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Table 4 The pharmacokinetic parameters of myrislignan in mice following oral or intraperitoneal administration (n = 6)

From: Determination of myrislignan levels in BALB/c mouse plasma by LC-MS/MS and a comparison of its pharmacokinetics after oral and intraperitoneal administration

Parameters (Units)

Mean ± SD

Intraperitoneal

Oral

Kel (h− 1)

1.19 ± 0.443

0.366 ± 0.0789

T1/2 (h)

0.692 ± 0.386

1.97 ± 0.426

Tmax (h)

0.167 ± 0.0915

1.04 ± 1.45

Cmax (ng/mL)

3870 ± 1200

105 ± 72.3

Cl_Fobs(mL/hr/kg)

45,123 ± 11,936

302,900 ± 442,668

Vz_Fobs(mL/kg)

24,198 ± 5987

970,149 ± 199,518

AUC0 − t (h/ng/mL)

2050 ± 532

157 ± 55.1

AUC0 − inf (h/ng/mL)

2060 ± 536

162 ± 52.9

AUMClast (hr*hr*ng/mL)

1006 ± 227

457 ± 240

MRT0 − t (h)

0.457 ± 0.0499

2.19 ± 0.841

MRT0 − inf (h)

0.466 ± 0.0485

2.57 ± 0.858

 F* = 1.97 %