Method for synthesizing silica nanoparticles

Patent metadata

Field	Value
Publication number	US-11512003-B2
Application number	US-201816620413-A
Country	US
Kind code	B2
Filing date	Jun 8, 2018
Priority date	Jun 9, 2017
Publication date	Nov 29, 2022
Grant date	Nov 29, 2022

Abstract

The invention relates to a method for synthesizing ultrasmall silica nanoparticles, useful in particular for diagnostics and/or therapy. More specifically, a method for synthesizing silica nanoparticles, said method comprising the mixing of at least one silane which is negatively charged at physiological pH with at least one silane which is neutral at physiological pH, and/or at least one silane which is positively charged at physiological pH, wherein: —the molar ratio A of neutral silane(s) to negatively charged silane(s) is defined as follows: 0≤A≤6, —the molar ratio B of positively charged silane(s) to negatively charged silane(s) is defined as follows: 0≤B≤5, —the molar ratio C of neutral and positively charged silanes to negatively charged silane(s) is defined as follows: 0<C≤8. The invention also relates to the obtained ultrasmall silica nanoparticles.

First claim

The invention claimed is:

1. A method for synthesizing silica nanoparticles, said method comprising the mixing of at least one silane which is negatively charged at physiological pH with
at least one silane which is neutral at physiological pH, and/or
at least one silane which is positively charged at physiological pH,

wherein:
the molar ratio A of neutral silane(s) to negatively charged silane(s) is defined as follows: 0≤A≤6;
the molar ratio B of positively charged silane(s) to negatively charged silane(s) is defined as follows: 0≤B≤5;
the molar ratio C of neutral and positively charged silanes to negatively charged silane(s) is defined as follows: 0<C≤8, wherein said nanoparticles, dispersed in water, have a mean hydrodynamic diameter between 0.5 and 15 nm, and wherein all the silanes represent at least 80% by weight of the total weight of the reagents.

2. The method according to claim 1 , wherein all the silanes are chosen among alkoxysilanes, hydroxysilanes, and mixture thereof.

3. The method according to claim 1 , wherein the mixing step is performed in a protic solvent.

4. The method according to claim 1 , wherein said method is a one-pot synthesis without any isolation or purification step of the intermediate product(s).

5. The method according to claim 1 , wherein the silica nanoparticles do not comprise a crystalline core.

6. The method according to claim 1 , wherein said negatively charged silane(s) includes silane(s) comprising at least one, two, or more negatively charged carboxylic acid functions.

7. The method according to claim 1 , wherein said negatively charged silane(s) includes silane(s) comprising at least one chelating agent.

8. The method according to claim 7 , wherein said chelating agent is chosen from polyamino polycarboxylic acids including without limitation:
DOTA (1,4,7,10-tetraazacyclododecane-N,N′,N″,N′″-tetraacetic acid), DOTAGA (2-(4,7,10-tris(carboxymethyl)-1,4,7,10-tetraazacyclododecan-1-yl)pentanedioic acid), DO3A-pyridine of formula (III) below:

DTPA (diethylenetriaminepentaacetic acid), CHX-DTPA (trans-cyclohexyl-diethylenetriaminepentaacetic acid), oxo-Do3A (1-oxa-4,7,10-triazacyclododecane-4,7,10-triacetic acid), SCN-Bz-DTPA (p-isothiocyanatobenzyl-DTPA), 1 B3M (1-(p-isothiocyanatobenzyl)-3-methyl-DTPA), MX-DTPA (1-(2)-methyl-4-isocyanatobenzyl-DTPA);
EDTA (2,2′,2″,2′″-(ethane-1,2-diyldinitrilo)tetraacetic acid);
EGTA (ethylene glycol-bis(2-aminoethylether)-N,N,N′,N′-tetraacetic acid), BAPTA (1,2-bis(o-aminophenoxy)ethane-N,N,N′,N′-tetraacetic acid);
NOTA (1,4,7-triazacyclononane-1,4,7-triacetic acid);
PCTA (3,6,9,15-tetraazabicyclo[9.3.1.]pentadeca-1(15),11,13-triene-3,6,9-triacetic acid);
TMPAC of formula (N) below:

and mixtures thereof.

9. The method according to claim 7 , wherein said chelating agent(s) is(are) free of metallic ions.

10. The method according to claim 7 , wherein said chelating agent(s) is(are) chelating a metallic ion including alkali metal ions and their radioactive isotopes, transition metal ions and their radioactive isotopes, post-transition metal ions and their radioactive isotopes, rare earth metal ions and their radioactive isotopes, and mixtures thereof.

11. The method according to claim 1 , wherein said positively charged silane(s) includes at least a silane with one positively charged amino function.

12. The method according to claim 1 , wherein the mixing step further includes at least one silane comprising at least one fluorophore, the molar ratio D of silane(s) comprising a fluorophore to neutral silane(s) being defined as follows: 0.001≤D≤0.2.

13. The method according to claim 1 , wherein the mixing step further includes at least one silane comprising at least one drug moiety, the molar ratio E of silane(s) comprising a drug to neutral silane(s) is defined as follows: 0.1≤E≤5.

14. Method according to claim 13 , wherein the nanoparticles comprise between 0.5 and 50% by weight of drug moiety as compared to the total weight of the nanoparticle.

15. The method of claim 1 , wherein the molar ratio A of neutral silane(s) to negatively charged silane(s) is defined as follows: 0.5≤A≤2.

16. The method of claim 1 , wherein the molar ratio B of positively charged silane(s) to negatively charged silane(s) is defined as follows: 0.25≤B≤3.

17. The method of claim 1 , wherein the molar ratio C of neutral and positively charged silanes to negatively charged silane(s) is defined as follows: 1<C≤4.

18. The method of claim 1 , wherein said nanoparticles, dispersed in water, have a mean hydrodynamic diameter between 0.5 and 10 nm.

19. The method of claim 13 , wherein the nanoparticles comprise between 2 and 10% by weight of drug moiety as compared to the total weight of the nanoparticle.

Assignees

• Nh Theraguix
• Univ Claude Bernard Lyon
• Centre National De La Rech Scientifique—Cnrs
• Centre National De La Rech Gantifote—Cnrs—

Inventors

• Lux François
• Tillement Olivier
• Rossetti Fabien
• Thakare Vivek
• Tran Vu Long

Classifications

• A61K49/1833 Primary

  having a (super)(para)magnetic core coated or functionalised with a small organic molecule (oligomeric, polymeric, dendrimeric A61K49/1851) · CPC title

• B82Y30/00

  Nanotechnology for materials or surface science, e.g. nanocomposites · CPC title

• A61K49/08

  characterised by the carrier · CPC title

• A61N5/1039

  using functional images, e.g. PET or MRI · CPC title

• C01P2004/64

  Nanometer sized, i.e. from 1-100 nanometer · CPC title