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. 2023 May 23;13:172. doi: 10.1038/s41398-023-02477-4

Table 2.

Pharmacokinetic parameters for DMT based on non–compartmental analyses [geometric mean (95% CI), range].

Low infusion (0.6 mg/min) High infusion (1.0 mg/min) Low bolus (15 mg) + low infusion (0.6 mg/min) High bolus (2 5 mg) + high infusion (1.0 mg/min)
Cmax (ng/ml) 24 (21–28) 39 (33–45) 29 (26–33)a 61 (51–73)a
11–48 15–83 14–56 11–107
Tmax (min) 72 (67–78) 73 (64–83) 2.5 (2.1–2.9)a 2.9 (2.4–3.6)a
40–90 15–90 2–5 2–10
t1/2α (min) 5.3 (4.5–6.1) 5.3 (4.7–5.9) 5.0 (4.4–5.6) 5.8 (5.1–6.5)
3.0–15 3.2–10.0 2.9–11 2.8–11
t1/2β (min) 15 (13–16) 15 (14–16) 14 (13–16) 16 (14–17)
7.8–29 10–22 7.5–23 10–22
CL (L/min) 39 (34–46) 39 (33–46) 36 (32–42) 36 (32–40)
16–97 16–91 21–82 22–61
Vz (L) 820 (671–1004) 831 (683–1012) 746 (639–871) 799 (693–922)
287–2765 284–2133 388–1945 379–1752
AUC (ngamin/ml) 1374 (1174–1607) 2303 (1966–2697) 1902 (1653–2189) 3220 (2889–3588)
554–3374 987–5764 839–3212 1883–5247

AUC area under the plasma concentration-time curve, AUC AUC from time zero to infinity, CL apparent total clearance, Cmax maximum observed plasma concentration, t1/2α early elimination plasma half-life, t1/2β late elimination plasma half-life, Tmax time to reach Cmax, 95%CI 95% confidence interval, Vz apparent volume of distribution, n = 27.

aIn the DMT bolus conditions, Cmax and Tmax values were calculated considering only plasma concentrations within the first 15 min after the bolus application.