Alternate-day dosing of itraconazole in healthy adult cats

被引:13
作者
Middleton, S. M. [1 ]
Kubier, A. [2 ]
Dirikolu, L. [1 ]
Papich, M. G. [3 ]
Mitchell, M. A. [1 ]
Rubin, S. I. [1 ]
机构
[1] Univ Illinois, Coll Vet Med, Dept Vet Clin Med, 1008 West Hazelwood M-C 004, Urbana, IL 61802 USA
[2] Vet Specialty Ctr, Melbourne, FL USA
[3] N Carolina State Univ, Coll Vet Med, Mol Biomed Sci Dept, Raleigh, NC 27695 USA
关键词
DOGS; PHARMACOKINETICS; DERMATOPHYTOSIS; BLASTOMYCOSIS; EFFICACY; FOOD;
D O I
10.1111/jvp.12231
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The current available formulations of itraconazole are not ideal for dosing in cats. The capsular preparation often does not allow for accurate dosing, the oral solution is difficult to administer and poorly tolerated, and the bioavailability of compounded formulations has been shown to be poor in other species. The aim of this study was to evaluate every other day dosing of 100 mg itraconazole capsule in healthy adult cats. Ten healthy adult cats received a 100 mg capsule of itraconazole orally every 48 h for 8 weeks. Peak and trough serum concentrations of itraconazole were measured weekly using high-performance liquid chromatography (HPLC). Physical examination, complete blood count (CBC), and chemistry profiles were performed weekly. The dosage regimen achieved average therapeutic trough concentrations (>0.5 mu g/mL) within 3 weeks. The protocol yielded no adverse effects in 8 of the 10 study cats, with affected cats recovering fully with discontinuation of the drug and supportive care. At 8 weeks, an average peak concentration of 1.79 +/- 0.952 mu g/mL (95% CI: 0.996-2.588) and an average trough concentration of 0.761 +/- 0.540 mu g/mL (95% CI: 0.314-1.216) were achieved. Overall, a 100 mg every other day oral dosage regimen for itraconazole in cats yielded serum concentrations with minimal fluctuation and with careful monitoring may be considered for treatment of cats with systemic fungal disease.
引用
收藏
页码:27 / 31
页数:5
相关论文
共 25 条
[1]  
Arceneaux KA, 1998, J AM VET MED ASSOC, V213, P658
[2]   FOOD INTERACTION AND STEADY-STATE PHARMACOKINETICS OF ITRACONAZOLE CAPSULES IN HEALTHY MALE-VOLUNTEERS [J].
BARONE, JA ;
KOH, JG ;
BIERMAN, RH ;
COLAIZZI, JL ;
SWANSON, KA ;
GAFFAR, MC ;
MOSKOVITZ, BL ;
MECHLINSKI, W ;
VANDEVELDE, V .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1993, 37 (04) :778-784
[3]  
Boothe DM, 1997, AM J VET RES, V58, P872
[4]  
BOOTHE DM, 2001, SMALL ANIMAL CLIN PH, P222
[5]   Liquid chromatographic-mass spectrometric determination of itraconazole and its major metabolite, hydroxyitraconazole, in dog plasma [J].
Carrier, A ;
Parent, J .
JOURNAL OF CHROMATOGRAPHY B, 2000, 745 (02) :413-420
[7]   Antifungal Treatment of Small Animal Veterinary Patients [J].
Foy, Daniel S. ;
Trepanier, Lauren A. .
VETERINARY CLINICS OF NORTH AMERICA-SMALL ANIMAL PRACTICE, 2010, 40 (06) :1171-+
[8]   Antifungal serum concentration monitoring: an update [J].
Goodwin, Megan L. ;
Drew, Richard H. .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2008, 61 (01) :17-25
[9]   Coccidioidomycosis in dogs and cats: A review [J].
Graupmann-Kuzma, Angela ;
Valentine, Beth A. ;
Shubitz, Lisa F. ;
Dial, Sharon M. ;
Watrous, Barbara ;
Tornquist, Susan J. .
JOURNAL OF THE AMERICAN ANIMAL HOSPITAL ASSOCIATION, 2008, 44 (05) :226-235
[10]  
Heykants J., 1987, Recent trends in the discovery, development and evaluation of antifungal agents., P223