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Antimicrobial Agents and Chemotherapy, September 2008, p. 3454-3456, Vol. 52, No. 9
0066-4804/08/$08.00+0 doi:10.1128/AAC.00396-08
Copyright © 2008, American Society for Microbiology. All Rights Reserved.

Department of Pharmacy and Pharmacokinetics, Aichi Medical University School of Medicine, Nagakute-cho, Aichi-gun, Aichi 480-1195,1 Department of Medical Technology, Nagoya University School of Health Sciences, 1-1-20 Daikominami, Higashi-ku, Nagoya 461-8672,2 Faculty of Pharmaceutical Sciences, Meijo University, 150 Yagotoyama, Tenpaku-ku, Nagoya 468-8503,3 Department of Critical Care Medicine, Aichi Medical University School of Medicine, Nagakute-cho, Aichi-gun, Aichi 480-1195, Japan4
Received 24 March 2008/ Returned for modification 30 April 2008/ Accepted 23 June 2008
There were no significant differences in the pharmacokinetics of micafungin and expression of hepatic multidrug resistance-associated protein 2 (ABCC2/Mrp2) between analbuminemic and Sprague-Dawley rats. Micafungin bound strongly to high-density lipoprotein (HDL) and moderately to gamma globulin. These results suggest that HDL and gamma globulin contribute to the pharmacokinetics of micafungin.
Published ahead of print on 30 June 2008.
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