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Antimicrobial Agents and Chemotherapy, July 2003, p. 2351-2353, Vol. 47, No. 7
0066-4804/03/$08.00+0 DOI: 10.1128/AAC.47.7.2351-2353.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.
Wolfgang Sadee,1,
and B. Joseph Guglielmo1*
Schools of Pharmacy,1 Medicine, University of California, San Francisco, California2
Received 22 November 2002/ Returned for modification 17 March 2003/ Accepted 24 April 2003
Variability in valacyclovir bioavailability and the potential for cephalexin-valacyclovir interaction were evaluated. The intraindividual acyclovir area under the concentration-time curve (AUC) varied minimally, whereas interindividual differences were substantial. Coadministration of the human peptide transporter 1 (hPEPT1) substrates valacyclovir and cephalexin minimally reduced the acyclovir AUC. These results suggest a stable valacyclovir absorption phenotype, significant interindividual variability, and minimal interaction between these hPEPT1 substrates.
Present address: ISREC, 1066 Epalinges, Switzerland.
Present address: Ohio State University, Columbus, OH 43210.
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