Linezolid absolute bioavailability and the effect of food on oral bioavailability

被引:97
作者
Welshman, IR [1 ]
Sisson, TA [1 ]
Jungbluth, GL [1 ]
Stalker, DJ [1 ]
Hopkins, NK [1 ]
机构
[1] Pharmacia, Dept Clin Pharmacol, Kalamazoo, MI 49007 USA
关键词
linezolid; bioavailability; food effect;
D O I
10.1002/bdd.255
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Linezolid is a novel oxazolidinone antibiotic that has a spectrum of activity encompassing a variety of Gram-positive bacteria. The objectives of this study were twofold: (1) to compare the absorption of linezolid tablets given immediately following a high-fat meal with the absorption of tablets administered While fasting, and (2) to assess the bioavailability of a 375-mg oral dose given while fasting relative to a 375-mg dose of linezolid sterile solution given intravenously. Venous blood samples were taken over the 48 h following the single dose administration of both the oral and intravenous (IV) treatment. Samples were subsequently frozen for the determination of linezolid concentrations by HPLC. The only statistically significant difference between the fasted and the fed treatment was in peak plasma concentration, with the mean C-max for fasted subjects being 23% greater than that for subjects after consumption of a high-fat meal. Comparable AUC(0-infinity) values were measured under both conditions, indicating that the overall extent of absorption is the same. Therefore, the difference in C-max, while statistically significant, should not affect the therapeutic efficacy of linezolid when it is administered with food. There were no statistically significant differences in AUC(0-infinity), CL or half-life between the fasted oral treatment and the intravenous treatment. As expected, C-max was statistically different between the two treatments. However, the mean absolute bioavailability (F) of the tablet, using the IV sterile solution as the reference treatment, was 103%(+/- 20%). Copyright (C) 2001 John Wiley & Sons, Ltd.
引用
收藏
页码:91 / 97
页数:7
相关论文
共 19 条
[1]   MECHANISM OF ACTION AND INVITRO AND INVIVO ACTIVITIES OF S-6123, A NEW OXAZOLIDINONE COMPOUND [J].
DALY, JS ;
ELIOPOULOS, GM ;
WILLEY, S ;
MOELLERING, RC .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1988, 32 (09) :1341-1346
[2]   ACTIVITY AND MECHANISM OF ACTION OF DUP-105 AND DUP-721, NEW OXAZOLIDINONE COMPOUNDS [J].
DALY, JS ;
ELIOPOULOS, GM ;
REISZNER, E ;
MOELLERING, RC .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1988, 21 (06) :721-730
[3]  
DEMYAN WF, 1997, 37 INT C ANT AG CHEM
[4]   THE MECHANISM OF ACTION OF DUP 721, A NEW ANTIBACTERIAL AGENT - EFFECTS ON MACROMOLECULAR-SYNTHESIS [J].
EUSTICE, DC ;
FELDMAN, PA ;
SLEE, AM .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1988, 150 (03) :965-971
[5]   MECHANISM OF ACTION OF DUP-721 - INHIBITION OF AN EARLY EVENT DURING INITIATION OF PROTEIN-SYNTHESIS [J].
EUSTICE, DC ;
FELDMAN, PA ;
ZAJAC, I ;
SLEE, AM .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1988, 32 (08) :1218-1222
[6]  
Gibaldi M. P., 1982, PHARMACOKINETICS
[7]   In vitro antimicrobial activities and spectra of U-100592 and U-100766, two novel fluorinated oxazolidinones [J].
Jones, RN ;
Johnson, DM ;
Erwin, ME .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1996, 40 (03) :720-726
[8]   The oxazolidinone eperezolid binds to the 50S ribosomal subunit and competes with binding of chloramphenicol and lincomycin [J].
Lin, AH ;
Murray, RW ;
Vidmar, TJ ;
Marotti, KR .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1997, 41 (10) :2127-2131
[9]   ESTIMATION OF GASTRIC RESIDENCE TIME OF THE HEIDELBERG CAPSULE IN HUMANS - EFFECT OF VARYING FOOD COMPOSITION [J].
MOJAVERIAN, P ;
FERGUSON, RK ;
VLASSES, PH ;
ROCCI, ML ;
OREN, A ;
FIX, JA ;
CALDWELL, LJ ;
GARDNER, C .
GASTROENTEROLOGY, 1985, 89 (02) :392-397
[10]  
PAWSEY SD, 1996, EUR C ANT CHEM