PHARMACEUTICAL COMPOSITIONS COMPRISING ANTIEMETICS AND ALPHA-2-ADRENERGIC RECEPTOR AGONISTS AND METHODS OF USING THE SAME FOR ANESTHESIOLOGICAL APPLICATIONS
Pharmaceutical compositions and methods for inducing conscious sedation using such compositions are described, the compositions including antiemetic(s) and a-2-adrenergic receptor agonist(s), and optionally β-blocker(s), NSAID(s), antihistamine(s), and/or pain reliever(s). The compositions may be incorporated into vehicles for extended release. Methods for fabricating the compositions and using them for anesthesiological applications are also described.
1 . A pharmaceutical composition, comprising a therapeutically effective quantity of a pharmaceutical formulation incorporated into a vehicle, wherein the pharmaceutical composition comprises:
(a) a therapeutically effective quantity of an at least one antiemetic medicament;
(b) a therapeutically effective quantity of an at least one α-2-adrenergic receptor agonist; and
(c) optionally, a pharmaceutically acceptable excipient,
wherein the vehicle further optionally provides for extended release of the pharmaceutical formulation.
2 . The pharmaceutical composition of claim 1 , wherein the antiemetic medicament is selected from the group consisting of ondansetron, dolasetron, granisetron, palonosetron, promethazine, imenhydrinate, and meclizine.
3 . The pharmaceutical composition of claim 2 , wherein the antiemetic medicament is ondansetron.
4 . The pharmaceutical composition of claim 1 , wherein the α-2-adrenergic receptor agonist is selected from the group consisting of dexmedetomidine hydrochloride, clonidine, guanfacine, xylazine, guanabenz, guanethidine, tizanidine, medetomidine, methylnorepinephrine, norepinephrine, 3-nitrobiphenyline, amitraz, detomidine, and lofexidine.
5 . The pharmaceutical composition of claim 4 , wherein the α-2-adrenergic receptor agonist is dexmedetomidine hydrochloride.
6 . The pharmaceutical composition of claim 1 , wherein the excipient is selected from the group consisting of extended release capsules ensconcing the pharmaceutical formulation and a matrix polymer structure holding the pharmaceutical formulation that is embedded into the matrix.
7 . The pharmaceutical composition of claim 6 , wherein the excipient is configured to allow the release of the pharmaceutical formulation in a period of time of between about 15 minutes and about 20 hours.
8 . The pharmaceutical composition of claim 6 , wherein the excipient comprises a polymer selected from the group consisting of esters of cellulose, poly(lactic-co-glycolic acid), polylactic acid, polyglycolide, dextrin, polyacetals, poly(N-(2-hydroxypropyl)methacrylamide), polycaprolactone, and poly-3-hydroxybutyrate.
9 . The pharmaceutical composition of claim 8 , wherein the esters of cellulose are selected from the group consisting of methyl cellulose and hydroxypropyl methyl cellulose.
10 . The pharmaceutical composition of claim 6 , wherein the excipient comprises a substance selected from the group consisting of gelatin, sodium saccharin, stevioside, peppermint oil, cherry flavor, lemon oil, raspberry flavor and combinations thereof.
11 . The pharmaceutical composition of claim 1 , wherein the pharmaceutical formulation further comprises a therapeutically effective quantity of one or more additional pharmaceutically active compounds selected from the group consisting of β-blockers, NSAIDs, antihistamines, pain relievers and combinations thereof, or pharmaceutically acceptable salts, hydrates, solvates or N-oxides thereof.
12 . The pharmaceutical composition of claim 11 , wherein the β-blocker or the pain reliever is selected from the group consisting of metoprolol, propranolol, acebutolol, nadolol, atenolol, betaxolol, esmolol, bi soprolol fumarate, carvedilol, nebivolol, penbutolol, timolol, sotalol, and acetaminophen.
13 . The pharmaceutical composition of claim 11 , wherein the NSAID is selected from the group consisting of bromfenac, ketorolac, etodolac, sulindac, diclofenac, aceclofenac, nepafenac, tolmetin, indomethacin, nabumetone, ketoprofen, dexketoprofen, ibuprofen, flurbiprofen, dexibuprofen, fenoprofen, loxoprofen, oxaprozin, naproxen, aspirin, salicylic acid, diflunisal, salsalate, mefenamic acid, meclofenamic acid, flufenamic acid, tolfenamic acid, meloxicam, piroxicam, ternoxicam, droxicam, lornoxicam, isoxicam, celecoxib, rofecoxib, valdecoxib, parecoxib, lumiracoxib, etoricoxib, firocoxib, nimesulide, clonixin, and licofelone.
14 . The pharmaceutical composition of claim 11 , wherein the antihistamine is selected from the group consisting of hydroxyzine pamoate, hydroxyzine hydrochloride, diphenhydramine hydrochloride, meclizine, chlorpheniramine, clemastine, promethazine, and prochlorperazine.
15 . A method for inducing conscious sedation, procedural sedation, analgesia, pre-sedation or non-general anesthesia in a patient comprising administering to a patient in need thereof the pharmaceutical composition of claim 1 prior to carrying out an invasive or a non-invasive medical procedure.
16 . The method of claim 15 , wherein the invasive or non-invasive medical procedure is selected from the group consisting of an ophthalmic surgery, a dental procedure, an outpatient medical procedure, an obstetric and gynecological procedure, a gastrointestinal procedure, an otolaryngological procedure, a cosmetic surgery procedure, a dermatological procedure, a podiatric procedure, an orthopedic procedure, an emergency medical treatment, a psychiatric treatment, a urological procedure, and a veterinarian procedure.
17 . The method of claim 16 , wherein the ophthalmic surgery is selected from the group consisting of a cataract surgery, a glaucoma surgery, corneal surgery, eyelid surgery, and retinal surgery.
18 . The method of claim 16 , wherein the dental procedure is selected from the group consisting of a tooth extraction, an oral surgery, and a root canal surgery.
19 . The method of claim 16 , wherein the outpatient surgical procedure is selected from the group consisting of a medical imaging procedure, biopsy, bone marrow harvesting, colonoscopy, endoscopy, and a laparoscopic procedure.
20 . The method of claim 16 , wherein the patient experiences or expects to experience high anxiety, bouts of panic attacks, disquietude, apprehension, or angst prior to, or during, the medical procedure.
21 . The method of claim 16 , wherein the pharmaceutical composition is administered by a method selected from the group consisting of sublingual administration, buccal administration, rectal administration, nasal spray administration, oral spray administration, transdermal administration, and transmucosal administration.