In Vitro Activities of Voriconazole as a Triazole Derivative and Caspofungin as an Echinocandin Were Compared with Those of Some Antifungal Agents against Candida Species Isolated from Clinical Specimens

We evaluated the in vitro activity of ketoconazole (KET), fluconazole (FLU), amphotericin B (AmpB), and flucytosine (FCU) in comparison to voriconazole (VOR) as a triazole derivative and caspofungin (CAS) as an echinocandin against 114 Candida spp. isolated from different cultures (blood, urine, spu...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Japanese Journal of Infectious Diseases 2007/09/27, Vol.60(5), pp.302-304
Hauptverfasser: Özçelik, Berrin, Kaynak, Fatma, Cesur, Salih, Sipahi, Bilge, Sultan, Nedim
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 304
container_issue 5
container_start_page 302
container_title Japanese Journal of Infectious Diseases
container_volume 60
creator Özçelik, Berrin
Kaynak, Fatma
Cesur, Salih
Sipahi, Bilge
Sultan, Nedim
description We evaluated the in vitro activity of ketoconazole (KET), fluconazole (FLU), amphotericin B (AmpB), and flucytosine (FCU) in comparison to voriconazole (VOR) as a triazole derivative and caspofungin (CAS) as an echinocandin against 114 Candida spp. isolated from different cultures (blood, urine, sputum). The most common species of identified Candida were C. albicans (88), followed by C. parapsilosis (8), C. glabrata (7), C. tropicalis (6), C. famata (2), C. kefyr (2), and C. sake (1). The Clinical and Laboratory Standards Institute M 27-A method was used to evaluate the activity of antifungal agents. The minimal inhibitory concentrations of the strains were evaluated by RPMI 1640 medium using a microdilution method. Of 114 isolates, 100% were sensitive to AmpB, VOR, and CAS, 1.75% showed intermediate resistant to FCU also 0.87% showed intermediate resistant to FLU, and 2.63% were fully resistant to FLU and FCU. These results suggest that KET, AmpB, CAS, and VOR demonstrated excellent activity against all Candida spp. Taken together; these antifungal agents should be effective in the treatment of a broad range of Candida infections.
doi_str_mv 10.7883/yoken.JJID.2007.302
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_68292293</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>68292293</sourcerecordid><originalsourceid>FETCH-LOGICAL-c504t-e6652e9643d5235c4b2fc9b6c230fd30cee077261bb36f77825b1efe1a3d96f53</originalsourceid><addsrcrecordid>eNpVkc1u1DAYRSMEoqXwBEjIK3YZ_JM4yXKUtpCqEosOZWk5zucZl8QOtqeovCIvhTMzKmLjv-_ck0g3y94TvKrqmn16cj_Arm5uussVxbhaMUxfZOekrouc1oy_TGdWFDlnuDjL3oTwgDEtS4JfZ2ckCUhdsfPsT2fRvYneobWK5tFEAwE5je6dN8pZ-duNgGRAEm28Od4uwZtHmeA0sANqZZid3tutsQfQoiu1M9apNExP38EDat00Sw8D-mXiDm12LsDykTs3AVrbaJa4HNF6CzYmxVYaG2IyJ8Mg0d0MavmtLrhRxmTR3k2oHY01KqUO4wlseJu90nIM8O60X2Tfrq827Zf89uvnrl3f5qrERcyB85JCwws2lJSVquipVk3PFWVYDwwrAFxVlJO-Z1xXVU3LnoAGItnQcF2yi-zj0Tt793MPIYrJBAXjKC24fRC8pg2lDUsgO4LKuxA8aDF7M0n_JAgWS4fi0KFYOhRLhyJ1mFIfTvp9P8HwL3MqLQHdEXgIUW7hGZA-GjXCScqxKJflP_kzo3bSC7DsL8hWt9k</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>68292293</pqid></control><display><type>article</type><title>In Vitro Activities of Voriconazole as a Triazole Derivative and Caspofungin as an Echinocandin Were Compared with Those of Some Antifungal Agents against Candida Species Isolated from Clinical Specimens</title><source>J-STAGE Free</source><source>MEDLINE</source><source>Freely Accessible Japanese Titles</source><source>EZB-FREE-00999 freely available EZB journals</source><creator>Özçelik, Berrin ; Kaynak, Fatma ; Cesur, Salih ; Sipahi, Bilge ; Sultan, Nedim</creator><creatorcontrib>Özçelik, Berrin ; Kaynak, Fatma ; Cesur, Salih ; Sipahi, Bilge ; Sultan, Nedim</creatorcontrib><description>We evaluated the in vitro activity of ketoconazole (KET), fluconazole (FLU), amphotericin B (AmpB), and flucytosine (FCU) in comparison to voriconazole (VOR) as a triazole derivative and caspofungin (CAS) as an echinocandin against 114 Candida spp. isolated from different cultures (blood, urine, sputum). The most common species of identified Candida were C. albicans (88), followed by C. parapsilosis (8), C. glabrata (7), C. tropicalis (6), C. famata (2), C. kefyr (2), and C. sake (1). The Clinical and Laboratory Standards Institute M 27-A method was used to evaluate the activity of antifungal agents. The minimal inhibitory concentrations of the strains were evaluated by RPMI 1640 medium using a microdilution method. Of 114 isolates, 100% were sensitive to AmpB, VOR, and CAS, 1.75% showed intermediate resistant to FCU also 0.87% showed intermediate resistant to FLU, and 2.63% were fully resistant to FLU and FCU. These results suggest that KET, AmpB, CAS, and VOR demonstrated excellent activity against all Candida spp. Taken together; these antifungal agents should be effective in the treatment of a broad range of Candida infections.</description><identifier>ISSN: 1344-6304</identifier><identifier>EISSN: 1884-2836</identifier><identifier>DOI: 10.7883/yoken.JJID.2007.302</identifier><identifier>PMID: 17881873</identifier><language>eng</language><publisher>Japan: National Institute of Infectious Diseases</publisher><subject>Antifungal Agents - pharmacology ; Candida - drug effects ; Candida - isolation &amp; purification ; Candidiasis - blood ; Candidiasis - microbiology ; Candidiasis - urine ; Drug Resistance, Fungal ; Echinocandins - pharmacology ; Humans ; Lipopeptides ; Microbial Sensitivity Tests ; Pyrimidines - pharmacology ; Sputum - microbiology ; Triazoles - pharmacology ; Voriconazole</subject><ispartof>Japanese Journal of Infectious Diseases, 2007/09/27, Vol.60(5), pp.302-304</ispartof><rights>2007 Authors</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c504t-e6652e9643d5235c4b2fc9b6c230fd30cee077261bb36f77825b1efe1a3d96f53</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,1877,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17881873$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Özçelik, Berrin</creatorcontrib><creatorcontrib>Kaynak, Fatma</creatorcontrib><creatorcontrib>Cesur, Salih</creatorcontrib><creatorcontrib>Sipahi, Bilge</creatorcontrib><creatorcontrib>Sultan, Nedim</creatorcontrib><title>In Vitro Activities of Voriconazole as a Triazole Derivative and Caspofungin as an Echinocandin Were Compared with Those of Some Antifungal Agents against Candida Species Isolated from Clinical Specimens</title><title>Japanese Journal of Infectious Diseases</title><addtitle>Jpn J Infect Dis</addtitle><description>We evaluated the in vitro activity of ketoconazole (KET), fluconazole (FLU), amphotericin B (AmpB), and flucytosine (FCU) in comparison to voriconazole (VOR) as a triazole derivative and caspofungin (CAS) as an echinocandin against 114 Candida spp. isolated from different cultures (blood, urine, sputum). The most common species of identified Candida were C. albicans (88), followed by C. parapsilosis (8), C. glabrata (7), C. tropicalis (6), C. famata (2), C. kefyr (2), and C. sake (1). The Clinical and Laboratory Standards Institute M 27-A method was used to evaluate the activity of antifungal agents. The minimal inhibitory concentrations of the strains were evaluated by RPMI 1640 medium using a microdilution method. Of 114 isolates, 100% were sensitive to AmpB, VOR, and CAS, 1.75% showed intermediate resistant to FCU also 0.87% showed intermediate resistant to FLU, and 2.63% were fully resistant to FLU and FCU. These results suggest that KET, AmpB, CAS, and VOR demonstrated excellent activity against all Candida spp. Taken together; these antifungal agents should be effective in the treatment of a broad range of Candida infections.</description><subject>Antifungal Agents - pharmacology</subject><subject>Candida - drug effects</subject><subject>Candida - isolation &amp; purification</subject><subject>Candidiasis - blood</subject><subject>Candidiasis - microbiology</subject><subject>Candidiasis - urine</subject><subject>Drug Resistance, Fungal</subject><subject>Echinocandins - pharmacology</subject><subject>Humans</subject><subject>Lipopeptides</subject><subject>Microbial Sensitivity Tests</subject><subject>Pyrimidines - pharmacology</subject><subject>Sputum - microbiology</subject><subject>Triazoles - pharmacology</subject><subject>Voriconazole</subject><issn>1344-6304</issn><issn>1884-2836</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkc1u1DAYRSMEoqXwBEjIK3YZ_JM4yXKUtpCqEosOZWk5zucZl8QOtqeovCIvhTMzKmLjv-_ck0g3y94TvKrqmn16cj_Arm5uussVxbhaMUxfZOekrouc1oy_TGdWFDlnuDjL3oTwgDEtS4JfZ2ckCUhdsfPsT2fRvYneobWK5tFEAwE5je6dN8pZ-duNgGRAEm28Od4uwZtHmeA0sANqZZid3tutsQfQoiu1M9apNExP38EDat00Sw8D-mXiDm12LsDykTs3AVrbaJa4HNF6CzYmxVYaG2IyJ8Mg0d0MavmtLrhRxmTR3k2oHY01KqUO4wlseJu90nIM8O60X2Tfrq827Zf89uvnrl3f5qrERcyB85JCwws2lJSVquipVk3PFWVYDwwrAFxVlJO-Z1xXVU3LnoAGItnQcF2yi-zj0Tt793MPIYrJBAXjKC24fRC8pg2lDUsgO4LKuxA8aDF7M0n_JAgWS4fi0KFYOhRLhyJ1mFIfTvp9P8HwL3MqLQHdEXgIUW7hGZA-GjXCScqxKJflP_kzo3bSC7DsL8hWt9k</recordid><startdate>20070927</startdate><enddate>20070927</enddate><creator>Özçelik, Berrin</creator><creator>Kaynak, Fatma</creator><creator>Cesur, Salih</creator><creator>Sipahi, Bilge</creator><creator>Sultan, Nedim</creator><general>National Institute of Infectious Diseases</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>20070927</creationdate><title>In Vitro Activities of Voriconazole as a Triazole Derivative and Caspofungin as an Echinocandin Were Compared with Those of Some Antifungal Agents against Candida Species Isolated from Clinical Specimens</title><author>Özçelik, Berrin ; Kaynak, Fatma ; Cesur, Salih ; Sipahi, Bilge ; Sultan, Nedim</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c504t-e6652e9643d5235c4b2fc9b6c230fd30cee077261bb36f77825b1efe1a3d96f53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Antifungal Agents - pharmacology</topic><topic>Candida - drug effects</topic><topic>Candida - isolation &amp; purification</topic><topic>Candidiasis - blood</topic><topic>Candidiasis - microbiology</topic><topic>Candidiasis - urine</topic><topic>Drug Resistance, Fungal</topic><topic>Echinocandins - pharmacology</topic><topic>Humans</topic><topic>Lipopeptides</topic><topic>Microbial Sensitivity Tests</topic><topic>Pyrimidines - pharmacology</topic><topic>Sputum - microbiology</topic><topic>Triazoles - pharmacology</topic><topic>Voriconazole</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Özçelik, Berrin</creatorcontrib><creatorcontrib>Kaynak, Fatma</creatorcontrib><creatorcontrib>Cesur, Salih</creatorcontrib><creatorcontrib>Sipahi, Bilge</creatorcontrib><creatorcontrib>Sultan, Nedim</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>Japanese Journal of Infectious Diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Özçelik, Berrin</au><au>Kaynak, Fatma</au><au>Cesur, Salih</au><au>Sipahi, Bilge</au><au>Sultan, Nedim</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>In Vitro Activities of Voriconazole as a Triazole Derivative and Caspofungin as an Echinocandin Were Compared with Those of Some Antifungal Agents against Candida Species Isolated from Clinical Specimens</atitle><jtitle>Japanese Journal of Infectious Diseases</jtitle><addtitle>Jpn J Infect Dis</addtitle><date>2007-09-27</date><risdate>2007</risdate><volume>60</volume><issue>5</issue><spage>302</spage><epage>304</epage><pages>302-304</pages><artnum>JJID.2007.302</artnum><issn>1344-6304</issn><eissn>1884-2836</eissn><abstract>We evaluated the in vitro activity of ketoconazole (KET), fluconazole (FLU), amphotericin B (AmpB), and flucytosine (FCU) in comparison to voriconazole (VOR) as a triazole derivative and caspofungin (CAS) as an echinocandin against 114 Candida spp. isolated from different cultures (blood, urine, sputum). The most common species of identified Candida were C. albicans (88), followed by C. parapsilosis (8), C. glabrata (7), C. tropicalis (6), C. famata (2), C. kefyr (2), and C. sake (1). The Clinical and Laboratory Standards Institute M 27-A method was used to evaluate the activity of antifungal agents. The minimal inhibitory concentrations of the strains were evaluated by RPMI 1640 medium using a microdilution method. Of 114 isolates, 100% were sensitive to AmpB, VOR, and CAS, 1.75% showed intermediate resistant to FCU also 0.87% showed intermediate resistant to FLU, and 2.63% were fully resistant to FLU and FCU. These results suggest that KET, AmpB, CAS, and VOR demonstrated excellent activity against all Candida spp. Taken together; these antifungal agents should be effective in the treatment of a broad range of Candida infections.</abstract><cop>Japan</cop><pub>National Institute of Infectious Diseases</pub><pmid>17881873</pmid><doi>10.7883/yoken.JJID.2007.302</doi><tpages>3</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1344-6304
ispartof Japanese Journal of Infectious Diseases, 2007/09/27, Vol.60(5), pp.302-304
issn 1344-6304
1884-2836
language eng
recordid cdi_proquest_miscellaneous_68292293
source J-STAGE Free; MEDLINE; Freely Accessible Japanese Titles; EZB-FREE-00999 freely available EZB journals
subjects Antifungal Agents - pharmacology
Candida - drug effects
Candida - isolation & purification
Candidiasis - blood
Candidiasis - microbiology
Candidiasis - urine
Drug Resistance, Fungal
Echinocandins - pharmacology
Humans
Lipopeptides
Microbial Sensitivity Tests
Pyrimidines - pharmacology
Sputum - microbiology
Triazoles - pharmacology
Voriconazole
title In Vitro Activities of Voriconazole as a Triazole Derivative and Caspofungin as an Echinocandin Were Compared with Those of Some Antifungal Agents against Candida Species Isolated from Clinical Specimens
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-08T01%3A40%3A22IST&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=In%20Vitro%20Activities%20of%20Voriconazole%20as%20a%20Triazole%20Derivative%20and%20Caspofungin%20as%20an%20Echinocandin%20Were%20Compared%20with%20Those%20of%20Some%20Antifungal%20Agents%20against%20Candida%20Species%20Isolated%20from%20Clinical%20Specimens&rft.jtitle=Japanese%20Journal%20of%20Infectious%20Diseases&rft.au=%C3%96z%C3%A7elik,%20Berrin&rft.date=2007-09-27&rft.volume=60&rft.issue=5&rft.spage=302&rft.epage=304&rft.pages=302-304&rft.artnum=JJID.2007.302&rft.issn=1344-6304&rft.eissn=1884-2836&rft_id=info:doi/10.7883/yoken.JJID.2007.302&rft_dat=%3Cproquest_cross%3E68292293%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=68292293&rft_id=info:pmid/17881873&rfr_iscdi=true