Physicochemical Characterization of Spray-Dried Phenylbutazone Polymorphs
A spray-drying method was applied to the recrystallization of phenylbutazone, and the resulting samples were examined by X-ray powder diffractometry, differential thermal analysis, IR spectrophotometry, scanning electron microscopy, and hot-stage photomicroscopy. Three different crystalline forms (δ...
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Veröffentlicht in: | Journal of pharmaceutical sciences 1984-02, Vol.73 (2), p.173-179 |
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creator | Matsuda, Yoshihisa Kawaguchi, Sachiyo Kobayashi, Hitomi Nishijo, Jujiro |
description | A spray-drying method was applied to the recrystallization of phenylbutazone, and the resulting samples were examined by X-ray powder diffractometry, differential thermal analysis, IR spectrophotometry, scanning electron microscopy, and hot-stage photomicroscopy. Three different crystalline forms (δ, β, and ϵ) could be prepared from methylene chloride solution by varying the drying temperature of sprayed droplets from 120°C to 30°C. Form ϵ, the fifth polymorph of phenylbutazone, was confirmed as a novel crystalline form which could not be prepared by recrystallization techniques. In this spray-drying system the composition of spray-dried samples was shown to be a function of the drying temperature. While the stable form δ was obtained at higher drying temperatures, form δ was obtained only under conditions affording a slower evaporation rate of the solvent. The dissolution properties of the pure modifications prepared by recrystallization techniques and the spray-dried samples were evaluated in simulated intestinal fluid. Form ϵ showed excellent in vitro availability and much higher solubility than any other of the forms. |
doi_str_mv | 10.1002/jps.2600730209 |
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Three different crystalline forms (δ, β, and ϵ) could be prepared from methylene chloride solution by varying the drying temperature of sprayed droplets from 120°C to 30°C. Form ϵ, the fifth polymorph of phenylbutazone, was confirmed as a novel crystalline form which could not be prepared by recrystallization techniques. In this spray-drying system the composition of spray-dried samples was shown to be a function of the drying temperature. While the stable form δ was obtained at higher drying temperatures, form δ was obtained only under conditions affording a slower evaporation rate of the solvent. The dissolution properties of the pure modifications prepared by recrystallization techniques and the spray-dried samples were evaluated in simulated intestinal fluid. Form ϵ showed excellent in vitro availability and much higher solubility than any other of the forms.</description><identifier>ISSN: 0022-3549</identifier><identifier>EISSN: 1520-6017</identifier><identifier>DOI: 10.1002/jps.2600730209</identifier><identifier>PMID: 6707878</identifier><identifier>CODEN: JPMSAE</identifier><language>eng</language><publisher>Washington: Elsevier Inc</publisher><subject>Biological and medical sciences ; Calorimetry - methods ; Chemical Phenomena ; Chemistry, Physical ; Crystallization ; General pharmacology ; Medical sciences ; Microscopy, Electron, Scanning ; Pharmaceutical technology. Pharmaceutical industry ; Pharmacology. Drug treatments ; Phenylbutazone ; Phenylbutazone-recrystallized polymorphs ; Phenylbutazone—recrystallized polymorphs, spray-drying technique, physicochemical characterization ; physicochemical characterization ; Recrystallization-polymorphs of phenylbutazone ; Recrystallization—polymorphs of phenylbutazone, spray-drying technique, physicochemical characterization ; Solubility ; Spectrophotometry, Infrared ; spray-drying technique ; Spray-drying-recrystallized polymorphs of phenylbutazone ; Spray-drying—recrystallized polymorphs of phenylbutazone, physicochemical characterization ; Thermodynamics ; X-Ray Diffraction</subject><ispartof>Journal of pharmaceutical sciences, 1984-02, Vol.73 (2), p.173-179</ispartof><rights>1984 Wiley-Liss, Inc., A Wiley Company</rights><rights>Copyright © 1984 Wiley‐Liss, Inc., A Wiley Company</rights><rights>1985 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5229-fac372e43b25106704f3a11f1bbf14854d7c562ec08a13ff3ec1ec749b99c7c73</citedby><cites>FETCH-LOGICAL-c5229-fac372e43b25106704f3a11f1bbf14854d7c562ec08a13ff3ec1ec749b99c7c73</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjps.2600730209$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjps.2600730209$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27923,27924,45573,45574</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=8903823$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/6707878$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Matsuda, Yoshihisa</creatorcontrib><creatorcontrib>Kawaguchi, Sachiyo</creatorcontrib><creatorcontrib>Kobayashi, Hitomi</creatorcontrib><creatorcontrib>Nishijo, Jujiro</creatorcontrib><title>Physicochemical Characterization of Spray-Dried Phenylbutazone Polymorphs</title><title>Journal of pharmaceutical sciences</title><addtitle>J. Pharm. Sci</addtitle><description>A spray-drying method was applied to the recrystallization of phenylbutazone, and the resulting samples were examined by X-ray powder diffractometry, differential thermal analysis, IR spectrophotometry, scanning electron microscopy, and hot-stage photomicroscopy. Three different crystalline forms (δ, β, and ϵ) could be prepared from methylene chloride solution by varying the drying temperature of sprayed droplets from 120°C to 30°C. Form ϵ, the fifth polymorph of phenylbutazone, was confirmed as a novel crystalline form which could not be prepared by recrystallization techniques. In this spray-drying system the composition of spray-dried samples was shown to be a function of the drying temperature. While the stable form δ was obtained at higher drying temperatures, form δ was obtained only under conditions affording a slower evaporation rate of the solvent. The dissolution properties of the pure modifications prepared by recrystallization techniques and the spray-dried samples were evaluated in simulated intestinal fluid. Form ϵ showed excellent in vitro availability and much higher solubility than any other of the forms.</description><subject>Biological and medical sciences</subject><subject>Calorimetry - methods</subject><subject>Chemical Phenomena</subject><subject>Chemistry, Physical</subject><subject>Crystallization</subject><subject>General pharmacology</subject><subject>Medical sciences</subject><subject>Microscopy, Electron, Scanning</subject><subject>Pharmaceutical technology. Pharmaceutical industry</subject><subject>Pharmacology. Drug treatments</subject><subject>Phenylbutazone</subject><subject>Phenylbutazone-recrystallized polymorphs</subject><subject>Phenylbutazone—recrystallized polymorphs, spray-drying technique, physicochemical characterization</subject><subject>physicochemical characterization</subject><subject>Recrystallization-polymorphs of phenylbutazone</subject><subject>Recrystallization—polymorphs of phenylbutazone, spray-drying technique, physicochemical characterization</subject><subject>Solubility</subject><subject>Spectrophotometry, Infrared</subject><subject>spray-drying technique</subject><subject>Spray-drying-recrystallized polymorphs of phenylbutazone</subject><subject>Spray-drying—recrystallized polymorphs of phenylbutazone, physicochemical characterization</subject><subject>Thermodynamics</subject><subject>X-Ray Diffraction</subject><issn>0022-3549</issn><issn>1520-6017</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1984</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkEFv1DAQRi0EKtvClRtSDohblrGdxPERbaEUrWClBYG4WI4zUVySOLWzlPTXY5TVIg6Ikw_zvpnPj5BnFNYUgL26GcOaFQCCAwP5gKxoziAtgIqHZBUBlvI8k4_JeQg3AFBAnp-Rs0KAKEW5Ite7dg7WONNib43ukk2rvTYTenuvJ-uGxDXJfvR6Ti-9xTrZtTjMXXWY9L0bMNm5bu6dH9vwhDxqdBfw6fG9IJ_fvvm0eZduP15db15vU5MzJtNGGy4YZrxiOYXYI2u4prShVdXQrMyzWpi8YGig1JQ3DUdD0YhMVlIaYQS_IC-XvaN3twcMk-ptMNh1ekB3CKoEKbN4KoLrBTTeheCxUaO3vfazoqB-u1PRnfrjLgaeHzcfqh7rE36UFecvjnMdoqrG68HYcMJKCbxkPGJywe5sh_N_jqr3u_1fFdIla8OEP09Z7b_HFlzk6suHK7WR--0llF_Vt8iXC4_R-A-LXgVjcTBYW49mUrWz__rtLw-dqgQ</recordid><startdate>198402</startdate><enddate>198402</enddate><creator>Matsuda, Yoshihisa</creator><creator>Kawaguchi, Sachiyo</creator><creator>Kobayashi, Hitomi</creator><creator>Nishijo, Jujiro</creator><general>Elsevier Inc</general><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley</general><general>American Pharmaceutical Association</general><scope>BSCLL</scope><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>198402</creationdate><title>Physicochemical Characterization of Spray-Dried Phenylbutazone Polymorphs</title><author>Matsuda, Yoshihisa ; Kawaguchi, Sachiyo ; Kobayashi, Hitomi ; Nishijo, Jujiro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5229-fac372e43b25106704f3a11f1bbf14854d7c562ec08a13ff3ec1ec749b99c7c73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1984</creationdate><topic>Biological and medical sciences</topic><topic>Calorimetry - methods</topic><topic>Chemical Phenomena</topic><topic>Chemistry, Physical</topic><topic>Crystallization</topic><topic>General pharmacology</topic><topic>Medical sciences</topic><topic>Microscopy, Electron, Scanning</topic><topic>Pharmaceutical technology. Pharmaceutical industry</topic><topic>Pharmacology. Drug treatments</topic><topic>Phenylbutazone</topic><topic>Phenylbutazone-recrystallized polymorphs</topic><topic>Phenylbutazone—recrystallized polymorphs, spray-drying technique, physicochemical characterization</topic><topic>physicochemical characterization</topic><topic>Recrystallization-polymorphs of phenylbutazone</topic><topic>Recrystallization—polymorphs of phenylbutazone, spray-drying technique, physicochemical characterization</topic><topic>Solubility</topic><topic>Spectrophotometry, Infrared</topic><topic>spray-drying technique</topic><topic>Spray-drying-recrystallized polymorphs of phenylbutazone</topic><topic>Spray-drying—recrystallized polymorphs of phenylbutazone, physicochemical characterization</topic><topic>Thermodynamics</topic><topic>X-Ray Diffraction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Matsuda, Yoshihisa</creatorcontrib><creatorcontrib>Kawaguchi, Sachiyo</creatorcontrib><creatorcontrib>Kobayashi, Hitomi</creatorcontrib><creatorcontrib>Nishijo, Jujiro</creatorcontrib><collection>Istex</collection><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>Journal of pharmaceutical sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Matsuda, Yoshihisa</au><au>Kawaguchi, Sachiyo</au><au>Kobayashi, Hitomi</au><au>Nishijo, Jujiro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Physicochemical Characterization of Spray-Dried Phenylbutazone Polymorphs</atitle><jtitle>Journal of pharmaceutical sciences</jtitle><addtitle>J. Pharm. Sci</addtitle><date>1984-02</date><risdate>1984</risdate><volume>73</volume><issue>2</issue><spage>173</spage><epage>179</epage><pages>173-179</pages><issn>0022-3549</issn><eissn>1520-6017</eissn><coden>JPMSAE</coden><abstract>A spray-drying method was applied to the recrystallization of phenylbutazone, and the resulting samples were examined by X-ray powder diffractometry, differential thermal analysis, IR spectrophotometry, scanning electron microscopy, and hot-stage photomicroscopy. Three different crystalline forms (δ, β, and ϵ) could be prepared from methylene chloride solution by varying the drying temperature of sprayed droplets from 120°C to 30°C. Form ϵ, the fifth polymorph of phenylbutazone, was confirmed as a novel crystalline form which could not be prepared by recrystallization techniques. In this spray-drying system the composition of spray-dried samples was shown to be a function of the drying temperature. While the stable form δ was obtained at higher drying temperatures, form δ was obtained only under conditions affording a slower evaporation rate of the solvent. The dissolution properties of the pure modifications prepared by recrystallization techniques and the spray-dried samples were evaluated in simulated intestinal fluid. Form ϵ showed excellent in vitro availability and much higher solubility than any other of the forms.</abstract><cop>Washington</cop><pub>Elsevier Inc</pub><pmid>6707878</pmid><doi>10.1002/jps.2600730209</doi><tpages>7</tpages></addata></record> |
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subjects | Biological and medical sciences Calorimetry - methods Chemical Phenomena Chemistry, Physical Crystallization General pharmacology Medical sciences Microscopy, Electron, Scanning Pharmaceutical technology. Pharmaceutical industry Pharmacology. Drug treatments Phenylbutazone Phenylbutazone-recrystallized polymorphs Phenylbutazone—recrystallized polymorphs, spray-drying technique, physicochemical characterization physicochemical characterization Recrystallization-polymorphs of phenylbutazone Recrystallization—polymorphs of phenylbutazone, spray-drying technique, physicochemical characterization Solubility Spectrophotometry, Infrared spray-drying technique Spray-drying-recrystallized polymorphs of phenylbutazone Spray-drying—recrystallized polymorphs of phenylbutazone, physicochemical characterization Thermodynamics X-Ray Diffraction |
title | Physicochemical Characterization of Spray-Dried Phenylbutazone Polymorphs |
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