JAC Advance Access published online on October 27, 2004
Journal of Antimicrobial Chemotherapy, doi:10.1093/jac/dkh460
© 2004 by The British Society for Antimicrobial Chemotherapy
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1 Department of Biological Sciences, California State Polytechnic University, Pomona, CA 91768, USA
* To whom correspondence should be addressed. Objectives: This study was done to determine whether high dose AmBisome (4-20 mg/kg), given intermittently, could reduce the frequency of dosing needed to treat murine systemic candidiasis when compared with conventional daily treatment. Methods: Mice were immunosuppressed with cyclophosphamide every 3 days, beginning day -3 before challenge with log10 5.0 cfu Candida albicans. Treatment was begun 48-72 h post-challenge with daily or intermittent dose regimens of AmBisome, followed by determination of kidney cfu for up to 1 month post-treatment. Results: A single AmBisome dose of 4 mg/kg was as effective as four daily, 1 mg/kg treatments. A total of 8 mg/kg, given as 4 mg/kg on days 2 and 4, or as 5 mg/kg on day 2 followed by 1 mg/kg on days 3, 4, and 5, also produced comparable efficacy. While 20 mg/kg given day 2, 4 and 6 post-challenge as a 1 week loading dose, followed by one 10 mg/kg treatment on day 13, decreased the fungal burden by up to 5 logs compared with controls (log10 2.3 cfu/g and log10 7.5 cfu/g, respectively), 20 mg/kg given Monday, Wednesday and Friday for 5 weeks, reduced the fungal burden to undetectable levels (i.e. log10 1.0 cfu). Conclusions: Significant reduction or clearance of kidney cfu, following intermittent, high dose AmBisome treatment, indicated that non-daily dosing regimens could be successfully used instead of conventional daily dosing to treat established C. albicans infection in immunosuppressed mice.
Revised August 20, 2004
Accepted September 12, 2004
Original article
Alternative dosing regimens of liposomal amphotericin B (AmBisome) effective in treating murine systemic candidiasis

Jill P. Adler-Moore, E-mail: jpadler{at}csupomona.edu
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