Empirical kinetic model of propafenone release from Hot Air Coating microparticles
Lipid microparticles, containing 30% and 50% (w/w) propafenone hydrochloride as the active molecule and cetearyl alcohol and Pluronic ® F68 as excipients, were prepared by Hot Air Coating (HAC). The aim of the work was to identify the kinetics and the mechanism of the drug release process from these...
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Veröffentlicht in: | International journal of pharmaceutics 2008-04, Vol.353 (1), p.124-130 |
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creator | Segale, L. Albertini, B. Giovannelli, L. Pattarino, F. |
description | Lipid microparticles, containing 30% and 50% (w/w) propafenone hydrochloride as the active molecule and cetearyl alcohol and Pluronic
® F68 as excipients, were prepared by Hot Air Coating (HAC).
The aim of the work was to identify the kinetics and the mechanism of the drug release process from these microparticulate systems. The application of the Weibull model to the release data from each single fraction of microparticles suggests that a diffusive mechanism governs drug release from microparticles. Thus, we proposed and applied a release kinetic model to the experimental data that takes into account the diffusion as the predominantly mechanism of drug release. The model proposed is a modified version of the exponential equation in which the product of the apparent release rate constant
K, specific for each drug/excipient mixture, and the area-to-volume ratio of particles was used.
The
K values of single fractions of HAC microparticles (coded
K
fr) are very similar to those of the mixtures of particles obtained from the process (coded
K
pool). Using the
K
pool constants, the release behaviour of ensembles of different size microparticles of well-known composition was predicted. The strength of the model was proved by the good fitting of the experimental release data versus those predicted (
R
2
≥
0.997). |
doi_str_mv | 10.1016/j.ijpharm.2007.11.022 |
format | Article |
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® F68 as excipients, were prepared by Hot Air Coating (HAC).
The aim of the work was to identify the kinetics and the mechanism of the drug release process from these microparticulate systems. The application of the Weibull model to the release data from each single fraction of microparticles suggests that a diffusive mechanism governs drug release from microparticles. Thus, we proposed and applied a release kinetic model to the experimental data that takes into account the diffusion as the predominantly mechanism of drug release. The model proposed is a modified version of the exponential equation in which the product of the apparent release rate constant
K, specific for each drug/excipient mixture, and the area-to-volume ratio of particles was used.
The
K values of single fractions of HAC microparticles (coded
K
fr) are very similar to those of the mixtures of particles obtained from the process (coded
K
pool). Using the
K
pool constants, the release behaviour of ensembles of different size microparticles of well-known composition was predicted. The strength of the model was proved by the good fitting of the experimental release data versus those predicted (
R
2
≥
0.997).</description><identifier>ISSN: 0378-5173</identifier><identifier>EISSN: 1873-3476</identifier><identifier>DOI: 10.1016/j.ijpharm.2007.11.022</identifier><identifier>PMID: 18162344</identifier><identifier>CODEN: IJPHDE</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>Biological and medical sciences ; General pharmacology ; Hot Air Coating ; Kinetics ; Mathematical modelling ; Medical sciences ; Microparticles ; Models, Theoretical ; Pharmaceutical technology. Pharmaceutical industry ; Pharmacology. Drug treatments ; Propafenone ; Propafenone - administration & dosage ; Propafenone - chemistry ; Release mechanism ; Solubility ; Technology, Pharmaceutical</subject><ispartof>International journal of pharmaceutics, 2008-04, Vol.353 (1), p.124-130</ispartof><rights>2007 Elsevier B.V.</rights><rights>2008 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c393t-5e924311ad7d4e03f8ce1e83b8684e0799386e222ade4d1250873f239c61c143</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.ijpharm.2007.11.022$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,27923,27924,45994</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=20226353$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18162344$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Segale, L.</creatorcontrib><creatorcontrib>Albertini, B.</creatorcontrib><creatorcontrib>Giovannelli, L.</creatorcontrib><creatorcontrib>Pattarino, F.</creatorcontrib><title>Empirical kinetic model of propafenone release from Hot Air Coating microparticles</title><title>International journal of pharmaceutics</title><addtitle>Int J Pharm</addtitle><description>Lipid microparticles, containing 30% and 50% (w/w) propafenone hydrochloride as the active molecule and cetearyl alcohol and Pluronic
® F68 as excipients, were prepared by Hot Air Coating (HAC).
The aim of the work was to identify the kinetics and the mechanism of the drug release process from these microparticulate systems. The application of the Weibull model to the release data from each single fraction of microparticles suggests that a diffusive mechanism governs drug release from microparticles. Thus, we proposed and applied a release kinetic model to the experimental data that takes into account the diffusion as the predominantly mechanism of drug release. The model proposed is a modified version of the exponential equation in which the product of the apparent release rate constant
K, specific for each drug/excipient mixture, and the area-to-volume ratio of particles was used.
The
K values of single fractions of HAC microparticles (coded
K
fr) are very similar to those of the mixtures of particles obtained from the process (coded
K
pool). Using the
K
pool constants, the release behaviour of ensembles of different size microparticles of well-known composition was predicted. The strength of the model was proved by the good fitting of the experimental release data versus those predicted (
R
2
≥
0.997).</description><subject>Biological and medical sciences</subject><subject>General pharmacology</subject><subject>Hot Air Coating</subject><subject>Kinetics</subject><subject>Mathematical modelling</subject><subject>Medical sciences</subject><subject>Microparticles</subject><subject>Models, Theoretical</subject><subject>Pharmaceutical technology. Pharmaceutical industry</subject><subject>Pharmacology. Drug treatments</subject><subject>Propafenone</subject><subject>Propafenone - administration & dosage</subject><subject>Propafenone - chemistry</subject><subject>Release mechanism</subject><subject>Solubility</subject><subject>Technology, Pharmaceutical</subject><issn>0378-5173</issn><issn>1873-3476</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE1LxDAQhoMoun78BCUXvbVmkjZpTyKLXyAI4j3EdKpZ26YmXcF_b5YtevQUBp538s5DyCmwHBjIy1XuVuO7CX3OGVM5QM443yELqJTIRKHkLlkwoaqsBCUOyGGMK8aY5CD2yQFUILkoigV5vulHF5w1Hf1wA07O0t432FHf0jH40bQ4-AFpwA5NRNoG39N7P9FrF-jSm8kNb7R3doOGlO4wHpO91nQRT-b3iLzc3rws77PHp7uH5fVjZkUtpqzEmhcCwDSqKZCJtrIIWInXSlZpVnUtKomcc9Ng0QAvWbqs5aK2EiwU4ohcbNemmp9rjJPuXbTYdWZAv45apetVLesEllswlYwxYKvH4HoTvjUwvXGpV3p2qTcuNYBOLlPubP5g_dpj85ea5SXgfAZMTALbYAbr4i_H0xIpSpG4qy2HycaXw6CjdThYbFxAO-nGu3-q_ABW95Rm</recordid><startdate>20080402</startdate><enddate>20080402</enddate><creator>Segale, L.</creator><creator>Albertini, B.</creator><creator>Giovannelli, L.</creator><creator>Pattarino, F.</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20080402</creationdate><title>Empirical kinetic model of propafenone release from Hot Air Coating microparticles</title><author>Segale, L. ; Albertini, B. ; Giovannelli, L. ; Pattarino, F.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c393t-5e924311ad7d4e03f8ce1e83b8684e0799386e222ade4d1250873f239c61c143</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Biological and medical sciences</topic><topic>General pharmacology</topic><topic>Hot Air Coating</topic><topic>Kinetics</topic><topic>Mathematical modelling</topic><topic>Medical sciences</topic><topic>Microparticles</topic><topic>Models, Theoretical</topic><topic>Pharmaceutical technology. Pharmaceutical industry</topic><topic>Pharmacology. Drug treatments</topic><topic>Propafenone</topic><topic>Propafenone - administration & dosage</topic><topic>Propafenone - chemistry</topic><topic>Release mechanism</topic><topic>Solubility</topic><topic>Technology, Pharmaceutical</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Segale, L.</creatorcontrib><creatorcontrib>Albertini, B.</creatorcontrib><creatorcontrib>Giovannelli, L.</creatorcontrib><creatorcontrib>Pattarino, F.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>International journal of pharmaceutics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Segale, L.</au><au>Albertini, B.</au><au>Giovannelli, L.</au><au>Pattarino, F.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Empirical kinetic model of propafenone release from Hot Air Coating microparticles</atitle><jtitle>International journal of pharmaceutics</jtitle><addtitle>Int J Pharm</addtitle><date>2008-04-02</date><risdate>2008</risdate><volume>353</volume><issue>1</issue><spage>124</spage><epage>130</epage><pages>124-130</pages><issn>0378-5173</issn><eissn>1873-3476</eissn><coden>IJPHDE</coden><abstract>Lipid microparticles, containing 30% and 50% (w/w) propafenone hydrochloride as the active molecule and cetearyl alcohol and Pluronic
® F68 as excipients, were prepared by Hot Air Coating (HAC).
The aim of the work was to identify the kinetics and the mechanism of the drug release process from these microparticulate systems. The application of the Weibull model to the release data from each single fraction of microparticles suggests that a diffusive mechanism governs drug release from microparticles. Thus, we proposed and applied a release kinetic model to the experimental data that takes into account the diffusion as the predominantly mechanism of drug release. The model proposed is a modified version of the exponential equation in which the product of the apparent release rate constant
K, specific for each drug/excipient mixture, and the area-to-volume ratio of particles was used.
The
K values of single fractions of HAC microparticles (coded
K
fr) are very similar to those of the mixtures of particles obtained from the process (coded
K
pool). Using the
K
pool constants, the release behaviour of ensembles of different size microparticles of well-known composition was predicted. The strength of the model was proved by the good fitting of the experimental release data versus those predicted (
R
2
≥
0.997).</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>18162344</pmid><doi>10.1016/j.ijpharm.2007.11.022</doi><tpages>7</tpages></addata></record> |
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source | MEDLINE; ScienceDirect Journals (5 years ago - present) |
subjects | Biological and medical sciences General pharmacology Hot Air Coating Kinetics Mathematical modelling Medical sciences Microparticles Models, Theoretical Pharmaceutical technology. Pharmaceutical industry Pharmacology. Drug treatments Propafenone Propafenone - administration & dosage Propafenone - chemistry Release mechanism Solubility Technology, Pharmaceutical |
title | Empirical kinetic model of propafenone release from Hot Air Coating microparticles |
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