R. Hallu
University of Buenos Aires
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Featured researches published by R. Hallu.
Veterinary Research Communications | 2004
L. Montoya; L. Ambros; V. Kreil; R. Bonafine; G. Albarellos; R. Hallu; A. Soraci
AbstractKetoprofen (KTP) and meloxicam (MLX) are non-steroidal anti-inflamatory drugs used extensively in veterinary medicine. The pharmacokinetics of these drugs were studied in eight dogs following a single oral dose of 1 mg/kg of KTP as a racemate or 0.2 mg/kg of MLX. The concentrations of the drugs in plasma were determined by high-performance liquid chromatography (HPLC). There were differences between the disposition curves of the KTP enantiomers, confirming that the pharmacokinetics of KTP is enantioselective. (S)-(+)-KTP was the predominant enantiomer; the S:R ratio in the plasma increased from 2.58±0.38 at 15 min to 5.72±2.35 at 1 h. The area under the concentration–time curve (AUC) of (S)-(+)-KTP was approximately 6 times greater than that of (R)-(–)-KTP. The mean (±SD) pharmacokinetic parameters for (S)-(+)-KTP were characterized as Tmax = 0.76±0.19 h, Cmax = 2.02±0.41 μg/ml, t
Laboratory Animals | 2003
G. Albarellos; R. Bonafine; V. Kreil; L. Ambros; L. Montoya; R. Hallu
Journal of Veterinary Pharmacology and Therapeutics | 2008
G. Albarellos; V. Kreil; L. Ambros; S. Waxman; L. Montoya; L. Tarragona; P. C. Quaine; R. Hallu; M. Rebuelto
t_{\frac{1}{2}{\text{el}}}
Archivos De Medicina Veterinaria | 2001
Kreil; C Luders; R. Hallu; M. Rebuelto; L Betancourt
Veterinary Medicine International | 2014
Ana Paula Prados; Paula Schaiquevich; V. Kreil; Agustina Monfrinotti; Pamela Quaine; Lisa Tarragona; R. Hallu; M. Rebuelto
= 1.65±0.48 h, AUC = 6.06±1.16 μg.h/ml, Vd/F = 0.39±0.07 L/kg, Cl/F = 170±39 ml/(kg.h). The mean (±SD) pharmacokinetic parameters of MLX were Tmax = 8.5±1.91 h, Cmax = 0.82±0.29 μg/ml, t
Journal of Veterinary Pharmacology and Therapeutics | 2011
L. Ambros; V. Kreil; L. Tarragona; Agustina Monfrinotti; R. Hallu; M. Rebuelto
Journal of Veterinary Pharmacology and Therapeutics | 2011
M. Rebuelto; L. Montoya; Ana Paula Prados; V. Kreil; P. C. Quaine; Agustina Monfrinotti; L. Tarragona; R. Hallu
t_{\frac{1}{2}\lambda ({\text{z)}}}
Archivos De Medicina Veterinaria | 2014
Kreil; Ana Paula Prados; L. Ambros; Agustina Monfrinotti; P. C. Quaine; R. Hallu; M. Rebuelto
Journal of Veterinary Pharmacology and Therapeutics | 2004
G. Albarellos; L. Montoya; L. Ambros; V. Kreil; R. Hallu; M. Rebuelto
= 12.13±2.15 h, AUCinf = 15.41±1.24 μg.h/ml, Vd/F = 0.23±0.03 L/kg, and Cl/F = 10±1.4 ml/(kg.h). Our results indicate significant pharmacokinetic differences between MLX and KTP after therapeutic doses.
Journal of Veterinary Pharmacology and Therapeutics | 2002
M. Rebuelto; G. Albarellos; L. Ambros; V. Kreil; L. Montoya; R. Bonafine; P. Otero; R. Hallu
In order to perform pharmacokinetic studies involving multiple blood sampling, repeated at variable intervals of time, a simple and reliable non-surgical jugular catheterization technique was developed. Six cats were catheterized 48 times using an indwelling through-the-needle type catheter (22G and 20.3 cm) placed into the jugular vein through an over-the-needle type (20G and 32 mm). Catheters remained in place for 1–13 days (median 3 days) without loss of patency until removal. Each jugular was catheterized a range of 2–6 times, with a total indwelling time of 4–33 days. No clinical signs of phlebitis, thrombosis or sepsis were observed either during or after the studies. This technique allows an easy, non-painful, non-stressful blood withdrawal during extended sampling periods, with minimal damage of the veins.