Lipobeads and their production
View Patent ↗Lipobeads (liposome-encapsulated hydrogels) combine properties of hydrogels and liposomes to create systems that are sensitive to environmental conditions and respond to changes in those conditions in a fast time scale. Lipobeads may be produced by polymerizing anchored or unanchored hydrogels within liposomes or by mixing anchored or unanchored hydrogels with liposomes. Giant lipobeads may be produced by shrinking unanchored nanogels in lipobeads and fusing the resulting lipobead aggregates, long-term aging of anchored or unanchored lipobeads, or mixing anchored or unanchored aggregated nanogels with liposomes. Poly(acrylamide), poly(N-isopropylacrylamide), and poly(N-isopropylacrylamide-co-1-vinylimidazole) lipobeads were produced and characterized.
1. A method for producing a lipobead defined by a hydrogel, having a diameter of less than 1 μm, encapsulated in a lipid bilayer, the method comprising:
a) encnpsulating hydrogel-forming components into liposomes, wherein the hydrogel-forming components include initiator, cross-linker, and polymer-forming monomers; and
b) polymerizing the polymer-forming monomers of the hydrogel-forming components by photo- or redox-polymerization, thereby forming lipobeads.
2. The method of claim 1 further comprising:
c) diluting a large unilamellar vesicles (LUV) suspension before polymerization to prevent polymerization outside the liposomes.
3. The method of claim 1 wherein the polymer-forming monomers contain a vinyl group.
4. The method of claim 1 wherein the polymer-forming monomers are selected from a group consisting of acrylamide, N-isopropylacrylamide, N, N-dimethylacrylamide, N,N-diethylacrylamide, 1-vinylimidazole, sodium acrylate, sodium methacrylate, 2-hydroxyethylmethacrylate (HEMA), N,N-dimethylaminoethyl methacrylate (DMAEMA), N-[tris(hydroxymethyl)methyl]acrylamide, 1-(3-methacryloxy)propylsulfonic acid (sodium salt), allylamine, N-acryloxysuccinimide, N-vinylcaprolactam, 1-vinyl-2-pyrrolidone, 2-acrylamide-2-methyl-1-propanesulfonic acid (sodium salt), (3-acrylamidopropyl) trimethylammonium chloride, and diallyldimethylammonium chloride.
5. The method of claim 1 wherein the liposome is selected from group consisting of egg yolk L-α-phosphatidylcholine (EPC), 1,2-dimyristoyl-sn-glycero-3-phosphatidylcholine (DMPC), 1,2-dipalmitoyl-sn-glycero-3-phosphatidylcholine (DPPC), 1,2-dioleoyl-sn-glycero-3-phosphatidylcholine (DOPC), 1,2-distearcyl-sn-glycero-3-phosphatidylcholine (DSPC), 1,2-dilauroyl-sn-glycero-3-phosphatidylcholine (DLPC), 1,2-dioleoyl-sn-glycero-3-phosphaethanolamine (DOPE), 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphaethanolamine (POPE), 1,2-dimyristoyl-sn-glycero-3-phosphaethanolamine (DMPE), 1,2-dipalmitoyl-sn-glycero-3-phosphaethanolamine (DPPE), and 1,2-distearoyl-sn-glycero-3-phospharthanolamnine (DSPE).
6. The method of claim 1 wherein the cross-linker is selected from a group consisting of N,N′-methylenebisacrylamide, N,N′-(1,2-dihydroxyethylene)bisacrylamide, ethylene glycol diacrylate, di(ethylene glycol) diacrylate, tri(ethylene glycol) diacrylate, tetra(ethylene glycol) diacrylate, ethylene glycol dimethacrylate, di(ethylene glycol) dimethacrylate, tri(ethylene glycol) dimethacrylate, tetra(ethylene glycol) dimethacrylate, and pentaerythritol triacrylate.
7. The method of claim 1 wherein photopolymerization is accomplished by a photoinitiator, and wherein the photoinitiator is selected from a group consisting of 2,2-diethoxyacetophenone, 2,2-dimethoxy-2-phenylacetophenone (IRGACURE 651), 1-[4-(2-hydroxyethoxy)phenyl]-2-hydroxy-2-methyl-1-propan-1-one (IRGACURE 2959), 2-hydroxy-2-methylpropiophenone, and 2-hydroxy-4′-(2-hydroxyethoxy)-2-methylpropiophenone.
8. The method of claim 1 wherein redox polymerization is accomplished by a redox initiator, and wherein the redox initiator is selected from a group consisting of ammonium persulfate, potassium persulfate, 2,2′-azobis[2-methyl-N-(2-hydroxyethyl)propionamide (VA-086), 2,2′-azobis(2-amidinopropane)dihydrochloride (V-50), 4,4′-azobis(4-cyanovaleric acid).
9. The method of claim 1 wherein the hydrogel has a diameter of approximately 30 nm to approximately 1000 nm.
10. The method of claim 1 wherein the lipobead generated has a diameter of approximately 30 nm to approximately 1000 nm.