Preparation method of nano gold immobilized pellets and application of nano gold immobilized pellets to ziram detection
A technology of immobilizing small balls and nano-gold, which is applied in the direction of analyzing materials through chemical reactions and observing the influence of chemical indicators on materials, etc., which can solve the problem of limited repeatability and reliability of test results. Poor repeatability and reliability, poor stability of the detection system, etc., to achieve the effect of convenient on-site detection, improved storage stability, and less sample volume
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[0037] The embodiment of the present invention provides a preparation method of nano-gold immobilized beads, comprising the following steps:
[0038] Step 1: Weigh di-tert-butyl dicarbonate tyrosine, N-hydroxysuccinimide and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride, add 2 - (N-morpholine) ethanesulfonic acid aqueous solution was stirred and dissolved, reacted for 96-144min, then added chitosan solution and stirred overnight, and the reacted solution was placed in an ultrafiltration tube for centrifugal ultrafiltration to obtain chitosan graft Tyrosine solution.
[0039] In this step, N-hydroxysuccinimide (NHS) and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDC) activate di-tert-butyldicarbonate The carboxyl group of ester tyrosine, 2-(N-morpholine) ethanesulfonic acid aqueous solution (being MES damping fluid) is used for providing the acidic environment required for activation reaction, the di-tert-butyl dicarbonate tyrosine through activ...
Embodiment 1
[0065] A preparation method for nano-gold immobilized beads, comprising the steps of:
[0066] Step 1: Weigh 0.5g chitosan, add 19.4g water and 0.63g acetic acid, mix well to obtain chitosan solution; weigh 7.67mg di-tert-butyl dicarbonate tyrosine, 8mg N-hydroxysuccinyl imine and 34mg of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride, add 5.6mL of 1mol / L 2-(N-morpholine)ethanesulfonic acid aqueous solution and stir to dissolve, With 1200r / min rotating speed stirring reaction 120min, then add the prepared chitosan solution stirring reaction overnight, the solution after the reaction is placed in the ultrafiltration tube (molecular weight cut-off is 10kDa), with the speed centrifugation ultrafiltration of 11000r / min 7min, And repeat 2-4 times to obtain chitosan grafted tyrosine solution.
[0067] Step 2: Add 40 mL of 0.5 mmol / L chloroauric acid aqueous solution to the chitosan-grafted tyrosine solution obtained in step 1, and adjust the pH value of the solution to...
Embodiment 2
[0070] Step 1: Weigh 0.4g chitosan, add 15.5g water and 0.504g acetic acid, mix well to obtain chitosan solution; weigh 6.13mg di-tert-butyl dicarbonate tyrosine, 6.4mg N-hydroxybutanediol imide and 27.2mg of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride, add 5.15mL of 0.87mol / L 2-(N-morpholine)ethanesulfonic acid aqueous solution Stir and dissolve, stir and react with 1100r / min rotating speed for 96min, then add the prepared chitosan solution and stir to react overnight, the solution after the reaction is placed in an ultrafiltration tube (molecular weight cut-off is 10kDa), and centrifuged at a speed of 10000r / min Filter for 5 minutes, and repeat 2-4 times to obtain chitosan grafted tyrosine solution.
[0071] Step 2: Add 35.56mL of 0.45mmol / L chloroauric acid aqueous solution to the chitosan grafted tyrosine solution obtained in step 1, and adjust the pH value of the solution to 11.5, shake it up, and let it stand at 37°C for reaction 24min, the chitosan-nano...
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