Intravenous curcumin and derivatives for treatment of neurodegenerative and stress disorders
Liposomal formulations and polymer conjugates of curcumin, curcumin analogs and derivatives thereof for parenteral administration are disclosed herein. The formulations are effective in the treatment of progressive supranuclear palsy, Alzheimer's disease (AD), Parkinson's disease (PD), Tauopathies or stress disorders including Post Traumatic Stress Disorder (PTSD). Curcumin crosses the blood brain barrier, localizes in the hippocampus and striata, prevents stress-induced neuronal cell damage, and stimulates neurogenesis and remediation of damaged neural circuits.
1. A method for ameliorating symptoms and/or treating one or more neurodegenerative diseases, in a subject comprising the steps of:
identifying the subject in need of ameliorating symptoms and/or treatment against one or more neurodegenerative diseases; and
administering intravenously a therapeutically effective amount of a pharmaceutical composition that ameliorates the symptoms or that treats a neurodegenerative disease comprising a curcuminoid, wherein the curcuminoid comprises curcumin dissolved or dispersed in a suitable aqueous or non-aqueous medium, wherein the curcumin is a poly-lactic-glycolic-acid (PLGA)-curcumin conjugate enclosed in one or more liposomes that cross the blood brain barrier and concentrate in the hippocampus and the striatum, the size being about 100 nanometer (nm), wherein the curcumin has been synthesized to a 99.2% purity and reaches the hippocampus at a concentration that is at least half the concentration in plasma at two hours, wherein the intravenous liposomal curcumin is administered at 20 mg/kg.
2. The method of claim 1 , further comprising the step of monitoring the efficacy of the amelioration of the symptoms or the treatment of the neurodegenerative diseases, in the subject.
3. The method of claim 1 , wherein the liposomes comprise a lipid or a phospholipid wall.
4. The method of claim 3 , wherein the lipids or the phospholipids are selected from the group consisting of phosphatidylcholine, lysolecithin, lysophosphatidylethanol-amine, phosphatidylserine, phosphatidylinositol, sphingomyelin, phosphatidylethanolamine, cardiolipin, phosphatidic acid, cerebrosides, dicetylphosphate, and dipalmitoyl-phosphatidylglycerol, stearylamine, dodecylamine, hexadecyl-amine, acetyl palmitate, glycerol ricinoleate, hexadecyl sterate, isopropyl myristate, amphoteric acrylic polymers, fatty acid, fatty acid amides, cholesterol, cholesterol ester, diacylglycerol, and diacylglycerol succinate.
5. The method of claim 1 , wherein the composition further comprises a biodegradable polymer is selected from the group consisting of polyesters, polylactides, polyglycolides, polycaprolactones, polyanhydrides, polyamides, polyurethanes, polyesteramides, polydioxanones, polyacetals, polyketals, polycarbonates, polyorthocarbonates, polyorthoesters, polyphosphoesters, polyphosphazenes, polyhydroxybutyrates, polyhydroxyvalerates, polyalkylene oxalates, polyalkylene succinates, poly(malic acid), poly(amino acids), copolymers, terpolymers, and combinations or mixtures thereof.
6. The method of claim 1 , wherein the therapeutically effective amount comprises 50 nM/kg of body weight of the subject.
7. The method of claim 1 , wherein the pharmaceutical composition is optionally administered along with related co-factors, proteins, antibodies, pain medications, and other pharmaceutically active agents.
8. The method of claim 7 , wherein the pharmaceutically active agents comprise a serotonin reuptake inhibitor, sertraline or, paroxetine.
9. A method of ameliorating symptoms and/or treating, Parkinson's disease (PD), in a subject comprising the steps of:
identifying the subject in need of amelioration and/or treatment against Parkinson's disease (PD); and
administering intravenously a therapeutically effective amount of a pharmaceutical composition that ameliorates the symptoms or that treats the PD comprising a curcuminoid, wherein the curcuminoid comprises curcumin and is a poly-lactic-glycolic-acid (PLGA)-curcumin conjugate enclosed in one or more liposomes sized to cross the blood brain barrier and concentrate in the hippocampus and the striatum, the size being about 100 nanometer (nm), wherein the curcumin has been synthesized to a 99.2% purity and a concentration level of curcumin that reaches the hippocampus at a concentration that is at least half the concentration in plasma at two hours, wherein the intravenous liposomal curcumin is administered at 20 mg/kg.
10. The method of claim 9 , further comprising the step of monitoring the efficacy of the amelioration of the symptoms or the treatment by improvements in memory, cognition, learning, speech, one or more motor skills, mood, behavior or combinations thereof in the subject.
11. The method of claim 9 , wherein the liposomes comprise a lipid or a phospholipid wall.
12. The method of claim 11 , wherein the lipids or the phospholipids are selected from the group consisting of phosphatidylcholine, lysolecithin, lysophosphatidylethanol-amine, phosphatidylserine, phosphatidylinositol, sphingomyelin, phosphatidylethanolamine, cardiolipin, phosphatidic acid, cerebrosides, dicetylphosphate, and dipalmitoyl-phosphatidylglycerol, stearylamine, dodecylamine, hexadecyl-amine, acetyl palmitate, glycerol ricinoleate, hexadecyl sterate, isopropyl myristate, amphoteric acrylic polymers, fatty acid, fatty acid amides, cholesterol, cholesterol ester, diacylglycerol, and diacylglycerol succinate.
13. The method of claim 9 , wherein the therapeutically effective amount comprises 50 nM/kg of body weight of the subject.
14. The method of claim 9 , wherein the pharmaceutical composition is optionally administered along with related co-factors, proteins, antibodies, pain medications, and other pharmaceutically active agents.
15. The method of claim 14 , wherein the one or more pharmaceutically active agents are selected from the group consisting of serotonin reuptake inhibitors sertraline, paroxetine, L-dopa, Carbidopa, benserazide, Tolcapone, dopamine agonists bromocriptine, pergolide, pramipexole, ropinirole, piribedil, cabergoline, apomorphine, lisuride, MAO inhibitors, selegiline, and rasagiline.