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. 2021 Nov 3;28(1):2313–2328. doi: 10.1080/10717544.2021.1995077

Table 2.

Pharmacokinetic parameters of PMX in rats after intravenous or oral administration of PMX or PMX/DL(1:1)-CD.

Test material PMX-IV (10) PMX-Oral (20) PMX/DL(1:1)-CD (10) PMX/DL(1:1)-CD (20) PMX/DL(1:1)-CD (40)
Administration route IV Oral Oral Oral Oral
PMX dose (mg/kg) 10 20 10 20 40
Tmax (h) 0.50 ± 0.00 0.50 ± 0.00 0.50 ± 0.00 0.50 ± 0.00
T1/2 (h) 0.954 ± 0.043 13.1 ± 1.82 15.3 ± 1.18 13.9 ± 1.25 8.11 ± 1.91
Cmax (μg/mL) 32.3 ± 1.22 0.579 ± 0.073 1.81 ± 0.225 3.85 ± 0.371 5.07 ± 0.624
AUClast (μg·h/mL) 25.1 ± 3.56 3.93 ± 0.380 7.02 ± 1.04 11.1 ± 1.71 12.7 ± 2.70
AUCinf (μg·h/mL) 25.3 ± 3.56 8.96 ± 0.089 19.7 ± 1.21 26.7 ± 4.65 20.7 ± 6.17
Bioavailability (%) 100 7.80 ± 0.755 27.9 ± 4.12 22.0 ± 3.40 12.6 ± 2.68

Tmax: time to reach the maximum plasma concentration of PMX; T1/2: plasma half-life of PMX; Cmax: maximum plasma PMX 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. Bioavailability (%) = (AUClast, oral/DosePMX, oral)/(AUClast, IV/DosePMX, IV) × 100. All values are means ± SDs (n = 4).