New formulation of in situ gelling Metolose-based liquid suppository
Context: An in situ gelling liquid suppository is liquid at room temperature but forms a gel at body temperature. In our work, Metolose® SM-4000 (methylcellulose) is studied that basically shows thermal gelation at 68°C (2%, w w). Objective: The objective was to study the potency of different factor...
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creator | Pásztor, E. Makó, Á. Csóka, G. Fenyvesi, Zs Benko, R. Prosszer, M. Marton, S. Antal, I. Klebovich, I. |
description | Context: An in situ gelling liquid suppository is liquid at room temperature but forms a gel at body temperature. In our work, Metolose® SM-4000 (methylcellulose) is studied that basically shows thermal gelation at 68°C (2%, w w). Objective: The objective was to study the potency of different factors (concentration, pH, additives) to change the value of thermal gelation temperature (T t) for Metolose® to form an in situ gelling liquid suppository. Materials and methods: We studied the effect of Metolose® concentration, pH, and salts (sodium chloride, potassium chloride, sodium hydrogen carbonate, and sodium monohydrogen phosphate) on T t by viscosimetry. To choose the appropriate compound, in vitro drug release was examined. Rectal safety test was performed on rats in vivo after 12-hour application. Results: Increasing the Metolose® concentrations (0.5-4%, w w), T t can be decreased, but it also altered the consistency of gel. pH does not affect the T t. The water-soluble salts allowed reducing the gelation temperature to 37°C. Sodium monohydrogen phosphate in 4.5% concentration was found to be the most appropriate. The impact of examined factors on in vitro drug release of piroxicam from the in situ-formed gel was characterized according to Fickian diffusion. Metolose® and the chosen salt did not cause any morphological damage on the rectal tissues. Discussion: According to our study, Metolose® has the physical and chemical potential to be used as base for liquid suppositories. |
doi_str_mv | 10.3109/03639045.2010.489558 |
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In our work, Metolose® SM-4000 (methylcellulose) is studied that basically shows thermal gelation at 68°C (2%, w w). Objective: The objective was to study the potency of different factors (concentration, pH, additives) to change the value of thermal gelation temperature (T t) for Metolose® to form an in situ gelling liquid suppository. Materials and methods: We studied the effect of Metolose® concentration, pH, and salts (sodium chloride, potassium chloride, sodium hydrogen carbonate, and sodium monohydrogen phosphate) on T t by viscosimetry. To choose the appropriate compound, in vitro drug release was examined. Rectal safety test was performed on rats in vivo after 12-hour application. Results: Increasing the Metolose® concentrations (0.5-4%, w w), T t can be decreased, but it also altered the consistency of gel. pH does not affect the T t. The water-soluble salts allowed reducing the gelation temperature to 37°C. Sodium monohydrogen phosphate in 4.5% concentration was found to be the most appropriate. The impact of examined factors on in vitro drug release of piroxicam from the in situ-formed gel was characterized according to Fickian diffusion. Metolose® and the chosen salt did not cause any morphological damage on the rectal tissues. Discussion: According to our study, Metolose® has the physical and chemical potential to be used as base for liquid suppositories.</description><identifier>ISSN: 0363-9045</identifier><identifier>EISSN: 1520-5762</identifier><identifier>DOI: 10.3109/03639045.2010.489558</identifier><identifier>PMID: 21073325</identifier><language>eng</language><publisher>England: Informa Healthcare</publisher><subject>Administration, Rectal ; Animals ; Anti-Inflammatory Agents, Non-Steroidal - administration & dosage ; Anti-Inflammatory Agents, Non-Steroidal - chemistry ; Chemistry, Pharmaceutical - methods ; Gels - chemistry ; Hydrogen-Ion Concentration ; In situ gelling suppository ; Male ; Methylcellulose - chemistry ; Metolose ; Models, Biological ; Phosphates - chemistry ; piroxicam ; Piroxicam - administration & dosage ; Piroxicam - chemistry ; Rats ; Rats, Wistar ; Suppositories - chemistry ; Temperature</subject><ispartof>Drug development and industrial pharmacy, 2011-01, Vol.37 (1), p.1-7</ispartof><rights>2011 Informa UK, Ltd. 2011</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c417t-29dc1ac5393e5017e13fe345a2dfb2c71c6567994d13b14b4ba4c842c12ef5913</citedby><cites>FETCH-LOGICAL-c417t-29dc1ac5393e5017e13fe345a2dfb2c71c6567994d13b14b4ba4c842c12ef5913</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21073325$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pásztor, E.</creatorcontrib><creatorcontrib>Makó, Á.</creatorcontrib><creatorcontrib>Csóka, G.</creatorcontrib><creatorcontrib>Fenyvesi, Zs</creatorcontrib><creatorcontrib>Benko, R.</creatorcontrib><creatorcontrib>Prosszer, M.</creatorcontrib><creatorcontrib>Marton, S.</creatorcontrib><creatorcontrib>Antal, I.</creatorcontrib><creatorcontrib>Klebovich, I.</creatorcontrib><title>New formulation of in situ gelling Metolose-based liquid suppository</title><title>Drug development and industrial pharmacy</title><addtitle>Drug Dev Ind Pharm</addtitle><description>Context: An in situ gelling liquid suppository is liquid at room temperature but forms a gel at body temperature. In our work, Metolose® SM-4000 (methylcellulose) is studied that basically shows thermal gelation at 68°C (2%, w w). Objective: The objective was to study the potency of different factors (concentration, pH, additives) to change the value of thermal gelation temperature (T t) for Metolose® to form an in situ gelling liquid suppository. Materials and methods: We studied the effect of Metolose® concentration, pH, and salts (sodium chloride, potassium chloride, sodium hydrogen carbonate, and sodium monohydrogen phosphate) on T t by viscosimetry. To choose the appropriate compound, in vitro drug release was examined. Rectal safety test was performed on rats in vivo after 12-hour application. Results: Increasing the Metolose® concentrations (0.5-4%, w w), T t can be decreased, but it also altered the consistency of gel. pH does not affect the T t. The water-soluble salts allowed reducing the gelation temperature to 37°C. Sodium monohydrogen phosphate in 4.5% concentration was found to be the most appropriate. The impact of examined factors on in vitro drug release of piroxicam from the in situ-formed gel was characterized according to Fickian diffusion. Metolose® and the chosen salt did not cause any morphological damage on the rectal tissues. Discussion: According to our study, Metolose® has the physical and chemical potential to be used as base for liquid suppositories.</description><subject>Administration, Rectal</subject><subject>Animals</subject><subject>Anti-Inflammatory Agents, Non-Steroidal - administration & dosage</subject><subject>Anti-Inflammatory Agents, Non-Steroidal - chemistry</subject><subject>Chemistry, Pharmaceutical - methods</subject><subject>Gels - chemistry</subject><subject>Hydrogen-Ion Concentration</subject><subject>In situ gelling suppository</subject><subject>Male</subject><subject>Methylcellulose - chemistry</subject><subject>Metolose</subject><subject>Models, Biological</subject><subject>Phosphates - chemistry</subject><subject>piroxicam</subject><subject>Piroxicam - administration & dosage</subject><subject>Piroxicam - chemistry</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Suppositories - chemistry</subject><subject>Temperature</subject><issn>0363-9045</issn><issn>1520-5762</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kMtOwzAQRS0EoqXwBwhlxyrFzzw2IFSeUoENrC3HcVpXTtzaiar-PY7SIrHpaqTRuXdGB4BrBKcEwfwOkoTkkLIphmFFs5yx7ASMEcMwZmmCT8G4R-KeGYEL71cQIhyoczDCCKaEYDYGT59qG1XW1Z0RrbZNZKtIN5HXbRctlDG6WUQfqrXGehUXwqsyMnrT6TLy3XptA2fd7hKcVcJ4dbWfE_Dz8vw9e4vnX6_vs8d5LClK2xjnpURCMpITxSBKFSKVIpQJXFYFlimSCUvSPKclIgWiBS0ElRnFEmFVsRyRCbgdetfObjrlW15rL8OXolG28zxDIU4hSwNJB1I6671TFV87XQu34wjyXh8_6OO9Pj7oC7Gb_YGuqFX5Fzr4CsDDAOimlya21pmSt2JnrKucaKT2ff3RE_f_GpZKmHYphVN8ZTvXBH_Hf_wF6mWR5g</recordid><startdate>201101</startdate><enddate>201101</enddate><creator>Pásztor, E.</creator><creator>Makó, Á.</creator><creator>Csóka, G.</creator><creator>Fenyvesi, Zs</creator><creator>Benko, R.</creator><creator>Prosszer, M.</creator><creator>Marton, S.</creator><creator>Antal, I.</creator><creator>Klebovich, I.</creator><general>Informa Healthcare</general><general>Taylor & Francis</general><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>201101</creationdate><title>New formulation of in situ gelling Metolose-based liquid suppository</title><author>Pásztor, E. ; Makó, Á. ; Csóka, G. ; Fenyvesi, Zs ; Benko, R. ; Prosszer, M. ; Marton, S. ; Antal, I. ; Klebovich, I.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c417t-29dc1ac5393e5017e13fe345a2dfb2c71c6567994d13b14b4ba4c842c12ef5913</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Administration, Rectal</topic><topic>Animals</topic><topic>Anti-Inflammatory Agents, Non-Steroidal - administration & dosage</topic><topic>Anti-Inflammatory Agents, Non-Steroidal - chemistry</topic><topic>Chemistry, Pharmaceutical - methods</topic><topic>Gels - chemistry</topic><topic>Hydrogen-Ion Concentration</topic><topic>In situ gelling suppository</topic><topic>Male</topic><topic>Methylcellulose - chemistry</topic><topic>Metolose</topic><topic>Models, Biological</topic><topic>Phosphates - chemistry</topic><topic>piroxicam</topic><topic>Piroxicam - administration & dosage</topic><topic>Piroxicam - chemistry</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Suppositories - chemistry</topic><topic>Temperature</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pásztor, E.</creatorcontrib><creatorcontrib>Makó, Á.</creatorcontrib><creatorcontrib>Csóka, G.</creatorcontrib><creatorcontrib>Fenyvesi, Zs</creatorcontrib><creatorcontrib>Benko, R.</creatorcontrib><creatorcontrib>Prosszer, M.</creatorcontrib><creatorcontrib>Marton, S.</creatorcontrib><creatorcontrib>Antal, I.</creatorcontrib><creatorcontrib>Klebovich, I.</creatorcontrib><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>Drug development and industrial pharmacy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pásztor, E.</au><au>Makó, Á.</au><au>Csóka, G.</au><au>Fenyvesi, Zs</au><au>Benko, R.</au><au>Prosszer, M.</au><au>Marton, S.</au><au>Antal, I.</au><au>Klebovich, I.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>New formulation of in situ gelling Metolose-based liquid suppository</atitle><jtitle>Drug development and industrial pharmacy</jtitle><addtitle>Drug Dev Ind Pharm</addtitle><date>2011-01</date><risdate>2011</risdate><volume>37</volume><issue>1</issue><spage>1</spage><epage>7</epage><pages>1-7</pages><issn>0363-9045</issn><eissn>1520-5762</eissn><abstract>Context: An in situ gelling liquid suppository is liquid at room temperature but forms a gel at body temperature. In our work, Metolose® SM-4000 (methylcellulose) is studied that basically shows thermal gelation at 68°C (2%, w w). Objective: The objective was to study the potency of different factors (concentration, pH, additives) to change the value of thermal gelation temperature (T t) for Metolose® to form an in situ gelling liquid suppository. Materials and methods: We studied the effect of Metolose® concentration, pH, and salts (sodium chloride, potassium chloride, sodium hydrogen carbonate, and sodium monohydrogen phosphate) on T t by viscosimetry. To choose the appropriate compound, in vitro drug release was examined. Rectal safety test was performed on rats in vivo after 12-hour application. Results: Increasing the Metolose® concentrations (0.5-4%, w w), T t can be decreased, but it also altered the consistency of gel. pH does not affect the T t. The water-soluble salts allowed reducing the gelation temperature to 37°C. Sodium monohydrogen phosphate in 4.5% concentration was found to be the most appropriate. The impact of examined factors on in vitro drug release of piroxicam from the in situ-formed gel was characterized according to Fickian diffusion. Metolose® and the chosen salt did not cause any morphological damage on the rectal tissues. Discussion: According to our study, Metolose® has the physical and chemical potential to be used as base for liquid suppositories.</abstract><cop>England</cop><pub>Informa Healthcare</pub><pmid>21073325</pmid><doi>10.3109/03639045.2010.489558</doi><tpages>7</tpages></addata></record> |
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subjects | Administration, Rectal Animals Anti-Inflammatory Agents, Non-Steroidal - administration & dosage Anti-Inflammatory Agents, Non-Steroidal - chemistry Chemistry, Pharmaceutical - methods Gels - chemistry Hydrogen-Ion Concentration In situ gelling suppository Male Methylcellulose - chemistry Metolose Models, Biological Phosphates - chemistry piroxicam Piroxicam - administration & dosage Piroxicam - chemistry Rats Rats, Wistar Suppositories - chemistry Temperature |
title | New formulation of in situ gelling Metolose-based liquid suppository |
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