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 stable, synthetic low density lipoprotein (LDL) solid 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; and 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 a taxane, abeo-taxane, camptothecin, epothilone, cucurbitacin, quassinoid and an anthracycline;
b) phospholipids (PL) wherein the phospholipids 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.
2. The LDL nanoparticle of claim 1 , wherein the LDL nanoparticle has a mean size distribution of 60 nm.
3. The LDL nanoparticle of claim 1 , further comprising cholesterol ester (CE) or cholesterol (C), or mixtures of cholesterol ester and cholesterol.
4. The LDL nanoparticle of claim 3 , wherein the cholesterol ester is selected from the group consisting of C 16-22 esters of cholesterol, and mixtures thereof; and the triglycerides is selected from the group consisting of soybean oil, triolein, glyceryl tripalmitate and mixtures thereof.
5. The LDL nanoparticle of claim 1 , further comprising an agent selected from the group consisting of triolein, BHT, ubiquinol, ubiquinol 10, vitamin E, alpha-tocopherol, gamma-tocopherol, lycopene, retinyl derivative and betacarotene, or mixtures thereof.
6. The LDL nanoparticle of claim 1 , wherein the lipophilic anti-cancer agent has a log P greater than 6.0 or greater than 8.0.
7. The LDL nanoparticle of claim 3 , 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, retinyl derivative and betacarotene, or mixtures thereof.
8. The LDL nanoparticle of claim 7 , wherein the weight ratio of PL:TG:CE:C is 77:10:2:1.
9. The LDL nanoparticle of claim 1 , further comprising a poloxamer 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.
10. A 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; and 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 a taxane, abeo-taxane, camptothecin, epothilone, cucurbitacin, quassinoid and an anthracycline;
b) phospholipids (PL) wherein the phospholipids 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) prepared by the process comprising:
1) combining the lipophilic anti-cancer agent, phospholipids and triglycerides to form a mixture;
2) homogenizing the mixture by dissolution in a volatile solvent;
3) removing the solvent;
4) forming a coarse emulsion by blending of the mixture in a buffer to form an emulsion mixture;
5) microfluidizing the emulsion mixture in a microfluidizer apparatus for a sufficient amount of time to produce a particle preparation of 100 nm or less; and
6) sterilizing the nanoparticle preparation through a 0.22 micron filter to obtain the synthetic LDL nanoparticles with a mean particle size range of 40 nm to 80 nm.