Importance of pharmacokinetic and physicochemical data in the discovery and development of novel anti-arrhythmic drugs

Abstract

1. The importance of pharmacokinetics and physicochemical data in the discovery and development of a new mono-cationic antiarrhythmic agent, bidisomide (pK_a 9.3), structurally related to the di-cationic anti-arrhythmic disobutamide (pK_a of 8.6 and 10.2) and a mono-cationic drug disopyramide (pK_a 10.4), is described.

2. In man, the di-cationic disobutamide was slowly eliminated with a mean terminal phase half-life of 54±18 h, a value >7 times longer than disopyramide. The long terminal phase half-life of disobutamide is attributed to high accumulation of the drug in the tissues, a phenomenon attributed to the di-cationic nature.

3. Structural modification of disobutamide resulted in the mono-cationic agent bidisomide, designed to minimize drug accumulation in the tissues. Human studies with bidisomide confirmed that the terminal phase elimination of this drug was much faster than that of disobutamide, with a half-life of about 11 h. The absolute bioavailability of bidisomide was 45-62% which is lower than that of disopyramide (60-90%).

4. Unlike disopyramide, absorption of bidisomide was complex, characterized by a lag period (0.75–1.5 h) before absorption, followed by occurrence of two peaks in the plasma concentration-time curves.

5. The characteristic double peaks found with bidisomide was attributed to two rapid absorption sites of the drug in the gastrointestinal tract.