Study on the Pharmacokinetics of Qianlietai Tablets after Oral Adminstration in Rabbits
DI Duo
Abstract
DI Duo
Abstract
An analytical method for the determination of stachydrine concentration in rabbits after oral administration with 4 % suspension of tablet powder was established. The pharmacokinetics in rabbits is a two compartment model. The main pharmacokinetic parameters are: C\- max is 6.29±0.84 μg/mL, T\- max is 3.36±0.64 h; T\- 1/2\+α is 5.35±3.79 h; T\- 1/2\+β is 32.38±24.33 h; AUC is 208.15±118.4 μg/(mL·h)
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.
An analytical method for the determination of stachydrine concentration in rabbits after oral administration with 4 % suspension of tablet powder was established. The pharmacokinetics in rabbits is a two compartment model. The main pharmacokinetic parameters are: C\- max is 6.29±0.84 μg/mL, T\- max is 3.36±0.64 h; T\- 1/2\+α is 5.35±3.79 h; T\- 1/2\+β is 32.38±24.33 h; AUC is 208.15±118.4 μg/(mL·h)
Key concepts: Pharmacokinetics, Oral administration, Pharmacology, Chemistry, Chromatography, Medicine