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Generally, the particular cation(s) and anion(s) used to prepare the disclosed ionic liquids are selected as described herein.
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The vagal neuromodulators are preferably in an amount sufficient to reduce a side-effect of the CNS active agent.
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Indication: Used in cardiovascular disease to treat arrhythmias, angina pectoris, and hypertension.
As noted, all of these delivery devices can be used in the methods disclosed herein.
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Both blueberry and I have and for me at least amisulpride was very different from other low-dose antipsychotics.
The term “in conjunction with” means that when the CNS and the neuromodulators are administered in separate dosage forms, there is at least some chronological overlap in their physiological activity.
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The amount of active ingredient that may be combined with the carrier materials to produce a single dosage form will vary depending upon the host treated and the particular mode of administration.
For example, prodrugs, ionic and neutral active molecules can be dissolved in the disclosed ionic liquid compositions.
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.
Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); bizarre behavior; black or bloody stools; chest pain; confusion; decreased bladder control; decreased concentration; decreased coordination; exaggerated reflexes; fainting; fast or irregular heartbeat; fever; hallucinations; memory loss; new or worsening agitation, panic attacks, aggressiveness, impulsiveness, irritability, hostility, exaggerated feeling of well-being, restlessness, or inability to sit still; persistent or severe ringing in the ears; persistent, painful erection; red, swollen, blistered, or peeling skin; seizures; severe or persistent anxiety or trouble sleeping; severe or persistent headache; stomach pain; suicidal thoughts or attempts; tremor; unusual bruising or bleeding; unusual or severe mental or mood changes; unusual weakness; vision changes; worsening of depression.
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Formulation and dosage of the pharmaceutical composition will now be described, with reference to a time-release component that makes possible overlapping effectiveness of the CNS active agent and the neuromodulators as are discussed above.
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Examples of those ionic liquid compositions made utilizing above protocol include, but are not limited to, the mixture of at least two components of functionalized 5-, 6-membered, and bicyclic fused ring heterocyclic cation precursors and anion precursors containing 1, 2, 3, 4, or 5 atoms of nitrogen in the ring structure.
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Therapeutically effective amount" also includes an amount that is effective for prophylaxis.
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Standard laboratory tests were performed at Screening Visit 1 including those of chemistry, hematology and urinalysis, urine test for drugs of abuse, HIV and hepatitis B and C serology tests, 12-lead resting electrocardiogram, and serum pregnancy test for females.
However, the combined CNS active agent comprising both chemoreceptor stimulator (PSE) and mechanoreceptor stimulator (GUA) was effective in reduction of the sedation outcome without disturbing anti-stress action of the drugs, In addition, delayed administration of GUA (at least for 10-30 minutes, preferably 15-20 minutes) was significant to synchronize between PK and PD of CNS active agent and neuromodulators.
The mean halflife is about 30 hours.
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Conversely, the disclosed ionic liquid compositions can be formed by reacting a salt of a desired anion, say YAnion where Y is an appropaite balancing cation, with a base to yield the ionic liquid and Ybase byproduct.
The kit form may be desirable when the separate components are preferably administered in different dosage forms (e.
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To introduce deuterium at one or more positions of R 16-R 17 and R 25-R 27, compound 12 with the corresponding deuterium substitutions can be used.
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For example, if the value "10" is disclosed, then "about 10" is also disclosed.
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Only the dextro-isomer has an analgesic effect; the levo-isomer appears to exert an antitussive effect.
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Such drugs can possess any therapeutic or prophylactic activity, many of which are described herein.
One or more kinds of anions with a desired property(ies) that is similar or different to that of the cation(s) can likewise be provided.
Indication: For symptomatic treatment of rheumatoid arthritis, juvenile rheumatoid arthritis and osteoarthritis.
Neuromodulators may also be used in combination with electrical stimulation.
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In one embodiment, CNS active agent particles, and particles from at least two vagal neuromodulators are formulated in a single solid dosage form, such as multi-layered tablets, suspension tablets, effervescent tablets, powder, pellets, granules or capsules comprising multiple beads.
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The method as recited in claim 19 wherein said antipsychotic is selected from the group consisting of chlorpromazine, levomepromazine, promazine, acepromazine, triflupromazine, cyamemazine, chlorproethazine, dixyrazine, fluphenazine, perphenazine, prochlorperazine, thiopropazate, trifluoperazine, acetophenazine, thioproperazine, butaperazine, perazine, periciazine, thioridazine, mesoridazine, pipotiazine, haloperidol, trifluperidol, melperone, moperone, pipamperone, bromperidol, benperidol, droperidol, fluanisone, oxypertine, molindone, sertindole, ziprasidone, flupentixol, clopenthixol, chlorprothixene, thiothixene, zuclopenthixol, fluspirilene, pimozide, penfluridol, loxapine, clozapine, olanzapine, quetiapine, tetrabenazine, sulpiride, sultopride, tiapride, remoxipride, amisulpride, veralipride, levosulpiride, lithium, prothipendyl, risperidone, clotiapine, mosapramine, zotepine, pripiprazole, and paliperidone.
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The following schemes can be used to practice the present invention.
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The term "allcyl" as used herein is a branched or unbranched saturated hydrocarbon group of 1 to 24 carbon atoms, such as metliyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, t-butyl, pentyl, hexyl, heptyl, octyl, nonyl, decyl, dodecyl, tetradecyl, hexadecyl, eicosyl, tetracosyl, and the like.
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From AMA Drug Evaluations Annual, 1994, p236) Indication: For the short-term treatment of insomnia.
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However, the drug soon appeared to reduce psychosis beyond this calming effect, and now some believe that it causes a reduction of psychosis unrelated to the sedating effect of the medication.
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In one aspect, disclosed herein are methods for using ionic liquid compositions that comprise administering an effective amount of at least one ionic liquid composition as disclosed herein.
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