix Interaction
title_short Analysis of Dissolution of Salicylamide from Carrageenan Based Hard-Shell Capsules: A Study of the Drug-Matrix Interaction
title_full Analysis of Dissolution of Salicylamide from Carrageenan Based Hard-Shell Capsules: A Study of the Drug-Matrix Interaction
title_fullStr Analysis of Dissolution of Salicylamide from Carrageenan Based Hard-Shell Capsules: A Study of the Drug-Matrix Interaction
title_full_unstemmed Analysis of Dissolution of Salicylamide from Carrageenan Based Hard-Shell Capsules: A Study of the Drug-Matrix Interaction
title_sort analysis of dissolution of salicylamide from carrageenan based hard-shell capsules: a study of the drug-matrix interaction
publisher Department of Chemistry, Universitas Gadjah Mada
publishDate 2020
url https://doaj.org/article/87754166cc6946c1bb1e2e1724d2d20f
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