Pharmacokinetics and bioavailability of domestic cefaclor
Bei Guo
Abstract
Bei Guo
Abstract
Objective:To determine the pharmacokinetics and relative availability of domestic cefaclor. Methods:The crossover study was conducted in 8 healthy, fast volunteers. They were treated randomly with domestic or imported cefaclor 1 000 mg and their serum and urine drug levels were measured by bioassay. RESULTS: The concentration time curves fitted to a two compartment model. The pharmacokinetic parameters of domestic cefaclor were: mean C max =(20.51±3.84) mg/L, T max =(0.84±0.13)h, t 1/2 β=(1.07±0.38)h, AUC=(27.27±2.88) mg·h/L. The cumulative excretion rate in urine within 24 h was (69.15±6.66)%. The relative bioavailability of domestic cefaclor was 108.43%. CONCLUSION: The domestic and the imported cefaclor are bioequivalent with similar bioavilability.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Objective:To determine the pharmacokinetics and relative availability of domestic cefaclor. Methods:The crossover study was conducted in 8 healthy, fast volunteers. They were treated randomly with domestic or imported cefaclor 1 000 mg and their serum and urine drug levels were measured by bioassay. RESULTS: The concentration time curves fitted to a two compartment model. The pharmacokinetic parameters of domestic cefaclor were: mean C max =(20.51±3.84) mg/L, T max =(0.84±0.13)h, t 1/2 β=(1.07±0.38)h, AUC=(27.27±2.88) mg·h/L. The cumulative excretion rate in urine within 24 h was (69.15±6.66)%. The relative bioavailability of domestic cefaclor was 108.43%. CONCLUSION: The domestic and the imported cefaclor are bioequivalent with similar bioavilability.
Key concepts: Cefaclor, Bioequivalence, Bioavailability, Pharmacokinetics, Crossover study, Pharmacology, Urine, Medicine