Study of sodium hyaluronate-based intranasal formulations containing micro- or nanosized meloxicam particles
[Display omitted] This article reports on the micro- and nanonization of meloxicam (MEL) with the aim of developing pre-dispersions as intermediates for the design of intranasal formulations. As a new approach, combined wet milling technology was developed in order to reduce the particle size of the...
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Veröffentlicht in: | International journal of pharmaceutics 2015-08, Vol.491 (1-2), p.198-207 |
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creator | Bartos, Csilla Ambrus, Rita Sipos, Péter Budai-Szűcs, Mária Csányi, Erzsébet Gáspár, Róbert Márki, Árpád Seres, Adrienn B. Sztojkov-Ivanov, Anita Horváth, Tamás Szabó-Révész, Piroska |
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This article reports on the micro- and nanonization of meloxicam (MEL) with the aim of developing pre-dispersions as intermediates for the design of intranasal formulations. As a new approach, combined wet milling technology was developed in order to reduce the particle size of the MEL. Different milling times resulted in micro- or nanosized MEL in the pre-dispersions with polyvinyl alcohol as stabilizer agent, which were directly used for preparing intranasal liquid formulations with the addition of sodium hyaluronate as mucoadhesive agent. Reduction of the MEL particle size into the nano range led to increased saturation solubility and dissolution velocities, and increased adhesiveness to surfaces as compared with microsized MEL particles. A linear correlation was demonstrated between the specific surface area of MEL and the AUC. The in vitro and in vivo studies indicated that the longer residence time and the uniform distribution of nano MEL spray throughout an artificial membrane and the nasal mucosa resulted in better diffusion and a higher AUC. Nanosized MEL may be suggested for the development of an innovative dosage form with a different dose of the drug, as a possible administration route for pain management. |
doi_str_mv | 10.1016/j.ijpharm.2015.06.046 |
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This article reports on the micro- and nanonization of meloxicam (MEL) with the aim of developing pre-dispersions as intermediates for the design of intranasal formulations. As a new approach, combined wet milling technology was developed in order to reduce the particle size of the MEL. Different milling times resulted in micro- or nanosized MEL in the pre-dispersions with polyvinyl alcohol as stabilizer agent, which were directly used for preparing intranasal liquid formulations with the addition of sodium hyaluronate as mucoadhesive agent. Reduction of the MEL particle size into the nano range led to increased saturation solubility and dissolution velocities, and increased adhesiveness to surfaces as compared with microsized MEL particles. A linear correlation was demonstrated between the specific surface area of MEL and the AUC. The in vitro and in vivo studies indicated that the longer residence time and the uniform distribution of nano MEL spray throughout an artificial membrane and the nasal mucosa resulted in better diffusion and a higher AUC. Nanosized MEL may be suggested for the development of an innovative dosage form with a different dose of the drug, as a possible administration route for pain management.</description><identifier>ISSN: 0378-5173</identifier><identifier>EISSN: 1873-3476</identifier><identifier>DOI: 10.1016/j.ijpharm.2015.06.046</identifier><identifier>PMID: 26142244</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Adhesiveness ; Administration, Intranasal ; Animals ; Anti-Inflammatory Agents, Non-Steroidal - administration & dosage ; Anti-Inflammatory Agents, Non-Steroidal - pharmacokinetics ; Area Under Curve ; AUC ; Chemistry, Pharmaceutical ; Combined wet milling ; Drug Compounding ; Excipients - chemistry ; Hyaluronic Acid - administration & dosage ; Hyaluronic Acid - chemistry ; Intranasal formulation ; Male ; Meloxicam ; Membranes, Artificial ; Mucoadhesivity ; Nanoparticles ; Nasal Mucosa - metabolism ; Particle Size ; Permeability ; Polyvinyl Alcohol ; Rats ; Rats, Sprague-Dawley ; Rheology ; Solubility ; Thiazines - administration & dosage ; Thiazines - pharmacokinetics ; Thiazoles - administration & dosage ; Thiazoles - pharmacokinetics</subject><ispartof>International journal of pharmaceutics, 2015-08, Vol.491 (1-2), p.198-207</ispartof><rights>2015 Elsevier B.V.</rights><rights>Copyright © 2015 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c365t-b9302fe46ec151060a72a9402b3163daf16a9bef476ca659c571e9862ded7b33</citedby><cites>FETCH-LOGICAL-c365t-b9302fe46ec151060a72a9402b3163daf16a9bef476ca659c571e9862ded7b33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0378517315300144$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26142244$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bartos, Csilla</creatorcontrib><creatorcontrib>Ambrus, Rita</creatorcontrib><creatorcontrib>Sipos, Péter</creatorcontrib><creatorcontrib>Budai-Szűcs, Mária</creatorcontrib><creatorcontrib>Csányi, Erzsébet</creatorcontrib><creatorcontrib>Gáspár, Róbert</creatorcontrib><creatorcontrib>Márki, Árpád</creatorcontrib><creatorcontrib>Seres, Adrienn B.</creatorcontrib><creatorcontrib>Sztojkov-Ivanov, Anita</creatorcontrib><creatorcontrib>Horváth, Tamás</creatorcontrib><creatorcontrib>Szabó-Révész, Piroska</creatorcontrib><title>Study of sodium hyaluronate-based intranasal formulations containing micro- or nanosized meloxicam particles</title><title>International journal of pharmaceutics</title><addtitle>Int J Pharm</addtitle><description>[Display omitted]
This article reports on the micro- and nanonization of meloxicam (MEL) with the aim of developing pre-dispersions as intermediates for the design of intranasal formulations. As a new approach, combined wet milling technology was developed in order to reduce the particle size of the MEL. Different milling times resulted in micro- or nanosized MEL in the pre-dispersions with polyvinyl alcohol as stabilizer agent, which were directly used for preparing intranasal liquid formulations with the addition of sodium hyaluronate as mucoadhesive agent. Reduction of the MEL particle size into the nano range led to increased saturation solubility and dissolution velocities, and increased adhesiveness to surfaces as compared with microsized MEL particles. A linear correlation was demonstrated between the specific surface area of MEL and the AUC. The in vitro and in vivo studies indicated that the longer residence time and the uniform distribution of nano MEL spray throughout an artificial membrane and the nasal mucosa resulted in better diffusion and a higher AUC. Nanosized MEL may be suggested for the development of an innovative dosage form with a different dose of the drug, as a possible administration route for pain management.</description><subject>Adhesiveness</subject><subject>Administration, Intranasal</subject><subject>Animals</subject><subject>Anti-Inflammatory Agents, Non-Steroidal - administration & dosage</subject><subject>Anti-Inflammatory Agents, Non-Steroidal - pharmacokinetics</subject><subject>Area Under Curve</subject><subject>AUC</subject><subject>Chemistry, Pharmaceutical</subject><subject>Combined wet milling</subject><subject>Drug Compounding</subject><subject>Excipients - chemistry</subject><subject>Hyaluronic Acid - administration & dosage</subject><subject>Hyaluronic Acid - chemistry</subject><subject>Intranasal formulation</subject><subject>Male</subject><subject>Meloxicam</subject><subject>Membranes, Artificial</subject><subject>Mucoadhesivity</subject><subject>Nanoparticles</subject><subject>Nasal Mucosa - metabolism</subject><subject>Particle Size</subject><subject>Permeability</subject><subject>Polyvinyl Alcohol</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Rheology</subject><subject>Solubility</subject><subject>Thiazines - administration & dosage</subject><subject>Thiazines - pharmacokinetics</subject><subject>Thiazoles - administration & dosage</subject><subject>Thiazoles - pharmacokinetics</subject><issn>0378-5173</issn><issn>1873-3476</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE1v1DAQhi1URLeFnwDysZcEfyTO5oRQVShSpR7auzWxJ9Qrfyy2g1h-Pal26bWnuTzvvDMPIR85aznj6vOudbv9E-TQCsb7lqmWdeoN2fDtIBvZDeqMbJgctk3PB3lOLkrZMcaU4PIdOReKd0J03Yb4h7rYA00zLcm6JdCnA_glpwgVmwkKWupizRChgKdzymHxUF2KhZoUK7jo4k8anMmpoSnTCDEV93eNBfTpjzMQ6B5ydcZjeU_ezuALfjjNS_L47ebx-ra5u__-4_rrXWOk6mszjZKJGTuFhvecKQaDgLFjYpJcSQszVzBOOK9PGlD9aPqB47hVwqIdJikvydVx7T6nXwuWqoMrBr2HiGkpmg9MsO3Iu35F-yO63l9KxlnvswuQD5oz_exZ7_TJs372rJnSq-c19-lUsUwB7Uvqv9gV-HIEcP3zt8Osi3EYDVqX0VRtk3ul4h81YJPX</recordid><startdate>20150801</startdate><enddate>20150801</enddate><creator>Bartos, Csilla</creator><creator>Ambrus, Rita</creator><creator>Sipos, Péter</creator><creator>Budai-Szűcs, Mária</creator><creator>Csányi, Erzsébet</creator><creator>Gáspár, Róbert</creator><creator>Márki, Árpád</creator><creator>Seres, Adrienn B.</creator><creator>Sztojkov-Ivanov, Anita</creator><creator>Horváth, Tamás</creator><creator>Szabó-Révész, Piroska</creator><general>Elsevier B.V</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>20150801</creationdate><title>Study of sodium hyaluronate-based intranasal formulations containing micro- or nanosized meloxicam particles</title><author>Bartos, Csilla ; Ambrus, Rita ; Sipos, Péter ; Budai-Szűcs, Mária ; Csányi, Erzsébet ; Gáspár, Róbert ; Márki, Árpád ; Seres, Adrienn B. ; Sztojkov-Ivanov, Anita ; Horváth, Tamás ; Szabó-Révész, Piroska</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c365t-b9302fe46ec151060a72a9402b3163daf16a9bef476ca659c571e9862ded7b33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Adhesiveness</topic><topic>Administration, Intranasal</topic><topic>Animals</topic><topic>Anti-Inflammatory Agents, Non-Steroidal - administration & dosage</topic><topic>Anti-Inflammatory Agents, Non-Steroidal - pharmacokinetics</topic><topic>Area Under Curve</topic><topic>AUC</topic><topic>Chemistry, Pharmaceutical</topic><topic>Combined wet milling</topic><topic>Drug Compounding</topic><topic>Excipients - chemistry</topic><topic>Hyaluronic Acid - administration & dosage</topic><topic>Hyaluronic Acid - chemistry</topic><topic>Intranasal formulation</topic><topic>Male</topic><topic>Meloxicam</topic><topic>Membranes, Artificial</topic><topic>Mucoadhesivity</topic><topic>Nanoparticles</topic><topic>Nasal Mucosa - metabolism</topic><topic>Particle Size</topic><topic>Permeability</topic><topic>Polyvinyl Alcohol</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Rheology</topic><topic>Solubility</topic><topic>Thiazines - administration & dosage</topic><topic>Thiazines - pharmacokinetics</topic><topic>Thiazoles - administration & dosage</topic><topic>Thiazoles - pharmacokinetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bartos, Csilla</creatorcontrib><creatorcontrib>Ambrus, Rita</creatorcontrib><creatorcontrib>Sipos, Péter</creatorcontrib><creatorcontrib>Budai-Szűcs, Mária</creatorcontrib><creatorcontrib>Csányi, Erzsébet</creatorcontrib><creatorcontrib>Gáspár, Róbert</creatorcontrib><creatorcontrib>Márki, Árpád</creatorcontrib><creatorcontrib>Seres, Adrienn B.</creatorcontrib><creatorcontrib>Sztojkov-Ivanov, Anita</creatorcontrib><creatorcontrib>Horváth, Tamás</creatorcontrib><creatorcontrib>Szabó-Révész, Piroska</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>International journal of pharmaceutics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bartos, Csilla</au><au>Ambrus, Rita</au><au>Sipos, Péter</au><au>Budai-Szűcs, Mária</au><au>Csányi, Erzsébet</au><au>Gáspár, Róbert</au><au>Márki, Árpád</au><au>Seres, Adrienn B.</au><au>Sztojkov-Ivanov, Anita</au><au>Horváth, Tamás</au><au>Szabó-Révész, Piroska</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Study of sodium hyaluronate-based intranasal formulations containing micro- or nanosized meloxicam particles</atitle><jtitle>International journal of pharmaceutics</jtitle><addtitle>Int J Pharm</addtitle><date>2015-08-01</date><risdate>2015</risdate><volume>491</volume><issue>1-2</issue><spage>198</spage><epage>207</epage><pages>198-207</pages><issn>0378-5173</issn><eissn>1873-3476</eissn><abstract>[Display omitted]
This article reports on the micro- and nanonization of meloxicam (MEL) with the aim of developing pre-dispersions as intermediates for the design of intranasal formulations. As a new approach, combined wet milling technology was developed in order to reduce the particle size of the MEL. Different milling times resulted in micro- or nanosized MEL in the pre-dispersions with polyvinyl alcohol as stabilizer agent, which were directly used for preparing intranasal liquid formulations with the addition of sodium hyaluronate as mucoadhesive agent. Reduction of the MEL particle size into the nano range led to increased saturation solubility and dissolution velocities, and increased adhesiveness to surfaces as compared with microsized MEL particles. A linear correlation was demonstrated between the specific surface area of MEL and the AUC. The in vitro and in vivo studies indicated that the longer residence time and the uniform distribution of nano MEL spray throughout an artificial membrane and the nasal mucosa resulted in better diffusion and a higher AUC. Nanosized MEL may be suggested for the development of an innovative dosage form with a different dose of the drug, as a possible administration route for pain management.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>26142244</pmid><doi>10.1016/j.ijpharm.2015.06.046</doi><tpages>10</tpages></addata></record> |
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subjects | Adhesiveness Administration, Intranasal Animals Anti-Inflammatory Agents, Non-Steroidal - administration & dosage Anti-Inflammatory Agents, Non-Steroidal - pharmacokinetics Area Under Curve AUC Chemistry, Pharmaceutical Combined wet milling Drug Compounding Excipients - chemistry Hyaluronic Acid - administration & dosage Hyaluronic Acid - chemistry Intranasal formulation Male Meloxicam Membranes, Artificial Mucoadhesivity Nanoparticles Nasal Mucosa - metabolism Particle Size Permeability Polyvinyl Alcohol Rats Rats, Sprague-Dawley Rheology Solubility Thiazines - administration & dosage Thiazines - pharmacokinetics Thiazoles - administration & dosage Thiazoles - pharmacokinetics |
title | Study of sodium hyaluronate-based intranasal formulations containing micro- or nanosized meloxicam particles |
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