Ligands for semiconductor nanocrystals
In this invention, polyimidazole ligands (PILs) incorporating pendant imidazole moieties for nanocrystal binding and either sulfonatebetaine, carboxybetaine, or phosphocholinebetaine moieties for water-solubilization have been developed. Greatly enhanced stability of nanocrystals (both over time and in wide pH range) was achieved by incorporating multi-dentate imidazole moieties which provide strong coordination of the ligand to the nanocrystal surface and prevent aggregation of nanocrystals. Synthesis of betaine PILs was developed by modifying the synthesis of recently developed PEG containing poly imidazole ligands (PEG PILs). These nanocrystals are compact, water soluble, and biocompatible.
1. A method of making a water-soluble semiconductor nanocrystal comprising:
purifying imidazole monomers;
purifying tertiary amine monomers;
polymerizing imidazole and tertiary amine monomers to form a copolymer; and
exchanging the ligand of a capped semiconductor nanocrystal with the imidazole polymer including a zwitterionic moiety,
wherein the zwitterionic moiety includes betaine,
wherein the copolymer on the each semiconductor nanocrystal increases a hydrodynamic diameter of the each semiconductor nanocrystal no more than 5 nm.
2. The method of claim 1 , further comprising betainisation of the imidazole polymer before deprotecting a BOC group.
3. The method of claim 2 , further comprising deprotecting the BOC group on the imidazole polymer before exchanging the ligand of a capped semiconductor nanocrystal.
4. The method of claim 1 , wherein betainisation of the imidazole polymer results in a sulfonate betaine polymer.
5. The method of claim 1 , wherein betainisation of the imidazole polymer results in a carboxylate betaine polymer.
6. The method of claim 1 , wherein betainisation of the imidazole polymer results in a phosphocholine betaine polymer.
7. The method of biological in vivo imaging comprising:
introducing a copolymer including a betaine polyimidazole ligand including a zwitterionic moiety coated semiconductor nanocrystals to the subject wherein the copolymer on the each semiconductor nanocrystal increases a hydrodynamic diameter of the each semiconductor nanocrystal no more than 5 nm;
allowing the semiconductor nanocrystals to diffuse; and
visualizing the image with photon laser scanning microscopy.
8. The method of claim 7 , wherein the photon laser scanning microscopy can be one-photon or two-photon.
9. The method of claim 7 , wherein the semiconductor nanocrystals are used to image the extravasation of the nanocrystals from microvessels into a tumor.
10. A method of biological in vitro imaging comprising:
introducing a copolymer including a betaine polyimidazole ligand including a zwitterionic moiety coated semiconductor nanocrystals to a biological sample wherein the copolymer on the each semiconductor nanocrystal increases a hydrodynamic diameter of the each semiconductor nanocrystal no more than 5 nm;
allowing the semiconductor nanocrystals to diffuse;
collecting data from the semiconductor nanocrystals; and
visualizing an image from the data.