IP Library Granted Patent US 7,368,086
Granted Patent B2
US 7,368,086 · App. 11/261,861 · Granted May 6, 2008

Functionalized fluorescent nanocrystals, and methods for their preparation and use

View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 7,368,086
App. No.
11/261,861
Granted
May 6, 2008
Kind
B2
Abstract

Functionalized fluorescent nanocrystal compositions and methods for making and using these compositions are disclosed. The compositions are fluorescent nanocrystals coated with at least one material. The coating material has chemical compounds or ligands with functional groups or moieties with conjugated electrons and moieties for imparting solubility to coated fluorescent nanocrystals in aqueous solutions. The coating material provides for functionalized fluorescent nanocrystal compositions which are water soluble, chemically stable, and emit light with a high quantum yield and/or luminescence efficiency when excited with light. The coating material may also have chemical compounds or ligands with moieties for bonding to target molecules and cells as well as moieties for cross-linking the coating. In the presence of reagents suitable for reacting to form capping layers, the compounds in the coating may form a capping layer on the fluorescent nanocrystal with the coating compounds operably bonded to the capping layer.

Claims (20)

1. A functionalized fluorescent nanocrystal comprising:

a fluorescent nanocrystal; and

a coating material comprising gylcyl histidine and histidyl leucine.

2. The functionalized fluorescent nanocrystal of claim 1 , wherein the fluorescent nanocrystal comprises a core and a shell.

3. The functionalized fluorescent nanocrystal of claim 1 , wherein the fluorescent nanocrystal comprises a CdS, CdSe, or CdTe core.

4. The functionalized fluorescent nanocrystal of claim 1 , wherein the fluorescent nanocrystal comprises a core and a ZnS, ZuSe, CdS, or CdSe shell.

5. The functionalized fluorescent nanocrystal of claim 1 , wherein the fluorescent nanocrystal comprises a CdS or CdSe core, and a ZnS or ZuSe shell.

6. The functionalized fluorescent nanocrystal of claim 1 , wherein the fluorescent nanocrystal comprises a CdSe core, and a ZnS shell.

7. The fluorescent nanocrystal of claim 1 , wherein the fluorescent nanocrystal is a doped metal oxide nanocrystal.

8. The functionalized fluorescent nanocrystal of claim 1 , characterized as emitting light with a quantum yield of greater than 10%.

9. The functionalized fluorescent nanocrystal of claim 1 , characterized as emitting light with a quantum yield of greater than 30%.

10. The functionalized fluorescent nanocrystal of claim 1 , characterized as emitting light with a quantum yield of greater than 50%.

11. The functionalized fluorescent nanocrystal of claim 1 , characterized as emitting light with a quantum yield of greater than 70%.

12. The functionalized fluorescent nanocrystal of claim 1 , characterized as being soluble in a fluid having a surface energy of greater than 35 dynes/cm.

13. The functionalized fluorescent nanocrystal of claim 1 , characterized as being soluble in an aqueous solution.

14. The functionalized fluorescent nanocrystal of claim 1 , further comprising a polynucleotide attached to the coating material.

15. The functionalized fluorescent nanocrystal of claim 1 , further comprising a polynucleotide covalently attached to the coating material.

16. The functionalized fluorescent nanocrystal of claim 1 , further comprising a biomolecule attached to the coating material, wherein the biomolecule is biotin, avidin, ConA, lectin, or IgG.

17. The functionalized fluorescent nanocrystal composition of claim 1 , further comprising avidin attached to the coating material.

18. The functionalized fluorescent nanocrystal composition of claim 1 , wherein the coating material is crosslinked with tris(hydroxy methyl) phosphine or beta-(tris(hydroxymethyl)phosphino) propionic acid.

Assignments (4)
LIEN RELEASE Recorded Apr 9, 2013
From: BANK OF AMERICA, N.A.
To: LIFE TECHNOLOGIES CORPORATION
Reel/Frame 030182/0461 →
CHANGE OF NAME Recorded Sep 30, 2010
From: INVITROGEN CORPORATION
To: LIFE TECHNOLOGIES CORPORATION
Reel/Frame 025066/0566 →
SECURITY AGREEMENT Recorded Dec 5, 2008
From: LIFE TECHNOLOGIES CORPORATION
To: BANK OF AMERICA, N.A., AS COLLATERAL AGENT
Reel/Frame 021975/0467 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 6, 2006
From: NAASANI, IMAD
To: INVITROGEN CORP.
Reel/Frame 016981/0669 →