Document Detail


Use of an in vitro absorption model system for predicting sustained release of verapamil.
MedLine Citation:
PMID:  1445475     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
It is shown that it is possible to characterize sustained release formulations in vitro using not only dissolution data but also an absorption model system. The mean dissolution time (MDT) has been shown to be a suitable parameter for evaluating sustained release formulations in vitro. t1/2 and mean residence time (MRT) have been shown to be convenient pharmacokinetic parameters for characterizing sustained release formulations. For comparing in vitro and in vivo results the quotients MDT normal/MDT retard and MRT normal/MRT retard do seem to be useful.
Authors:
R Neubert; F Fahr; C Mäder; L Lücke; G Fries; G Rostock
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Publication Detail:
Type:  Journal Article    
Journal Detail:
Title:  Arzneimittel-Forschung     Volume:  42     ISSN:  0004-4172     ISO Abbreviation:  Arzneimittelforschung     Publication Date:  1992 Sep 
Date Detail:
Created Date:  1992-12-17     Completed Date:  1992-12-17     Revised Date:  2004-11-17    
Medline Journal Info:
Nlm Unique ID:  0372660     Medline TA:  Arzneimittelforschung     Country:  GERMANY    
Other Details:
Languages:  eng     Pagination:  1098-100     Citation Subset:  IM    
Affiliation:
Department of Pharmacy, Martin-Luther-University, Halle/Saale, Fed. Rep. of Germany.
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MeSH Terms
Descriptor/Qualifier:
Adult
Delayed-Action Preparations
Female
Half-Life
Humans
Intestinal Absorption
Male
Middle Aged
Models, Biological
Solubility
Verapamil / administration & dosage,  pharmacokinetics*
Chemical
Reg. No./Substance:
0/Delayed-Action Preparations; 52-53-9/Verapamil

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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