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In one embodiment, the CNS active agent administered is in a time-dependent release form, preferably before the vagal neuromodulator's administration in order to ensure that the CNS active agent (already absorbed into the blood from the intestines) will be available for modulation of vagal afferent or efferent receptors while the neuromodulators are active in the stomach.

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In fact, many of the compounds disclosed herein as being suitable ions for the disclosed ionic liquids have already been proven to be effective alone or in some other preparation.

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The release of carbon dioxide from the ethylcellulose-coated sodium bicarbonate core causes particle buoyancy, thereby delaying the release of vagal neuromodulators from the particles.

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Yes, doses above 200mg result in D2 and D3 antagonism the atypical antipsychotic fashion while low doses seem to facilitate dopamine activity, now I don't really know if one can range between 50 and 200mg for antidepressant action, my pdoc states that amisulpride at 100mg dose already acts like antipsychotic but I'm not not sure.

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In this embodiment the CNS agent maybe in an amount that is substantially the same as the conventionally accepted effective dosage, yet still have a reduction in at least one side-effect of the CNS.

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CNS active agents of the present invention also include “serotonin- and noradrenalin-reuptake inhibitors” (SNRIs).

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The Tmax of CNS agent will allow release of CNS agent once the vagal afferent neurons have already been stimulated and therefore, will prevent sedation-related effects associated with the CNS agent.

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Other delayed gastric-emptying approaches may be used in order to delay the release of vagal neuromodulators in the stomach.

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