Clinical pharmacokinetics of norfloxacin-glycine acetate after intravenous and oral administration in pigs

The pharmacokinetics and dosage regimen of norfloxacin-glycine acetate (NFLXGA) was investigated in pigs after a single intravenous (i.v.) or oral (p.o.) administration at a dosage of 7.2 mg/kg body weight. After both i.v. and p.o. administration, plasma drug concentrations were best fitted to an op...

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Veröffentlicht in:Journal of veterinary science (Suwŏn-si, Korea) 2007, 8(4), , pp.353-356
Hauptverfasser: Chang, Zhi-Qiang (Kyungpook National University, Daegu, Republic of Korea), Oh, B.C. (Gachon University of Medicine and Science, Incheon, Republic of Korea), Kim, J.C. (Chonnam National University, Gwangju, Republic of Korea), Jeong, K.S. (Kyungpook National University, Daegu, Republic of Korea), Lee, M.H. (National Veterinary Research and Quarantine Service, Anyang, Republic of Korea), Yun, H.I. (Chungnam National University, Daejeon, Republic of Korea), Hwang, M.H. (Kyungpook National University, Daegu, Republic of Korea), Park, S.C. (Kyungpook National University, Daegu, Republic of Korea), E-mail: parksch@knu.ac.kr
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Sprache:eng
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Zusammenfassung:The pharmacokinetics and dosage regimen of norfloxacin-glycine acetate (NFLXGA) was investigated in pigs after a single intravenous (i.v.) or oral (p.o.) administration at a dosage of 7.2 mg/kg body weight. After both i.v. and p.o. administration, plasma drug concentrations were best fitted to an open two-compartment model with a rapid distribution phase. After i.v. administration of NFLXGA, the distribution (t∧1/2α) and elimination half-life (t∧1/2β) were 0.36±0.07 h and 7.42±3.55 h, respectively.
ISSN:1229-845X
1976-555X
DOI:10.4142/jvs.2007.8.4.353