Nanosizing: a formulation approach for poorly-water-soluble compounds
Poorly-water-soluble compounds are difficult to develop as drug products using conventional formulation techniques and are frequently abandoned early in discovery. The use of media milling technology to formulate poorly-water-soluble drugs as nanocrystalline particles offers the opportunity to addre...
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Veröffentlicht in: | European Journal of Pharmaceutical Sciences 2003-02, Vol.18 (2), p.113-120 |
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creator | Merisko-Liversidge, Elaine Liversidge, Gary G Cooper, Eugene R |
description | Poorly-water-soluble compounds are difficult to develop as drug products using conventional formulation techniques and are frequently abandoned early in discovery. The use of media milling technology to formulate poorly-water-soluble drugs as nanocrystalline particles offers the opportunity to address many of the deficiencies associated with this class of molecules. NanoCrystal
® Technology is an attrition process wherein large micron size drug crystals are media milled in a water-based stabilizer solution. The process generates physically stable dispersions consisting of nanometer-sized drug crystals. Nanocrystalline particles are a suitable delivery system for all commonly used routes of administration, i.e. oral, injectable (IV, SC, and IM) and topical applications. In addition, aqueous dispersions of nanoparticles can be post-processed into tablets, capsules, fast-melts and lyophilized for sterile product applications. The technology has been successfully incorporated into all phases of the drug development cycle from identification of new chemical entities to refurbishing marketed products for improving their performance and value. |
doi_str_mv | 10.1016/S0928-0987(02)00251-8 |
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® Technology is an attrition process wherein large micron size drug crystals are media milled in a water-based stabilizer solution. The process generates physically stable dispersions consisting of nanometer-sized drug crystals. Nanocrystalline particles are a suitable delivery system for all commonly used routes of administration, i.e. oral, injectable (IV, SC, and IM) and topical applications. In addition, aqueous dispersions of nanoparticles can be post-processed into tablets, capsules, fast-melts and lyophilized for sterile product applications. The technology has been successfully incorporated into all phases of the drug development cycle from identification of new chemical entities to refurbishing marketed products for improving their performance and value.</description><identifier>ISSN: 0928-0987</identifier><identifier>EISSN: 1879-0720</identifier><identifier>DOI: 10.1016/S0928-0987(02)00251-8</identifier><identifier>PMID: 12594003</identifier><language>eng</language><publisher>Shannon: Elsevier B.V</publisher><subject>Animals ; Biological and medical sciences ; General pharmacology ; Humans ; Medical sciences ; Nanoparticles and drug delivery ; Nanotechnology - instrumentation ; Nanotechnology - methods ; Pharmaceutical Preparations - chemistry ; Pharmaceutical technology. Pharmaceutical industry ; Pharmacology. Drug treatments ; Poorly-water-soluble compounds ; Solubility ; Water - chemistry</subject><ispartof>European Journal of Pharmaceutical Sciences, 2003-02, Vol.18 (2), p.113-120</ispartof><rights>2002 Elsevier Science B.V.</rights><rights>2003 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c509t-b93d65693141011f41d78b0fbd0618350383ad24b23c74d49f8f697cf2bf20783</citedby><cites>FETCH-LOGICAL-c509t-b93d65693141011f41d78b0fbd0618350383ad24b23c74d49f8f697cf2bf20783</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/S0928-0987(02)00251-8$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>313,314,780,784,792,3550,27922,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=14546648$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12594003$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Merisko-Liversidge, Elaine</creatorcontrib><creatorcontrib>Liversidge, Gary G</creatorcontrib><creatorcontrib>Cooper, Eugene R</creatorcontrib><title>Nanosizing: a formulation approach for poorly-water-soluble compounds</title><title>European Journal of Pharmaceutical Sciences</title><addtitle>Eur J Pharm Sci</addtitle><description>Poorly-water-soluble compounds are difficult to develop as drug products using conventional formulation techniques and are frequently abandoned early in discovery. The use of media milling technology to formulate poorly-water-soluble drugs as nanocrystalline particles offers the opportunity to address many of the deficiencies associated with this class of molecules. NanoCrystal
® Technology is an attrition process wherein large micron size drug crystals are media milled in a water-based stabilizer solution. The process generates physically stable dispersions consisting of nanometer-sized drug crystals. Nanocrystalline particles are a suitable delivery system for all commonly used routes of administration, i.e. oral, injectable (IV, SC, and IM) and topical applications. In addition, aqueous dispersions of nanoparticles can be post-processed into tablets, capsules, fast-melts and lyophilized for sterile product applications. The technology has been successfully incorporated into all phases of the drug development cycle from identification of new chemical entities to refurbishing marketed products for improving their performance and value.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>General pharmacology</subject><subject>Humans</subject><subject>Medical sciences</subject><subject>Nanoparticles and drug delivery</subject><subject>Nanotechnology - instrumentation</subject><subject>Nanotechnology - methods</subject><subject>Pharmaceutical Preparations - chemistry</subject><subject>Pharmaceutical technology. Pharmaceutical industry</subject><subject>Pharmacology. Drug treatments</subject><subject>Poorly-water-soluble compounds</subject><subject>Solubility</subject><subject>Water - chemistry</subject><issn>0928-0987</issn><issn>1879-0720</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkM1P1kAQhzdGIi_gnyDpRYKH4uxH94MLMQSVhOABPW-2-6FL2m7dbTH419vyvoGjp0kmz_xm5kHoHYYzDJh_vANFZA1KilMgHwBIg2v5Cm2wFKoGQeA12jwj--iglHsA4FLAG7SPSaMYAN2gq1szpBL_xuHneWWqkHI_d2aKaajMOOZk7K-1WY0p5e6x_mMmn-uSurntfGVTP6Z5cOUI7QXTFf92Vw_Rj89X3y-_1jffvlxffrqpbQNqqltFHW-4opgtP-DAsBOyhdA64FjSBqikxhHWEmoFc0wFGbgSNpA2EBCSHqKTbe5y2e_Zl0n3sVjfdWbwaS5aUKCKcrqAzRa0OZWSfdBjjr3JjxqDXv3pJ396laOB6Cd_el1wvFswt713L1M7YQvwfgeYYk0XshlsLC8caxjnbA262HJ-0fEQfdbFRj9Y72L2dtIuxf-c8g8bSovg</recordid><startdate>20030201</startdate><enddate>20030201</enddate><creator>Merisko-Liversidge, Elaine</creator><creator>Liversidge, Gary G</creator><creator>Cooper, Eugene R</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>20030201</creationdate><title>Nanosizing: a formulation approach for poorly-water-soluble compounds</title><author>Merisko-Liversidge, Elaine ; Liversidge, Gary G ; Cooper, Eugene R</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c509t-b93d65693141011f41d78b0fbd0618350383ad24b23c74d49f8f697cf2bf20783</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>General pharmacology</topic><topic>Humans</topic><topic>Medical sciences</topic><topic>Nanoparticles and drug delivery</topic><topic>Nanotechnology - instrumentation</topic><topic>Nanotechnology - methods</topic><topic>Pharmaceutical Preparations - chemistry</topic><topic>Pharmaceutical technology. Pharmaceutical industry</topic><topic>Pharmacology. Drug treatments</topic><topic>Poorly-water-soluble compounds</topic><topic>Solubility</topic><topic>Water - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Merisko-Liversidge, Elaine</creatorcontrib><creatorcontrib>Liversidge, Gary G</creatorcontrib><creatorcontrib>Cooper, Eugene R</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>European Journal of Pharmaceutical Sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Merisko-Liversidge, Elaine</au><au>Liversidge, Gary G</au><au>Cooper, Eugene R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Nanosizing: a formulation approach for poorly-water-soluble compounds</atitle><jtitle>European Journal of Pharmaceutical Sciences</jtitle><addtitle>Eur J Pharm Sci</addtitle><date>2003-02-01</date><risdate>2003</risdate><volume>18</volume><issue>2</issue><spage>113</spage><epage>120</epage><pages>113-120</pages><issn>0928-0987</issn><eissn>1879-0720</eissn><abstract>Poorly-water-soluble compounds are difficult to develop as drug products using conventional formulation techniques and are frequently abandoned early in discovery. The use of media milling technology to formulate poorly-water-soluble drugs as nanocrystalline particles offers the opportunity to address many of the deficiencies associated with this class of molecules. NanoCrystal
® Technology is an attrition process wherein large micron size drug crystals are media milled in a water-based stabilizer solution. The process generates physically stable dispersions consisting of nanometer-sized drug crystals. Nanocrystalline particles are a suitable delivery system for all commonly used routes of administration, i.e. oral, injectable (IV, SC, and IM) and topical applications. In addition, aqueous dispersions of nanoparticles can be post-processed into tablets, capsules, fast-melts and lyophilized for sterile product applications. The technology has been successfully incorporated into all phases of the drug development cycle from identification of new chemical entities to refurbishing marketed products for improving their performance and value.</abstract><cop>Shannon</cop><pub>Elsevier B.V</pub><pmid>12594003</pmid><doi>10.1016/S0928-0987(02)00251-8</doi><tpages>8</tpages></addata></record> |
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subjects | Animals Biological and medical sciences General pharmacology Humans Medical sciences Nanoparticles and drug delivery Nanotechnology - instrumentation Nanotechnology - methods Pharmaceutical Preparations - chemistry Pharmaceutical technology. Pharmaceutical industry Pharmacology. Drug treatments Poorly-water-soluble compounds Solubility Water - chemistry |
title | Nanosizing: a formulation approach for poorly-water-soluble compounds |
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