Enhancement of the efficacy of nifedipine by deuteration

• US 5,846,514 A
• Filed: 10/04/1996
• Issued: 12/08/1998
• Est. Priority Date: 03/25/1994
• Status: Expired due to Fees

• Current Assignee: Isotechnika Inc. (Endo International PLC)
• Original Assignee: Isotechnika Inc. (Endo International PLC)
• Inventors: Foster, Robert T., Caille, Gilles, Lewanczuk, Richard
• Primary Examiner(s): Hollinden, Gary E.
• Assistant Examiner(s): Hartley, Michael G.
• Application Number:
  US08/725,992
• Time in Patent Office: 795 Days
• Field of Search: 424/1.81, 514/356, 514/458, 546/167, 546/256, 546/263, 546/321
• US Class Current: 424/1.81
• CPC Class Codes: A61P 9/12 Antihypertensives
• CPC Class Codes: C07B 59/002 Heterocyclic compounds

Abstract

A method of enhancing the efficiency and increasing the duration of action of drugs (e.g. dihydropyridines and anti-bacterials) and particularly of nifedipine and penicillins wherein one or more hydrogen atoms are deuterated and wherein the deuterated drug has unexpectedly improved properties when used in much lower concentrations than unmodified drug. A method for determining the identity and bioequivalency of a new drug is also disclosed wherein the molecular and isotope structure of a new drug is determined by isotope ratio mass spectrometry and compared with the molecular and isotope structure of a known human drug.

Claims

1. A pharmaceutical composition comprising:

a dihydropyridine compound which is enriched with deuterium having the formula;

##STR19## wherein R is either hydrogen or deuterium and at least one R is deuterium and a pharmaceutically acceptable carrier.

2. The pharmaceutical composition according to claim 1 wherein at least one of the methyl groups attached to position 2 and 6 of the dihydropyridine ring is substituted with CD₃.

3. The pharmaceutical composition according to claim 2, wherein said deuterated dihydropyridine is deuterated nifedipine having the formula ##STR20##

8. A method for the treatment of hypertension in an animal suffering therefrom comprising:

administering to said animal a therapeutically effective amount of the pharmaceutical composition of claim 1.

9. A method for the prolongation of the duration of action of a drug comprising,

administering to a patient in need thereof a pharmaceutical preparation as in claim 1, wherein the active ingredient thereof is a deuterated pharmacologically active compound.

10. A method for the treatment of hypertension in an animal suffering therefrom comprising:

administering to said animal a therapeutically effective amount of the pharmaceutical composition of claim 3.

4. Deuterated nifedipine having the formula ##STR21##

5. A method for making the deuterated nifedipine of claim 4, said method comprising:

dissolving nifedipine in a mixture of deuterochloroform and deuterium oxide to form a solution,

adding trifluoroacetic anhydride and deuteroacetone to said solution,

freezing and sealing said solution within a vessel,

heating said solution at a temperature and for a period of time sufficient to deuterate all of the hydrogen atoms at the 2 and 6 position on said nifedipine, and recovering said deuterated nifedipine.

6. A pharmaceutical preparation comprising as the active component the deuterated nifedipine of claim 4 and a pharmaceutically acceptable carrier.

7. The method according to claim 5, said method comprising:

dissolving 80 mg of nifedipine in a mixture of about 2 ml of deuterochloroform and about 0.5 ml of deuterium oxide to form a solution,

adding about 0.2 ml of trifluoracetic anhydride and 2 ml of deuteroacetone to said solution and mixing therewith,

freezing and sealing said solution within a vessel,

heating said solution at a temperature of about 50°

to about 65°

C. for a period of time of about 150 to 180 hours,

cooling said heated solution and recovering said deutrated nifedipine.