IP Library Granted Patent US 8,367,042
Granted Patent B2
US 8,367,042 · App. 12/576,193 · Granted Feb 5, 2013

Nanoparticles of light emissive polymers and preparation method thereof

Inventors: Sehoon Kim (Seoul, KR); Ick Chan Kwon (Seoul, KR); Kwangmeyung Kim (Seoul, KR); Kuiwon Choi (Seoul, KR); Chang-Keun Lim (Seoul, KR)
Assignee: Korea Institute of Science and Technology
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Quick Facts
Patent No.
US 8,367,042
App. No.
12/576,193
Granted
Feb 5, 2013
Kind
B2
Abstract

Disclosed are nanoparticles of a light emissive polymer, comprising nanoparticles of a cyano-substituted poly(arylene vinylene) polymer; and a biocompatible surfactant adsorbed to the surface of the nanoparticles of the polymer, and preparation method thereof, wherein the method comprises: (1) uniformly mixing a dialdehyde monomer represented by a general formula OHC—Ar 1 —CHO, a dicyanide monomer represented by a general formula NC—Ar 2 —CN, and a liquid surfactant; (2) adding water to the resulting mixture to prepare an aqueous micelle dispersion; and (3) adding a polymerization catalyst to the aqueous micelle dispersion, followed by carrying out colloidal polymerization of the resulting mixture at room temperature under an atmosphere. The nanoparticles of the light emissive polymer of the invention are stabilized with a biocompatible surfactant, so that it can form a stable aqueous dispersion phase, and has particle size and fluorescence efficiency suitable for a biomolecular marker or a cell or in vivo imaging; therefore, it can be used as a cell or in vivo light emission contrast agent.

Claims (23)

1. Nanoparticles of a light emissive polymer, comprising nanoparticles of cyano-substituted poly(arylene vinylene) polymer represented by Formula 1 below; and a biocompatible liquid surfactant adsorbed to the surface of the nanoparticles of the polymer:

wherein n is an integer of 10 to 10,000, and

wherein Ar 1 is selected from the groups represented by Formula 2:

wherein Ar 2 is phenylene.

2. The nanoparticles according to claim 1 , wherein a ratio between the nanoparticles of the cyano-substituted poly(arylene vinylene) polymer represented by Formula 1 and the biocompatible surfactant is 1:7 to 1:12 by weight.

3. The nanoparticles according to claim 1 , wherein the surfactant is selected from the group consisting of Tween® 20, Tween® 60, Tween® 80, Triton® X-100, Span® 20, Span® 60 and Span® 80.

4. The nanoparticles according to claim 1 , having a diameter in the range of from 5 nm to 500 nm.

5. The nanoparticles according to claim 1 , having an absorption wavelength in the range of from 300 nm to 800 nm.

6. The nanoparticles according to claim 1 , having a light emission wavelength in the range of from 400 nm to 900 nm.

7. The nanoparticles according to claim 6 , having a light emitting wavelength of 450 nm or higher, and used as a fluorescence contrast agent for cell imaging.

8. The nanoparticles according to claim 6 , having a light emission wavelength of 530 nm or higher, and used as a fluorescence contrast agent for in vivo imaging.

9. The nanoparticles according to claim 6 , having a diameter of from 10 nm to 50 nm and a light emission wavelength of 600 nm or higher, and used as a contrast agent for fluorescence detection of sentinel lymph node.

10. A method to prepare the nanoparticles of claim 1 , comprising:

(1) uniformly mixing a monomer of formula OHC—Ar 1 —CHO, a monomer of formula NC—Ar 2 —CN, and a liquid surfactant;

(2) adding water to the resulting mixture to prepare an aqueous micelle dispersion; and

(3) adding a polymerization catalyst to the aqueous micelle dispersion, followed by carrying out colloidal polymerization of the resulting mixture at room temperature under an atmosphere, to obtain the nanoparticles of the light emissive polymer, surface of which is stabilized with the surfactant.

11. The method according to claim 10 , further comprising dialysis of the nanoparticles of the light emissive polymer obtained in step ( 3 ) for removing excessive amount of surfactant, catalyst and non-reacted monomers.

12. The method according to claim 10 , wherein the monomer of formula OHC—Ar 1 —CHO and the monomer of formula NC—Ar 2 —CN are used in molar ratio of 1:1 in step ( 1 ), and the liquid surfactant used is 20 to 100 times by weight of the total weight of the monomers.

13. The method according to claim 10 , wherein in step ( 1 ), the monomer of formula OHC—Ar 1 —CHO and the monomer of formula NC—Ar 2 —CN are uniformly dissolved in the liquid surfactant without an organic solvent.

14. The method according to claim 10 or 11 , wherein the polymerization catalyst is selected from the group consisting of tetrabutylammonium hydroxide, tetramethylammonium hydroxide and tetraethylammonium hydroxide.

15. The method according to claim 10 , wherein diameter of the nanoparticles of the light emissive polymer obtained in step ( 3 ) is in the range of from 5 nm to 500 nm.

16. The method according to claim 10 , wherein an absorption wavelength of the nanoparticles of the light emissive polymer obtained in step ( 3 ) is in the range of from 300 nm to 800 nm.

17. The method according to claim 10 , wherein a light emission wavelength of the nanoparticles of the light emissive polymer obtained in step ( 3 ) is in the range of from 400 nm to 900 nm.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 12, 2009
From: KIM, SEHOON; KWON, ICK CHAN; KIM, KWANGMEYUNG; CHOI, KUIWON; LIM, CHANG-KEUN
To: KOREA INSTITUTE OF SCIENCE AND TECHNOLOGY
Reel/Frame 023512/0744 →
Priority Claims (1)
KR 10-2009-0041898 · May 13, 2009 · national
Continuity (1)
Related Publication 20100290999A1 · Nov 18, 2010