Dissolution Profile of Nimesulide from Pharmaceutical Preparations for Oral Use

Nimesulide belongs to the group of semi-selective COX-2 inhibitors, widely used in solid oral formulations. In the present work the influence of surfactants among other drug excipients, as well as particle size of the active substance and the effects of medium pH on the dissolution rate of nimesulid...

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Main Authors: Biljana Tubić, Alija Uzunović, Saša Pilipović, Žarko Gagić
Format: Article
Language:English
Published: Slovenian Chemical Society 2016-02-01
Series:Acta Chimica Slovenica
Subjects:
Online Access:https://journals.matheo.si/index.php/ACSi/article/view/2168
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spelling doaj-580fa468ea7748e292706907bce394502020-11-25T01:28:54ZengSlovenian Chemical SocietyActa Chimica Slovenica1318-02071580-31552016-02-0163119319910.17344/acsi.2015.2168331Dissolution Profile of Nimesulide from Pharmaceutical Preparations for Oral UseBiljana Tubić0Alija UzunovićSaša PilipovićŽarko GagićAgency for medicines and medical devices of Bosnia and Herzegovina and Faculty of medicine - study program PharmaciaNimesulide belongs to the group of semi-selective COX-2 inhibitors, widely used in solid oral formulations. In the present work the influence of surfactants among other drug excipients, as well as particle size of the active substance and the effects of medium pH on the dissolution rate of nimesulide from solid pharmaceutical forms. For that purpose, four different preparations containing 100 mg nimesulide per tablet and available in the market of Bosnia and Herzegovina (labeled here as A, B, C and D) were studied. The test for the assessment of dissolution profiles of the formulations was performed in surfactant-free dissolution medium pH 7.5. The dissolution profiles were compared by calculating difference (f1), and similarity (f2) factors. The increasing dissolution medium pH value from 7.5 to 7.75 resulted in a significant increase of nimesulide dissolution rate from the examined formulations. Also, the results showed that particle size affects to a great extent the dissolution rate and the best results were achieved with micronized nimesulide. The presence of the surfactants among the other excipients expressed a negligible effect on the dissolution profile.https://journals.matheo.si/index.php/ACSi/article/view/2168nimesulidedissolution ratebioavailability
collection DOAJ
language English
format Article
sources DOAJ
author Biljana Tubić
Alija Uzunović
Saša Pilipović
Žarko Gagić
spellingShingle Biljana Tubić
Alija Uzunović
Saša Pilipović
Žarko Gagić
Dissolution Profile of Nimesulide from Pharmaceutical Preparations for Oral Use
Acta Chimica Slovenica
nimesulide
dissolution rate
bioavailability
author_facet Biljana Tubić
Alija Uzunović
Saša Pilipović
Žarko Gagić
author_sort Biljana Tubić
title Dissolution Profile of Nimesulide from Pharmaceutical Preparations for Oral Use
title_short Dissolution Profile of Nimesulide from Pharmaceutical Preparations for Oral Use
title_full Dissolution Profile of Nimesulide from Pharmaceutical Preparations for Oral Use
title_fullStr Dissolution Profile of Nimesulide from Pharmaceutical Preparations for Oral Use
title_full_unstemmed Dissolution Profile of Nimesulide from Pharmaceutical Preparations for Oral Use
title_sort dissolution profile of nimesulide from pharmaceutical preparations for oral use
publisher Slovenian Chemical Society
series Acta Chimica Slovenica
issn 1318-0207
1580-3155
publishDate 2016-02-01
description Nimesulide belongs to the group of semi-selective COX-2 inhibitors, widely used in solid oral formulations. In the present work the influence of surfactants among other drug excipients, as well as particle size of the active substance and the effects of medium pH on the dissolution rate of nimesulide from solid pharmaceutical forms. For that purpose, four different preparations containing 100 mg nimesulide per tablet and available in the market of Bosnia and Herzegovina (labeled here as A, B, C and D) were studied. The test for the assessment of dissolution profiles of the formulations was performed in surfactant-free dissolution medium pH 7.5. The dissolution profiles were compared by calculating difference (f1), and similarity (f2) factors. The increasing dissolution medium pH value from 7.5 to 7.75 resulted in a significant increase of nimesulide dissolution rate from the examined formulations. Also, the results showed that particle size affects to a great extent the dissolution rate and the best results were achieved with micronized nimesulide. The presence of the surfactants among the other excipients expressed a negligible effect on the dissolution profile.
topic nimesulide
dissolution rate
bioavailability
url https://journals.matheo.si/index.php/ACSi/article/view/2168
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