Related Experiment Video
Updated: Jul 25, 2026

Screening for Thermotoga maritima Membrane-Bound Pyrophosphatase Inhibitors
Published on: November 23, 2019
Inhibition of thrombin by iopromide in vitro
L L Graf1, D A Young, D C Kressin
1Department of Research, Veterans Affairs Medical Center, Denver, Colorado, USA.
Iopromide, a nonionic contrast agent, partially inhibits thrombin activity in vitro. This interaction is rapid, reversible, and specific, but less potent than known inhibitors.
Area of Science:
- Biochemistry
- Pharmacology
- Medical Imaging
Background:
- Nonionic contrast media like iopromide are used in angiography.
- Concerns exist regarding their potential to increase thrombogenicity compared to ionic media.
Purpose of the Study:
- To characterize iopromide's interaction with thrombin.
- To determine the inhibition rate, extent, specificity, and reversibility.
- To assess thrombin-iopromide complex integrity and inhibitory potency.
Main Methods:
- Iopromide was incubated with purified thrombin or pooled serum.
- Thrombin activity was measured spectrophotometrically after substrate addition.
- Trypsin inhibition was assessed to determine specificity.
- Iopromide's potency was compared to Thromstop.
Main Results:
- Iopromide inhibited thrombin immediately, reversibly, and dose-proportionally.
- Mean thrombin inhibition was 44.5% at 184 mmol/L iopromide.
- Iopromide's inhibitory potency was significantly lower than Thromstop.
- Inhibition was specific to thrombin, not trypsin.
Conclusions:
- Iopromide partially inhibits thrombin activity in vitro at clinically relevant concentrations.
- The in vitro findings do not account for in vivo coagulation factors.
Related Concept Videos
Anticoagulant Drugs: Low-Molecular-Weight Heparins
Anticoagulant Drugs: Vitamin K Antagonists and Direct Oral Anticoagulants
Warfarin, a prominent vitamin K antagonist family member, exerts its effect by inhibiting the enzyme VKORC1 (vitamin K epoxide reductase complex 1). By hindering this enzyme, warfarin...
Antiplatelet Drugs: Prostaglandin Synthesis, P2Y12 and Glycoprotein IIb/IIIa Inhibitors
Prostaglandin synthesis inhibitors, exemplified by the widely known aspirin, wield their power by irreversibly acetylating...
Treatment for Pulmonary Arterial Hypertension: Prostacyclin Receptor Agonists
These agonists bind to the IPR receptor situated on the plasma membrane of the pulmonary artery smooth muscle cells. This binding triggers a cascade of reactions known as the GS-AC-cAMP-PKA pathway. This pathway results in the relaxation of smooth muscle...
Venous Thrombosis I: Introduction
Venous Thrombosis III: Interprofessional Care

