مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

video

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

sound

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Persian Version

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

View:

355
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Download:

242
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Cites:

Information Journal Paper

Title

THE PHARMACOKINETICS OF RAFOXANIDE FOLLOWING SINGLE DOSE INTRAVENOUS AND ORAL ADMINISTRATION IN GOATS

Pages

  26-29

Abstract

 The study was conducted to determine the plasma concentrations and pharmacokinetic parameters of RAFOXANIDE after a single INTRAVENOUS (10 mg/kg) and ORAL (22.5 mg/kg) administrations in black Bengal female GOATS. Maximum (87.63±11.71 µg/ml) and minimum (1.8±0.24 µg/ml) plasma concentrations of RAFOXANIDE were recorded at 0.08 and 12 h respectively after Lv. administration. The elimination half life (t1.2) , total body clearance (GIB)and volume of distribution (Vdarea)values were 2.89±0.26 h, 0.05 ± 0.002 mg/h and 0.19±0.02 Lkg respectively. An adequate plasma level of RAFOXANIDE (14.63±2.12  mg/ml) was detected at 1h followed by gradual increase and peak concentration level (30.88±4.30 mg/ml) was recorded at 36 h after ORAL administration. The rate of absorption (Ka), elimination half life (t112 P), total body clearance (GIB) and volume of distribution (Vdarea) values were 0.07±0.009 h-1,138.02± 13.99 h, 0.003±0.0003 L/kg/h, and 0.57±0.06L/kg/h respectively. Plasma protein binding percentages of RAFOXANIDE varied from 81.06 to 92.28 and its association and dissociation constants were 1.26 x 107 ± 0.18 X 107 L/mol and 0.83 x 10-7±0.12 x 10-7mol/L respectively. On conclusion, RAFOXANIDE is slowly absorbed from the gastrointestinal tract, slowly eliminated; highly protein bound and persists for long time in blood of goat.

Multimedia

  • No record.
  • Cites

  • No record.
  • References

    Cite

    APA: Copy

    PAL, S., GHANDRA DEBNATH, SH., KUMAR DAS, SH., KUMAR GHAKRABORTY, A., & KUMAR MANDAL, T.. (2004). THE PHARMACOKINETICS OF RAFOXANIDE FOLLOWING SINGLE DOSE INTRAVENOUS AND ORAL ADMINISTRATION IN GOATS. IRANIAN JOURNAL OF PHARMACOLOGY AND THERAPEUTICS (IJPT), 3(1), 26-29. SID. https://sid.ir/paper/297052/en

    Vancouver: Copy

    PAL S., GHANDRA DEBNATH SH., KUMAR DAS SH., KUMAR GHAKRABORTY A., KUMAR MANDAL T.. THE PHARMACOKINETICS OF RAFOXANIDE FOLLOWING SINGLE DOSE INTRAVENOUS AND ORAL ADMINISTRATION IN GOATS. IRANIAN JOURNAL OF PHARMACOLOGY AND THERAPEUTICS (IJPT)[Internet]. 2004;3(1):26-29. Available from: https://sid.ir/paper/297052/en

    IEEE: Copy

    S. PAL, SH. GHANDRA DEBNATH, SH. KUMAR DAS, A. KUMAR GHAKRABORTY, and T. KUMAR MANDAL, “THE PHARMACOKINETICS OF RAFOXANIDE FOLLOWING SINGLE DOSE INTRAVENOUS AND ORAL ADMINISTRATION IN GOATS,” IRANIAN JOURNAL OF PHARMACOLOGY AND THERAPEUTICS (IJPT), vol. 3, no. 1, pp. 26–29, 2004, [Online]. Available: https://sid.ir/paper/297052/en

    Related Journal Papers

  • No record.
  • Related Seminar Papers

  • No record.
  • Related Plans

  • No record.
  • Recommended Workshops






    Move to top
    telegram sharing button
    whatsapp sharing button
    linkedin sharing button
    twitter sharing button
    email sharing button
    email sharing button
    email sharing button
    sharethis sharing button