Background: Clindamycin is frequently used for the treatment of bacterial pyoderma. Objective: To compare the pharmacokinetics of clindamycin in whole skin homogenates of normal dogs when administered orally at two dosage regimens (5.5 mg/kg BW, twice daily and 11 mg/kg BW, once daily). Animals and Methods: Skin biopsies were obtained from six laboratory beagles before, 3, 6 and 12 h after the first and the fifth dose of clindamycin at the former regimen, as well as before, 3, 6, 12 and 24 h after the first and third dose at the latter regimen. Tissue was homogenized and clindamycin concentrations were measured by reverse-phase high-performance liquid chromatography coupled with mass spectrometry. Results were analyzed using Student's t-test at a level of significance of 0.05. Results: Maximal concentration and area under the concentration-time curve, but not their relevant dose-normalized values, were higher at the dosage regimen of 11 mg/kg BW, once daily than at 5.5 mg/kg BW twice daily. Conclusions: The pharmacokinetic profile of clindamycin is at least equal, if not better, when this antimicrobial is administered at 11 mg/kg BW, once daily. © 2013 Copyright Taylor and Francis Group, LLC.
CITATION STYLE
Saridomichelakis, M. N., Athanasiou, L. V., Chatzis, M. K., Salame, M., Katsoudas, V., & Pappas, I. S. (2013). Concentrations of clindamycin hydrochloride in homogenates of normal dog skin when administered at two oral dosage regimens. Veterinary Quarterly, 33(1), 8–14. https://doi.org/10.1080/01652176.2013.772315
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