Effect of grapefruit juice on serum voriconazole concentrations in the mouse

被引:70
作者
Sugar, AM
Liu, XP
机构
[1] Boston Med Ctr, EBRC, Evans Mem Dept Clin Res, Boston, MA 02118 USA
[2] Boston Med Ctr, Dept Med, Boston, MA 02118 USA
关键词
antifungal therapy; cytochrome P450; grapefruit juice; voriconazole;
D O I
10.1080/714030944
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Voriconazole is a broad spectrum, triazole antifungal drug now well into the final phases of clinical trials in humans. During preclinical phases of development, it was found that when administered to mice, one of the more important animals used in the in vivo evaluation of antifungal compounds, serum voriconazole concentrations were very low at best and often undetectable. This was due to a combination of high clearance and extensive metabolism by cytochrome P450 enzymes. As a result, mice were abandoned as being suitable for further study of voriconazole and most subsequent work with voriconazole has been performed in the guinea pig. In this study, we show that the administration of grapefruit juice, a known inhibitor of cytochrome P450 enzymes, is effective in producing measurable serum concentrations of voriconazole in mice when the drug is administered once daily. Serum voriconazole concentrations were <3 mu g ml(-1) at all time points in mice not receiving grapefruit juice. In contrast, grapefruit juice administered by once daily gavage or continuously in lieu of water in the water bottle resulted in serum voriconazole concentrations ranging 0.4-2.6 and 1.8-5.8 mu g ml(-1), respectively, with increasing concentrations observed over the 10-day evaluation period. Further studies to elucidate the precise mechanism of action and optimal dosing schedule in mice can now be performed to improve our understanding of the pharmacokinetics of voriconazole in the mouse.
引用
收藏
页码:209 / 212
页数:4
相关论文
共 18 条
[1]   ANIMAL-MODELS - USEFULNESS FOR STUDIES OF FUNGAL PATHOGENESIS AND DRUG EFFICACY IN ASPERGILLOSIS [J].
ANDRIOLE, VT ;
MINITER, P ;
GEORGE, D ;
KORDICK, D ;
PATTERSON, TF .
CLINICAL INFECTIOUS DISEASES, 1992, 14 :S134-S138
[2]   In vitro studies of two triazole antifungal agents (Voriconazole [UK-109,496] and fluconazole) against Candida species [J].
Barry, AL ;
Brown, SD .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1996, 40 (08) :1948-1949
[3]   Mechanism-based inactivation of human cytochrome P450 3A4 by grapefruit juice and red wine [J].
Chan, WK ;
Nguyen, LT ;
Miller, VP ;
Harris, RZ .
LIFE SCIENCES, 1998, 62 (10) :PL135-PL142
[4]   Drug interactions with grapefruit juice - Extent, probable mechanism and clinical relevance [J].
Fuhr, U .
DRUG SAFETY, 1998, 18 (04) :251-272
[5]   Efficacy of UK-109496, a new azole antifungal agent, in an experimental model of invasive aspergillosis [J].
George, D ;
Miniter, P ;
Andriole, VT .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1996, 40 (01) :86-91
[6]   Antifungal activity of voriconazole (UK-109,496), fluconazole and amphotericin B against hematogenous Candida krusei infection in neutropenic guinea pig model [J].
Ghannoum, MA ;
Okogbule-Wonodi, I ;
Bhat, N ;
Sanati, H .
JOURNAL OF CHEMOTHERAPY, 1999, 11 (01) :34-39
[7]   Use of voriconazole in treatment of Scedosporium apiospermum infection:: Case report [J].
Girmenia, C ;
Luzi, G ;
Monaco, M ;
Martino, P .
JOURNAL OF CLINICAL MICROBIOLOGY, 1998, 36 (05) :1436-1438
[8]   Inactivation of cytochrome P450 3A4 by bergamottin, a component of grapefruit juice [J].
He, K ;
Iyer, KR ;
Hayes, RN ;
Sinz, MW ;
Woolf, TF ;
Hollenberg, PF .
CHEMICAL RESEARCH IN TOXICOLOGY, 1998, 11 (04) :252-259
[9]  
Hegener P, 1998, AIDS, V12, P2227
[10]  
JEZQUEL S, 1995, 36 INT C ANT AG CHEM