KP-103, a Novel Triazole Derivative, Is Effective in Preventing Relapse and Successfully Treating Experimental Interdigital Tinea Pedis and Tinea Corporis in Guinea Pigs

The therapeutic efficacy of KP‐103, a triazole derivative, for 10 guinea pigs with interdigital tinea pedis or tinea corporis was investigated. Topical KP‐103 solution (0.25 to 1%) was dose‐dependently effective in treating both dermatophytoses. A 1% KP‐103‐treatment rendered all infected skins cult...

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Veröffentlicht in:Microbiology and immunology 2002-01, Vol.46 (7), p.425-432
Hauptverfasser: Tatsumi, Yoshiyuki, Yokoo, Mamoru, Arika, Tadashi, Yamaguchi, Hideyo
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creator Tatsumi, Yoshiyuki
Yokoo, Mamoru
Arika, Tadashi
Yamaguchi, Hideyo
description The therapeutic efficacy of KP‐103, a triazole derivative, for 10 guinea pigs with interdigital tinea pedis or tinea corporis was investigated. Topical KP‐103 solution (0.25 to 1%) was dose‐dependently effective in treating both dermatophytoses. A 1% KP‐103‐treatment rendered all infected skins culture‐negative on day‐2 posttreatment. A high negative‐culture rate was obtained with 1% solutions of butenafine and lanoconazole but not with 1% neticonazole solution. The follow up study performed on day‐30 and day‐9 posttreatment demonstrated that the relapse rates for 1% KP‐103‐treated animals with tinea pedis and for those with tinea corporis were 20 and 30%, respectively, and that these values were the same as those for 1% butenafine‐treated animals, but lower than those for 1% lanoconazole‐treated animals (55 and 80%, respectively). When a single dose of 1% KP‐103 was applied to the back skin 48 hr before fungal inoculation, 9 of the 10 animals were protected from the dermatophytosis, suggesting that active KP‐103 is retained in skin tissue for at least 48 hr after dosing. Moreover, it was suggested that KP‐103 retains a high activity in the horny layer because of its lower keratin‐affinity. The effectiveness of KP‐103 against dermatophytoses may be due to the favorable pharmacokinetic properties in the skin tissues, together with its potent antifungal activity.
doi_str_mv 10.1111/j.1348-0421.2002.tb02716.x
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Topical KP‐103 solution (0.25 to 1%) was dose‐dependently effective in treating both dermatophytoses. A 1% KP‐103‐treatment rendered all infected skins culture‐negative on day‐2 posttreatment. A high negative‐culture rate was obtained with 1% solutions of butenafine and lanoconazole but not with 1% neticonazole solution. The follow up study performed on day‐30 and day‐9 posttreatment demonstrated that the relapse rates for 1% KP‐103‐treated animals with tinea pedis and for those with tinea corporis were 20 and 30%, respectively, and that these values were the same as those for 1% butenafine‐treated animals, but lower than those for 1% lanoconazole‐treated animals (55 and 80%, respectively). When a single dose of 1% KP‐103 was applied to the back skin 48 hr before fungal inoculation, 9 of the 10 animals were protected from the dermatophytosis, suggesting that active KP‐103 is retained in skin tissue for at least 48 hr after dosing. Moreover, it was suggested that KP‐103 retains a high activity in the horny layer because of its lower keratin‐affinity. The effectiveness of KP‐103 against dermatophytoses may be due to the favorable pharmacokinetic properties in the skin tissues, together with its potent antifungal activity.</description><identifier>ISSN: 0385-5600</identifier><identifier>EISSN: 1348-0421</identifier><identifier>DOI: 10.1111/j.1348-0421.2002.tb02716.x</identifier><identifier>PMID: 12222928</identifier><identifier>CODEN: MIIMDV</identifier><language>eng</language><publisher>Tokyo: Blackwell Publishing Ltd</publisher><subject>Animals ; Antibiotic Prophylaxis - trends ; Antifungal Agents - pharmacology ; Antifungal Agents - therapeutic use ; Aspergillus flavus - growth &amp; development ; Aspergillus flavus - pathogenicity ; Bacterial diseases ; Bacteriology ; Biological and medical sciences ; dermatophytoses ; Disease Models, Animal ; Drug Evaluation, Preclinical ; Experimental bacterial diseases and models ; Fundamental and applied biological sciences. 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Topical KP‐103 solution (0.25 to 1%) was dose‐dependently effective in treating both dermatophytoses. A 1% KP‐103‐treatment rendered all infected skins culture‐negative on day‐2 posttreatment. A high negative‐culture rate was obtained with 1% solutions of butenafine and lanoconazole but not with 1% neticonazole solution. The follow up study performed on day‐30 and day‐9 posttreatment demonstrated that the relapse rates for 1% KP‐103‐treated animals with tinea pedis and for those with tinea corporis were 20 and 30%, respectively, and that these values were the same as those for 1% butenafine‐treated animals, but lower than those for 1% lanoconazole‐treated animals (55 and 80%, respectively). When a single dose of 1% KP‐103 was applied to the back skin 48 hr before fungal inoculation, 9 of the 10 animals were protected from the dermatophytosis, suggesting that active KP‐103 is retained in skin tissue for at least 48 hr after dosing. 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Psychology</topic><topic>Guinea Pigs</topic><topic>Infectious diseases</topic><topic>Keratins - agonists</topic><topic>Keratins - metabolism</topic><topic>KP-103</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Microbial Sensitivity Tests</topic><topic>Microbiology</topic><topic>relapse-preventing effect</topic><topic>Secondary Prevention</topic><topic>Tinea - classification</topic><topic>Tinea - drug therapy</topic><topic>Tinea - prevention &amp; control</topic><topic>Tinea Pedis - drug therapy</topic><topic>Tinea Pedis - prevention &amp; control</topic><topic>Toes</topic><topic>Treatment Outcome</topic><topic>triazole antifungal agent</topic><topic>Triazoles - pharmacokinetics</topic><topic>Triazoles - therapeutic use</topic><topic>Trichophyton - drug effects</topic><topic>Trichophyton - growth &amp; development</topic><topic>Trichophyton - pathogenicity</topic><topic>Vaccines, antisera, therapeutical immunoglobulins and monoclonal antibodies</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tatsumi, Yoshiyuki</creatorcontrib><creatorcontrib>Yokoo, Mamoru</creatorcontrib><creatorcontrib>Arika, Tadashi</creatorcontrib><creatorcontrib>Yamaguchi, Hideyo</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>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>MEDLINE - Academic</collection><jtitle>Microbiology and immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tatsumi, Yoshiyuki</au><au>Yokoo, Mamoru</au><au>Arika, Tadashi</au><au>Yamaguchi, Hideyo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>KP-103, a Novel Triazole Derivative, Is Effective in Preventing Relapse and Successfully Treating Experimental Interdigital Tinea Pedis and Tinea Corporis in Guinea Pigs</atitle><jtitle>Microbiology and immunology</jtitle><addtitle>Microbiology and Immunology</addtitle><date>2002-01-01</date><risdate>2002</risdate><volume>46</volume><issue>7</issue><spage>425</spage><epage>432</epage><pages>425-432</pages><issn>0385-5600</issn><eissn>1348-0421</eissn><coden>MIIMDV</coden><abstract>The therapeutic efficacy of KP‐103, a triazole derivative, for 10 guinea pigs with interdigital tinea pedis or tinea corporis was investigated. Topical KP‐103 solution (0.25 to 1%) was dose‐dependently effective in treating both dermatophytoses. A 1% KP‐103‐treatment rendered all infected skins culture‐negative on day‐2 posttreatment. A high negative‐culture rate was obtained with 1% solutions of butenafine and lanoconazole but not with 1% neticonazole solution. The follow up study performed on day‐30 and day‐9 posttreatment demonstrated that the relapse rates for 1% KP‐103‐treated animals with tinea pedis and for those with tinea corporis were 20 and 30%, respectively, and that these values were the same as those for 1% butenafine‐treated animals, but lower than those for 1% lanoconazole‐treated animals (55 and 80%, respectively). When a single dose of 1% KP‐103 was applied to the back skin 48 hr before fungal inoculation, 9 of the 10 animals were protected from the dermatophytosis, suggesting that active KP‐103 is retained in skin tissue for at least 48 hr after dosing. Moreover, it was suggested that KP‐103 retains a high activity in the horny layer because of its lower keratin‐affinity. The effectiveness of KP‐103 against dermatophytoses may be due to the favorable pharmacokinetic properties in the skin tissues, together with its potent antifungal activity.</abstract><cop>Tokyo</cop><pub>Blackwell Publishing Ltd</pub><pmid>12222928</pmid><doi>10.1111/j.1348-0421.2002.tb02716.x</doi><tpages>8</tpages></addata></record>
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subjects Animals
Antibiotic Prophylaxis - trends
Antifungal Agents - pharmacology
Antifungal Agents - therapeutic use
Aspergillus flavus - growth & development
Aspergillus flavus - pathogenicity
Bacterial diseases
Bacteriology
Biological and medical sciences
dermatophytoses
Disease Models, Animal
Drug Evaluation, Preclinical
Experimental bacterial diseases and models
Fundamental and applied biological sciences. Psychology
Guinea Pigs
Infectious diseases
Keratins - agonists
Keratins - metabolism
KP-103
Male
Medical sciences
Microbial Sensitivity Tests
Microbiology
relapse-preventing effect
Secondary Prevention
Tinea - classification
Tinea - drug therapy
Tinea - prevention & control
Tinea Pedis - drug therapy
Tinea Pedis - prevention & control
Toes
Treatment Outcome
triazole antifungal agent
Triazoles - pharmacokinetics
Triazoles - therapeutic use
Trichophyton - drug effects
Trichophyton - growth & development
Trichophyton - pathogenicity
Vaccines, antisera, therapeutical immunoglobulins and monoclonal antibodies
title KP-103, a Novel Triazole Derivative, Is Effective in Preventing Relapse and Successfully Treating Experimental Interdigital Tinea Pedis and Tinea Corporis in Guinea Pigs
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