Nanoparticulate compositions for targeted delivery of acid labile, lipophilic prodrugs of cancer chemotherapeutics and their preparation
In one embodiment, the present application discloses synthetic LDL nanoparticles comprising mixtures of components selected from the group consisting of phospholipids, triglycerides, cholesterol ester and free cholesterol; optionally further comprising an agent selected from the group consisting of natural antioxidants, ubiquinol and vitamin E, and methods for preparing the synthetic nanoparticles. The disclosed synthetic LDL nanoparticles are capable of selectively delivering lipophilic drugs and prodrugs to cellular targets expressing LDL receptors after intra venous injection.
1. A method for the treatment of cancer in a patient in need of such treatment comprising administering to the patient a therapeutically effective amount of the stable, synthetic low density lipoprotein (LDL) nanoparticle comprising:
a) a lipophilic anti-cancer agent of the formula 1a, 1b or formula 2a:
wherein:
for formula 1a or 1b R 1 is hydrogen, C 1 -C 4 alkyl or C 5 -C 22 alkyl; and R 2 is C 5 -C 22 alkyl;
for formula 2a: R 2 is C 1 -C 22 alkyl; and X is hydrogen or is selected from the group consisting of Cl, Br and I; and
R is a hydroxyl bearing cancer chemotherapeutic agent (HBCCA) selected from the group consisting of paclitaxel and docetaxel;
b) phospholipids (PL) wherein the phospholipid is selected from the group consisting of phosphotidylcholine, phosphotidylethanolamine, symmetric or asymmetric 1,2-diacyl-sn-glycero-3-phosphorylcholines, 1,2-dimyristoyl-sn-glycero-3-phosphorylcholine, 1,2-dimyristoyl-sn-glycero-3-phosphorylethanolamine, egg phospholipids, egg phosphatidyl glycerol, dipalmitoylphosphatidyl glycerol, egg lecithin, soy lecithin, lecithin (NOS) and mixtures thereof; and
c) triglycerides (TG);
wherein the LDL nanoparticle has a mean particle size of 40-80 nm;
wherein the cancer is breast cancer.
2. The method of claim 1 , wherein the lipophilic anti-cancer agent of the formula 1a, 1b or formula 2a is ALLMC of paclitaxel or ALLMC of docetaxel:
wherein -ALL 1 is hydrogen;
wherein for the formula ALLMC of paclitaxel, -ALL 2 is hydrogen; and
wherein for the formula ALLMC of docetaxel, -ALL 2 is hydrogen and -ALL 3 is hydrogen.
3. The method of claim 1 or 2 , wherein the lipophilic anti-cancer agent of the formula 1a is:
4. The method of claim 1 , wherein the LDL nanoparticle has a mean size distribution of 60 nm.
5. The method of claim 1 , further comprising cholesterol ester (CE) or cholesterol (C), or mixtures of cholesterol ester and cholesterol.
6. The method of claim 5 , wherein the cholesterol ester (CE) is selected from the group consisting of C 16-22 esters of cholesterol and mixtures thereof; and the triglyceride is selected from the group consisting of soybean oil, triolein, glyceryl tripalmitate and mixtures thereof.
7. The method of claim 1 , wherein the stable, synthetic low density lipoprotein (LDL) nanoparticle further comprises an agent selected from the group consisting of triolein, BHT, ubiquinol, ubiquinol 10, vitamin E, alpha-tocopherol, gamma-tocopherol, lycopene, and betacarotene, or mixtures thereof.
8. The method of claim 5 , wherein the weight ratio of PL:TG:CE:C ranges from 73:12:2:1 to 78:12:2:1; optionally further comprising an additive selected from the group consisting of triolein, BHT, ubiquinol, ubiquinol 10, vitamin E, alpha-tocopherol, gamma-tocopherol, lycopene, and betacarotene, or mixtures thereof.
9. The method of claim 8 , wherein the weight ratio of PL:TG:CE:C is 77:10:2:1.
10. The method of claim 1 , wherein the stable, synthetic low density lipoprotein (LDL) nanoparticle further comprises poloxamers that are nonionic triblock copolymers composed of a central hydrophobic chain of polyoxypropylene (poly(propylene oxide)) flanked by two hydrophilic chains of polyoxyethylene (poly(ethylene oxide)), or mixtures thereof.