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Infrared ii region fluorescent gold nanoclusters and its preparation and application

A technology of fluorescent gold nanometers and gold nanoclusters, which is applied in the field of fluorescent materials in the infrared II region, can solve the problems of non-compliance, cytotoxic side effects, the preparation and imaging application of gold nanomaterials without research, and achieves improved biocompatibility. sexual effect

Active Publication Date: 2021-08-24
SUZHOU UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

[0006] The significant cytotoxic side effects of the above two types of infrared II materials are the shortcomings and deficiencies of the existing technologies. Therefore, how to synthesize and prepare infrared II region nano-imaging materials with good biocompatibility is an important issue in the field of nano-biological imaging research. Scientific question
[0007] Although gold nanomaterials have microwave absorption properties, high surface activity, optical properties, photocatalytic properties, photoelectrochemical properties and photothermal properties, and optical conversion properties (absorption, emission, scattering, plasmon resonance), although gold nanomaterials have unique It has potential application value in a variety of biomedical imaging due to its physical and chemical properties, but there is no research on the preparation and imaging application of gold nanomaterials in the infrared II region.
This is due to the fact that gold nanomaterials have fluorescence properties that depend on the particle size, and their emission spectra can be tuned in different bands (visible light region to infrared region) by adjusting the size, but the near-infrared region (especially 800- 1000nm) luminescent gold nanomaterials do not comply with the quantum size effect theory, and it is difficult to realize their emission spectrum in the near-infrared II region through size regulation.

Method used

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  • Infrared ii region fluorescent gold nanoclusters and its preparation and application
  • Infrared ii region fluorescent gold nanoclusters and its preparation and application
  • Infrared ii region fluorescent gold nanoclusters and its preparation and application

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Experimental program
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Effect test

Embodiment 1

[0061] (1) The ligand-template molecule RNase-A was dissolved in water to prepare a ligand-template solution with a concentration of 10 mg / mL. Further, tetrachloroauric acid was dissolved in water to obtain a chloroauric acid solution having a concentration of 15 mM. Both solutions were prepared in 500 μL.

[0062] (2) Add 50 μL of 1M sodium hydroxide aqueous solution dropwise into the chloroauric acid solution, and observe that the golden yellow chloroauric acid solution fades, and then add the ligand template solution to it to form a mixed solution. The pH of the mixed solution is about 11.

[0063] (3) After mixing thoroughly for 5 minutes, add 10 μL of reducing agent NaBH 4 An aqueous solution (concentration 15 mM) was added dropwise to the above mixed solution. The mixed solution was placed in a refrigerator at 4°C overnight, and a dark brown transparent and clear mixed solution was obtained, indicating that the reaction was complete, and the solution contained a large...

Embodiment 2

[0066] Prepare gold nanoclusters according to the method of Example 1, the difference is that RNase-A is replaced by equimolar amounts of β-lactoglobulin, bovine blood serum albumin (BSA), dihydrolipoic acid, dihydrosulfur-sulfur betaine, glutathione, mercaptoethanol or bioengineering custom polypeptide (its amino acid sequence structure is shown in Table 1).

[0067] Test the fluorescence properties of the infrared II region of several gold nanoclusters prepared in the above examples, the structures are as shown in Table 1, and N in the table 巯基 / N 共轭 Represents the molar ratio of the total number of sulfhydryl groups in the ligand molecule to the total number of conjugated molecules. It can be seen from the table that the eight kinds of ligand molecules can emit fluorescence in the infrared region II, and ribonuclease, β-lactoglobulin, dihydrosulfur-sulfobetaine, and bioengineered polypeptides (containing sulfhydryl and The fluorescence emission peaks of gold nanoclusters pr...

Embodiment 3

[0077] Prepare gold nanomaterials according to the method of Example 1, the difference is that RNase-A is replaced by small molecule amino acids: cysteine, histidine and tyrosine, and the molar ratio of the three amino acids is changed to prepare different gold nanomaterials.

[0078] Table 2 shows the effects of different amino acid ratios on the emission peaks and morphology of gold nanomaterials. In Table 2, NA represents no fluorescence emission. It can be seen that only a specific ratio of amino acids can make the emission peak of the gold nanoclusters red-shift to the infrared II region.

[0079] Table 2 Effects of different ratios of amino acids on the emission peaks and morphology of gold nanoclusters

[0080]

[0081]

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Abstract

The invention relates to the preparation and application of a fluorescent gold nanocluster in the infrared II region. The aqueous phase synthesis method is used to prepare tetrachloroauric acid HAuCl 4 Soluble in a strong alkaline aqueous solution, and use a reducing agent to convert trivalent gold ions Au 3+ Reduction to gold atoms Au 0 , select protein ligand template molecules containing sulfhydryl groups (cysteine) and conjugated functional groups, change the temperature and reaction time and other conditions through microwave-assisted synthesis equipment, so that gold atoms grow and aggregate in the corresponding ligand templates to form gold nanoparticles clusters. The gold nano-cluster of the invention can emit fluorescence in infrared II region, has higher fluorescence quantum yield and good biological safety.

Description

technical field [0001] The invention relates to the technical field of fluorescent materials in the infrared II region, in particular to a fluorescent gold nanocluster in the infrared II region and its preparation and application. Background technique [0002] Infrared II region fluorescence imaging technology refers to the imaging research technology that uses infrared laser (>808nm) to excite materials to emit near-infrared II region fluorescence (1000nm-1700nm), and performs real-time and dynamic detection at the level of living organisms. This technology originated from an important scientific hypothesis in the biological imaging research of fluorescent quantum dots by Carroll et al. in 2006: the fluorescent biological imaging effect in the near-infrared II region (1000nm-1700nm) is better than that in the visible light region and infrared I region (400-1000nm). Once this hypothesis was put forward, it was recognized by many scholars. Compared with traditional optical...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C09K11/58B82Y20/00B82Y40/00B22F9/24B22F1/00G01N21/64
CPCC09K11/58B82Y20/00B82Y40/00B22F9/24G01N21/6402B22F1/102
Inventor 李瑞宾王威力
Owner SUZHOU UNIV