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. 2022 Nov 23;29(1):3397–3413. doi: 10.1080/10717544.2022.2149896

Table 3.

Pharmacokinetic parameters of ATV in rats after intraperitoneal (IP) or oral administration of ATV or ATV-NEs.

Test material ATV-IP (2) ATV in water (40) ATV in 10% DMF (40) ATV-NE#1 (40) ATV-NE#6 (40)
Administration route IP Oral Oral Oral Oral
ATV dose (mg/kg) 2 40 40 40 40
Tmax (h) 0.50 ± 0.00 4.00 ± 0.00 4.00 ± 0.00 4.00 ± 0.00 4.00 ± 0.00
T1/2 (h) 1.77 ± 0.04 2.45 ± 0.26 2.97 ± 0.53 6.75 ± 0.33 9.72 ± 2.68
Cmax (ng/mL) 82.5 ± 2.28 28.1 ± 2.94 39.2 ± 3.95 99.1 ± 0.92 141 ± 8.79
AUClast (ng·h/mL) 211 ± 4.84 117 ± 7.03 256 ± 49.9 768 ± 34.7 1396 ± 43.1
AUCinf (ng·h/mL) 220 ± 4.94 149 ± 13.5 283 ± 32.5 873 ± 29.4 1751 ± 170
Relative bioavailability (%) 100 2.78 ± 0.17 6.06 ± 1.18 18.2 ± 0.82 33.1 ± 1.02

Relative bioavailability (%) = (AUClast, oral/DoseATV, oral)/(AUClast, IP/DoseATV, IP) × 100. All values are shown as means ± SDs (n = 4). Tmax, time to reach maximum plasma concentration of ATV; T1/2, plasma half-life of ATV; Cmax, maximum plasma ATV concentration; AUClast, area under the plasma concentration–time curve between zero and the last measurable plasma concentration; AUCinf, area under the plasma concentration–time curve between zero and infinity.