IP Library Granted Patent US 9,174,186
Granted Patent B2
US 9,174,186 · App. 12/672,447 · Granted Nov 3, 2015

Supercrystalline colloidal particles and method of production

Inventors: Y. Charles Cao (Gainesville, FL); Jiaqi Zhuang (Gainesville, FL); Huimeng Wu (Gainesville, FL); Yongan Yang (Golden, CO)
Assignee: UNIVERSITY OF FLORIDA RESEARCH FOUNDATION, INC.
B01J13/0026B01J13/0043
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Quick Facts
Patent No.
US 9,174,186
App. No.
12/672,447
Granted
Nov 3, 2015
Kind
B2
Abstract

The present invention concerns size- and shape-controlled, colloidal superparticles (SPs) and methods for synthesizing the same. Ligand-functionalized nanoparticles such as nonpolar-solvent-dispersible nanoparticles, are used, and the solvophobic interactions can be controlled. Advantageously, supercrystalline SPs having a superlattice structure, such as a face-centered cubic structure, can be produced. Further, the methods of the invention can provide SPs that self-assemble and are monodisperse. The SPs can be doped with organic dyes and further assembled into more complex structures.

Claims (32)

1. A colloidal superparticle (SP) of controlled shape and size, comprising an aggregate of nanoparticles, wherein the nanoparticles have a diameter of less than 100 nm and wherein adjacent nanoparticles are bound together through non-covalent interactions, wherein the SP comprises a superlattice structure and the SP is dispersible in a polar solvent.

2. The colloidal SP of claim 1 , wherein the superlattice structure is a face-centered cubic (fcc) superlattice structure.

3. The colloidal SP of claim 1 , wherein the SP comprises one type of nanoparticle.

4. The colloidal SP of claim 1 , wherein the SP comprises two or more types of nanoparticle.

5. The colloidal SP of claim 1 , wherein the nanoparticles are doped.

6. The colloidal SP of claim 1 , wherein the SP comprises a dye inside or outside the nanoparticles.

7. The colloidal SP of claim 1 , wherein the SP is synthesized by mixing a first solution comprising ligand-functionalized nanoparticles with a surfactant under aqueous conditions to form a second solution comprising nanoparticle-micelles; and mixing the second solution with a solvent to form a third solution comprising colloidal SPs.

8. The colloidal SP of claim 1 , wherein the SP is spherical or partially spherical in shape.

9. The colloidal SP of claim 1 , comprising one or more drugs or biologically active molecules.

10. The colloidal SP of claim 9 , wherein the one or more drugs are analgesics, anesthetics, anti-inflammatory agents, anthelmintics, anti-arrhythmic agents, antiasthma agents, antibiotics, anticancer agents, anticoagulants, antidepressants, antidiabetic agents, antiepileptics, antihistamines, antitussives, antihypertensive agents, antimuscarinic agents, antimycobacterial agents, antineoplastic agents, antioxidant agents, antipyretics, immunosuppressants, immunostimulants, antithyroid agents, antiviral agents, anxiolytic sedatives, astringents, bacteriostatic agents, beta-adrenoceptor blocking agents, blood products and substitutes, bronchodilators, buffering agents, cardiac inotropic agents, chemotherapeutics, contrast media, corticosteroids, cough suppressants, diagnostic agents, diagnostic imaging agents, diuretics, dopaminergics, free radical scavenging agents, growth factors, haemostatics, immunological agents, lipid regulating agents, muscle relaxants, proteins, peptides and polypeptides, parasympathomimetics, parathyroid calcitonin and biphosphonates, prostaglandins, radio-pharmaceuticals, hormones, sex hormones, time release binders, anti-allergic agents, stimulants and anoretics, steroids, sympathomimetics, thyroid agents, vaccines, vasodilators, or xanthines.

11. The colloidal SP of claim 9 , wherein the one or more biologically active molecules are chemotherapeutics, toxins, radiotherapeutics, radiosensitizing agents, gene therapy vectors, antisense nucleic acid constructs, transcription factor decoys, imaging agents, diagnostic agents, agents known to interact with an intracellular protein, polypeptides, or polynucleotides.

12. The colloidal SP of claim 1 , wherein the SP is supercrystalline comprising a superlattice structure.

13. The colloidal SP of claim 1 , wherein the nanoparticles are semiconductor nanoparticles, alloy semiconductor nanoparticles, doped semiconductor nanoparticles, core-shell semiconductor nanoparticles, metal nanoparticles, or metal oxide nanoparticles, or a combination of two or more semiconductor nanoparticles, alloy semiconductor nanoparticles, doped semiconductor nanoparticles, core-shell semiconductor nanoparticles, metal nanoparticles, or metal oxide nanoparticles.

14. The colloidal SP of claim 13 , wherein the semiconductor nanoparticles comprise CdSe, CdS, CdTe, ZnS, ZnSe, ZnTe, HgS, HgSe, HgTe, PbS, PbSe, PbTe, InAs, InP, GaP, GaAs, FeS, CuS, Ag2S, or MnS nanoparticles.

15. The colloidal SP of claim 13 , wherein the alloy semiconductor nanoparticles comprise CdZnS, CdZnSe, CdZnTe CdHgS, CdHgSe, CdHgTe, ZnSSe, CdSSe, HgSSe, CdSeTe, HgSeTe, InGaAs, or InGaP nanoparticles.

16. The colloidal SP of claim 13 , wherein the core-shell semiconductor nanoparticles comprise CdS/ZnS, CdSe/ZnS, CdSe/CdS, CdSe/CdS/ZnS, PbSe/PbS, InAs/InP, InP/ZnS, or InP/CdS nanoparticles.

17. The colloidal SP of claim 13 , wherein the doped semiconductor nanoparticles comprise Mn-doped ZnSe, Mn-doped CdS/ZnS, Mn-doped ZnSe/ZnS, or In-doped CdSe/ZnS nanoparticles.

18. The colloidal SP of claim 13 , wherein the metal nanoparticles comprise Au, Ag, Cu, Pt, Cr, Pd, Fe, Co, Ni, Ru, W, Pt/Fe, Pt/Ni, Pt/Co, Ag/Au, or Cu/Ag nanoparticles.

19. The colloidal SP of claim 13 , wherein the metal oxide nanoparticles comprise Fe 2 O 3 , Fc 3 O 4 , FeMnO 3 , Fe 2 MnO 3 , NiO, MnO, TiO 2 , ZrO 2 , MoO 3 , WO 3 , V 2 O 5 , CrO 3 , ZnO, Al 2 O 3 , Ga 2 O 3 , In 2 O 3 , SnO, SiO 2 , GeO 2 , or rare earth oxides nanoparticles.

20. The colloidal SP of claim 1 , wherein the nanoparticles comprise Fe 3 O 4 nanoparticles.

21. The colloidal SP of claim 20 , wherein the Fe 3 O 4 nanoparticles are about 5.8 nm or about 8.9 nm in diameter.

22. The colloidal SP of claim 20 , wherein the Fe 3 O 4 nanoparticles are oleic acid-functionalized.

23. The colloidal SP of claim 1 , wherein the SP are between 0.02 micron and 1.0 micron in diameter.

24. The colloidal SP of claim 1 , wherein the SP comprises nanoparticles of two or more different sizes.

25. The colloidal SP of claim 24 , wherein the nanoparticles of two or more different sizes comprise Fe 3 O 4 nanoparticles of about 5.8 nm and 8.9 nm in diameter.

26. An article of manufacture or a film or a stacked superparticle (SP) of controlled shape and size comprising a colloidal SP comprising an aggregate of nanoparticles, wherein the nanoparticles have a diameter of less than 100 nm and wherein adjacent nanoparticles are bound together through non-covalent interactions, wherein the SP comprises a superlattice structure and the SP is dispersible in a polar solvent.

27. The article of manufacture of claim 26 , wherein the colloidal SP is provided as a coating on the article of manufacture.

28. The article of manufacture of claim 26 , wherein the article of manufacture is a medical device, or an LED, or a solar cell, or a MRI contrast reagent, or a fluorescent label, or a gas sensor.

29. A pharmaceutical composition comprising a) a colloidal superparticle (SP) of controlled shape and size comprising an aggregate of nanoparticles, wherein the nanoparticles have a diameter of less than 100 nm and wherein adjacent nanoparticles are bound together through non-covalent interactions, wherein the SP comprises a superlattice structure and the SP is dispersible in a polar solvent, and b) a pharmaceutically acceptable carrier.

30. The pharmaceutical composition of claim 29 , wherein the colloidal SP comprises one or more drugs or biologically active molecules.

31. The pharmaceutical composition of claim 30 , wherein the one or more drugs are analgesics, anesthetics, anti-inflammatory agents, anthelmintics, anti-arrhythmic agents, antiasthma agents, antibiotics, anticancer agents, anticoagulants, antidepressants, antidiabetic agents, antiepileptics, antihistamines, antitussives, antihypertensive agents, antimuscarinic agents, antimycobacterial agents, antineoplastic agents, antioxidant agents, antipyretics, immunosuppressants, immunostimulants, antithyroid agents, antiviral agents, anxiolytic sedatives, astringents, bacteriostatic agents, beta-adrenoceptor blocking agents, blood products and substitutes, bronchodilators, buffering agents, cardiac inotropic agents, chemotherapeutics, contrast media, corticosteroids, cough suppressants, diagnostic agents, diagnostic imaging agents, diuretics, dopaminergics, free radical scavenging agents, growth factors, haemostatics, immunological agents, lipid regulating agents, muscle relaxants, proteins, peptides and polypeptides, parasympathomimetics, parathyroid calcitonin and biphosphonates, prostaglandins, radio-pharmaceuticals, hormones, sex hormones, time release binders, anti-allergic agents, stimulants and anoretics, steroids, sympathomimetics, thyroid agents, vaccines, vasodilators, or xanthines.

32. The pharmaceutical composition of claim 30 , wherein the one or more biologically active molecules are chemotherapeutics, toxins, radiotherapeutics, radiosensitizing agents, gene therapy vectors, antisense nucleic acid constructs, transcription factor decoys, imaging agents, diagnostic agents, agents known to interact with an intracellular protein, polypeptides, or polynucleotides.

Assignments (3)
CONFIRMATORY LICENSE Recorded Feb 7, 2017
From: FLORIDA, UNIVERSITY OF
To: NAVY, SECRETARY OF THE UNITED STATES OF AMERICA
Reel/Frame 041683/0471 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 21, 2011
From: CAO, Y. CHARLES; ZHUANG, JIAQI; WU, HUIMENG; YANG, YONGAN
To: UNIVERSITY OF FLORIDA RESEARCH FOUNDATION, INC.
Reel/Frame 026165/0266 →
CONFIRMATORY LICENSE Recorded May 13, 2010
From: UNIVERSITY OF FLORIDA
To: NATIONAL SCIENCE FOUNDATION
Reel/Frame 024381/0427 →
Continuity (2)
Provisional Application 60956625 · Aug 17, 2007
Related Publication 20110150938A1 · Jun 23, 2011