Source:http://linkedlifedata.com/resource/pubmed/id/19000278
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
2008-11-12
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pubmed:abstractText |
The purpose of this study was to determine an oral dosing regimen of zonisamide in healthy dogs such that therapeutic concentrations would be safely reached and maintained at steady-state. Adult hound dogs (n = 8) received a single IV (6.9) and an oral (PO) dose (10.3 mg/kg) using a randomized cross-over design. Zonisamide was then administered at 10.3 mg/kg PO every 12 h for 8 weeks. Zonisamide was quantitated in blood compartments or urine by HPLC and data were subjected to noncompartmental pharmacokinetic analysis. Comparisons were made among blood compartments (one-way anova; P </= 0.05). Differences among blood compartments occurred in all derived pharmacokinetic paramenters for each route of administration after single and multiple dosing. After single PO dosing, plasma C(max) was 14.4 +/- 2.3 mcg/mL and elimination half-life was 17.2 +/- 3.6 h. After IV dosing, volume of distribution was 1.1 +/- 0.25 L/kg, clearance was 58 +/- 11 mL/h/kg and elimination t(1/2) was 12.9 +/- 3.6 h. Oral bioavailability was 68 +/- 12%; fraction of unbound drug approximated 60%. At steady-state (4 days), differences occurred for for all parameters except C(max) and C(min.) Plasma C(max) at steady-state was 56 +/- 12 mcg/mL, with 10% fluctuation between C(max) and C(min.) Plasma t(1/2) (h) was 23.52 +/- 5.76 h. Clinical laboratory tests remained normal, with the exception of total T4, which was below normal limits at study end. In conclusion, 10 mg/kg twice daily results in peak plasma zonisamide which exceeds the recommended human therapeutic range (10 to 40 microg/mL) and is associated with suppression of thyroid hormone synthesis. A reasonable b.i.d starting dose for canine epileptics would be 3 mg/kg. Zonisamide monitored in either serum or plasma should be implemented at approximately 7 days.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
1365-2885
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
31
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
544-53
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pubmed:meshHeading |
pubmed-meshheading:19000278-Administration, Oral,
pubmed-meshheading:19000278-Animals,
pubmed-meshheading:19000278-Anticonvulsants,
pubmed-meshheading:19000278-Area Under Curve,
pubmed-meshheading:19000278-Biological Availability,
pubmed-meshheading:19000278-Dogs,
pubmed-meshheading:19000278-Drug Toxicity,
pubmed-meshheading:19000278-Female,
pubmed-meshheading:19000278-Half-Life,
pubmed-meshheading:19000278-Injections, Intravenous,
pubmed-meshheading:19000278-Isoxazoles,
pubmed-meshheading:19000278-Linear Models,
pubmed-meshheading:19000278-Male,
pubmed-meshheading:19000278-Metabolic Clearance Rate,
pubmed-meshheading:19000278-Protein Binding,
pubmed-meshheading:19000278-Thyroid Hormones
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pubmed:year |
2008
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pubmed:articleTitle |
Disposition and safety of zonisamide after intravenous and oral single dose and oral multiple dosing in normal hound dogs.
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pubmed:affiliation |
Department of Anatomy, Physiology and Pharmacology, College of Veterinary Medicine, Auburn University, AL 36849-5518, USA. boothdm@auburn.edu
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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