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2010 | 13 | 4 |

Tytuł artykułu

Pharmacokinetics of tramadol and metabolites after injective administrations in dogs

Treść / Zawartość

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
The aim of this study was to determine the pharmacokinetics of tramadol and its main metabolites after IV and IM injections. The pharmacokinetic cross-over study was carried out on 6 healthy male beagle dogs. Tramadol was administered by intravenous (IV) and intramuscular (IM) injection at 4 mg/kg. Tramadol and its main metabolites O-desmethyl-tramadol (M1), N-,N-didesmethyl-tramadol (M2) and N-,O-didesmethyl-tramadol (M5) concentrations were measured in plasma samples by a HPLC coupled with fluorimetric detection; pharmacokinetic evaluations were carried out with a compartmental and non-compartmental model for tramadol and its metabolites, respectively. The bioavailability of the drug, ranging between 84-102% (mean 92%), was within the generally accepted values for a positive bioequivalence decision of (80-125%). After the IM injection the mean plasma drug concentration peak was reached after a Tmax of 0.34 h with a Cmax of 2.52 μg/mL. No therapeutic relevant differences were observed between IM and IV administration. The minimal effective plasma concentration was reached after a few minutes and maintained for about 6-7 h in both administrations. M1 plasma concentration was low and the amounts of the other metabolites produced were analogous in both routes of administration. In conclusion, tramadol was rapidly and almost completely absorbed after IM administration and its systemic availability was equivalent to the IV injection. The different onset time and duration of action observed were very small and probably therapeutically irrelevant. The IM injection is a useful alternative to IV injection in the dog.

Wydawca

-

Rocznik

Tom

13

Numer

4

Opis fizyczny

p.639-644,fig.,ref.

Twórcy

autor
  • Department of Veterinary Clinics, University of Pisa, Via Livornese (lato monte) 1, San Piero a Grado, 56010 Pisa, Italy
autor

Bibliografia

  • de Sousa AB, Santos AC, Schramm SG, Porta V, Górniak SL, Florio JC, de Souza Spinosa H (2008) Pharmacokinetics of tramadol and o-desmethyltramadol in goats after intravenous and oral administration. J Vet Pharmacol Ther 31: 45-51.
  • Elghazali M, Barezaik IM, Abdel Hadi AA, Eltayeb FM, Al Masri J, Wasfi IA (2008) The pharmacokinetics, metabolism and urinary detection time of tramadol in camels. Vet J 178: 272-277.
  • Garrido MJ, Sayar O, Segura C, Rapado J, Dios-Vieitez MC, Renedo MJ, Troconiz IF (2003) Pharmacokinetic/ pharmacodynamic modeling of the antinociceptive effects of (+)-tramadol in the rat: role of cytochrome P450 2D activity. J Pharmacol Exp Ther 305: 710-718.
  • Giorgi M, Del Carlo S, Saccomanni G, Łebkowska-Wieruszewska B, Kowalski CJ (2009a) Pharmacokinetics of tramadol and its major metabolites following rectal and intravenous administration in dogs. N Z Vet J 57: 146-152.
  • Giorgi M, Del Carlo S, Saccomanni G, Łebkowska-Wieruszewska B, Kowalski CJ (2009b) Pharmacokinetic and urine profile of tramadol and its major metabolites following oral immediate release capsules administration in dogs. Vet Res Commun 33: 875-885.
  • Giorgi M, Del Carlo S, Sgorbini M, Saccomanni G (2009c) Pharmacokinetics of tramadol and its metabolites M1, M2 and M5 in donkeys following intravenous and oral immediate release single dose administration. J Equine Vet Sci 29: 569-574.
  • Giorgi M, Saccomanni G, Lebkowska-Wieruszewska B, Kowalski C (2009d) Pharmacokinetic evaluation of tramadol and its major metabolites after single oral sustained tablet administration in the dog: a pilot study. Vet J 180: 253-255.
  • Giorgi M, Soldani G, Manera C, Ferrarini PL, Sgorbini M, Saccomanni G (2007) Pharmacokinetics of tramadol and its metabolites M1, M2 and M5 in horses following intravenous, immediate release (fasted/fed) and sustained release single dose administration. J Equine Vet Sci 27: 481-488.
  • Grond S, Meuser T, Uragg H, Stahlberg HJ, Lehmann KA (1999) Serum concentrations of tramadol enantiomers during patient-controlled analgesia. Br J Clin Pharmacol 48:254-257.
  • Grond S, Sablotzki A (2004) Clinical pharmacology of tramadol. Clin Pharmacokinet 43: 879-923.
  • Kukanich B, Papich MG (2004) Pharmacokinetics of tramadol and the metabolite O-desmethyltramadol in dogs. J Vet Pharmacol Ther 27: 239-246.
  • Lintz W, Beier H, Gerloff J (1999) Bioavailability of tramadol after i.m. injection in comparison to i.v. infusion. Int J Clin Pharmacol Ther 37: 175-183.
  • McMillan CJ, Livingston A, Clark CR, Dowling PM, Taylor SM, Duke T, Terlinden R (2008) Pharmacokinetics of intravenous tramadol in dogs. Can J Vet Res 72: 325-331.
  • Pypendop BH, Ilkiw JE (2008) Pharmacokinetics of tramadol, and its metabolite O-desmethyl-tramadol, in cats. J Vet Pharmacol Ther 31: 52-59.
  • Raffa RB, Friderichs E, Reimann W, Shank RP, Codd EE, Vaught JL (1992) Opioid and nonopioid components independently contribute to the mechanism of action of tramadol, an ‘atypical’ opioid analgesic. J Pharmacol Exp Ther 260: 275-285.
  • Shilo Y, Britzi M, Eytan B, Lifschitz T, Soback S, Steinman A (2008) Pharmacokinetics of tramadol in horses after intravenous, intramuscular and oral administration. J Vet Pharmacol Ther 31: 60-65.
  • Shipton EA (2000) Tramadol – present and future. Anaesth Intensive Care 28: 363-374.

Typ dokumentu

Bibliografia

Identyfikatory

Identyfikator YADDA

bwmeta1.element.agro-91ab52db-192d-4e17-88d1-1f7af127c2dc
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