Influence of Fungicidal Activity against Candida tropicalis on the Efficacy of Micafungin and Liposomal Amphotericin B in a Neutropenic Murine Lethal Infection Model
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作者:
Takemoto, Koji
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Dainippon Sumitomo Pharma Co Ltd, Pharmacol Res Labs, Konohana Ku, Osaka 5540022, JapanDainippon Sumitomo Pharma Co Ltd, Pharmacol Res Labs, Konohana Ku, Osaka 5540022, Japan
Takemoto, Koji
[1
]
Nakayama, Tatsuo
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机构:Dainippon Sumitomo Pharma Co Ltd, Pharmacol Res Labs, Konohana Ku, Osaka 5540022, Japan
Nakayama, Tatsuo
Kanazawa, Katsunori
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Dainippon Sumitomo Pharma Co Ltd, Prod Management & Promot Planning, Osaka 5540022, JapanDainippon Sumitomo Pharma Co Ltd, Pharmacol Res Labs, Konohana Ku, Osaka 5540022, Japan
Kanazawa, Katsunori
[2
]
Ueda, Yutaka
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机构:Dainippon Sumitomo Pharma Co Ltd, Pharmacol Res Labs, Konohana Ku, Osaka 5540022, Japan
Ueda, Yutaka
机构:
[1] Dainippon Sumitomo Pharma Co Ltd, Pharmacol Res Labs, Konohana Ku, Osaka 5540022, Japan
[2] Dainippon Sumitomo Pharma Co Ltd, Prod Management & Promot Planning, Osaka 5540022, Japan
Objectives: To investigate the correlation between in vitro killing activity and in vivo efficacy of micafungin (MCFG) and liposomal amphotericin B (L-AMB) against Candida tropicalis in a neutropenic murine lethal infection model. Methods: Candida albicans (one strain) and C. tropicalis (three strains) were tested in time-kill studies. Cyclophosphamide-treated mice were inoculated intravenously with each strain. One day after inoculation, antifungals were administered intravenously once daily for 1 or 3 days. Results: MCFG exhibited fungicidal activity against C. albicans ATCC 90029 and C. tropicalis SP-20142, and fungistatic activity against C. tropicalis ATCC 42678 and SP-20047. The ED(50)s (dosage that results in 50% survival) of MCFG for C. tropicalis ATCC 42678 and SP-20047 (4.1-50 mg/kg) were higher than those for other strains (1.6-12 mg/kg). A 1-day course of MCFG was not effective against C. tropicalis ATCC 42678 and SP-20047 at the clinical dose (5 mg/kg), which achieved an AUC level almost equal to that of 100 mg in humans, whereas a 3-day course of 5 mg/kg MCFG was efficacious against all strains. In contrast, L-AMB showed fungicidal activity against all strains tested and the ED(50)s of L-AMB were 0.08-0.65 mg/kg. In both treatment regimens, the minimum effective doses of L-AMB (<= 0.5 mg/kg) were less than the clinical dosage (<= 5 mg/kg). Conclusions: The in vivo efficacy of MCFG and L-AMB showed a correlation with the in vitro killing activity. At the clinical dose, L-AMB exerted anti-C. tropicalis activity within a shorter treatment period than MCFG. Copyright (c) 2012 S. Karger AG, Basel
机构:
Dainippon Sumitomo Pharma Co Ltd, Pharmacol Res Labs, Konohana Ku, Osaka 5540022, JapanDainippon Sumitomo Pharma Co Ltd, Pharmacol Res Labs, Konohana Ku, Osaka 5540022, Japan
Takemoto, Koji
Yamamoto, Yutaka
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Dainippon Sumitomo Pharma Co Ltd, Prod Management & Promot Planning, Chuo Ku, Tokyo 1048356, JapanDainippon Sumitomo Pharma Co Ltd, Pharmacol Res Labs, Konohana Ku, Osaka 5540022, Japan
Yamamoto, Yutaka
Kanazawa, Katsunori
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Dainippon Sumitomo Pharma Co Ltd, Pharmacol Res Labs, Konohana Ku, Osaka 5540022, JapanDainippon Sumitomo Pharma Co Ltd, Pharmacol Res Labs, Konohana Ku, Osaka 5540022, Japan
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UNIV TEXAS,MD ANDERSON CANCER CTR,DEPT MED SPECIALTIES,INFECT DIS SECT,HOUSTON,TX 77030UNIV TEXAS,MD ANDERSON CANCER CTR,DEPT MED SPECIALTIES,INFECT DIS SECT,HOUSTON,TX 77030
KARYOTAKIS, NC
ANAISSIE, EJ
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UNIV TEXAS,MD ANDERSON CANCER CTR,DEPT MED SPECIALTIES,INFECT DIS SECT,HOUSTON,TX 77030UNIV TEXAS,MD ANDERSON CANCER CTR,DEPT MED SPECIALTIES,INFECT DIS SECT,HOUSTON,TX 77030