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Polymers prepared using smart templates

Inactive Publication Date: 2015-12-31
SELLERGREN BOERJE
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

The patent proposes a method to make molecularly imprinted polymers (MIPs) in high yield, in the form of nano- or micro-particles, with a unique affinity for a specific target molecule. These MIPs can be made using a scalable process that allows for practical and economic recycling and reuse of the template. The method uses nanosized, multifunctional, and recyclable placeholder templates, which allow for easy enrichment of imprinted particles based on their affinity in a template-free form. This approach also allows multiple parallel reactions to be performed using a scalable process, which is more efficient than alternative techniques involving solid phase synthesis of MIP nanoparticles.

Problems solved by technology

One recurring problem associated with molecularly imprinted polymers (MIPs) is viewed when testing the reuptake of template to the empty binding sites.
The low yield of binding sites results in a strong dependence of selectivity and binding uptake on sample load.
Template occlusion is another recurring problem in traditional molecular imprinting.
Typically a small fraction of the template added to the monomer mixture remains entrapped or bound in the polymer matrix which can result in bleeding—a process detrimental when using the MIPs as enrichment phases in trace analysis.
Moreover, template recovery is not straightforward requiring multiple purification steps.
This is unpractical and costly in cases where expensive templates are used.
Hardly avoidable, the kinetically controlled formation of the polymer network leads to a statistical distribution of binding site microenvironments.
In spite of the above individually promising results, none of the reported methods address the remaining problems i.e. 1) template occlusion and recycling and 2) process scalability and 3) parallelism and miniaturization There is therefore a need for new techniques allowing simultaneously interfacial imprinting, nanoparticle production, template recycling and parallelism and scalability.

Method used

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Examples

Experimental program
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Effect test

example 1

Preparation of a Magnetic Core Silica Shell Nanoparticles (magNP@SiO2)

[0095]Synthesis of magnetic core particles: 6 g FeSO4.7H2O and 7 g anhydrous FeCl3. were dissolved in 200 ml millipore water under N2 with vigorous stirring at 85° C. 15 mL of 25% ammonia (aq) were added quickly into the solution. The solution turned from orange to black due to the precipitation of the magnetite nano-particles. The solution was stirred for 30 min at elevated temperature and then allowed to cool down to RT. Afterwards, the magnetic particles were collected using a magnet and washed with 3×50 mL water and finally with 50 mL 0.2M NaCl solution. The particles were dried at 80° C. under vacuum.

[0096]Synthesis of magnetic core silica shell particles (magNP@SiO2): 2 g of dry magNP were dispersed in 50 mL water by sonication. Then they were collected by a magnet and the supernatant was removed. Then, a 10% (v / v)TEOS-solution (230 mL) was added followed by 200 mL glycerol. The pH was adjusted to 4.6 with g...

example 2

Functionalization of the Magnetic Silica Core-Shell Beads with Glycidoxypropyltrimethoxysilane (GPTMS) to Give magNPepoxy

[0097]3,25 g magNP@SiO2 were dispersed in 50 mL dry toluene under N2-atmosphere by sonication. 1 mL GPTMS was added to the solution and the mixture was heated to reflux under positive nitrogen pressure and stirred using an overhead-stirrer for 30 h. Then, the particles were collected using a magnetic separator and washed with 3 times with 50 mL toluene and 3 time with 50 mL acetone and dried under vacuum at 40° C.

example 3

Immobilization of the Decapeptides NH2—O—K—S-L-S-L-S—P-G-K—COOH (T10) and NH2—O-L-S—K—S—K—S—P-G-L-COOH (R10) on the magnetic nanoparticles to give magNP-T10 and magNP-R10 (FIG. 3).

[0098]1 g of epoxy-functionalized magnetic particles were dispersed In buffer (phosphate buffer, pH 7.4)(5 mL) by sonication. They were separated using a magnet and the supernatant was discarded. Then, a solution of 5.3 mg T10 or R10 in 5mL of the same buffer was added to the magnetic particles. Also a blank sample was prepared by adding 5mL pure buffer. The three samples were incubated over night at RT on a shaker. MALDI TOF analysis of the nanoparticle samples with reference to free peptide demonstrated the successful immobilization (FIG. 4).

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Abstract

New molecularly imprinted polymers are described, and a method for their production using novel particle technology based on multifunctional placeholder templates.

Description

CROSS-REFERENCE TO RELATED APPLICATION[0001]This application claims priority under the provisions of 35 USC 119 to Swedish Patent Application No. 1430090-9 filed on Jun. 26, 2014. The disclosure of Swedish Patent Application No. 1430090-9 is hereby incorporated herein by reference, in its entirety, for all purposes.TECHNICAL FIELD[0002]The present describes new molecularly imprinted polymers and a method for their production using novel particle technology based on multifunctional placeholder templates.BACKGROUND ART[0003]Molecular imprinting refers to a templating technique for producing inverse replicas of individual molecules in network polymer. This approach has been used to generate porous materials exhibiting receptor-like affinity for a large variety of template structures. Commonly referred to as plastic antibodies, these can now be produced of a similar size and featuring binding properties resembling antibodies. Their ability to function in complex environments including b...

Claims

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Application Information

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IPC IPC(8): C08F222/10G01N33/545C08F220/56
CPCG01N33/545C08F220/56C08F292/00C08F220/54C08F222/14G01N2600/00C08F220/06C08F222/385C08F2/44
Inventor SELLERGREN, BOERJEBERGHAUS, MELANIE
Owner SELLERGREN BOERJE
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