Hollow silica nanospheres and methods of making same
The disclosure provide hollow nanospheres and methods of making and using the same. The methods and compositions of the disclosure are useful for drug delivery and gene transfer.
1. A method for preparing a colloidal dispersion of nanospheres comprising:
(a) depositing a silica-shell precursor on a polyamino acid or carboxylate functionalized template particle at a pH range from 5.5 to 9.5 to afford core-shell nanospheres;
(b) subjecting said core-shell nanospheres to calcination or washing with an organic solvent to remove the template particle and to form hollow silica nanospheres; and
(c) sonicating a solution comprising said hollow silica nanospheres to prepare a colloidal dispersion, wherein the colloidal dispersion of nanospheres is suitable for in vivo administration by injection.
2. The method of claim 1 , further comprising hydrolyzing a silicon-containing compound to synthesize the silica shell precursor.
3. The method of claim 1 , wherein the template particle is a polymer particle.
4. The method of claim 1 , wherein the silica-shell precursor comprises a mixture of silicon and iron ethoxide.
5. The method of claim 3 , wherein the template particle comprises polystyrene.
6. The method of claim 1 , wherein the size of the template particle is from about 10 nm to 1 μm.
7. The method of claim 2 , wherein the silicon-containing compound is selected from the group consisting of tetraalkoxysilanes, trialkoxysilanes, dialkoxysilanes, tetrapropoxysilane, tetraethoxysilane, tetramethoxysilane and any combination thereof.
8. The method of claim 2 , wherein the silicon-containing compound is hydrolyzed in an acidic solution.
9. The method of claim 1 , wherein the polyamino acids comprise homo- or co-polymers of amino acids with primary amine groups on the polymer backbone.
10. The method of claim 1 , wherein the polyamino acid is selected from the group consisting of poly-L-lysine, poly-L-arginine and polyornithine.
11. The method of claim 1 , wherein the calcination comprises heating to about 450° C.
12. The method of claim 11 , wherein heating is achieved by employing a temperature ramp rate of from about 0.1° C./min to about 10° C./min.
13. The method of claim 8 , wherein the acidic solution comprises hydrochloric acid, sulfuric acid, nitric acid or any combination thereof.
14. The method of claim 8 , wherein the silicon-containing compound is hydrolyzed in an aqueous solution comprising about 0.01 M hydrochloric acid.
15. The method of claim 8 , wherein the concentration of the silicon-containing compound in the acidic solution is about 0.1-10 M.
16. The method of claim 8 , wherein the concentration of the silicon-containing compound in the acidic solution is about 1 M.
17. The method of claim 5 , wherein the depositing the silica shell precursor on the polystyrene template particle is conducted at room temperature.
18. The method of claim 17 , wherein the depositing the silica-shell precursor on the polystyrene template particle occurs at about pH 7.4.
19. The method of claim 17 , wherein the depositing the silica-shell precursor on the polystyrene template particle occurs in a phosphate buffer.
20. The method of claim 17 , wherein the polystyrene core is removed by heating in air at about 400-900° C. for 3-6 hours.
21. The method of claim 5 , wherein the washing with the organic solvents to remove the template particle core utilizes an organic solvent selected from the group consisting of toluene, dichloromethane, chloroform, tetrahydrofuran, dimethylformamide, and any combination thereof.
22. The method of claim 21 , wherein the polystyrene core is removed by washing the core-shell nanospheres in toluene.
23. The method of claim 1 , wherein the template particle comprises latex.