Pharmacokinetics of azithromycin tablet after a single oral dose in Chinese healthy volunteers
Yan Xiao
Abstract
Yan Xiao
Abstract
Objective To study the pharmacokinetics of azithromycin tablet in Chinese healthy volunteers. Methods Ten healthy volunteers were given a single oral dose of 500 mg azithromycin tablet. The serum concentrations of azithromycin were determined by HPLC - UV. The compartment model was fitted by AIC - F test method The pharmacoki-netic parameters were calculated by DAS program. Results The main pharmacokinetic parameters of azithromycin for orally administered tablet were as follows: Ka was (0.87 ±0.27)h-1 ,t1/2β was (39.66 ± 10. 85) h,tmax was (2.60 ±0.52) h,Cmax was (451. 19 ±67.72) μg · L-1 ,CL/ F was (0.56±0.13)L · (h · kg)-1 ,AUC0-144 was (13.68 ±2.92) mg · h ·L-1 and AUC0-β was (13.71 ±2.91) mg · h · L-1. Conclusion The pharmacokinetics was best fitted to a two - compartment model.
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 study the pharmacokinetics of azithromycin tablet in Chinese healthy volunteers. Methods Ten healthy volunteers were given a single oral dose of 500 mg azithromycin tablet. The serum concentrations of azithromycin were determined by HPLC - UV. The compartment model was fitted by AIC - F test method The pharmacoki-netic parameters were calculated by DAS program. Results The main pharmacokinetic parameters of azithromycin for orally administered tablet were as follows: Ka was (0.87 ±0.27)h-1 ,t1/2β was (39.66 ± 10. 85) h,tmax was (2.60 ±0.52) h,Cmax was (451. 19 ±67.72) μg · L-1 ,CL/ F was (0.56±0.13)L · (h · kg)-1 ,AUC0-144 was (13.68 ±2.92) mg · h ·L-1 and AUC0-β was (13.71 ±2.91) mg · h · L-1. Conclusion The pharmacokinetics was best fitted to a two - compartment model.
Key concepts: Azithromycin, Pharmacokinetics, Cmax, Pharmacology, Medicine, Oral dose, Chemistry, Antibiotics