Literature DB >> 18297309

Comparative pharmacokinetics of ivermectin alone and a novel formulation of ivermectin and rafoxanide in calves and sheep.

H A El-Banna1, A Goudah, H El-Zorba, S Abd-El-Rahman.   

Abstract

This study investigated the comparative serum disposition kinetics of ivermectin (IVM) after a single subcutaneous dose of 200 microg/kg body weight of IVM alone or in combination with an anthelmintic consisting of ivermectin and rafoxanide (200 microg/kg of IVM and 2.5 mg/kg rafoxanide) for use in calves and sheep. The IVM concentrations in serum samples were analyzed by high-performance liquid chromatography with fluorescence detection. In sheep serum, rafoxanide induced a rapid absorption of IVM when given in combined form manifested by a shorter absorption half-life time of IVM by 68.49% when given in combination as compared with IVM when given alone. In addition, there is an increase in the value of the area under the concentration curve (AUC) by 15.48% while the value of elimination rate constant was decreased by 38.2% and significantly increased the half-life time of elimination from 2.04 days for IVM alone to 3.3 days when given in combination with rafoxanide. In calves serum, the mean t1/2ab for IVM/rafoxanide was 0.131 days and for the control formulation 0.16 days, and t1/2el was 5.78 and 4.95, respectively. IVM Cmax for IVM/rafoxanide was 22.4 ng/ml and for the control formulation 19.1 ng/ml. T (max) values were 0.99 and 1.12 days, and the mean AUC values were 188.9 and 165.4 ng/ml/day. The difference in Cmax, AUC, Kab, K el, and t1/2el was significant. However, there was no statistical difference between the Tmax and t1/2ab. These findings revealed that the combination of rafoxanide with IVM in sheep and calves increased the absorption of IVM and delayed its elimination.

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Year:  2008        PMID: 18297309     DOI: 10.1007/s00436-008-0915-6

Source DB:  PubMed          Journal:  Parasitol Res        ISSN: 0932-0113            Impact factor:   2.289


  22 in total

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Journal:  J Vet Pharmacol Ther       Date:  1997-04       Impact factor: 1.786

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4.  Comparative pharmacokinetics of doramectin and ivermectin in cattle.

Authors:  P L Toutain; D W Upson; T N Terhune; M E McKenzie
Journal:  Vet Parasitol       Date:  1997-09       Impact factor: 2.738

Review 5.  Avermectins and milbemycins.

Authors:  Q A McKellar; H A Benchaoui
Journal:  J Vet Pharmacol Ther       Date:  1996-10       Impact factor: 1.786

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Review 7.  The absorption, distribution and elimination of anthelmintic drugs: the role of pharmacokinetics.

Authors:  J D Baggot; Q A McKellar
Journal:  J Vet Pharmacol Ther       Date:  1994-12       Impact factor: 1.786

8.  The pharmacodynamics of ivermectin in sheep and cattle.

Authors:  J A Bogan; Q A McKellar
Journal:  J Vet Pharmacol Ther       Date:  1988-09       Impact factor: 1.786

9.  Pharmacokinetics of doramectin and ivermectin after oral administration in horses.

Authors:  R Pérez; I Cabezas; C Godoy; L Rubilar; L Muñoz; M Arboix; G Castells; M Alvinerie
Journal:  Vet J       Date:  2002-03       Impact factor: 2.688

10.  Influence of verapamil on the pharmacokinetics of the antiparasitic drugs ivermectin and moxidectin in sheep.

Authors:  M B Molento; A Lifschitz; J Sallovitz; C Lanusse; R Prichard
Journal:  Parasitol Res       Date:  2003-11-21       Impact factor: 2.289

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  2 in total

Review 1.  P-glycoproteins and other multidrug resistance transporters in the pharmacology of anthelmintics: Prospects for reversing transport-dependent anthelmintic resistance.

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Journal:  Int J Parasitol Drugs Drug Resist       Date:  2011-11-07       Impact factor: 4.077

2.  A controlled study on gastrointestinal nematodes from two Swedish cattle farms showing field evidence of ivermectin resistance.

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  2 in total

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