Mathematical methods for quantification and comparison of dissolution testing data

In recent years, drug release/dissolution from solid dosage forms has been the subject of intense and profitable scientific developments. Whenever a new solid dosage form is developed or produced, it is necessary to ensure that drug dissolutionoccurs in an appropriate manner. The pharmaceutical indu...

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Main Authors: Edina Vranić, Aida Mehmedagić, Sabira Hadžović
Format: Article
Language:English
Published: Association of Basic Medical Sciences of Federation of Bosnia and Herzegovina 2002-02-01
Series:Bosnian Journal of Basic Medical Sciences
Subjects:
Online Access:http://www.bjbms.org/ojs/index.php/bjbms/article/view/3581
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spelling doaj-3a67c666fea04a4a8ffb6ebda38a56832020-11-24T21:17:55ZengAssociation of Basic Medical Sciences of Federation of Bosnia and HerzegovinaBosnian Journal of Basic Medical Sciences1512-86011840-48122002-02-0121-210.17305/bjbms.2002.3581Mathematical methods for quantification and comparison of dissolution testing dataEdina Vranić0Aida Mehmedagić1Sabira Hadžović2Department of Pharmaceutical TechnologyDepartment of Pharmacokinetics, University of Sarajevo, Faculty of PharmacyDepartment of Pharmaceutical TechnologyIn recent years, drug release/dissolution from solid dosage forms has been the subject of intense and profitable scientific developments. Whenever a new solid dosage form is developed or produced, it is necessary to ensure that drug dissolutionoccurs in an appropriate manner. The pharmaceutical industry and the registration authorities do focus, nowadays, on drug dissolution studies. The quantitative analysis of the values obtained in dissolution/release tests is easier when mathematicalformulas that express the dissolution results as a function of some of the dosage forms characteristics are used. This work discusses the analysis of data obtained for dissolution profiles under different media pH conditions using mathematical methodsof analysis described by Moore and Flanner. These authors have described difference factor (f1) and similarity factor (f2), which can be used to characterise drug dissolution/release profiles. In this work we have used these formulas for evaluation of dissolution profiles of the conventional tablets in different pH of dissolution medium (range of physiological variations).http://www.bjbms.org/ojs/index.php/bjbms/article/view/3581dissolution testingdifference factorsimilarity factorquantificationcomparisonsolid dosage forms
collection DOAJ
language English
format Article
sources DOAJ
author Edina Vranić
Aida Mehmedagić
Sabira Hadžović
spellingShingle Edina Vranić
Aida Mehmedagić
Sabira Hadžović
Mathematical methods for quantification and comparison of dissolution testing data
Bosnian Journal of Basic Medical Sciences
dissolution testing
difference factor
similarity factor
quantification
comparison
solid dosage forms
author_facet Edina Vranić
Aida Mehmedagić
Sabira Hadžović
author_sort Edina Vranić
title Mathematical methods for quantification and comparison of dissolution testing data
title_short Mathematical methods for quantification and comparison of dissolution testing data
title_full Mathematical methods for quantification and comparison of dissolution testing data
title_fullStr Mathematical methods for quantification and comparison of dissolution testing data
title_full_unstemmed Mathematical methods for quantification and comparison of dissolution testing data
title_sort mathematical methods for quantification and comparison of dissolution testing data
publisher Association of Basic Medical Sciences of Federation of Bosnia and Herzegovina
series Bosnian Journal of Basic Medical Sciences
issn 1512-8601
1840-4812
publishDate 2002-02-01
description In recent years, drug release/dissolution from solid dosage forms has been the subject of intense and profitable scientific developments. Whenever a new solid dosage form is developed or produced, it is necessary to ensure that drug dissolutionoccurs in an appropriate manner. The pharmaceutical industry and the registration authorities do focus, nowadays, on drug dissolution studies. The quantitative analysis of the values obtained in dissolution/release tests is easier when mathematicalformulas that express the dissolution results as a function of some of the dosage forms characteristics are used. This work discusses the analysis of data obtained for dissolution profiles under different media pH conditions using mathematical methodsof analysis described by Moore and Flanner. These authors have described difference factor (f1) and similarity factor (f2), which can be used to characterise drug dissolution/release profiles. In this work we have used these formulas for evaluation of dissolution profiles of the conventional tablets in different pH of dissolution medium (range of physiological variations).
topic dissolution testing
difference factor
similarity factor
quantification
comparison
solid dosage forms
url http://www.bjbms.org/ojs/index.php/bjbms/article/view/3581
work_keys_str_mv AT edinavranic mathematicalmethodsforquantificationandcomparisonofdissolutiontestingdata
AT aidamehmedagic mathematicalmethodsforquantificationandcomparisonofdissolutiontestingdata
AT sabirahadzovic mathematicalmethodsforquantificationandcomparisonofdissolutiontestingdata
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