Method of systematically delivering SSRIs
Methods and compositions are disclosed for the intravaginal or rectal delivery of selected serotonin reuptake inhibitors (SSRIs) to the systemic circulation. Such methods and compositions are useful in the treatment of depression, migraine headaches, chronic pain, psychoactive substance abuse disorders, pre-menstrual dysphoric disorder (PMDD) and obsessive compulsive disorders. The compositions may be formulated for the immediate release or controlled release of SSRIs over an extended period of time. A preferred SSRI is fluoxetine.
1. A device, suitable for insertion into the vaginal canal of a female, for delivering and controllably releasing a selective serotonin reuptake inhibitor (SSRI) intravaginally over an extended period of time in a single application, to treat a disorder selected from the group consisting of depression, eating disorders, migraine headaches, pain, psychoactive substance use disorders, pre-menstrual dysphoric disorders (PMDD) and obsessive compulsive disorders, said device adapted to receive a pharmaceutical composition consisting of said SSRI as the sole active ingredient and suitable excipients, such that upon insertion of said device into the vaginal canal, a therapeutically effective amount of said SSRI is controllably released from said device over an extended period of time to treat said disorder.
2. A device in accordance with claim 1 , wherein said SSRI is selected from the group consisting of fluoxetine, sertraline, paroxeline, fluvoxamine, citalopram and pharmaceutically acceptable salts thereof.
3. A device in accordance with claim 2 , wherein said SSRI is fluoxetine or a pharmaceutically acceptable salt thereof and said composition consists of from about 4–60% by weight fluoxetine and from about 40–96% by weight of said suitable excipients.
4. A device, suitable for insertion into the vaginal canal of a female, for immediate delivery of a selective serotonin reuptake inhibitor (SSRI) intravaginally to treat a disorder selected from the group consisting of depression, eating disorders, migraine headaches, pain, psychoactive substance use disorders, pre-menstrual dysphoric disorders (PMDD) and obsessive compulsive disorders, said device adapted to receive a pharmaceutical composition consisting of said SSRI as the sole active ingredient and suitable excipients, such that upon insertion of said device into the vaginal canal, a therapeutically effective amount of said SSRI is immediately released from said device.
5. A device in accordance with claim 4 , wherein said SSRI is selected from the group consisting of fluoxetine, sertraline, paroxetine, fluvoxamine, citalopram and pharmaceutically acceptable salts thereof.
6. A device in accordance with claim 5 , wherein said SSRI is fluoxetine or a pharmaceutically acceptable salt thereof and said composition consists of from about 4–60% by weight fluoxetine and from about 40–96% by weight of said suitable excipients.
7. A device in accordance with claim 1 , wherein said device is a vaginal ring.
8. A vaginal ring in accordance with claim 7 , wherein said SSRI is selected from the group consisting of fluoxetine, sertraline, paroxetine, fluvoxamine, citalopram and pharmaceutically acceptable salts thereof.
9. A vaginal ring in accordance with claim 8 , wherein said SSRI is fluoxetine or a pharmaceutically acceptable salt thereof said composition consists of from about 4–60% by weight fluoxetine and from about 40–96% by weight of said suitable excipients.
10. A device in accordance with claim 4 , wherein said device is a vaginal ring.
11. A vaginal ring in accordance with claim 10 , wherein said SSRI is selected from the group consisting of fluoxetine, sertraline, paroxetine, fluvoxamine, citalopram and pharmaceutically acceptable salts thereof.
12. A vaginal ring in accordance with claim 11 , wherein said SSRI is fluoxetine or a pharmaceutically acceptable salt thereof and said composition consists of from about 4–60% by weight fluoxetine and from about 40–96% by weight of said suitable excipients.