PHARMACOKINETIC PROFILE OF AMPICILLIN AND CLINDAMYCIN IN RABBITS | ||||
| Veterinary Medical Journal (Giza) | ||||
| Volume 42, Issue 1, January 1994, Page 51-56 PDF (1.97 MB) | ||||
| Document Type: Original Article | ||||
| DOI: 10.21608/vmjg.1994.372019 | ||||
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| Authors | ||||
| A RAMADAN* 1; NEHAL AFIFI1; T ABBAS2; A EMARA2 | ||||
| 1Department of Pharmacology, Faculty of Veterinary medicine, Cairo University, Giza, Egypt. | ||||
| 2Department of Oral Surgery, Faculty of Oral and Dental Medicine, Cairo University, Giza, Egypt. | ||||
| Abstract | ||||
| Ampicillin and clindamycin were once administered in rabbits via oral and i.v. routes in doses of 25 andl6 mg/kg b.wt., respectively, to determine blood concentration, kinetic behaviour and bioavailability. Following a single i.v. injection, the blood concentration-time curve indicated a two compartment open model, with an climination half-life value (to.5, (B),) of 103.03 and 209.41 minutes for ampicillin and clindamycin, respectively. The apparent volume of distribution of ampicillin in rabbits was less than 1 litre/kg and suggesting a lower distribution in tissues than in blood. While, the apparent volume of distribution of clindamycin in rabbits was more than 1 litre/kg and suggesting a higher distribution in tissues than in blood. After oral administration the peak plasma concentration of ampicillin and clindamycin were 11.03 and 2.25ug/ml at 2.45 and 0.96 hours, respectively. The average bioavailability of ampicillin and clindamycin given by oral administration, were 0.44 and 0.56%, respectively. | ||||
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