Ibuprofen
Category: pharmacological
Aliases: Advil, Motrin, Brufen
Pharmacological Mechanism
Reversible non-selective arachidonic acid cascade COX inhibitor. Reduces prostaglandin synthesis → analgesia, anti-inflammation, antipyresis. Reversibility means antiplatelet effect is dose-dependent + reversible (unlike aspirin's irreversible acetylation).
Half-Life (t½)
PO: 1.9h, IV: 1.9h
Dosing Guidelines
- PO: Typical 400 mg (Range: 200–800 mg)
- IV: Typical 400 mg (Range: 200–800 mg)
- TD: Typical 400 mg (Range: 200–800 mg)
Target Organ Systems
Interactions
- Acetaminophen (synergistic): Complementary mechanisms — APAP + ibuprofen outperforms either alone for post-op/dental pain.
- Apixaban (caution): Additive GI bleed risk; avoid chronic co-use. [Holbrook 2005]
- Aspirin (caution): Ibuprofen may block aspirin's COX-1 acetylation site if taken within 2 h prior — reduces cardioprotective effect.
- Dabigatran (caution): Additive GI bleeding; avoid chronic combination. [Holbrook 2005]
- Rivaroxaban (caution): Additive GI bleed risk; avoid chronic co-use. [Holbrook 2005]
- Warfarin (caution): Plasma protein-binding displacement at HSA. Chan 1989 (PMID:2724076) equilibrium dialysis: free warfarin 5–9% with ibuprofen vs 2.5–6% baseline. Low-end Δfu = (5 − 4.25)/4.25 ≈ 0.18. In-vitro magnitude; clinical effect smaller. Dominant clinical concern is COX-1/platelet additive bleed risk + GI mucosal injury, not displacement.
Pathways It Modulates
Chemical Identifiers
- PubChem CID: 3672
- Formula: C13H18O2
- Molecular weight: 206.28 g/mol
- InChIKey: HEFNNWSXXWATRW-UHFFFAOYSA-N
- SMILES: CC(C)CC1=CC=C(C=C1)C(C)C(=O)O
References