Nanoparticles, nanoparticle delivery methods, and systems of delivery
In accordance with the purpose(s) of the present disclosure, as embodied and broadly described herein, embodiments of the present disclosure, in one aspect, relate to nanoparticles, compositions including nanoparticles, methods of making nanoparticles, and the like. In particular, embodiments of the present disclosure include nanoparticles and compositions for the sustained release (e.g., release at a predetermined rate to maintain a certain concentration for a certain period of time) of an agent, such as a small interfering RNA (siRNA) from the nanoparticle.
1. A composition comprising:
a nanoparticle including a siRNA-cationic lipid conjugate, wherein the nanoparticle has a lipid monolayer enclosing a nanoparticle core, wherein the siRNA-cationic lipid conjugate is disposed within the nanoparticle core, wherein the lipid monolayer is selected from the group consisting of: lecithin, phosphatidylcholines, phosphatidic acid, phosphatidylethanolamines, phosphatidylglycerols, phosphatidylserines, phosphatidylinositols, cardiolipins, lipid-polyethyleneglycol conjugates, and a combination thereof,
wherein the nanoparticle core includes a liquid lipid, and
wherein the liquid lipid is a lipid extracted from adipose tissue.
2. The composition of claim 1 , wherein the liquid lipid is a lipid extracted from human adipose tissue.
3. The composition of claim 1 , wherein the nanoparticle has a diameter of about 150 to 800 nm.
4. The composition of claim 1 , wherein the nanoparticle core includes an agent selected from the group consisting of: a drug, an imaging agent, a nonionic surfactant, other types of lipids, and a combination thereof.
5. The composition of claim 1 , wherein the outside surface of the lipid monolayer includes an agent selected from the group consisting of: a drug, an imaging agent, a biocompatibility agent, a targeting agent, and a combination thereof.
6. A composition, comprising a nanoparticle including a siRNA-cationic lipid conjugate, wherein the nanoparticle has a lipid monolayer enclosing a nanoparticle core, wherein the siRNA-cationic lipid conjugate is disposed within the nanoparticle core,
wherein the nanoparticle core includes a liquid lipid, and
wherein the liquid lipid is a lipid extracted from adipose tissue,
wherein the cationic lipid is selected from the group consisting of: DOTAP, DC-Cholesterol, DODAP, DDAB, Ethyl PC, DOTMA, and a combination thereof.