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. 2020 Sep 28;13(10):276. doi: 10.3390/ph13100276

Table 2.

Pharmacological comparisons between PPI and Vonoprazan.

Parameter PPI Vonoprazan
First Generation PPI Second Generation PPI
Acid activation Yes No
Active drug No Yes
Acid Stability No Yes
Main P450 metabolizer CYP2C19 CYP3A4
Meal’s influence Yes No
Mechanism of Action Covalent bond to gastric proton pump Potassium ion competitive reversible inhibitor to gastric proton pump
Days required for reaching maximal acid suppression 3–5 1
pH > 4 holding time (%) OMZ 30.4
LPZ 39.1
ESO 43.1
RPZ 42.8
10 mg 38.4–43.1
20 mg 62.7–63.3
Time Needed to Reach Maximum Plasma Concentration (h) OMZ 1–4
LPZ 1.2–2.1
ESO 1–3.5
RPZ 1.14
10 mg 1.75
20 mg 1.50
Half-life (h) OMZ 0.5–1.2
LPZ 0.9–2.1
ESO 1.3–1.6
RPZ 0.6–1.4
10 mg 6.95 ± 1.03
20 mg 6.85 ± 0.80
Cmax (μmol/L) OMZ 0.23–23.2
LPZ 1.62–3.25
ESO 2.1–2.4
RPZ 1.14
10 mg 9.7 ± 2.1 μg/L
20 mg 25.0 ± 5.6 μg/L
AUC (μmol.h/L) OMZ 0.58–3.47
LPZ 4.60–13.5
ESO 4.2
RPZ 2.22
10 mg 60.1 ± 9.0 μg.h/L
20 mg 160.3 ± 38.6 μg.h/L

AUC: Area Under Curve; Cmax: Maximum Plasma Concentration; CYP: Cytochrome P450 OMZ: Omeprazole 20 mg; LPZ: Lansoprazole 30 mg; ESO: Esomeprazole 40 mg; RPZ: Rabeprazole 20 mg.