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Comparative Pharmacokinetics Study of Three Commercial Preparation of 10% Enrofloxacin in Goats


Affiliations
1 Department of Animal Husbandry and Veterinary Science, Tirhut College of Agriculture (R.A.U.), Dholi, Muzaffarpur, Bihar, India
2 Department of Veterinary Pharmacology and Toxicology, Bihar Veterinary College, Patna, Bihar, India
     

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Antimicrobial therapy constitutes a major component of modern medical and veterinary practices. Enrofloxacin has been developed exclusively for veterinary. In the present investigation, five clinically healthy female goats of non-descript were used. Three commercial preparations of enrofloxacin (10%) were used@5mg/kg b.wt .The samples of plasma were collected at different time interval i.e. 0.042, 0.083, 0.125, 0.333, 0.5, 0.75, 1, 1.5, 2, 3, 4, 6, 8, 10, 12 and 24 h after IM administration of drugs. Estimation of enrofloxacin were done by HPLC method at the flow rate was 0.6 ml.min-1,. Loop size was 200 ml, injection volume was 400 ml, the chart speed was 0.25 mm.min-1 and the detector sensitivity was 2.000 A.U.F.S. The mobile phase comprised of acetonitrile : methanol : water (17 : 3 : 80 v/v/v) containing 0.4% phosphoric acid (85% v/v) and 0.4% triethylamine (v/v). The pH of mobile phase was 3 (approx). The drug is present significantly at a lower concentration in brand II (0.07 ± 0.02 μg.ml-1) as compared to brand I (1.58 ± 0.41μg.ml-1) at 0.042 h. Similarly, brand II show lower concentrations upto 12 h .The drug maintained its therapeutic concentration (³ 0.125 μg.ml-1) upto 12 h in all the three brands. The value of absorption half-life (t1/2 Ka) of brand I, II and III were noted to be non-significant with a mean of 0.31 ± 0.04, 0.66 ± 0.13 and 0.83 ± 0.31 h, respectively. Brand I showed rapid absorption as compared to brand II and III but statistically it is non-significant. Elimination half life (t1/2 â) of brand I (3.10 ± 0.34 h) was found to be lower as compared to brand II and brand III (4.25 ± 0.71 and 3.84 ± 0.55 h, respectively), Mean residential time (MRT) of brand I, brand II and brand III were noted to be non-significant with a mean of 5.54 ± 1.13, 7.22 ± 0.86 and 6.52 ± 0.83 h, respectively. The values of mean absorption time (MAT) of brand I, brand II and brand III were noted to be non significant with a mean of 2.61 ± 0.98, 2.70 ± 0.92 and 2.61 ± 1.26 h, respectively. Maximum attainable concentrations (Cmax) was found to be significantly lower in brand II (1.94 ± 0.16 μg.ml-1) as compared to brand I (5.35 ± 0.87 μg.ml-1). However in case of time to reach maximum concentration (Tmax) there was no significant difference between different brands.In conclusion,all these three brands of enrofloxacin interchangeable and substituted for each other.

Keywords

Pharmacokinetics, Enrofloxacin, Antibacterial, Brands, HPLC, Goats
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  • Comparative Pharmacokinetics Study of Three Commercial Preparation of 10% Enrofloxacin in Goats

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Authors

V. K. Gond
Department of Animal Husbandry and Veterinary Science, Tirhut College of Agriculture (R.A.U.), Dholi, Muzaffarpur, Bihar, India
R. K. Nirala
Department of Veterinary Pharmacology and Toxicology, Bihar Veterinary College, Patna, Bihar, India
Archana
Department of Veterinary Pharmacology and Toxicology, Bihar Veterinary College, Patna, Bihar, India
C. Jayachandran
Department of Veterinary Pharmacology and Toxicology, Bihar Veterinary College, Patna, Bihar, India

Abstract


Antimicrobial therapy constitutes a major component of modern medical and veterinary practices. Enrofloxacin has been developed exclusively for veterinary. In the present investigation, five clinically healthy female goats of non-descript were used. Three commercial preparations of enrofloxacin (10%) were used@5mg/kg b.wt .The samples of plasma were collected at different time interval i.e. 0.042, 0.083, 0.125, 0.333, 0.5, 0.75, 1, 1.5, 2, 3, 4, 6, 8, 10, 12 and 24 h after IM administration of drugs. Estimation of enrofloxacin were done by HPLC method at the flow rate was 0.6 ml.min-1,. Loop size was 200 ml, injection volume was 400 ml, the chart speed was 0.25 mm.min-1 and the detector sensitivity was 2.000 A.U.F.S. The mobile phase comprised of acetonitrile : methanol : water (17 : 3 : 80 v/v/v) containing 0.4% phosphoric acid (85% v/v) and 0.4% triethylamine (v/v). The pH of mobile phase was 3 (approx). The drug is present significantly at a lower concentration in brand II (0.07 ± 0.02 μg.ml-1) as compared to brand I (1.58 ± 0.41μg.ml-1) at 0.042 h. Similarly, brand II show lower concentrations upto 12 h .The drug maintained its therapeutic concentration (³ 0.125 μg.ml-1) upto 12 h in all the three brands. The value of absorption half-life (t1/2 Ka) of brand I, II and III were noted to be non-significant with a mean of 0.31 ± 0.04, 0.66 ± 0.13 and 0.83 ± 0.31 h, respectively. Brand I showed rapid absorption as compared to brand II and III but statistically it is non-significant. Elimination half life (t1/2 â) of brand I (3.10 ± 0.34 h) was found to be lower as compared to brand II and brand III (4.25 ± 0.71 and 3.84 ± 0.55 h, respectively), Mean residential time (MRT) of brand I, brand II and brand III were noted to be non-significant with a mean of 5.54 ± 1.13, 7.22 ± 0.86 and 6.52 ± 0.83 h, respectively. The values of mean absorption time (MAT) of brand I, brand II and brand III were noted to be non significant with a mean of 2.61 ± 0.98, 2.70 ± 0.92 and 2.61 ± 1.26 h, respectively. Maximum attainable concentrations (Cmax) was found to be significantly lower in brand II (1.94 ± 0.16 μg.ml-1) as compared to brand I (5.35 ± 0.87 μg.ml-1). However in case of time to reach maximum concentration (Tmax) there was no significant difference between different brands.In conclusion,all these three brands of enrofloxacin interchangeable and substituted for each other.

Keywords


Pharmacokinetics, Enrofloxacin, Antibacterial, Brands, HPLC, Goats