Claims
- 1. A method of ameliorating sexual dysfunction in a human female which comprises administering to said human female apomorphine in an amount sufficient to increase intraclitoral blood flow and vaginal wall blood flow on stimulation of said female but less than the amount that induces substantial nausea.
- 2. The method in accordance with claim 1 wherein the apomorphine is administered in a sublingual dosage form containing about 2 milligrams to about 12 milligrams of apomorphine.
- 3. The method in accordance with claim 1 wherein the amount of apomorphine administered is in the range of about 25 to about 80 micrograms per kilogram of body weight.
- 4. The method in accordance with claim 1 wherein the apomorphine is administered as the hydrochloride salt.
- 5. The method in accordance with claim 1 wherein the apomorphine is administered together with a β-cyclodextrin.
- 6. The method in accordance with claim 1 wherein the β-cyclodextrin is hydroxypropyl-β-cyclodextrin.
- 7. A method of stimulating dopamine receptors in the mid-brain region of a human female to cause clitoral erectogenesis and vaginal engorgement which comprises administering to the human female apomorphine about 25 to about 80 micrograms of apomorphine per kilogram of body weight and at a rate so as to maintain a plasma concentration of apomorphine of no more than about 5.5 nanograms per milliliter during sexual activity.
- 8. The method in accordance with claim 7 wherein the plasma concentration of apomorphine is maintained in the range of about 0.3 to about 4 nanograms per milliliter during sexual activity.
- 9. The method in accordance with claim 7 wherein the plasma concentration of apomorphine is maintained in the range of about 1 to about 2 nanograms per milliliter during sexual activity.
- 10. A method of ameliorating sexual dysfunction in a human female which comprises administering to said human female apomorphine in an amount sufficient to stimulation induce clitoral erectogenesis and vaginal engorgement and to maintain a plasma concentration of apomorphine at a level of no more than about 5.5 nanograms per milliliter.
- 11. The method in accordance with claim 10 wherein the plasma concentration of apomorphine is maintained at a level of about 0.3 to about 4 nanograms per milliliter.
- 12. The method in accordance with claim 10 wherein the plasma concentration of apomorphine is maintained at a level of about 1 to about 2 nanograms per milliliter.
- 13. The method in accordance with claim 10 wherein the amount of apomorphine administered is in the range of about 2 milligrams to about 12 milligrams.
- 14. The method in accordance with claim 10 wherein the amount of apomorphine administered is in the range of about 25 to about 80 micrograms per kilogram of body weight.
- 15. The method in accordance with claim 10 wherein apomorphine is administered as the hydrochloride salt.
- 16. The method in accordance with claim 1 wherein the administration is effected by a transdermal patch.
- 17. The method in accordance with claim 1 wherein the administration is effected by the application of a cream to the clitoral region of the patient.
- 18. The method in accordance with claim 1 wherein the administration is effected by a buccal patch.
CROSS-REFERENCE TO RELATED APPLICATION
This application is a continuation-in-part of U.S. Ser. No. 09/016,252, filed on Jan. 30, 1998, now U.S. Pat. No. 5,945,117.
US Referenced Citations (2)
Number |
Name |
Date |
Kind |
5562917 |
Durif et al. |
Oct 1996 |
|
5945117 |
El-Rashidy et al. |
Aug 1999 |
|
Continuation in Parts (1)
|
Number |
Date |
Country |
Parent |
09/016252 |
Jan 1998 |
US |
Child |
09/345009 |
|
US |