disposition kinetics of amoxicillin in healthy, hepatopathic and nephropathic conditions in chicken after single oral administration

Authors

moloy kumar bhar

bakul kumar datta

pabitra hridoy patra

jeevan ranjan dash

tapas kumar sar

abstract

fifteen broiler chickens (cobb 400) of 42 days of age weighing 1.8 to 2.0 kg were equally divided into 3 groups, each consisting of 5 birds. hepatopathy was induced by oral administration of paracetamol while nephropathy was induced by intravenous administration of uranyl nitrate. kinetic study was investigated in healthy, hepatopathic and nephropathic birds following single oral administration of amoxicillin at 40 mg kg-1. blood samples were collected at different time schedule. plasma concentrations of amoxicillin in healthy, hepatopathic and nephropathic birds were 41.90 ± 5.59, 9.93 ± 0.76 and 38.75 ± 6.08 μg ml-1, respectively at 1 hr; 15.34 ± 1.99, 18.57 ± 1.66 and 67.40 ± 2.62 μg ml-1, respectively at 4 hr and 2.03 ± 0.28, 15.54 ± 0.82 and 30.63 ± 1.58 μg ml-1, respectively at 24 hr. maximum plasma concentration was detected at 1 hr in healthy birds (41.90 ± 5.59 μg ml-1 ), at 8 hr in hepatopathic birds (23.51 ± 1.64 μg ml-1) and at 4 hr in nephropathic birds (67.40 ± 2.62 μg ml-1). the drug could not be detected in plasma beyond 24 hr in healthy, 72 hr in both hepatopathic and nephropathic birds. the concentration of amoxicillin was significantly (p < 0.01) higher in most of the samples of hepatopathic and nephropathic birds compared to healthy birds. significant higher values (p < 0.01) of t1/2 k, auc, and mrt and lower values of k and clb in the hepatopathic and nephropathic birds in comparison to healthy birds were observed.

Upgrade to premium to download articles

Sign up to access the full text

Already have an account?login

similar resources

Disposition Kinetics of Amoxicillin in Healthy, Hepatopathic and Nephropathic Conditions in Chicken after Single Oral Administration

Fifteen broiler chickens (COBB 400) of 42 days of age weighing 1.8 to 2.0 kg were equally divided into 3 groups, each consisting of 5 birds. Hepatopathy was induced by oral administration of paracetamol while nephropathy was induced by intravenous administration of uranyl nitrate. Kinetic study was investigated in healthy, hepatopathic and nephropathic birds following single oral administration...

full text

Disposition kinetics of orbifloxacin in tissues of crucian carp (Carassius auratus) following a single intramuscular administration

Background: Orbifloxacin is being widely used in China to treat fish infections in an extra-label manner, which may cause its potential residues in edible tissues. Aims: The purpose of this study was to determine the disposition kinetics of orbifloxacin in crucian carp (Carassius auratus) following intramuscular administration for its further safe appl...

full text

Pharmacokinetics of Amoxicillin/Clavulanic Acid Combination after Oral Administration of New Suspension Formulations in Human Volunteers

      The pharmacokinetic properties of amoxicillin and clavulanic acid when used alone or in combination may be different and show interaction between these two agents that might decrease the absolute bioavailability of clavulanic acid. In an open, randomized, replicated Latin square under fasting condition, pharmacokinetics of new formulations of amoxicillin/clavulanic acid were compared with...

full text

Bioavailability and Disposition Kinetics of Amoxicillin

.. OBJECTIVE: The study was planned to observe the bioavailability and disposition kinetics of amoxicillin in adult rabbits (irrespective of sex) under healthy and dehydrated conditions. Design: Comparative. Place and duration of study: The study was conducted at the department of pharmacology, University of Veterinary and Animal Sciences, Lahore from April 2013 to October 2013. Methodology: In...

full text

Disposition Kinetic of Amoxicillin in Healthy and Nephropathic Goats with Immunological and Residual Level in Blood and Tissues

Pharmacokinetic is concerned with study and characterization of time course of drug absorption, distribution, metabolism and excretion [2]. Disease states alter the pharmacokinetic parameters of many drugs. It has been reported that the kinetic behavior of many drugs were altered following administration by different routes in experimentally induced diseased models of goats and dogs [3-5]. The ...

full text

The Disposition of C-labeled Tacrolimus after Intravenous and Oral Administration in Healthy Human Subjects

Tacrolimus is a macrolide lactone with potent immunosuppressive properties. It has been shown in clinical studies to prevent allograft rejection. The pharmacokinetics of tacrolimus in healthy subjects and transplant patients has been described in earlier studies using immunoassay methods; however, detailed information on the absorption, distribution, metabolism, and excretion of tacrolimus usin...

full text

My Resources

Save resource for easier access later


Journal title:
veterinary research forum

Publisher: faculty of veterinary medicine, urmia university

ISSN 2008-8140

volume 1

issue 3 2012

Hosted on Doprax cloud platform doprax.com

copyright © 2015-2023