Document Detail


Analysis of formulation effects in the dissolution of ibuprofen pellets.
MedLine Citation:
PMID:  14726117     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
In this work the effects of citric acid and of two common fillers, lactose (soluble) and tricalcium phosphate (insoluble) are examined on the release profiles from pellets, using ibuprofen as a model drug with pH-dependent solubility. Also studied is the dependence of these profiles on the specific surface area, bulk density, apparent density, porosity and porosity parameters (pore size distribution, total pore surface area, mean pore diameter and pore shape), as determined by mercury intrusion porosimetry. Pellets with high porosity and total pore surface area but small median pore diameter (tricalcium phosphate pellets-IPM) are found to produce similar dissolution results to those of low porosity and low total pore surface area, but having a high median pore diameter (lactose pellets-ILM), irrespective of the solubility of excipients. Addition of citric acid causes a delay in the initial dissolution for both formulations. During dissolution, however, citric acid reduces the median pore diameter of lactose-based pellets. In contrast, in tricalcium phosphate/citric acid pellets (CIPM), this parameter increases considerably during dissolution, when compared to the IPM formulation. These findings may justify the contrasting dissolution behaviors of CIPM and CILM (lactose/citric acid) pellets, after their common behavior in the initial stages, and show that porosity and its related parameters, along with physical properties of excipients such as solubility, density and specific surface area, are helpful to predict pellet behavior in drug release profiles.
Authors:
F O Costa; A A C C Pais; J J S Sousa
Related Documents :
17136437 - The viability of a nonenzymatic reductive citric acid cycle--kinetics and thermochemistry.
16269757 - Fate and role of ammonium ions during fermentation of citric acid by aspergillus niger.
15356277 - Integrating the universal metabolism into a phylogenetic analysis.
18459307 - Inactivation of avian influenza virus using common detergents and chemicals.
1701007 - Prevalence of cryptosporidium in rawalpindi/islamabad a comparison of saline, iodine an...
7800117 - Brain, liver, and adipose tissue erucic and very long chain fatty acid levels in adreno...
Publication Detail:
Type:  Comparative Study; Journal Article    
Journal Detail:
Title:  International journal of pharmaceutics     Volume:  270     ISSN:  0378-5173     ISO Abbreviation:  Int J Pharm     Publication Date:  2004 Feb 
Date Detail:
Created Date:  2004-01-16     Completed Date:  2004-05-11     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  7804127     Medline TA:  Int J Pharm     Country:  Netherlands    
Other Details:
Languages:  eng     Pagination:  9-19     Citation Subset:  IM    
Affiliation:
Faculdade de Farmácia, Universidade de Coimbra, P-3004-535 Coimbra Codex, Portugal.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Calcium Phosphates / chemistry
Chemistry, Pharmaceutical
Citric Acid / chemistry
Compressive Strength
Excipients / chemistry*
Hydrogen-Ion Concentration
Ibuprofen / chemistry*
Lactose / chemistry
Microscopy, Electron, Scanning
Porosity
Solubility
Surface Properties
Tablets
Chemical
Reg. No./Substance:
0/Calcium Phosphates; 0/Excipients; 0/Tablets; 0/beta-tricalcium phosphate; 15687-27-1/Ibuprofen; 63-42-3/Lactose; 77-92-9/Citric Acid; 7758-87-4/tricalcium phosphate

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


Previous Document:  Pharmacokinetic evaluation of an azithromycin controlled release dosage form in healthy human volunt...
Next Document:  New screening method for the determination of stability of pharmaceuticals.