The pharmacokinetics of linezolid are not affected by concomitant intake of the antioxidant vitamins C and E

被引:9
|
作者
Gordi, T
Tan, LH
Hong, C
Hopkins, NJ
Francom, SE
Slatter, JG
Antal, EJ
机构
[1] Pharmacia & Upjohn Inc, Clin Pharmacol, Kalamazoo, MI 49001 USA
[2] Pharmacia & Upjohn Inc, Clin Biostat, Kalamazoo, MI 49001 USA
[3] Pharmacia & Upjohn Inc, Global Drug Metab, Kalamazoo, MI 49001 USA
[4] Pharmacia, Clin Pharmacol, Singapore, Singapore
[5] Singapore Gen Hosp, Pharmacia Clin Res Unit, Singapore 0316, Singapore
来源
JOURNAL OF CLINICAL PHARMACOLOGY | 2003年 / 43卷 / 10期
关键词
linezolid; pharmacokinetics; vitamins C and E; drug interactions;
D O I
10.1177/0091270003257455
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In vitro metabolism experiments have suggested a possible role for endogenous reactive oxygen species (ROS) in the in 0 vivo clearance of linezolid, a synthetic antibiotic of the oxozolidinone class. This observation has resulted in the hypothesis that dietary antioxidant supplements might disturb the balance of ROS in vivo and thereby lower the clearance of linezolid, The purpose of this open-label, two-group parallel design study was to investigate whether continuous intake of widely used vitamin C or vitamin E will affect the pharmacokinetics of linezolid. A total of 28 healthy volunteers (27 male and I female), including 22 of Chinese origin, were administered a single oral dose of 600 mg linezolid on do 1 and 8. Half of the Subjects received daily oral doses of 1000 mg vitamin C on days 2 through 9, whereas the other half were administered daily oral doses of 800 IU vitamin E during the some time period. Serial blood samples for assessment of the pharmacokinetic parameters of linezolid and its two inactive metabolites were collected on days 1 and 8, whereas vitamin concentrations were measured prior to and after the vitamin intake on these days. Urine was collected oil days 1 and 8 to assess the fraction of dose excreted as linezolid and its major metabolites. All linezolid samples were analyzed according to validated HPLC/MS/MS methods. Linezolid was well tolerated in both groups with no reported clinically significant adverse events. No significant changes were found between the day I and day 8 AUC({}-infinity) and C-max values of linezolid in either the vitamin C treatment group (P = 0.55 and p = 0.64, respectively) or the vitamin E treatment group (p = 0.06 and p = 0.49, respectively). Assessment of other pharmacokinetic parameters did not imply any change across the study groups. In conclusion, linezolid pharmacokinetics are not affected by concomitant administration with vitamins C and E. Therefore, no dose adjustment is necessary in patients taking vitamin C or vitamin E. These no-effect drug interaction data are in accord with current literature indicating that antioxidant vitamins hove only subtle effects on overall ROS balance in vivo.
引用
收藏
页码:1161 / 1167
页数:7
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