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Preparation method and application of electrochemiluminescent polymer nanoparticles

A technology of light-emitting polymers and conductive polymers, which is applied in the fields of chemiluminescence/bioluminescence, chemical instruments and methods, and analysis through chemical reactions of materials, etc. To achieve the effects of enhanced electrochemiluminescent signal, stable retention of solution suspension uniformity, and stable structure

Active Publication Date: 2019-04-26
SUZHOU UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0004] The above-mentioned immobilization method relies on weak force, and the prepared nanoparticles have disadvantages such as unstable structure, easy leakage of ECL small molecules, and rapid decay of luminescence signal with storage time, and will obviously affect the intensity of ECL signal
Usually due to the influence of the shell outside the ECL small molecule, the luminescent signal of the ECL small molecule component immobilized inside the nanoparticle is obviously weakened. However, if the method of surface immobilized ECL small molecule is used, the immobilization capacity is small
The above problems are extremely unfavorable for biomarkers, especially detection reagents

Method used

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  • Preparation method and application of electrochemiluminescent polymer nanoparticles
  • Preparation method and application of electrochemiluminescent polymer nanoparticles
  • Preparation method and application of electrochemiluminescent polymer nanoparticles

Examples

Experimental program
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Embodiment 1

[0037]Chemically link bis(2,2'-bipyridyl)(5,6-epoxy-5,6-dihydro-[1,10]phenanthroline) ruthenium to the carboxyl group of polyacrylic acid (PAA) to obtain a ruthenium complex Polymer grafted with polyacrylic acid, that is, electrochemiluminescent polymer (ECL polymer). The specific plan is as follows:

[0038] Weigh 108 mg of bis(2,2'-bipyridyl)(5,6-epoxy-5,6-dihydro-[1,10]phenanthroline) ruthenium and dissolve it in 20 mL of NaHCO 3 Aqueous solution (1mmol / L) to obtain ECL complex stock solution. Weigh 2g of PAA (molecular weight is 30000g / mol) and dissolve in 10mL of NaHCO 3 Aqueous solution (1mmol / L), get PAA stock solution. Take 3 mL of the above ECL complex stock solution and place it in a 10 mL single-neck round bottom flask, and add 1 mL of PAA stock solution. Vacuumize and fill with nitrogen, repeat three times. In an oil bath at 110° C. in the dark, under the protection of nitrogen, the reaction was carried out with magnetic stirring for 24 h. After the reaction,...

Embodiment 2

[0042] Take 1.6mL of the electrochemiluminescent polymer solution prepared in Example 1 and place it in a round bottom flask, add 0.2mL PAA (molecular weight: 30000g / mol) aqueous solution (0.4mg / mL) to it, mix well, add 0.1mLPEI (molecular weight 1800g / mol) aqueous solution (0.01mg / mL), then add 20mg of cross-linking agent trimethylolpropane-tris(3-aziridinyl)propionate, place in 60°C water bath, stir (400 rpm min) to react for 10h. Finally, the reaction solution was dialyzed in water for 24 hours to remove excess cross-linking agent to obtain electrochemiluminescent polymer nanoparticles. In this example, the electrochemiluminescent polymer and PAA undergo a cross-linking reaction, and PEI is electrostatically assembled on the ECL polymer or (and) PAA, and then cross-linked and fixed in the structure of nanoparticles, at this time PEI It is doped inside the nanoparticles by electrostatic interaction.

Embodiment 3

[0044] 1.6 mL of the electrochemiluminescent polymer solution prepared in Example 1 was placed in a round bottom flask, and 0.2 mL of an aqueous solution (0.4 mg / mL) of PAA (molecular weight: 30000 g / mol) was added. Add 1mg EDC to 0.1mL PEI (molecular weight: 1800g / mol) aqueous solution (0.01mg / mL), shake well, then add to the above-mentioned round bottom flask, EDC activates the carboxyl groups in the electrochemiluminescence polymer and PAA. Stir (400 rpm) at room temperature for 1 h to make the activated carboxyl groups react with the amino groups on PEI to undergo a cross-linking reaction. Finally, the reaction solution was dialyzed in water for 24 hours to remove excess activator, and then the electrochemiluminescent polymer nanoparticles were obtained. In this example, the electrochemiluminescence polymer, PAA and PEI all underwent a cross-linking reaction and were immobilized in nanoparticles.

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Abstract

The invention relate to a preparation method of an electrochemical luminescence polymer nanoparticle. The preparation method comprises the following steps: mixing an electrochemical luminescence polymer and a non-luminescence polymer in a solvent, generating a cross-linking reaction to obtain the electrochemical luminescence polymer nanoparticle, and the non-luminescence polymer is an electric conductive polymer. The invention further provides an application of the prepared electrochemical luminescence polymer nanoparticle to a biomarker. With the adoption of the method provided by the invention, the signal enhanced stable-structure electrochemical luminescence polymer nanoparticle is prepared, the electrochemical luminescence polymer nanoparticle is excellent in water solubility, the grain size is uniform and is about 20 nm, a large number of active groups existing on the surface are beneficial for biological marking, and the electrochemical luminescence polymer nanoparticle has extensive applications in the high-sensitivity biomedical detection.

Description

technical field [0001] The invention relates to the field of electrochemiluminescence materials, in particular to a preparation method and application of electrochemiluminescence polymer nanoparticles. Background technique [0002] In small molecule electrochemiluminescent (ECL) substances, ruthenium terpyridine Ru(bpy) 3 2+ As a luminescent component, derivatize active genes and then label biomolecules to realize ECL bioanalysis, which is the main detection method in current clinical medicine. Theoretically, for each labeled biomacromolecule (such as an antibody), the more small ECL molecules on the label, the stronger the detection signal and the higher the detection sensitivity. But in fact, if there are too many labeled signal molecules, the reactivity of biomacromolecules will be significantly reduced, and the detection sensitivity will deteriorate instead, that is, "over-labeling". [0003] In order to achieve highly sensitive biomedical detection, people often use ...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C08J3/24C08J3/12C08F120/06C08F8/42C08L33/02C08L79/02C08L79/04C08L77/04C08K5/3412C08G73/02C09K11/06G01N21/76
CPCC08F8/42C08G73/0206C08J3/12C08J3/246C08J2333/02C08J2379/02C08J2433/02C08J2479/02C08J2479/04C08L33/02C08L79/02C08L2205/02C08L2205/025C08L2205/03C09K11/06C09K2211/185G01N21/76C08F120/06C08K5/3412C08L79/04C08L77/04
Inventor 谢洪平魏同洪
Owner SUZHOU UNIV