EFFECT OF ESCHERICHIA COLI ENDOTOXIN INDUCED FEVER ON THE KINETICS AND DOSAGE REGIMEN OF CEFUROXIME IN GOATS

S
Shahid Prawez
R
Rajinder Raina
1Division of Pharmacology and Toxicology, F. V. Sc. and A.H., SKUAST-J, R.S. Pura, Jammu - 181 102, India
  • Submitted|

  • First Online |

  • doi

Cite article:- Prawez Shahid, Raina Rajinder (2026). EFFECT OF ESCHERICHIA COLI ENDOTOXIN INDUCED FEVER ON THE KINETICS AND DOSAGE REGIMEN OF CEFUROXIME IN GOATS. Indian Journal of Animal Research. 40(2): 131 - 134. doi: .
The pharmacokinetics and dosage regimen of cefuroxime were determined in normal and
febrile goats following its single intravenous administration @ 20 mg/kg. Fever was induced by
a single intravenous injection of Escherichia coli endotoxin @ 1.0 μg kg-1. The distribution half
life (t½ α) and total body clearance (ClB) were found significantly lower in febrile goats (t½ α =
0.23 ± 0.03 hr and ClB = 11.23 ± 0.57ml kg-1 min-1) as compared to healthy goats (t½ α =
0.58 ± 0.09 hr and ClB = 20.23 ± 1.39 ml kg-1 min-1). The elimination half life (t½ β) and
apparent volume of distribution (Vdarea) were found significantly higher in febrile goats (t½ β =
8.07 ± 0.34 hr and Vdarea = 7.78 ± 0.24 L kg-1) compared to healthy goats (t½ β = 3.35 ± 0.09
hr and Vdarea = 5.88 ± 0.48 L kg-1). An intravenous dosage regimen suitable for maintaining the
minimum therapeutic plasma concentration of 1.0 μg ml-1 in febrile animal would be @ 22 mg/
kg body weight as loading dose (D*) and @ 15 mg/kg as maintenance dose(D0) repeated at 12
hourly dosage intervals
    1. Arret, B. et al. (1971). J. Pharm. Sci., 60: 1689 -1694.
    2. Caprile, K.A. (1988). J. Vet. Pharmacol. Ther., 11: 1-32.
    3. Chaudhary, R.K. et al. (1999). Vet. Res. Comm., 23: 361-368.
    4. Chaudhary, R.K. et al. (2001). Indian J. Pharmacol., 33: 425-430.
    5. Gibaldi, M. and Perrier, D. (1982). Pharmacokinetics. Marcel Dekker Inc., New York, pp. 433-444.
    6. Mandell, G.L. and Sande, M.A. (1991). Goodman and Oilman’s The Pharmacological Basis of Therapeutics.
    7. Singapore, Maxwell Macmillan, pp. 1065-97.
    8. Smith, B.R. and Lefrock, J.L. (1983). Thera. Drug Monit., 5: 149-160.
    9. Snedecor, W.G. and Cochran (1967). Statistical Method. 6th edn., Oxford and IBH publishing Co., New Delhi.

    EFFECT OF ESCHERICHIA COLI ENDOTOXIN INDUCED FEVER ON THE KINETICS AND DOSAGE REGIMEN OF CEFUROXIME IN GOATS

    S
    Shahid Prawez
    R
    Rajinder Raina
    1Division of Pharmacology and Toxicology, F. V. Sc. and A.H., SKUAST-J, R.S. Pura, Jammu - 181 102, India
    • Submitted|

    • First Online |

    • doi

    Cite article:- Prawez Shahid, Raina Rajinder (2026). EFFECT OF ESCHERICHIA COLI ENDOTOXIN INDUCED FEVER ON THE KINETICS AND DOSAGE REGIMEN OF CEFUROXIME IN GOATS. Indian Journal of Animal Research. 40(2): 131 - 134. doi: .
    The pharmacokinetics and dosage regimen of cefuroxime were determined in normal and
    febrile goats following its single intravenous administration @ 20 mg/kg. Fever was induced by
    a single intravenous injection of Escherichia coli endotoxin @ 1.0 μg kg-1. The distribution half
    life (t½ α) and total body clearance (ClB) were found significantly lower in febrile goats (t½ α =
    0.23 ± 0.03 hr and ClB = 11.23 ± 0.57ml kg-1 min-1) as compared to healthy goats (t½ α =
    0.58 ± 0.09 hr and ClB = 20.23 ± 1.39 ml kg-1 min-1). The elimination half life (t½ β) and
    apparent volume of distribution (Vdarea) were found significantly higher in febrile goats (t½ β =
    8.07 ± 0.34 hr and Vdarea = 7.78 ± 0.24 L kg-1) compared to healthy goats (t½ β = 3.35 ± 0.09
    hr and Vdarea = 5.88 ± 0.48 L kg-1). An intravenous dosage regimen suitable for maintaining the
    minimum therapeutic plasma concentration of 1.0 μg ml-1 in febrile animal would be @ 22 mg/
    kg body weight as loading dose (D*) and @ 15 mg/kg as maintenance dose(D0) repeated at 12
    hourly dosage intervals
      1. Arret, B. et al. (1971). J. Pharm. Sci., 60: 1689 -1694.
      2. Caprile, K.A. (1988). J. Vet. Pharmacol. Ther., 11: 1-32.
      3. Chaudhary, R.K. et al. (1999). Vet. Res. Comm., 23: 361-368.
      4. Chaudhary, R.K. et al. (2001). Indian J. Pharmacol., 33: 425-430.
      5. Gibaldi, M. and Perrier, D. (1982). Pharmacokinetics. Marcel Dekker Inc., New York, pp. 433-444.
      6. Mandell, G.L. and Sande, M.A. (1991). Goodman and Oilman’s The Pharmacological Basis of Therapeutics.
      7. Singapore, Maxwell Macmillan, pp. 1065-97.
      8. Smith, B.R. and Lefrock, J.L. (1983). Thera. Drug Monit., 5: 149-160.
      9. Snedecor, W.G. and Cochran (1967). Statistical Method. 6th edn., Oxford and IBH publishing Co., New Delhi.
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