Modelling of diclofenac sodium diffusion from swellable and water-soluble polyethylene oxide matrices
The main objective of this study was to develop a mathematical model for the characterization of diclofenac sodium diffusion from polyethylene oxide (PEO) matrices. A model was developed on the basis of the diffusion theory accounting for the characteristics of the polymer: swelling with subsequent...
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Veröffentlicht in: | Journal of pharmacy and pharmacology 2009-11, Vol.61 (11), p.1449-1456 |
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creator | Petrović, Jelena Jocković, Jelena Ibrić, Svetlana Durić, Zorica |
description | The main objective of this study was to develop a mathematical model for the characterization of diclofenac sodium diffusion from polyethylene oxide (PEO) matrices. A model was developed on the basis of the diffusion theory accounting for the characteristics of the polymer: swelling with subsequent dissolution in water. The concentration-dependent diffusion of drug and water was taken into account. Experimental data were analysed using a computer software program as an aid for solving partial differential equations.
Six formulations of matrix tablets with different drug-excipient ratios were prepared using low-molecular-weight PEO as a matrix-forming material. For obtaining drug release data, dissolution studies were performed and water uptake by pure PEO matrices was studied as well.
A good agreement of the developed model with experimental results was demonstrated. Some anomalies in drug diffusion were observed and their origin was questioned. Changes in the parameters characterizing the process of diffusion are attributed to glassy-rubbery polymer transitions. Additional interpretation of this phenomenon on the basis of percolation theory is also provided.
The obtained model has the ability to predict the required characteristics of matrices for desired drug release. The composition of batches with undesirable release properties can be predetermined and avoided in manufacturing. |
doi_str_mv | 10.1211/jpp/61.11.0003 |
format | Article |
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Six formulations of matrix tablets with different drug-excipient ratios were prepared using low-molecular-weight PEO as a matrix-forming material. For obtaining drug release data, dissolution studies were performed and water uptake by pure PEO matrices was studied as well.
A good agreement of the developed model with experimental results was demonstrated. Some anomalies in drug diffusion were observed and their origin was questioned. Changes in the parameters characterizing the process of diffusion are attributed to glassy-rubbery polymer transitions. Additional interpretation of this phenomenon on the basis of percolation theory is also provided.
The obtained model has the ability to predict the required characteristics of matrices for desired drug release. The composition of batches with undesirable release properties can be predetermined and avoided in manufacturing.</description><identifier>EISSN: 2042-7158</identifier><identifier>DOI: 10.1211/jpp/61.11.0003</identifier><identifier>PMID: 19903369</identifier><language>eng</language><publisher>England</publisher><subject>Anti-Inflammatory Agents, Non-Steroidal - chemistry ; Diclofenac - chemistry ; Diffusion ; Drug Delivery Systems - standards ; Excipients - chemistry ; Excipients - standards ; Models, Theoretical ; Molecular Weight ; Polyethylene Glycols ; Solubility ; Tablets - chemistry ; Tablets - standards ; Water</subject><ispartof>Journal of pharmacy and pharmacology, 2009-11, Vol.61 (11), p.1449-1456</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19903369$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Petrović, Jelena</creatorcontrib><creatorcontrib>Jocković, Jelena</creatorcontrib><creatorcontrib>Ibrić, Svetlana</creatorcontrib><creatorcontrib>Durić, Zorica</creatorcontrib><title>Modelling of diclofenac sodium diffusion from swellable and water-soluble polyethylene oxide matrices</title><title>Journal of pharmacy and pharmacology</title><addtitle>J Pharm Pharmacol</addtitle><description>The main objective of this study was to develop a mathematical model for the characterization of diclofenac sodium diffusion from polyethylene oxide (PEO) matrices. A model was developed on the basis of the diffusion theory accounting for the characteristics of the polymer: swelling with subsequent dissolution in water. The concentration-dependent diffusion of drug and water was taken into account. Experimental data were analysed using a computer software program as an aid for solving partial differential equations.
Six formulations of matrix tablets with different drug-excipient ratios were prepared using low-molecular-weight PEO as a matrix-forming material. For obtaining drug release data, dissolution studies were performed and water uptake by pure PEO matrices was studied as well.
A good agreement of the developed model with experimental results was demonstrated. Some anomalies in drug diffusion were observed and their origin was questioned. Changes in the parameters characterizing the process of diffusion are attributed to glassy-rubbery polymer transitions. Additional interpretation of this phenomenon on the basis of percolation theory is also provided.
The obtained model has the ability to predict the required characteristics of matrices for desired drug release. The composition of batches with undesirable release properties can be predetermined and avoided in manufacturing.</description><subject>Anti-Inflammatory Agents, Non-Steroidal - chemistry</subject><subject>Diclofenac - chemistry</subject><subject>Diffusion</subject><subject>Drug Delivery Systems - standards</subject><subject>Excipients - chemistry</subject><subject>Excipients - standards</subject><subject>Models, Theoretical</subject><subject>Molecular Weight</subject><subject>Polyethylene Glycols</subject><subject>Solubility</subject><subject>Tablets - chemistry</subject><subject>Tablets - standards</subject><subject>Water</subject><issn>2042-7158</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo1kM9LwzAYhoMgbk6vHiU3T93yNU2WHGX4CyZe9FzS5otmpE1tWub-ezucpxceHl5eXkJugC0hB1jtum4lYQmwZIzxMzLPWZFnaxBqRi5T2k10LaW8IDPQmnEu9Zzga7QYgm8_aXTU-jpEh62paYrWj81EnBuTjy11fWxo2k-yqQJS01q6NwP2WYphPJIuhgMOX4eALdL44y3Sxgy9rzFdkXNnQsLrUy7Ix-PD--Y52749vWzut1kHig2ZkFYJENwwJllRGVFZBdzVXOlCO1lJp6EoKlsUOleK2zw3ApyoOQqurAa-IHd_vV0fv0dMQ9n4VB8ntxjHVK45XwOAEJN5ezLHqkFbdr1vTH8o_5_hv97oZJs</recordid><startdate>200911</startdate><enddate>200911</enddate><creator>Petrović, Jelena</creator><creator>Jocković, Jelena</creator><creator>Ibrić, Svetlana</creator><creator>Durić, Zorica</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>200911</creationdate><title>Modelling of diclofenac sodium diffusion from swellable and water-soluble polyethylene oxide matrices</title><author>Petrović, Jelena ; Jocković, Jelena ; Ibrić, Svetlana ; Durić, Zorica</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p180t-56d85153a00604ba5bd813fc38949f6b6f9144bd4492883d22a51f5c3e538d913</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Anti-Inflammatory Agents, Non-Steroidal - chemistry</topic><topic>Diclofenac - chemistry</topic><topic>Diffusion</topic><topic>Drug Delivery Systems - standards</topic><topic>Excipients - chemistry</topic><topic>Excipients - standards</topic><topic>Models, Theoretical</topic><topic>Molecular Weight</topic><topic>Polyethylene Glycols</topic><topic>Solubility</topic><topic>Tablets - chemistry</topic><topic>Tablets - standards</topic><topic>Water</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Petrović, Jelena</creatorcontrib><creatorcontrib>Jocković, Jelena</creatorcontrib><creatorcontrib>Ibrić, Svetlana</creatorcontrib><creatorcontrib>Durić, Zorica</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of pharmacy and pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Petrović, Jelena</au><au>Jocković, Jelena</au><au>Ibrić, Svetlana</au><au>Durić, Zorica</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Modelling of diclofenac sodium diffusion from swellable and water-soluble polyethylene oxide matrices</atitle><jtitle>Journal of pharmacy and pharmacology</jtitle><addtitle>J Pharm Pharmacol</addtitle><date>2009-11</date><risdate>2009</risdate><volume>61</volume><issue>11</issue><spage>1449</spage><epage>1456</epage><pages>1449-1456</pages><eissn>2042-7158</eissn><abstract>The main objective of this study was to develop a mathematical model for the characterization of diclofenac sodium diffusion from polyethylene oxide (PEO) matrices. A model was developed on the basis of the diffusion theory accounting for the characteristics of the polymer: swelling with subsequent dissolution in water. The concentration-dependent diffusion of drug and water was taken into account. Experimental data were analysed using a computer software program as an aid for solving partial differential equations.
Six formulations of matrix tablets with different drug-excipient ratios were prepared using low-molecular-weight PEO as a matrix-forming material. For obtaining drug release data, dissolution studies were performed and water uptake by pure PEO matrices was studied as well.
A good agreement of the developed model with experimental results was demonstrated. Some anomalies in drug diffusion were observed and their origin was questioned. Changes in the parameters characterizing the process of diffusion are attributed to glassy-rubbery polymer transitions. Additional interpretation of this phenomenon on the basis of percolation theory is also provided.
The obtained model has the ability to predict the required characteristics of matrices for desired drug release. The composition of batches with undesirable release properties can be predetermined and avoided in manufacturing.</abstract><cop>England</cop><pmid>19903369</pmid><doi>10.1211/jpp/61.11.0003</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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source | Oxford University Press Journals All Titles (1996-Current); MEDLINE; Wiley Online Library Journals Frontfile Complete |
subjects | Anti-Inflammatory Agents, Non-Steroidal - chemistry Diclofenac - chemistry Diffusion Drug Delivery Systems - standards Excipients - chemistry Excipients - standards Models, Theoretical Molecular Weight Polyethylene Glycols Solubility Tablets - chemistry Tablets - standards Water |
title | Modelling of diclofenac sodium diffusion from swellable and water-soluble polyethylene oxide matrices |
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