2002Unpublished venueRequires access

Study on the Pharmacokinetics of Qianlietai Tablets after Oral Adminstration in Rabbits

DI Duo

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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)

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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)

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Available 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)

Key concepts: Pharmacokinetics, Oral administration, Pharmacology, Chemistry, Chromatography, Medicine

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