In vitro and in vivo activities of SCH 56592 (posaconazole), a new triazole antifungal agent, against Aspergillus and Candida

被引:78
作者
Cacciapuoti, A [1 ]
Loebenberg, D [1 ]
Corcoran, E [1 ]
Menzel, F [1 ]
Moss, EL [1 ]
Norris, C [1 ]
Michalski, M [1 ]
Raynor, K [1 ]
Halpern, J [1 ]
Mendrick, C [1 ]
Arnold, B [1 ]
Antonacci, B [1 ]
Parmegiani, R [1 ]
Yarosh-Tomaine, T [1 ]
Miller, GH [1 ]
Hare, RS [1 ]
机构
[1] Schering Plough Corp, Res Inst, Kenilworth, NJ 07033 USA
关键词
D O I
10.1128/AAC.44.8.2017-2022.2000
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
SCH 56592 (posaconazole), a new triazole antifungal agent, was tested in vitro, and its activity was compared to that of itraconazole against 39 Aspergillus strains and to that of fluconazole against 275 Candida and 9 Cryptococcus strains. The SCH 56592 MICs for Aspergillus ranged from less than or equal to 0.002 to 0.5 mu g/ml, and those of itraconazole ranged from less than or equal to 0.008 to 1 mu g/ml. The SCH 56592 MICs for Candida and Cryptococcus strains ranged from less than or equal to 0.004 to 16 mu g/ml, and those of fluconazole ranged from less than or equal to 0.062 to >64 mu g/ml. SCH 56592 showed excellent activity against Aspergillus fumigatus and Aspergillus flavus in a pulmonary mouse infection model. When administered therapeutically, the 50% protective doses (PD(50)s) of SCH 56592 ranged from 3.6 to 29.9 mg/kg of body weight, while the PD(50)s of SCH 56592 administered prophylactically ranged from 0.9 to 9.0 mg/kg; itraconazole administered prophylactically was ineffective (PD(50)s, >75 mg/kg). SCH 56592 was also very efficacious against fluconazole-susceptible, -susceptible dose-dependent, or -resistant Candida albicans strains In immunocompetent or immunocompromised mouse models of systemic infection. The PD(50)s of SCH 56592 administered therapeutically ranged from 0.04 to 15.6 mg/kg, while the PD(50)s of SCH 56592 administered prophylactically ranged from 1.5 to 19.3 mg/kg. SCH 56592 has excellent potential for therapy against serious Aspergillus or Candida infections.
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页码:2017 / 2022
页数:6
相关论文
共 38 条
[1]   Characterization and quantitation of the pharmacodynamics of fluconazole in a neutropenic murine disseminated candidiasis infection model [J].
Andes, D ;
van Ogtrop, H .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1999, 43 (09) :2116-2120
[2]  
[Anonymous], 1977, MED MYCOL
[3]  
Armstrong D, 1989, REV INFECT DIS S7, V11, ps1591, DOI [10.1093/clinids/11.Supplement_7.S1591, 10.1093/clinids/11.supplement_7.s1591]
[4]   COMPARISON OF SCH-39304, FLUCONAZOLE, AND KETOCONAZOLE FOR TREATMENT OF SYSTEMIC INFECTIONS IN MICE [J].
CACCIAPUOTI, A ;
LOEBENBERG, D ;
PARMEGIANI, R ;
ANTONACCI, B ;
NORRIS, C ;
MOSS, EL ;
MENZEL, F ;
YAROSHTOMAINE, T ;
HARE, RS ;
MILLER, GH .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1992, 36 (01) :64-67
[5]   CORRELATION OF IN-VITRO FLUCONAZOLE RESISTANCE OF CANDIDA ISOLATES IN RELATION TO THERAPY AND SYMPTOMS OF INDIVIDUALS SEROPOSITIVE FOR HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 [J].
CAMERON, ML ;
SCHELL, WA ;
BRUCH, S ;
BARTLETT, JA ;
WASKIN, HA ;
PERFECT, JR .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1993, 37 (11) :2449-2453
[6]  
CASTALDO P, 1991, ARCH SURG-CHICAGO, V126, P149, DOI 10.1001/archsurg.1991.01410260033005
[7]   Comparison of a new triazole antifungal agent, Schering 56592, with itraconazole and amphotericin B for treatment of histoplasmosis in immunocompetent mice [J].
Connolly, P ;
Wheat, J ;
Schnizlein-Bick, C ;
Durkin, M ;
Kohler, S ;
Smedema, M ;
Goldberg, J ;
Brizendine, E ;
Loebenberg, D .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1999, 43 (02) :322-328
[8]   Invasive aspergillosis [J].
Denning, DW .
CLINICAL INFECTIOUS DISEASES, 1998, 26 (04) :781-803
[9]   Comparison of in vitro activities of the new triazole SCH56592 and the echinocandins MK-0991 (L-743,872) and LY303366 against opportunistic filamentous and dimorphic fungi and yeasts [J].
Espinel-Ingroff, A .
JOURNAL OF CLINICAL MICROBIOLOGY, 1998, 36 (10) :2950-2956
[10]   DEVELOPMENT OF RESISTANCE IN CANDIDA ISOLATES FROM PATIENTS RECEIVING PROLONGED ANTIFUNGAL THERAPY [J].
FANHAVARD, P ;
CAPANO, D ;
SMITH, SM ;
MANGIA, A ;
ENG, RHK .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1991, 35 (11) :2302-2305