PARTICLES WITH HIGH UNIFORM LOADING OF NANOPARTICLES AND METHODS OF PREPARATION THEREOF

• US 20090311295A1
• Filed: 05/14/2007
• Published: 12/17/2009
• Est. Priority Date: 05/12/2006
• Status: Abandoned Application

• Current Assignee: Brown University
• Original Assignee: Brown University
• Inventors: Reineke, Joshua James, Harrison, Michael W., Morello, A. Peter, Mathiowitz, Edith, Kundakovic, Ljiljana
• Application Number:
  US12/300,304
• Publication Number:
  US 20090311295A1
• Time in Patent Office: Days
• US Class Current: 424/401
• CPC Class Codes: A61K 2800/412 Microsized, i.e. having sizes between 0.1 and 100 microns
• CPC Class Codes: A61K 49/0021 the fluorescent group being a small organic molecule
• CPC Class Codes: A61K 49/0034 Indocyanine green, i.e. ICG, cardiogreen
• CPC Class Codes: A61K 49/0036 Porphyrins used in photodynamic therapy A61K41/0071 or A61K41/0076; used as targeting group or modifying agent for targeting a therapeutic compound A61K47/546
• CPC Class Codes: A61K 49/0091 Microparticle, microcapsule, microbubble, microsphere, microbead, i.e. having a size or diameter higher or equal to 1 micrometer
• CPC Class Codes: A61K 49/0093 Nanoparticle, nanocapsule, nanobubble, nanosphere, nanobead, i.e. having a size or diameter smaller than 1 micrometer, e.g. polymeric nanoparticle
• CPC Class Codes: A61K 8/11 Encapsulated compositions
• CPC Class Codes: A61K 9/1694 resulting in granules or microspheres of the matrix type containing more than 5% of excipient
• CPC Class Codes: A61P 43/00 Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
• CPC Class Codes: A61Q 1/02 Preparations containing skin colorants, e.g. pigments preparations in powder form A61Q1/12
• CPC Class Codes: A61Q 19/00 Preparations for care of the skin
• CPC Class Codes: C09C 1/00 Treatment of specific inorganic materials other than fibrous fillers tenebrescent materials C09K9/00; luminescent materials C09K11/00; Preparation of carbon black

Abstract

Methods to produce polymeric microparticles containing nanoparticles such, as pigments, dyes and other chromophores for cosmetic use, plastic surgery therapeutic use, and tattoos have been developed. The microparticles contain within the polymer a very uniform dispersion of dye particles. The methods by which the particles are made ensure a homogeneous mixture and high loading. The microparticles are made using air, one of a number of known methods such as phase inversion, solvent evaporation, and melt processing. The improvement is in the use of a method that makes, a stable dispersion of the nanoparticles in the liquid polymer before formation of the microparticles. This is achieved through selection of appropriate solvent, optionally including surfactant, and then subjecting the dispersion to mechanical processing that stabilizes the dispersion within the polymer solvent, so that the nanoparticles remain suspended for at least thirty minutes, in some cases two hours to 48 hours, sometimes up to three months. The mechanical processing can be sonication and/or production of shear forces, for examples, resulting from use of an open blade or rotor stator mixer or milling with a concentric shaft, at a speed such as between 5000 and 25,000 RPM.

Claims

1. A method for enhancing uniformity of dispersion and increasing loading of nanoparticles in a polymeric microparticle comprising

(a) forming a homogeneous dispersion of nanoparticles in a polymer solution optionally containing surfactant,

(b) sonicating or exposing the polymer solution to shear forces effective to crease a stabilized dispersion of the polymer solution wherein the nanoparticles remain suspended for at least thirty minutes, preferably at least two hours, and

(c) forming microcapsules by a process selected from the group consisting of spray drying, solvent evaporation, interfacial polymerization, hot melt encapsulation, phase separation encapsulation, spontaneous emulsion, solvent evaporation microencapsulation, solvent removal microencapsulation, coacervation, low temperature microsphere formation, and phase inversion nanoencapsulation.

2. The method of claim 1 wherein the nanoparticle-polymer solution is mixed with an open blade or rotor stator type mixer at between 5000 and 25,000 RPM.

3. The method of claim 1 wherein the nanoparticle-polymer solution is milled with a concentric shaft type device.

4. The method of claim 1 wherein the polymer solvent is removed by solvent evaporation or extraction.

5. The method of claim 1 comprising

(a) dispersing nanoparticles to be encapsulated in a molten polymer,

(b) allowing the mixture of step (a) to cool to room temperature,

(c) dissolving the mixture of step (b) in an organic solvent,

(d) mixing the solution of step (c) using continual high shear stirring at between 3000-30,000 RPM and/or sonication for between about 1 minutes and about 30 minutes, and

(e) adding the result of step (d) to a non-solvent for the polymer, and optionally evaporating the solvent, to further precipitate the polymer in the form of microparticles containing a uniform distribution of nanoparticles.

6. The method of claim 5 wherein the non-solvent comprises surfactant in a concentration from about 0.001% w/v (surfactant to non-solvent) to about 5% w/v (surfactant to non-solvent).

7. The method of claim 1 comprising a surfactant, wherein the surfactant is selected to have a similar hydrophobicity or hydrophilicity as the nanoparticles to be incorporated.

8. The method of claim 7, wherein the non-solvent is water or a mixture of water and organic solvents which are miscible with water.

9. The method of claim 8, wherein the surfactant is selected from the group consisting of polyvinylalcohol, polyethylene glycol, and combinations thereof.

10. The method of claim 5, wherein the polymer is a water-insoluble polymer.

11. The method of claim 9, wherein the non-solvent is an oil comprising a surfactant.

12. The method of claim 11, wherein the surfactant is selected from the group consisting of fatty acids, cholesterol and cholesterol derivatives, polysorbates, lecithin and combinations thereof.

13. The method of claim 5, wherein the nanoparticles are in the polymer when it is melted.

14. The method of claim 1, wherein the microparticles are formed by precipitation.

15. The method of claim 1 wherein the polymer is selected from the group consisting of biodegradable polymer and non-biodegradable polymer.

16. The method of claim 1 comprising forming a dispersion having uniformly dispersed therein nanoparticles of less than one micron in diameter.

17. The method of claim 1 comprising forming microparticles having a diameter of less than 10 microns, between about 2 and about 3 microns, or between about 1 and about 2 microns.

18. The method of claim 1 wherein the nanoparticles comprise an agent selected from the group consisting of dye or chromophore, cosmetic, therapeutic, prophylactic, diagnostic, fragrant, nutraceutical, and flavoring agents.

19. The method of claim 18 wherein the nanoparticles comprise uniformly distributed active agent(s) at a low loading of about 1-2% by weight of the nanoparticles.

20. The method of claim 18 wherein the nanoparticles comprise a dye or chromophore selected from the group consisting of fluorescent, chemiluminescent, reflective, amorphous, crystalline, spherical or reflective particles, metals, magnetic, and colorless activatable particles.

21. The method of claim 1 wherein the microparticles comprise between approximately 1 and 80% nanoparticle by weight of microparticle, between approximately 10 and 60% nanoparticle by weight of microparticle, or between approximately 10 and 40% nanoparticle by weight of microparticle.

22. The method of claim 1 wherein the microparticles are made by solvent evaporation microencapsulation using a high oil to aqueous phase ratio effective to produce particles in combination with surfactant effective to improve dispersion of the pigment in the oil phase.

23. The method of claim 22, wherein the surfactant is soluble in the organic oil phase.

24. The method of claim 22 wherein the solvent is a mixed solvent containing a mixture of at least one water-immiscible solvent and water containing a surfactant in a ratio of from about 0.001% to about 5% surfactant (v/v), wherein the ratio of the water-immiscible solvents to the water is from 5 to 95%.

25. The method of claim 1, comprising a surfactant wherein the surfactant is selected from the group consisting of fatty acids, cholesterol and cholesterol derivatives, polysorbates, lecithin and combinations thereof.

26. Polymeric microparticles having nanoparticles uniformly dispersed therein, produced by the method of claim 1, the microparticles having a homogenous size distribution, uniform nanoparticle distribution and high nanoparticle loading.

27. The microparticles of claim 26 suitable for use in tissue marking, cosmetic use, therapeutic uses, or plastic surgery.

28. A method of marking skin comprising administering into or onto the skin the microparticles of claim 27.