Eureka AIR delivers breakthrough ideas for toughest innovation challenges, trusted by R&D personnel around the world.

Fluorescence labeling biological material and preparation method thereof

A biological material and fluorescent labeling technology, applied in the direction of luminescent materials, chemical instruments and methods, etc., can solve the problems of high biological toxicity and achieve the effect of broad application prospects

Inactive Publication Date: 2020-05-12
苏州永沁泉智能设备有限公司
View PDF3 Cites 3 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Fluorescent particles are mostly stored in emulsion, use more organic solvents, and have high biological toxicity after adding materials

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Fluorescence labeling biological material and preparation method thereof
  • Fluorescence labeling biological material and preparation method thereof
  • Fluorescence labeling biological material and preparation method thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0023] Example 1 Preparation of fluorescently labeled methacrylic anhydride modified gelatin (GelMA)

[0024] (1) Preparation of GelMA: Dissolve 10 g of gelatin in 0.01M PBS (pH=7.4) solution at 50 °C, slowly add 0.4 g of methacrylic anhydride to the solution, and at the same time adjust and maintain the pH of the solution with sodium hydroxide solution. Between 8 and 9. After the dropwise addition of methacrylic anhydride was completed, the reaction was continued for 2 hours, and then the pH of the reaction solution was adjusted to 7.4 with hydrochloric acid solution. The reaction solution was transferred into a dialysis bag with a molecular weight cut-off of 10 kDa, dialyzed in deionized water for 3 days, and then freeze-dried to obtain GelMA. Product amino substitution degree is 60%.

[0025] (2) Dissolve 1 g of rhodamine B in DMF at 10 mg / mL, then add 1.2 g of NHS and 2 g of EDC.HCl in sequence, and react at room temperature for 4 hours to obtain an activated fluorescent...

Embodiment 7

[0031] Example 7 Preparation of fluorescently labeled methacrylic anhydride modified chitosan (CSMA)

[0032] (1) Preparation of CSMA: Dissolve 10 g of chitosan in 500 mL of 2% v / v acetic acid solution. Heat to 50° C., and slowly drop 0.4 g of methacrylic anhydride into the solution. After the dropwise addition of methacrylic anhydride was completed, the reaction was continued for 2 hours, and then the pH of the reaction solution was adjusted to 7.4 with hydrochloric acid solution. The reaction solution was transferred into a dialysis bag with a molecular weight cut-off of 10 kDa, dialyzed in deionized water for 3 days, and then freeze-dried to obtain CSMA. The amino substitution degree of the product is 50%.

[0033] (2) Dissolve 1 g of Rhodamine B in DMF at 10 mg / mL, then add 1.2 g of NHS and 2 g of EDC.HCl in sequence, and react at room temperature for 4 hours to obtain an activated fluorescent molecule solution. Rhodamine B / NHS / EDC.HCl molar ratio is 1 / 1 / 1.

[0034] (3...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

No PUM Login to View More

Abstract

The invention discloses a fluorescence labeling biological material and a preparation method thereof. The method comprises the following steps: (1) activating fluorescent molecules; (2) carrying out areaction on a polymer and activated fluorescent molecules; (3) dialyzing the solution after the reaction in the step (2) with deionized water, and freeze-drying to obtain a fluorescence labeling biological material, wherein the polymer is a polyamino acid-based polymer or a chitosan-based polymer. According to the invention, the carboxyl on a fluorescent molecule is activated into active ester, then the active ester and the amino on a biopolymer are subjected to an amidation reaction, and the fluorescent molecule is chemically coupled to the biopolymer, so that the fluorescence labeling material has different fluorescence colors due to different labeled fluorescence molecules, and the chemical labeling method avoids the defect that fluorescent molecules or particles thereof are easy to diffuse out of a system in physical mixing or electrostatic adsorption and other methods; and the fluorescence labeling biological material has a wide application prospect in the research fields of in-vitro and in-vivo imaging, tracing, material degradation, biosensing, 3D printing and the like.

Description

technical field [0001] The invention belongs to the technical field of biological materials, and in particular relates to a fluorescent-labeled biological material and a preparation method thereof. Background technique [0002] Since the concept of tissue engineering was put forward, people have developed many types of biomaterials, some of which are polyamino acid materials such as collagen, gelatin and polylysine, etc., and polysaccharide materials such as chitosan are rich in amino groups in their molecular structures. It not only provides positively charged adhesion sites for cell adhesion and proliferation, but also provides active groups for chemical modification. [0003] Fluorescent probes have important applications in in vivo and in vitro imaging, material tracking, biosensing and other fields. Currently commercially available fluorescent probes are mostly quantum dots and polymer microspheres. Combining them with biological materials has a good fluorescent effect...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
IPC IPC(8): C08H1/00C08B37/08C09K11/06
CPCC08B37/003C08H1/00C09K11/06C09K2211/145
Inventor 简宇航贺永高庆王鹏谭振龙郑雅婷
Owner 苏州永沁泉智能设备有限公司
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Eureka Blog
Learn More
PatSnap group products