Bioequivalence of a Dosage form of the New Drug Mefebut

The bioequivalence of mefebut drug substance and its tablet dosage form was investigated by studying the main pharmacokinetic parameters and calculating the relative bioavailability. The results showed that mefebut circulated for up to 4 h in rabbit blood after peroral administration. The relative b...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Pharmaceutical chemistry journal 2018-09, Vol.52 (6), p.495-496
Hauptverfasser: Smirnova, L. A., Suchkov, E. A., Ryabukha, A. F., Kuznetsov, K. A., Velikopol’skaya, M. V., Tyurenkov, I. N., Bakulin, D. A., Stepanova, É. F., Shevchenko, A. M.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 496
container_issue 6
container_start_page 495
container_title Pharmaceutical chemistry journal
container_volume 52
creator Smirnova, L. A.
Suchkov, E. A.
Ryabukha, A. F.
Kuznetsov, K. A.
Velikopol’skaya, M. V.
Tyurenkov, I. N.
Bakulin, D. A.
Stepanova, É. F.
Shevchenko, A. M.
description The bioequivalence of mefebut drug substance and its tablet dosage form was investigated by studying the main pharmacokinetic parameters and calculating the relative bioavailability. The results showed that mefebut circulated for up to 4 h in rabbit blood after peroral administration. The relative bioavailability was 97.4%.
doi_str_mv 10.1007/s11094-018-1846-x
format Article
fullrecord <record><control><sourceid>gale_cross</sourceid><recordid>TN_cdi_gale_infotracacademiconefile_A554974313</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A554974313</galeid><sourcerecordid>A554974313</sourcerecordid><originalsourceid>FETCH-LOGICAL-c392t-e55e7bc1f8790eef79a49d3357ceb751de7c7035668ca1ff969f6c7522913ba3</originalsourceid><addsrcrecordid>eNp9kM9OwzAMhyMEEmPwANz6Ahlx0zTNcWz8kwZcduAWpZlTOm0NJC2MtydTOSMfLP3kz7I_Qq6BzYAxeRMBmCoog4pCVZT0cEImICSninE4JRPGFFAQ7O2cXMS4ZSxRPJ8Qedt6_BzaL7PDzmLmXWaypY-mwcz5sD8G_TtmL_idLcPQZM_osB76S3LmzC7i1V-fkvX93XrxSFevD0-L-YparvKeohAoawuukoohOqlMoTacC2mxlgI2KK1kXJRlZQ04p0rlSitFnivgteFTMhvXNuk-3XbO98HYVBvct9Z36NqUz4UolCw48ATACNjgYwzo9Edo9yb8aGD6aEqPpnQypY-m9CEx-cjENNs1GPTWD6FLb_0D_QJCf2rW</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Bioequivalence of a Dosage form of the New Drug Mefebut</title><source>SpringerLink Journals</source><creator>Smirnova, L. A. ; Suchkov, E. A. ; Ryabukha, A. F. ; Kuznetsov, K. A. ; Velikopol’skaya, M. V. ; Tyurenkov, I. N. ; Bakulin, D. A. ; Stepanova, É. F. ; Shevchenko, A. M.</creator><creatorcontrib>Smirnova, L. A. ; Suchkov, E. A. ; Ryabukha, A. F. ; Kuznetsov, K. A. ; Velikopol’skaya, M. V. ; Tyurenkov, I. N. ; Bakulin, D. A. ; Stepanova, É. F. ; Shevchenko, A. M.</creatorcontrib><description>The bioequivalence of mefebut drug substance and its tablet dosage form was investigated by studying the main pharmacokinetic parameters and calculating the relative bioavailability. The results showed that mefebut circulated for up to 4 h in rabbit blood after peroral administration. The relative bioavailability was 97.4%.</description><identifier>ISSN: 0091-150X</identifier><identifier>EISSN: 1573-9031</identifier><identifier>DOI: 10.1007/s11094-018-1846-x</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Medicine ; Organic Chemistry ; Pharmacology/Toxicology ; Pharmacy</subject><ispartof>Pharmaceutical chemistry journal, 2018-09, Vol.52 (6), p.495-496</ispartof><rights>Springer Science+Business Media, LLC, part of Springer Nature 2018</rights><rights>COPYRIGHT 2018 Springer</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c392t-e55e7bc1f8790eef79a49d3357ceb751de7c7035668ca1ff969f6c7522913ba3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s11094-018-1846-x$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s11094-018-1846-x$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids></links><search><creatorcontrib>Smirnova, L. A.</creatorcontrib><creatorcontrib>Suchkov, E. A.</creatorcontrib><creatorcontrib>Ryabukha, A. F.</creatorcontrib><creatorcontrib>Kuznetsov, K. A.</creatorcontrib><creatorcontrib>Velikopol’skaya, M. V.</creatorcontrib><creatorcontrib>Tyurenkov, I. N.</creatorcontrib><creatorcontrib>Bakulin, D. A.</creatorcontrib><creatorcontrib>Stepanova, É. F.</creatorcontrib><creatorcontrib>Shevchenko, A. M.</creatorcontrib><title>Bioequivalence of a Dosage form of the New Drug Mefebut</title><title>Pharmaceutical chemistry journal</title><addtitle>Pharm Chem J</addtitle><description>The bioequivalence of mefebut drug substance and its tablet dosage form was investigated by studying the main pharmacokinetic parameters and calculating the relative bioavailability. The results showed that mefebut circulated for up to 4 h in rabbit blood after peroral administration. The relative bioavailability was 97.4%.</description><subject>Medicine</subject><subject>Organic Chemistry</subject><subject>Pharmacology/Toxicology</subject><subject>Pharmacy</subject><issn>0091-150X</issn><issn>1573-9031</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp9kM9OwzAMhyMEEmPwANz6Ahlx0zTNcWz8kwZcduAWpZlTOm0NJC2MtydTOSMfLP3kz7I_Qq6BzYAxeRMBmCoog4pCVZT0cEImICSninE4JRPGFFAQ7O2cXMS4ZSxRPJ8Qedt6_BzaL7PDzmLmXWaypY-mwcz5sD8G_TtmL_idLcPQZM_osB76S3LmzC7i1V-fkvX93XrxSFevD0-L-YparvKeohAoawuukoohOqlMoTacC2mxlgI2KK1kXJRlZQ04p0rlSitFnivgteFTMhvXNuk-3XbO98HYVBvct9Z36NqUz4UolCw48ATACNjgYwzo9Edo9yb8aGD6aEqPpnQypY-m9CEx-cjENNs1GPTWD6FLb_0D_QJCf2rW</recordid><startdate>20180901</startdate><enddate>20180901</enddate><creator>Smirnova, L. A.</creator><creator>Suchkov, E. A.</creator><creator>Ryabukha, A. F.</creator><creator>Kuznetsov, K. A.</creator><creator>Velikopol’skaya, M. V.</creator><creator>Tyurenkov, I. N.</creator><creator>Bakulin, D. A.</creator><creator>Stepanova, É. F.</creator><creator>Shevchenko, A. M.</creator><general>Springer US</general><general>Springer</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20180901</creationdate><title>Bioequivalence of a Dosage form of the New Drug Mefebut</title><author>Smirnova, L. A. ; Suchkov, E. A. ; Ryabukha, A. F. ; Kuznetsov, K. A. ; Velikopol’skaya, M. V. ; Tyurenkov, I. N. ; Bakulin, D. A. ; Stepanova, É. F. ; Shevchenko, A. M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c392t-e55e7bc1f8790eef79a49d3357ceb751de7c7035668ca1ff969f6c7522913ba3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Medicine</topic><topic>Organic Chemistry</topic><topic>Pharmacology/Toxicology</topic><topic>Pharmacy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Smirnova, L. A.</creatorcontrib><creatorcontrib>Suchkov, E. A.</creatorcontrib><creatorcontrib>Ryabukha, A. F.</creatorcontrib><creatorcontrib>Kuznetsov, K. A.</creatorcontrib><creatorcontrib>Velikopol’skaya, M. V.</creatorcontrib><creatorcontrib>Tyurenkov, I. N.</creatorcontrib><creatorcontrib>Bakulin, D. A.</creatorcontrib><creatorcontrib>Stepanova, É. F.</creatorcontrib><creatorcontrib>Shevchenko, A. M.</creatorcontrib><collection>CrossRef</collection><jtitle>Pharmaceutical chemistry journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Smirnova, L. A.</au><au>Suchkov, E. A.</au><au>Ryabukha, A. F.</au><au>Kuznetsov, K. A.</au><au>Velikopol’skaya, M. V.</au><au>Tyurenkov, I. N.</au><au>Bakulin, D. A.</au><au>Stepanova, É. F.</au><au>Shevchenko, A. M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Bioequivalence of a Dosage form of the New Drug Mefebut</atitle><jtitle>Pharmaceutical chemistry journal</jtitle><stitle>Pharm Chem J</stitle><date>2018-09-01</date><risdate>2018</risdate><volume>52</volume><issue>6</issue><spage>495</spage><epage>496</epage><pages>495-496</pages><issn>0091-150X</issn><eissn>1573-9031</eissn><abstract>The bioequivalence of mefebut drug substance and its tablet dosage form was investigated by studying the main pharmacokinetic parameters and calculating the relative bioavailability. The results showed that mefebut circulated for up to 4 h in rabbit blood after peroral administration. The relative bioavailability was 97.4%.</abstract><cop>New York</cop><pub>Springer US</pub><doi>10.1007/s11094-018-1846-x</doi><tpages>2</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0091-150X
ispartof Pharmaceutical chemistry journal, 2018-09, Vol.52 (6), p.495-496
issn 0091-150X
1573-9031
language eng
recordid cdi_gale_infotracacademiconefile_A554974313
source SpringerLink Journals
subjects Medicine
Organic Chemistry
Pharmacology/Toxicology
Pharmacy
title Bioequivalence of a Dosage form of the New Drug Mefebut
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-19T10%3A09%3A26IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Bioequivalence%20of%20a%20Dosage%20form%20of%20the%20New%20Drug%20Mefebut&rft.jtitle=Pharmaceutical%20chemistry%20journal&rft.au=Smirnova,%20L.%20A.&rft.date=2018-09-01&rft.volume=52&rft.issue=6&rft.spage=495&rft.epage=496&rft.pages=495-496&rft.issn=0091-150X&rft.eissn=1573-9031&rft_id=info:doi/10.1007/s11094-018-1846-x&rft_dat=%3Cgale_cross%3EA554974313%3C/gale_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rft_galeid=A554974313&rfr_iscdi=true