Method for preparing a monolithic support on which uranyl cations are immobilised, and associated methods for capture and recovery
A method for preparing, in the internal volume of at least one channel, a monolithic support on which uranyl cations are immobilised. The method comprises: (a) activating the inner surface of the channel(s); (b) introducing, into the internal volume of the channel(s), a polymerisation solution comprising: a monomer comprising a phosphate group, at least one crosslinking agent, several solvents, and a radical polymerisation initiator; (c) polymerising the polymerisation solution; (d) rinsing the monolithic support obtained in step (c); and (e) contacting the monolithic support previously rinsed, with a solution comprising uranyl cations. A method for capturing proteins that selectively bind uranium by means of a monolithic support prepared by the above-mentioned method, as well as to a method for recovering proteins that selectively bind uranium with the capture method.
1 . A method for preparing, in an internal volume of at least one channel of a miniaturised analytical system, a monolithic support on which UO 2 2+ cations are immobilised, which method comprises the following successive steps (a) to (e) of:
(a) activating the inner surface of the channel(s);
(b) introducing a polymerisation solution for synthesising a monolithic support into the internal volume of the channel(s), the polymerisation solution comprising:
a monomer comprising a phosphate group,
at least one crosslinking agent
several solvents, and
a radical polymerisation initiator;
(c) polymerising the polymerisation solution obtained in step (b), whereby a monolithic support anchored onto the walls of the channel(s) is obtained;
(d) rinsing the monolithic support obtained in step (c); and
(e) contacting the rinsed monolithic support obtained in step (d) with a solution comprising UO 2 2+ cations, whereby a monolithic support on which the UO 2 2+ cations are immobilized is obtained.
2 . The method according to claim 1 , wherein the monomer comprising a phosphate group is a methacrylate monomer.
3 . The method according to claim 1 , wherein the crosslinking agent is consisting of a mixture of acrylamide/bisacrylamide.
4 . The method according to claim 1 , wherein the solvents are selected from dodecanol, dimethylformamide and dimethylsulphoxide.
5 . The method according to claim 1 , wherein the radical polymerisation initiator is azobisisobutyronitrile (AIBN).
6 . The method according to claim 5 , wherein the polymerisation solution comprises, based on the total mass of the polymerisation solution:
from 0.05 mass % to 0.2 mass % of azobisisobutyronitrile,
from 3 mass % to 8 mass % of acrylamide and bisacrylamide,
from 4 mass % to 10 mass % of polyethylene glycol methacrylate phosphate,
from 22 mass % to 53 mass % of dimethylsulphoxide,
from 28 mass % to 59 mass % of dodecanol, and
from 7 mass % to 9 mass % dimethylformamide.
7 . The method according to claim 1 , wherein the polymerisation step (c) is carried out by irradiation by means of ultraviolet rays.
8 . The method according to claim 7 , wherein, in step (c), the duration of irradiation by means of the ultraviolet rays is between 5 min and 60 min.
9 . The method according to claim 1 , wherein the rinsing step (d) is carried out successively with an alcohol and then with water.
10 . The method according to claim 1 , wherein, the channel(s) being made of glass, the activation step (a) is carried out by silanisation.
11 . The method according to claim 1 , wherein the internal diameter of the channel(s) is less than or equal to 300 μm.
12 . The method according to claim 1 , wherein the solution comprising the UO 2 2+ cations is prepared in an aqueous solution of ammonium acetate.
13 . The method according to claim 1 , wherein step (e) of contacting the monolithic support with the solution comprising the UO 2 2+ cations is carried out by circulating this solution comprising the UO 2 2+ cations on the monolithic support.
14 . A method for capturing proteins that selectively bind uranium, these proteins being contained in a biological sample, this method comprising the following steps (i) and (ii) of:
(i) preparing, in an internal volume of at least one channel of a miniaturised analytical system, a monolithic support on which UO22+cations are immobilised, by implementing the preparation method according to claim 1 , and
(ii) at least circulating a solution containing the biological sample through the monolithic support on which UO 2 2+ cations are immobilised, obtained at the end of step (i), whereby the capture of the proteins that selectively bind uranium on the monolithic support is achieved.
15 . A method for recovering proteins that selectively bind uranium, these proteins being contained in a biological sample, this method comprising the following steps (1) to (3) of:
(1) capturing the proteins that selectively bind uranium by implementing the capture method of claim 14 ,
(2) removing the unbound proteins by rinsing the monolithic support by circulating a solution containing no proteins, and
(3) at least one elution step, by circulating an eluting solution through the monolithic support obtained at the end of step (2), whereby the proteins that selectively bind uranium are recovered in the eluting solution.
16 . The method according to claim 2 , wherein the monomer comprising a phosphate group is polyethylene glycol methacrylate phosphate.
17 . The method according to claim 7 , wherein the wavelength of these ultraviolet rays is between 320 nm and 380 nm.
18 . The method according to claim 9 , wherein the alcohol is methanol.
19 . The method according to claim 10 , wherein the activation step (a) is carried out by means of gamma-methacryloxypropyltrimethoxysilane (γ-MAPS) as silanising agent.
20 . The method according to claim 11 , wherein the internal diameter of the channel(s) is between 50 μm and 90 μm.