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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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 |
_version_ |
1726011294917591040 |