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Preparation of cysteine ​​and cu2+ fluorescent probes based on au/ag core/shell quantum dots

A technology of cysteine ​​and fluorescent probes, applied in fluorescence/phosphorescence, chemical instruments and methods, luminescent materials, etc., can solve problems such as cysteine ​​fluorescent probes that have not yet been seen, and achieve simple methods and low cost Effect

Inactive Publication Date: 2015-09-09
SHANGHAI JIAOTONG UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

So far, there is no cysteine ​​fluorescent probe based on bovine serum albumin-stabilized biocompatible Au / Ag core / shell quantum dots, and this probe can be used for Cu 2+ Relevant Chinese patent reports on efficient detection of

Method used

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  • Preparation of cysteine ​​and cu2+ fluorescent probes based on au/ag core/shell quantum dots
  • Preparation of cysteine ​​and cu2+ fluorescent probes based on au/ag core/shell quantum dots
  • Preparation of cysteine ​​and cu2+ fluorescent probes based on au/ag core/shell quantum dots

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Embodiment 1

[0023] Cysteine ​​and Cu based on Au / Ag core / shell quantum dots 2+ For the preparation process of fluorescent probe, see figure 1 The detailed preparation steps are as follows: Dissolve chloroauric acid and BSA in 20mL deionized water, adjust the molar concentration of chloroauric acid to 2mM, and the dosage of BSA to 10mg / mL, at 20℃ and magnetic stirring, at pH 7.5 After reacting in phosphate buffer for 6 hours, BSA stabilized Au nanoparticles were prepared. Add this Au nanoparticles to a 20mL homogeneous aqueous solution containing silver nitrate and BSA, adjust the molar concentration of silver nitrate to 1mM, the amount of BSA to 5mg / mL, and the amount of Au nanoparticles to 0.2mg / mL at 20℃. Under magnetic stirring, react for 12h in pH 7.5 phosphate buffer to prepare BSA stable Au / Ag core / shell quantum dots. Through dialysis, rotary evaporation, centrifugal separation, and vacuum drying, the dry quantum dot powder is then dissolved in deionized water and configured into a 0...

Embodiment 2

[0027] The detailed preparation steps are as follows: Dissolve chloroauric acid and BSA in 20mL of deionized water, adjust the molar concentration of chloroauric acid to 5mM, and the dosage of BSA to 20mg / mL, at 25℃ and magnetic stirring, in phosphoric acid at pH 8.0 After reacting in the buffer for 12 hours, BSA stable Au nanoparticles were prepared. Add the Au nanoparticles to a 20mL homogeneous aqueous solution containing silver nitrate and BSA, adjust the molar concentration of silver nitrate to 2mM, the dosage of BSA to 10mg / mL, and the dosage of Au nanoparticles to 0.5mg / mL at 25℃. Under magnetic stirring, it was reacted in a phosphate buffer of pH 8.0 for 24 hours to prepare BSA-stable Au / Ag core / shell quantum dots. Through dialysis, rotary evaporation, centrifugal separation, and vacuum drying, the dry quantum dot powder is then dissolved in deionized water and configured into a 0.5 mg / mL quantum dot solution for later use. Add different molar concentrations of cystein...

Embodiment 3

[0029] The detailed preparation steps are as follows: Dissolve chloroauric acid and BSA in 20mL of deionized water, adjust the molar concentration of chloroauric acid to 8mM, and the dosage of BSA to 30mg / mL, at 37°C and magnetic stirring, in phosphoric acid at pH 8.5 After 18 hours of reaction in the buffer, BSA stable Au nanoparticles were prepared. Add the Au nanoparticles to a 20mL homogeneous aqueous solution containing silver nitrate and BSA, adjust the molar concentration of silver nitrate to 3mM, the dosage of BSA to 15mg / mL, and the dosage of Au nanoparticles to 0.8mg / mL at 37℃. Under magnetic stirring, the reaction was carried out in a phosphate buffer of pH 8.5 for 36 hours to prepare BSA-stable Au / Ag core / shell quantum dots. Through dialysis, rotary evaporation, centrifugal separation, and vacuum drying, the dry quantum dot powder is then dissolved in deionized water and configured into a 0.5 mg / mL quantum dot solution for later use. Add different molar concentrati...

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Abstract

The invention relates to a making method of an Au / Ag core / shell quantum dot-based cysteine-Cu2<+> fluorescent probe. The method comprises the steps of: (1) selecting bovine serum albumin (BSA) as a reducing agent / stabilizer, and reacting it with chloroauric acid in an alkaline aqueous solution to prepare Au nanoparticles; 2) mixing the nanoparticles with BSA and silver nitrate, and letting the mixture to react in an alkaline aqueous solution to prepare Au / Ag core / shell quantum dots; 3) establishing a linear relation between the fluorescence intensity of the Au / Ag core / shell quantum dots and the mole concentration of additional cysteine / Cu2<+>, and developing the novel cysteine / Cu2<+> fluorescent probe. Compared with the prior art, the method provided in the invention is simple, the prepared product has biocompatibility and can be developed into a bifunctional fluorescent probe for detection of mixed water samples and biological samples. The detection process is fast, the sensitivity is high, the selectivity is good, and the detection limit is low, thus having certain reference value to design and application of other biocompatible fluorescent probes.

Description

Technical field [0001] The invention belongs to the technical field of biochemical analysis and detection, and specifically relates to cysteine ​​and Cu based on Au / Ag core / shell quantum dots 2+ Fluorescent probe and its preparation method. Background technique [0002] Cysteine ​​is an amino acid containing a sulfhydryl group and is one of the twenty amino acids that make up protein. Since the sulfhydryl group in the molecular structure of cysteine ​​has high protic activity and is easily oxidized, it has strong reducibility. Cysteine ​​also has the ability to resist oxidation, detoxification and scavenging free radicals, and plays an irreplaceable role in the physiological processes of many cells. In addition, cysteine ​​is an essential molecule for the growth of cells and tissues. The lack of cysteine ​​can lead to a series of complex diseases, such as hair fading, edema, skin damage, liver damage, and stunted growth in young children. Therefore, the detection of cysteine ​​...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): G01N21/64C09K11/58
Inventor 万锕俊桂日军李慧丽金辉
Owner SHANGHAI JIAOTONG UNIV