Skip to main content

Table 1 Pharmacokinetic parameters (mean ± SEM) after single intraperitoneal/oral dose of three (1, 2 & 3) chalcone derivatives

From: Pharmacokinetic evaluation of Chalcone derivatives with antimalarial activity in New Zealand White Rabbits

Pharmacokinetic Parameters

Derivative 1

(mean ± SEM)

Derivative 2

(mean ± SEM)

Derivative 3

(mean ± SEM)

Administered Dose (mg/1.5 kg Rabbits)

5.46

7.28

5.46

Administration Route

Intraperitoneal

Oral

Oral

C0 (µg/mL)

0.966 ± 0.025

0.986 ± 0.004

0.944 ± 0.007

Cmax (µg/mL)

1.96 ± 0.46

69.89 ± 5.49

3.74 ± 1.64

tmax (h)

0.33 ± 0.05

3.4 ± 0.79

2.83 ± 0.87

t1/2 (h)

12.60 ± 2.09

93.32 ± 32.59

13.30 ± 1.67

AUC0–48 (µg.h/mL)

2.94 ± 0.83

3755.16 ± 738.71

14.16 ± 3.78

Ke

− 0.035 ± 0.026

− 0.013 ± 0.004

− 0.056 ± 0.007

CL (mL/min)

0.28 ± 0.08

0.15 ± 0.05

0.53 ± 0.10

Vd (L)

7.31 ± 0.29

10.72 ± 0.66

9.12 ± 0.73

  1. C0 Concentration of administrated drug at time zero, Cmax Peak plasma concentration, tmax time to reach the peak plasma concentration, t1/2 elimination half-life, AUC Area under the total plasma concentration–time curve, Ke Elimination rate constant, CL Plasma clearance, Vd Volume of distribution