Population Pharmacokinetic Modeling of the Unbound Levofloxacin Concentrations in Rat Plasma and Prostate Tissue Measured by Microdialysis

被引:24
作者
Hurtado, Felipe K. [1 ]
Weber, Benjamin [2 ]
Derendorf, Hartmut [2 ]
Hochhaus, Guenther [2 ]
Dalla Costa, Teresa [1 ]
机构
[1] Univ Fed Rio Grande do Sul, Fac Farm, Programa Posgrad Ciencias Farmaceut, Porto Alegre, RS, Brazil
[2] Univ Florida, Coll Pharm, Dept Pharmaceut, Gainesville, FL 32610 USA
关键词
INFECTED WISTAR RATS; ANTIINFECTIVE AGENTS; SKELETAL-MUSCLE; SEMINAL FLUID; PENETRATION; LUNG; MOXIFLOXACIN; HEALTHY; FLUOROQUINOLONES; GATIFLOXACIN;
D O I
10.1128/AAC.01884-13
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Levofloxacin is a broad-spectrum fluoroquinolone used in the treatment of both acute and chronic bacterial prostatitis. Currently, the treatment of bacterial prostatitis is still difficult, especially due to the poor distribution of many antimicrobials into the prostate, thus preventing the drug to reach effective interstitial concentrations at the infection site. Newer fluoroquinolones show a greater penetration into the prostate. In the present study, we compared the unbound levofloxacin prostate concentrations measured by microdialysis to those in plasma after a 7-mg/kg intravenous bolus dose to Wistar rats. Plasma and dialysate samples were analyzed using a validated high-pressure liquid chromatography-fluorescence method. Both noncompartmental analysis (NCA) and population-based compartmental modeling (NONMEM 6) were performed. Unbound prostate tissue concentrations represented 78% of unbound plasma levels over a period of 12 h by comparing the extent of exposure (unbound AUC(0-infinity)) of 6.4 and 4.8 h.mu g/ml in plasma and tissue, respectively. A three-compartment model with simultaneous passive diffusion and saturable distribution kinetics from the prostate to the central compartment gave the best results in terms of curve fitting, precision of parameter estimates, and model stability. The following parameter values were estimated by the population model: V-1 (0.38 liter; where V-1 represents the volume of the central compartment), C-L (0.22 liter/h), k(12) (2.27h(-1)), k(21) (1.44 h(-1)), k(13) (0.69h(-1)), V-max (7.19 mu g/h), k(M) (0.35 mu g/ml), V-3/fu(prostate) (0.05 liter; where fuprostate represents the fraction unbound in the prostate), and k(31) (3.67 h(-1)). The interindividual variability values for V-1, C-L, V-max, and k(M) were 21, 37, 42, and 76%, respectively. Our results suggest that levofloxacin is likely to be substrate for efflux transporters in the prostate.
引用
收藏
页码:678 / 686
页数:9
相关论文
共 37 条
[1]   Comparison of Fluconazole Renal Penetration Levels in Healthy and Candida albicans-Infected Wistar Rats [J].
Azeredo, Francine Johansson ;
de Araujo, Bibiana Verlindo ;
Haas, Sandra Elisa ;
Torres, Bruna ;
Pigatto, Maiara ;
de Andrade, Cristiane ;
Dalla Costa, Teresa .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2012, 56 (11) :5852-5857
[2]   Key elements of bioanalytical method validation for small molecules [J].
Bansal, Surendra ;
DeStefano, Anthony .
AAPS JOURNAL, 2007, 9 (01) :E109-E114
[3]   Population Pharmacokinetics and Penetration into Prostatic, Seminal, and Vaginal Fluid for Ciprofloxacin, Levofloxacin, and Their Combination [J].
Bulitta, Jurgen B. ;
Kinzig, Martina ;
Naber, Christoph K. ;
Wagenlehner, Florian M. E. ;
Sauber, Christian ;
Landersdorfer, Cornelia B. ;
Soergel, Fritz ;
Naber, Kurt G. .
CHEMOTHERAPY, 2011, 57 (05) :402-416
[4]   Levofloxacin - A review of its use in the treatment of bacterial infections in the United States [J].
Croom, KF ;
Goa, KL .
DRUGS, 2003, 63 (24) :2769-2802
[5]   PK-PD modeling of β-lactam antibiotics: In vitro or in vivo models? [J].
de Araujo, Bibiana Verlindo ;
Diniz, Andrea ;
Palma, Eduardo Celia ;
Buffe, Candida ;
Costa, Teresa Dalla .
JOURNAL OF ANTIBIOTICS, 2011, 64 (06) :439-446
[6]   Free renal levels of voriconazole determined by microdialysis in healthy and Candida sp.-infected Wistar rats [J].
de Araujo, Bibiana Verlindo ;
da Silva, Cristofer Farias ;
Haas, Sandra Elisa ;
Dalla Costa, Teresa .
INTERNATIONAL JOURNAL OF ANTIMICROBIAL AGENTS, 2009, 33 (02) :154-159
[7]   Methodological issues in microdialysis sampling for pharmacokinetic studies [J].
de Lange, ECM ;
de Boer, AG ;
Breimer, DD .
ADVANCED DRUG DELIVERY REVIEWS, 2000, 45 (2-3) :125-148
[8]   A population pharmacokinetic analysis of the penetration of the prostate by levofloxacin [J].
Drusano, GL ;
Preston, SL ;
Van Guilder, M ;
North, D ;
Gombert, M ;
Oefelein, M ;
Boccumini, L ;
Weisinger, B ;
Corrado, M ;
Kahn, J .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2000, 44 (08) :2046-2051
[9]   Application of microdialysis in pharmacokinetic studies [J].
Elmquist, WF ;
Sawchuk, RJ .
PHARMACEUTICAL RESEARCH, 1997, 14 (03) :267-288
[10]   Determination of norfloxacin free interstitial levels in skeletal muscle by microdialysis [J].
Freddo, RJ ;
Costa, TD .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2002, 91 (11) :2433-2440