Charged lipoprotein complexes and their uses
The present disclosure provides charged lipoprotein complexes that include as one component a negatively charged phospholipid that is expected to impart the complexes with improved therapeutic properties.
1. A method of treating dyslipidemia in a subject, comprising administering to a subject in need thereof an effective amount of a lipoprotein complex comprising an apolipoprotein fraction and a lipid fraction, wherein said lipid fraction consists essentially of (i) a sphingomyelin, (ii) about 0.2 to 6 wt % of one or more negatively charged phospholipids, and, optionally (iii) lecithin.
2. The method according to claim 1 , wherein the lipid fraction includes lecithin and lecithin and sphingomyelin are present in a molar ratio ranging from 1:20 to 3:10.
3. The method according to claim 1 , wherein the one or more negatively charged phospholipids of the lipoprotein complex are about 1 to 4 wt % of the lipid fraction.
4. The method according to claim 1 , wherein the negatively charged phospholipid of the lipoprotein complex is selected from phosphatidylinositol, phosphatidylserine, phosphatidic acid, phosphatidylglycerol, and mixtures thereof.
5. The method according to claim 1 , wherein the apolipoprotein of the lipoprotein complex comprises ApoA-I.
6. The method according to claim 1 , wherein the sphingomyelin in the lipoprotein complex is selected from D-erythrose-sphingomyelin, D-erythrose-dihydrosphingomyelin and mixtures thereof.
7. The method according to claim 1 , wherein the acyl chains of the sphingomyelin, and/or negatively charged phospholipids in the lipoprotein complex are each, independently of one another, selected from a saturated, a mono-unsaturated and a polyunsaturated hydrocarbon containing from 6 to 24 carbon atoms.
8. The method according to claim 1 , wherein the lipid fraction includes lecithin and the acyl chains of the lecithin are selected from a saturated, a mono-unsaturated and a polyunsaturated hydrocarbon containing from 6 to 24 carbon atoms.
9. The method according to claim 1 , wherein the lipid fraction includes lecithin and the lecithin is selected from 1-palmitoyl-2-oleoyl-phosphatidylcholine (POPC), dipalmitoyl-phosphatidylcholine (DPPC), and mixtures thereof.
10. The method according to claim 1 , wherein the amount of the charged lipoprotein complex administered ranges from about 1 to 100 mg/kg ApoA-I equivalents per injection.
11. The method according to claim 1 , wherein the lipoprotein complex is administered intravenously.
12. The method according to claim 1 , wherein the lipoprotein complex is adjunctively administered with a bile-acid resin, niacin, a statin, a fibrate and/or an inhibitor of cholesterol absorption.
13. The method according to claim 1 , wherein the lipoprotein complex is administered in the form of a pharmaceutical composition comprising the lipoprotein complex and a pharmaceutically acceptable carrier, diluent and/or excipient.
14. The method according to claim 1 , wherein the dyslipidemia in the subject is characterized by lipoprotein lipase deficiency and the lipoprotein lipase deficiency is hypertriglyceridemia, hypoalphalipoproteinemia, or hypercholesterolemialipoprotein.
15. The method according to claim 1 , wherein the dyslipidemia in the subject is characterized by atherosclerosis, acute coronary syndrome, myocardial infarction, angina, or stroke.