Lipid emulsions and uses thereof
The present disclosure provides lipid emulsions comprising at least 20 percent (w/v) lipid with an average particle size of about 200 to about 300 nm, and use thereof to treat subjects in need of lipid emulsion therapy.
1 . A lipid emulsion composition suitable for intraoperative administration consisting of at least 20 percent (w/v) lipid, about 1 to about 5 percent (w/v) emulsifier, about 1 to about 5 percent (w/v) tonicity modifier, optionally an inotrope, and water, wherein particles of the lipid emulsion have an average particle diameter of about 200 nm to less than 230 nm, and wherein the particle size standard deviation is about 150 nm or less.
2 . The composition of claim 1 , wherein the composition comprises about 24 percent (w/v) lipid.
3 . The composition of claim 1 , wherein at least 50% of the particles have a particle diameter less than 250 nm.
4 . The composition of claim 3 , wherein at least 60% of the particles have a particle diameter less than 250 nm.
5 . The composition of claim 4 , wherein at least 70% of the particles have a particle diameter less than 250 nm.
6 . The composition of claim 5 , wherein at least 75% of the particles have a particle diameter less than 250 nm.
7 . The composition of claim 1 , wherein at least 50% of the particles have a particle diameter of about 240 nm or less.
8 . The composition of claim 1 , wherein at least 50% of the particles have a particle diameter of about 230 nm or less.
9 . The composition of claim 1 , wherein at least 90% of the particles have a particle diameter less than 250 nm, and at least 50% of the particles have a diameter of about 240 nm or less.
10 . The composition of claim 1 , wherein the average particle diameter of the composition changes by 25% or less following storage at 25° C. for 3 months.
11 . The composition of claim 1 , wherein the particle size standard deviation is about 75 nm or less.
12 . The composition of claim 1 , wherein the particle size standard deviation is about 25 nm or less.
13 . The composition of claim 1 , wherein the particles have an increased surface area as compared to the particles of a composition having the same mass having an average particle diameter of 330 nm.
14 . The composition of claim 1 , wherein the particles have a more negative zeta potential as compared to a composition having an average particle diameter of 330 nm.
15 . The composition of claim 14 , wherein the particles have a zeta potential of −57.4 mV.
16 . The composition of claim 1 , wherein the lipid is soybean oil, avocado oil, flaxseed oil, coconut oil, cottonseed oil, squalene oil, groundnut oil, olive oil, canola oil, corn oil, rapeseed oil, safflower oil, sunflower oil, an animal oil, fish oil, flavor oil, water insoluble vitamins, mineral oil, or any combination thereof.
17 . The composition of claim 1 , wherein the emulsifier is a synthetic lecithin comprising dihexanoyl-L-a-lecithin, or a phospholipid chosen from phosphatidylcholine, phosphatidylethanolamine, phosphatidylserine, phosphatidylinositol, phosphatidylglycerol, phosphatidic acid, lysophospholipids, egg or soybean phospholipid or combinations thereof and the emulsifier may be in any form, including salted or desalted, hydrogenated or partially hydrogenated, or natural, modified, semisynthetic or synthetic.
18 . The composition of claim 1 , wherein the tonicity modifier is glycerin, sorbitol, a polyoxyethylated hydrocarbon, a C 6 -C 20 saturated aliphatic acid, or a C 6 -C 20 unsaturated aliphatic acid.
19 . The composition of claim 1 , wherein the lipid is soybean oil, the emulsifier is egg yolk phospholipids, and the tonicity modifier is glycerin.
20 . The composition of claim 1 , wherein the lipid emulsion has a pH between about 4 to about 10.
21 . The composition of claim 1 , further comprising an inotrope.
22 . The composition of claim 21 , wherein the inotrope is selected from the group consisting of insulin, glucose, levosimendan, epinephrine, neosynephrine, norepinephrine, dobutamine, dopamine, and combinations thereof.
23 . A lipid emulsion suitable for intravenous administration consisting of at least 20 percent (w/v) lipid, about 1 to about 5 percent (w/v) emulsifier, about 1 to about 5 percent (w/v) tonicity modifier, optionally an inotrope, and water, wherein particles of the lipid emulsion have an average particle diameter of about 200 nm to less than 230 nm.