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. Author manuscript; available in PMC: 2019 Jun 1.
Published in final edited form as: Biopharm Drug Dispos. 2018 Jun;39(6):289–297. doi: 10.1002/bdd.2136

Table 1.

Pharmacokinetic (PK) parameters of curcumin in Rat plasma.

Final Population Pharmacokinetic Parameters
Parameter Estimate (CV%) Description
CL(L/h/kg) 55.1 (1.76) Elimination clearance
CLD(L/h/kg) 30.3 (3.12) Distribution clearance
VC (L/kg) 14.2 (1.05) Volume of distribution in the central compartment
VP (L/kg) 48.5 (8.89) Volume of distribution in the peripheral compartment
Non-Compartmental Analysis
AUC(0–6)(ng/mL*h) 767 (37.4) Area under the curve from 0 to 6h
AUC(0–∞)(ng/mL*h) 785 (35.9) Area under the curve from 0 to infinity
AUMC(0–6)(ng/mL*h2) 962 (26.4) Area under the first moment curve 0 to 6h
AUMC(0–∞)(ng/mL*h2) 1265 (3.7) Area under the first moment curve 0 to infinity
MRT (h) 1.75 (33.0) Mean residence time
CL (L/h/kg) 55.7 (36.5) Total clearance
T1/2(h) 3.36 (42.9) Elimination half-life