Loading…
Preparation and dissolution rate of gliquidone-PVP K30 solid dispersions
Solid dispersions of gliquidone in PVP K30 were prepared by the solvent method. These dispersions were characterized using X-ray diffraction. In comparison with the drug alone, the physical mixtures and even more the solid dispersions showed an increase in the dissolution rate. Moreover these solid...
Saved in:
Published in: | European journal of drug metabolism and pharmacokinetics 1998-04, Vol.23 (2), p.113-117 |
---|---|
Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c311t-f09d01a3d7e34b7febbd35c9b310fa47f4c690a2c53cfd9a8fae082681eab7b73 |
---|---|
cites | cdi_FETCH-LOGICAL-c311t-f09d01a3d7e34b7febbd35c9b310fa47f4c690a2c53cfd9a8fae082681eab7b73 |
container_end_page | 117 |
container_issue | 2 |
container_start_page | 113 |
container_title | European journal of drug metabolism and pharmacokinetics |
container_volume | 23 |
creator | MARTNEZ, P GONI, M. M CANTERA, R. G MARTIN, C DIOS-VIEITEZ, C MARTINEZ-OHARRIZ, C |
description | Solid dispersions of gliquidone in PVP K30 were prepared by the solvent method. These dispersions were characterized using X-ray diffraction. In comparison with the drug alone, the physical mixtures and even more the solid dispersions showed an increase in the dissolution rate. Moreover these solid dispersions were stable during storage. |
doi_str_mv | 10.1007/BF03189325 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_73892104</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>73892104</sourcerecordid><originalsourceid>FETCH-LOGICAL-c311t-f09d01a3d7e34b7febbd35c9b310fa47f4c690a2c53cfd9a8fae082681eab7b73</originalsourceid><addsrcrecordid>eNpFkE1Lw0AQhhdRaqm9eBdyEA9CdDabZLNHLdaKBXtQr2GyH7KSJulucvDfu7ahzmWYmYcX5iHkksIdBeD3j0tgtBAsyU7INKHAY6AFnJIpMF7EXOT5OZl7_w2hWCGyLJ-QieBJluZ8SlYbpzt02Nu2ibBRkbLet_Wwn8NaR62Jvmq7G6xqGx1vPjfRK4MoMHYPd9r5wPoLcmaw9no-9hn5WD69L1bx-u35ZfGwjiWjtI8NCAUUmeKapRU3uqoUy6SoGAWDKTepzAVgIjMmjRJYGNRQJHlBNVa84mxGbg65nWt3g_Z9ubVe6rrGRreDL3n4MVhIA3h7AKVrvXfalJ2zW3Q_JYXyz1z5by7AV2PqUG21OqKjp3C_Hu_oJdbGYSOtP2JJGjISyn4B6Qd04w</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>73892104</pqid></control><display><type>article</type><title>Preparation and dissolution rate of gliquidone-PVP K30 solid dispersions</title><source>Springer Link</source><creator>MARTNEZ, P ; GONI, M. M ; CANTERA, R. G ; MARTIN, C ; DIOS-VIEITEZ, C ; MARTINEZ-OHARRIZ, C</creator><creatorcontrib>MARTNEZ, P ; GONI, M. M ; CANTERA, R. G ; MARTIN, C ; DIOS-VIEITEZ, C ; MARTINEZ-OHARRIZ, C</creatorcontrib><description>Solid dispersions of gliquidone in PVP K30 were prepared by the solvent method. These dispersions were characterized using X-ray diffraction. In comparison with the drug alone, the physical mixtures and even more the solid dispersions showed an increase in the dissolution rate. Moreover these solid dispersions were stable during storage.</description><identifier>ISSN: 0378-7966</identifier><identifier>EISSN: 2107-0180</identifier><identifier>DOI: 10.1007/BF03189325</identifier><identifier>PMID: 9725467</identifier><language>eng</language><publisher>Genève: Médecine et hygiène</publisher><subject>Biological and medical sciences ; Drug Stability ; Drug Storage ; Hormones. Endocrine system ; Hypoglycemic Agents - chemistry ; Medical sciences ; Pharmacology. Drug treatments ; Povidone - chemistry ; Solubility ; Sulfonylurea Compounds - chemistry</subject><ispartof>European journal of drug metabolism and pharmacokinetics, 1998-04, Vol.23 (2), p.113-117</ispartof><rights>1998 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c311t-f09d01a3d7e34b7febbd35c9b310fa47f4c690a2c53cfd9a8fae082681eab7b73</citedby><cites>FETCH-LOGICAL-c311t-f09d01a3d7e34b7febbd35c9b310fa47f4c690a2c53cfd9a8fae082681eab7b73</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>309,310,314,780,784,789,790,23930,23931,25140,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2425321$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9725467$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>MARTNEZ, P</creatorcontrib><creatorcontrib>GONI, M. M</creatorcontrib><creatorcontrib>CANTERA, R. G</creatorcontrib><creatorcontrib>MARTIN, C</creatorcontrib><creatorcontrib>DIOS-VIEITEZ, C</creatorcontrib><creatorcontrib>MARTINEZ-OHARRIZ, C</creatorcontrib><title>Preparation and dissolution rate of gliquidone-PVP K30 solid dispersions</title><title>European journal of drug metabolism and pharmacokinetics</title><addtitle>Eur J Drug Metab Pharmacokinet</addtitle><description>Solid dispersions of gliquidone in PVP K30 were prepared by the solvent method. These dispersions were characterized using X-ray diffraction. In comparison with the drug alone, the physical mixtures and even more the solid dispersions showed an increase in the dissolution rate. Moreover these solid dispersions were stable during storage.</description><subject>Biological and medical sciences</subject><subject>Drug Stability</subject><subject>Drug Storage</subject><subject>Hormones. Endocrine system</subject><subject>Hypoglycemic Agents - chemistry</subject><subject>Medical sciences</subject><subject>Pharmacology. Drug treatments</subject><subject>Povidone - chemistry</subject><subject>Solubility</subject><subject>Sulfonylurea Compounds - chemistry</subject><issn>0378-7966</issn><issn>2107-0180</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><recordid>eNpFkE1Lw0AQhhdRaqm9eBdyEA9CdDabZLNHLdaKBXtQr2GyH7KSJulucvDfu7ahzmWYmYcX5iHkksIdBeD3j0tgtBAsyU7INKHAY6AFnJIpMF7EXOT5OZl7_w2hWCGyLJ-QieBJluZ8SlYbpzt02Nu2ibBRkbLet_Wwn8NaR62Jvmq7G6xqGx1vPjfRK4MoMHYPd9r5wPoLcmaw9no-9hn5WD69L1bx-u35ZfGwjiWjtI8NCAUUmeKapRU3uqoUy6SoGAWDKTepzAVgIjMmjRJYGNRQJHlBNVa84mxGbg65nWt3g_Z9ubVe6rrGRreDL3n4MVhIA3h7AKVrvXfalJ2zW3Q_JYXyz1z5by7AV2PqUG21OqKjp3C_Hu_oJdbGYSOtP2JJGjISyn4B6Qd04w</recordid><startdate>19980401</startdate><enddate>19980401</enddate><creator>MARTNEZ, P</creator><creator>GONI, M. M</creator><creator>CANTERA, R. G</creator><creator>MARTIN, C</creator><creator>DIOS-VIEITEZ, C</creator><creator>MARTINEZ-OHARRIZ, C</creator><general>Médecine et hygiène</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>19980401</creationdate><title>Preparation and dissolution rate of gliquidone-PVP K30 solid dispersions</title><author>MARTNEZ, P ; GONI, M. M ; CANTERA, R. G ; MARTIN, C ; DIOS-VIEITEZ, C ; MARTINEZ-OHARRIZ, C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c311t-f09d01a3d7e34b7febbd35c9b310fa47f4c690a2c53cfd9a8fae082681eab7b73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Biological and medical sciences</topic><topic>Drug Stability</topic><topic>Drug Storage</topic><topic>Hormones. Endocrine system</topic><topic>Hypoglycemic Agents - chemistry</topic><topic>Medical sciences</topic><topic>Pharmacology. Drug treatments</topic><topic>Povidone - chemistry</topic><topic>Solubility</topic><topic>Sulfonylurea Compounds - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>MARTNEZ, P</creatorcontrib><creatorcontrib>GONI, M. M</creatorcontrib><creatorcontrib>CANTERA, R. G</creatorcontrib><creatorcontrib>MARTIN, C</creatorcontrib><creatorcontrib>DIOS-VIEITEZ, C</creatorcontrib><creatorcontrib>MARTINEZ-OHARRIZ, C</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 drug metabolism and pharmacokinetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>MARTNEZ, P</au><au>GONI, M. M</au><au>CANTERA, R. G</au><au>MARTIN, C</au><au>DIOS-VIEITEZ, C</au><au>MARTINEZ-OHARRIZ, C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Preparation and dissolution rate of gliquidone-PVP K30 solid dispersions</atitle><jtitle>European journal of drug metabolism and pharmacokinetics</jtitle><addtitle>Eur J Drug Metab Pharmacokinet</addtitle><date>1998-04-01</date><risdate>1998</risdate><volume>23</volume><issue>2</issue><spage>113</spage><epage>117</epage><pages>113-117</pages><issn>0378-7966</issn><eissn>2107-0180</eissn><abstract>Solid dispersions of gliquidone in PVP K30 were prepared by the solvent method. These dispersions were characterized using X-ray diffraction. In comparison with the drug alone, the physical mixtures and even more the solid dispersions showed an increase in the dissolution rate. Moreover these solid dispersions were stable during storage.</abstract><cop>Genève</cop><pub>Médecine et hygiène</pub><pmid>9725467</pmid><doi>10.1007/BF03189325</doi><tpages>5</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0378-7966 |
ispartof | European journal of drug metabolism and pharmacokinetics, 1998-04, Vol.23 (2), p.113-117 |
issn | 0378-7966 2107-0180 |
language | eng |
recordid | cdi_proquest_miscellaneous_73892104 |
source | Springer Link |
subjects | Biological and medical sciences Drug Stability Drug Storage Hormones. Endocrine system Hypoglycemic Agents - chemistry Medical sciences Pharmacology. Drug treatments Povidone - chemistry Solubility Sulfonylurea Compounds - chemistry |
title | Preparation and dissolution rate of gliquidone-PVP K30 solid dispersions |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-28T03%3A56%3A51IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Preparation%20and%20dissolution%20rate%20of%20gliquidone-PVP%20K30%20solid%20dispersions&rft.jtitle=European%20journal%20of%20drug%20metabolism%20and%20pharmacokinetics&rft.au=MARTNEZ,%20P&rft.date=1998-04-01&rft.volume=23&rft.issue=2&rft.spage=113&rft.epage=117&rft.pages=113-117&rft.issn=0378-7966&rft.eissn=2107-0180&rft_id=info:doi/10.1007/BF03189325&rft_dat=%3Cproquest_cross%3E73892104%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c311t-f09d01a3d7e34b7febbd35c9b310fa47f4c690a2c53cfd9a8fae082681eab7b73%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=73892104&rft_id=info:pmid/9725467&rfr_iscdi=true |