Effect of a Kampo preparation, byakkokaninjinto, on pharmacokinetics of ciprofloxacin and tetracycline
Autor: | Hiroko Saito, Shunsuke Kurono, Masayuki Nadai, Fumie Abe, Kotaro Hitoshi, Masayuki Haniuda, Masafumi Ohnishi, Takaaki Hasegawa, Miki Katoh |
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Rok vydání: | 2009 |
Předmět: |
Adult
Male Time Factors Tetracycline Kampo Cmax Pharmaceutical Science Administration Oral Biological Availability Urine Pharmacology Drug Administration Schedule Young Adult Pharmacokinetics Ciprofloxacin medicine Humans Chromatography High Pressure Liquid Cross-Over Studies business.industry General Medicine Drug interaction Bioavailability Anti-Bacterial Agents Medicine Kampo business medicine.drug Drugs Chinese Herbal |
Zdroj: | Biologicalpharmaceutical bulletin. 32(6) |
ISSN: | 0918-6158 |
Popis: | The effect on the bioavailability of the antimicrobial agents (ciprofloxacin and tetracycline), which are well known to form chelates with cationic metals such as calcium, was evaluated in 20 healthy male volunteers according to an open, random crossover fashion using a Kampo preparation, byakkokaninjinto (TJ-34) which contains various cationic metals including calcium. Each subject received a single oral dose of tetracycline (250 mg) alone or ciprofloxacin (200 mg) alone along with a single coadministration of one pack (3 g) of the Kampo preparation, at one-week intervals. Concentrations of the drugs in plasma and urine were analyzed by HPLC. Concomitant administration of the Kampo preparation significantly decreased the peak plasma concentration (C(max)) and area under the plasma concentration-time curves (AUC), but not time to reach C(max) (T(max)), of ciprofloxacin and tetracycline. However, the decrease in bioavailability of ciprofloxacin was slight (15%) compared with that of tetracycline (30%). The Kampo preparation significantly decreased the urinary recovery of tetracycline, but not ciprofloxacin, and it had no effect on the renal clearance of either ciprofloxacin or tetracycline. These results indicate that the Kampo preparation tested in this study reduces the extent of bioavailability of ciprofloxacin and tetracycline, but not renal excretion, by decreasing the gastrointestinal absorption due to the formation of insoluble chelates with calcium. We recommend that the dose timing of the Kampo preparation should be carefully controlled to avoid therapeutic failure especially for patients receiving the treatment with tetracycline. |
Databáze: | OpenAIRE |
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