Bioavailable polyamines
Disclosed herein are pharmaceutical salts of a cationic protonated polyamine pharmaceutical agent and an anionic organic carboxylate which is hydrophobic when in protonated form, particularly suited for oral administration, where these salts have good bioavailability in solid dosage forms and may be used in the treatment of cancer and other medical conditions for which the pharmaceutical agent is intended.
1. A salt of formula AMXT 1501:(caprate) 2 , wherein AMXT 1501 has formula
2. The salt of claim 1 having chemical structure (I)
3. The salt of claim 1 which is not in admixture with more than 5 wt % of any other solid or liquid chemical.
4. A pharmaceutical composition comprising the salt of formula AMXT 1501:(caprate) 2 according to claim 1 and a pharmaceutically acceptable inert component.
5. The pharmaceutical composition of claim 4 in a solid oral dosage form.
6. The pharmaceutical composition of claim 5 wherein the solid dosage form is enterically coated.
7. A method of forming the salt of formula AMXT 1501:(caprate) 2 according to claim 1 , the method comprising:
combining AMXT-1501, capric acid and a solvent so as to provide a solution; and
isolating a solid residue from the solution,
wherein the solid residue comprises AMXT 1501:(caprate) 2 .
8. The method of claim 7 wherein the solvent comprises water, methanol or a combination thereof.
9. The method of claim 7 wherein 1.8-2.2 moles of capric acid are combined with each 1.0 mole of AMXT-1501.
10. The method of claim 7 wherein the solid residue is formed by precipitation from the solution.
11. A method of treating cancer comprising administering to a subject in need thereof a therapeutically effective amount of AMXT 1501:(caprate) 2 of claim 1 .
12. The method of claim 11 wherein the therapeutically effective amount of AMXT 1501:(caprate) 2 is administered to the subject as a solid oral dosage form.