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Table 1 Pharmacokinetic parameters of 8 mg/kg FLQY2 in different formulations after intragastric administration

From: Preparation of a camptothecin analog FLQY2 self-micelle solid dispersion with improved solubility and bioavailability

Parameters (unit)

FLQY2-SD, 1:15

FLQY2-SD, 1:10

FLQY2-PM, 1:15

Cyclodextrin suspension

Cmax (ng/mL)

835.0 ± 53.6a

206.3 ± 40.9a

133.2 ± 18.6a

37.9 ± 4.9

Tmax (h)

1.3 ± 0.5

1.7 ± 0.5

1.7 ± 0.5

1(12)

MRT (h)

15.1 ± 1.4

19.69 ± 3.2

21.4 ± 2.7

25.4 ± 3.4

T1/2 (h)

10.0 ± 1.2

10.2 ± 1.6

12.4 ± 2.1

10.3 ± 1.4

AUC0-72 h (h·ng/mL)

10820.2 ± 936.3a

3507.8 ± 388.8a

3242.3 ± 353.2a

875.6 ± 58.6

  1. aRepresents
  2. p < 0.0001, compared with the cyclodextrin suspension group