LIPOSOME DELIVERY OF PSYCHEDELICS
A composition of a psychedelic in a liposome formulation, wherein the composition provides preferential distribution of the psychedelic at the CNS and blood, and reduced distribution at peripheral organs. A method of treating a patient, by administering a composition of a psychedelic in a liposome formulation to the patient, and preferentially distributing the psychedelic at the CNS with a reduced exposure in target peripheral organs (e.g., heart).
1 . A composition comprising a psychedelic in a liposome formulation, wherein said composition provides preferential distribution of the psychedelic at the CNS and blood, and reduced distribution at peripheral organs.
2 . The composition of claim 1 , wherein said psychedelic is chosen from the group consisting of ibogaine, noribogaine, lysergic acid diethylamide (LSD), psilocybin, psilocin, mescaline, 5-methoxy-N,N-dimethyltryptamine (5-MeO-DMT), dimethyltryptamine (DMT), 2,5-dimethoxy-4-iodoamphetamine (DOI), 2,5-dimethoxy-4-bromoamphetamie (DOB), salts thereof, solvates thereof, tartrates thereof, analogs thereof, and homologues thereof.
3 . The composition of claim 1 , wherein said liposome formulation is made from liposomes chosen from the group consisting of conventional liposomes, sterically-stabilized liposomes, ligand-targeted liposomes, and combinations thereof.
4 . The composition of claim 1 , wherein said liposome formulation is designed to preferentially target the CNS and provide a low concentration in peripheral organs.
5 . The composition of claim 4 , wherein said liposome formulation includes a mechanism to deliver the psychedelic across the blood brain barrier chosen from the group consisting of passive targeting and active targeting.
6 . The composition of claim 1 , wherein said psychedelic is chosen from the group consisting of ibogaine and noribogaine, and said composition reduces side effects of hERG inhibition, cardiotoxicity, and the development of cardiac arrhythmias by reducing distribution and exposure at the heart.
7 . A method of treating a patient, including the steps of:
administering a composition of a psychedelic in a liposome formulation to the patient; and
preferentially distributing the psychedelic at the CNS and blood and reducing distribution to target peripheral organs.
8 . The method of claim 7 , wherein the psychedelic is chosen from the group consisting of ibogaine, noribogaine, lysergic acid diethylamide (LSD), psilocybin, psilocin, mescaline, 5-methoxy-N,N-dimethyltryptamine (5-MeO-DMT), dimethyltryptamine (DMT), 2,5-dimethoxy-4-iodoamphetamine (DOI), 2,5-dimethoxy-4-bromoamphetamie (DOB), salts thereof, solvates thereof, tartrates thereof, analogs thereof, and homologues thereof.
9 . The method of claim 7 , wherein the liposome formulation is made from liposomes chosen from the group consisting of conventional liposomes, sterically-stabilized liposomes, ligand-targeted liposomes, and combinations thereof.
10 . The method of claim 7 , wherein said preferentially distributing step is accomplished by the liposome formulation.
11 . The method of claim 10 , wherein the liposome formulation includes a mechanism to deliver the psychedelic across the blood brain barrier chosen from the group consisting of passive targeting and active targeting.
12 . The method of claim 7 , wherein the composition stays bound at a receptor in the CNS long enough to provide a beneficial effect.
13 . The method of claim 7 , wherein the psychedelic is chosen from the group consisting of ibogaine and noribogaine, and further including the steps of reducing side effects of hERG inhibition, cardiotoxicity, and the development of cardiac arrhythmias by reducing distribution and exposure at the heart.
14 . The method of claim 7 , wherein the patient has a condition or disease chosen from the group consisting of anxiety disorders, depression, headache disorder, obsessive compulsive disorder (OCD), personality disorders, stress disorders, drug disorders, gambling disorder, eating disorder, body dysmorphic disorder, pain, neurodegenerative disorders, autism spectrum disorder, eating disorders, and neurological disorders.