Diblock copolymer vesicles and separation membranes comprising aquaporin water channels and methods of making and using them
A vesicle in a liquid composition including an amphiphilic diblock copolymer of the PMOXA a-b -PDMS c-d type as vesicle membrane forming material, further including as an additive from about 0.05% to about 1% v/v of reactive end group functionalised PDMS e-f , and a transmembrane protein. The vesicle optionally includes about 1 to about 12% v/v of triblock copolymer of the PMOXA a-b -PDMS c-d -PMOXA a-b type as membrane forming material.
1. A vesicle in a liquid composition, the vesicle comprising an amphiphilic diblock copolymer of the poly(2-methyloxazoline)-block-poly(dimethyl siloxane) (PMOXA-PDMS) type as vesicle membrane forming material, an additive from about 0.05% to about 1% (v/v) based on the liquid composition, of reactive end group functionalized poly(dimethyl siloxane) (PDMS), and a transmembrane protein, wherein the reactive end group is one, two, or more of amine, carboxylic, and/or hydroxy group(s).
2. The vesicle according to claim 1 , wherein said PMOXA-PDMS is selected from the group consisting of PMOXA 10-40 -PDMS 25-70 and mixtures thereof.
3. The vesicle according to claim 2 , wherein the mixture comprises at least a first amphiphilic diblock copolymer of the general formula PMOXA 10-28 -PDMS 25-70 and a second amphiphilic diblock copolymer of the general formula PMOXA 28-40 -PDMS 25-70 .
4. The vesicle according to claim 3 , wherein the weight proportion between the first and the second amphiphilic diblock copolymer is in the range of 0.1:1 to 1:0.1.
5. The vesicle according to claim 1 , wherein said reactive end group functionalized PDMS is PDMS 30-50 functionalized with one or more of amine, carboxylic acid, and/or hydroxy group(s).
6. The vesicle according to claim 5 , wherein the reactive end group functionalized PDMS is poly(dimethylsiloxane), bis(3-aminopropyl).
7. The vesicle according to claim 1 , wherein the transmembrane protein is an aquaporin water channel.
8. The vesicle according to claim 1 further comprising from about 1% (v/v) to about 12% (v/v) based on the liquid composition, of a triblock copolymer of the PMOXA-PDMS-PMOXA type.
9. The vesicle according to claim 8 , wherein said triblock copolymer of the PMOXA-PDMS-PMOXA type is selected from PMOXA 10-20 -PDMS 25-70 -PMOXA 10-20 .
10. The vesicle according to claim 1 , wherein the liquid composition further comprises a flux improving agent.
11. The vesicle according to claim 10 , wherein the flux improving agent is an alkylene glycol monoalkyl ether alkylate, beta cyclodextrin, or polyethylene glycol (15)-hydroxystearate.
12. The vesicle according to claim 10 , wherein the flux improving agent is present in an amount of 0.1% to 10% by weight of the liquid composition.
13. A separation membrane comprising a vesicle according to claim 1 .
14. The separation membrane according to claim 13 , wherein the separation membrane comprises an active layer incorporating the vesicle and a porous support membrane.
15. The separation membrane according to anyone of claim 14 , wherein the active layer comprises the vesicle incorporated in a thin film composite (TFC) layer formed on a porous substrate membrane.
16. A method of preparing vesicles in a liquid composition incorporating a transmembrane protein comprising the step of stirring a mixture of a solution of an amphiphilic diblock copolymer of the poly(2-methyloxazoline)-block-poly(dimethyl siloxane) (PMOXA-PDMS) type, 0.05% to about 1% (v/v) based on the of liquid composition, of reactive end group functionalized poly(dimethyl siloxane) (PDMS), and a transmembrane protein, wherein the reactive end group is one, two, or more of amine, carboxylic, and/or hydroxy group(s).
17. The method according to claim 16 , further comprising a flux improving agent selected among the group comprising alkylene glycol monoalkyl ether alkylate, beta cyclodextrin, and polyethylene glycol (15)-hydroxystearate.
18. A method of preparing a thin film composite layer immobilizing vesicles incorporating a transmembrane protein on a porous substrate membrane, comprising the steps of
a. providing a mixture of vesicles in a liquid composition prepared in accordance with claim 16 and a di-amine or tri-amine compound,
b. covering the surface of a porous support membrane with the mixture of step a,
c. applying a hydrophobic solution comprising an acyl halide compound, and
d. allowing the aqueous solution and the hydrophobic solution to perform an interfacial polymerization reaction to form the thin film composite layer.
19. The method according to claim 18 , wherein the porous support membrane is a flat sheet.
20. The method according to claim 19 , comprising the further step of producing a spiral wound membrane module by winding the flat sheet membrane.