2003
DOI: 10.1023/a:1025789607863
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Abstract: The pharmacokinetics of diphenhydramine (DPHM) was compared in camels (n = 8) and horses (n = 6) following intravenous (i.v.) administration of a dose of 0.625 mg/kg body weight. In addition, the metabolism and urinary detection time of DPHM was evaluated in camels. The data obtained (median and range in brackets) in camels and horses, respectively, were as follows. The terminal elimination half lives (h) were 1.58 (1.13-2.58) and 6.11 (4.80-14.1), and the total body clearances (L/h per kg) were 1.42 (1.13-1.7… Show more

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Cited by 12 publications
(4 citation statements)
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“…The maximum plasma con- Table 6. Studies on the pharmacokinetics of diphenhydramine have been reported in rabbits [9], sheep [20], human beings [19], camels and horses [33], except beagle dogs. There is only one literature on the pharmacokinetics of amphetamine in beagle dogs, reported by March et al [11], and the pharmacokinetic parameters after an oral administration of 10 mg of 'immediate- 11.6 ± 3.9 6.5 ± 0.8 AUC 0− (g h/mL) 3.8 ± 1.6 9.2 ± 3.1 AUC 0−∞ (g h/mL) 4.1 ± 2.1 9.5 ± 3.2 release' amphetamine dose are as follows: C max = 86.6 ng/mL, T max = 1 h, AUC 0− = 0.56 g h/mL, AUC 0−∞ = 0.67 g h/mL.…”
Section: Application Of the Assaymentioning
confidence: 99%
“…The maximum plasma con- Table 6. Studies on the pharmacokinetics of diphenhydramine have been reported in rabbits [9], sheep [20], human beings [19], camels and horses [33], except beagle dogs. There is only one literature on the pharmacokinetics of amphetamine in beagle dogs, reported by March et al [11], and the pharmacokinetic parameters after an oral administration of 10 mg of 'immediate- 11.6 ± 3.9 6.5 ± 0.8 AUC 0− (g h/mL) 3.8 ± 1.6 9.2 ± 3.1 AUC 0−∞ (g h/mL) 4.1 ± 2.1 9.5 ± 3.2 release' amphetamine dose are as follows: C max = 86.6 ng/mL, T max = 1 h, AUC 0− = 0.56 g h/mL, AUC 0−∞ = 0.67 g h/mL.…”
Section: Application Of the Assaymentioning
confidence: 99%
“…Pharmacokinetics of intravenously administered diphenhydramine have been previously reported in horses (Wasfi et al, 2003). When pharmacokinetic parameters are normalized for dose, most results are not similar between our study and the one by Wasfi et al Several differences exist to the current study including a higher dose administered in the current study (0.625 versus 1.0 mg/kg BW), method of analysis (gas chromatography-mass spectrometry versus liquid chromatography-tandem mass spectrometry), pharmacokinetic compartmental model utilized, and duration of sampling after administration (12 vs. 48 h).…”
Section: Discussionmentioning
confidence: 99%
“…diphenhydramine, and cetirizine, knowledge of their pharmacokinetics and pharmacodynamics is gradually being elucidated (Knych et al, 2016(Knych et al, , 2019Olsén et al, 2007Olsén et al, , 2008Olsén et al, , 2011. Pharmacokinetics of intravenously administered diphenhydramine have been evaluated in adult horses in one study (Wasfi et al, 2003); however, this is not a feasible route of administration for long-term use or by laypersons. In the study by Wasfi et al,a 0.625 mg/kg dose was utilized, whereas a maximum intravenous (IV) dose of 1 mg/kg has been reported for horses.…”
mentioning
confidence: 99%
“…In small animal medicine, the antihistamine diphenhydramine is the drug commonly used to prevent acute febrile and allergic transfusion reactions (25). Currently, there are no pharmacokinetic studies describing diphenhydramine in goats, although there are references among ruminant species for sheep (26) and camels (27). Future work should consider evaluating the effect of an antihistamine on reactions from xenotransfusion in goats (28).…”
Section: Idmentioning
confidence: 99%