Unlock instant, AI-driven research and patent intelligence for your innovation.

Method for quickly, simply and conveniently evaluating potential toxicity of molecules with planar structures

A planar structure and molecular technology, which is applied in the field of quick and easy evaluation of the potential toxicity of planar structure molecules, and can solve problems such as cumbersome operation, toxicity, and cumbersome detection operations

Inactive Publication Date: 2012-10-24
GUANGXI UNIVERSITY OF TECHNOLOGY
View PDF0 Cites 1 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0003] Many natural and synthetic molecules have a planar structure and are widely used in food additives, medicine, pesticides, and chemical industries, but have significant toxicity
At present, the research on the potential toxicity of related compounds is very weak, and the existing detection techniques are usually cumbersome and time-consuming, such as the in vitro test of sister chromatid exchange in mammalian animal cells, the micronucleus test in mammalian erythrocytes, and the chromosomal aberration in mammalian cells in vitro Tests, natural killer cell activity tests, etc., require complex detection equipment, cumbersome operations or take a long time

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
  • Method for quickly, simply and conveniently evaluating potential toxicity of molecules with planar structures
  • Method for quickly, simply and conveniently evaluating potential toxicity of molecules with planar structures
  • Method for quickly, simply and conveniently evaluating potential toxicity of molecules with planar structures

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0035] Example 1: Determination of the saturation value of EB (ethidium bromide) binding to DNA.

[0036] Take 6 10mL colorimetric tubes (sequentially numbered ①②③④⑤⑥), add 1mL BR buffer solution, 0.1mL 1.00×10 -3 mol / L EB solution, then add 0, 0.1, 0.13, 0.15, 0.18, 0.21mL 3.78×10 -5 mol / L DNA solution, take another 10mL colorimetric tube, add 1mL BR buffer solution and 0.15mL 3.78×10 -5 mol / L DNA solution. Then dilute the 7 colorimetric tubes with water to the scale of 5mL, eliminate the bubbles and mix them with a vortex mixer, place them in a 37°C water bath for 60 minutes, and perform synchronous scanning on a fluorescence spectrophotometer to obtain RLS spectra (resonance scattering spectra), emission and The excitation slit is 15nm, and the scanning range is 220-700nm. Through the measurement of resonance scattering spectroscopy, it can be seen that the colorimetric tube numbered ⑤ has the strongest resonance scattering signal. The DNA concentration at this time is the sat...

Embodiment 2

[0037] Example 2: Determination of the saturation value of doxorubicin and DNA binding.

[0038] Take 6 10mL colorimetric tubes (sequentially numbered ①②③④⑤⑥), add 1mL BR buffer, 0.1mL 2.00×10 -4 mol / L doxorubicin solution, add 0, 0.3, 0.4, 0.5, 0.6, 0.7mL 3.78×10 -6 mol / L DNA solution, take another 10mL colorimetric tube, add 1mL BR buffer solution and 0.4mL 3.78×10 -6 mol / L DNA solution. Then dilute 7 colorimetric tubes with water to the scale of 5mL, eliminate bubbles and mix them with a vortex mixer, place them in a 37°C water bath for 60 minutes, and perform synchronous scanning on a fluorescence spectrophotometer to obtain RLS spectra. The emission and excitation slits are 15nm. The scanning range is 220-700nm. Through resonance scattering spectroscopy, it can be seen that the colorimetric tube numbered ④ has the strongest resonance scattering signal. At this time, the DNA concentration is the saturation concentration of doxorubicin molecule and DNA binding. At this time, t...

Embodiment 3

[0039] Example 3: Determination of the saturation value of mitoxantrone and DNA binding.

[0040] Take 6 10mL colorimetric tubes (sequentially numbered ①②③④⑤⑥), add 1mL BR buffer, 0.1mL 1.00×10 -4 mol / L Mitoxantrone solution, add 0, 0.2, 0.4, 0.6, 0.8, 1mL 3.78×10 -6 mol / L DNA solution, take another 10mL colorimetric tube, add 1mL BR buffer solution and 0.4mL 3.78×10 -6 mol / L DNA solution. Then dilute 7 colorimetric tubes with water to the scale of 5mL, eliminate bubbles and mix them with a vortex mixer, place them in a 37°C water bath for 60 minutes, and perform synchronous scanning on a fluorescence spectrophotometer to obtain RLS spectra. The emission and excitation slits are 15nm. The scanning range is 220-700nm. Through resonance scattering spectroscopy, it can be seen that the resonance scattering signal of the colorimetric tube number ⑤ is the strongest. The DNA concentration at this time is the saturation concentration of mitoxantrone molecules and DNA binding. At this ti...

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 relates to a method for quickly, simply and conveniently evaluating potential toxicity of molecules with planar structures. A DNA (deoxyribonucleic acid) medicine intercalation theory is introduced into the method, an interaction relation of the molecules with the planar structures and DNA is researched by resonance light scattering technology, a corresponding binding saturation value of molecules with the planar structure and the DNA is calculated according to a measurement result of a resonance light scattering spectrum, and the corresponding potential toxicity of the molecules with the planar structures is further evaluated by means of adopting the binding saturation value of the molecules with the planar structures and the DNA as an evaluation index. By the aid of the method, the potential safety hazards of the planar molecules can be quickly, simply and conveniently evaluated, chemicals, medicines, healthcare food, food additives and food compositions with molecules with similarly planar structures can be quickly predicted and alerted, pharmacological and toxicological research for relevant pharmaceutical ingredients are supported technically, and the method effectively guides application of the molecules with the planar structures.

Description

Technical field [0001] The invention relates to a method for quickly and simply evaluating the potential toxicity of planar structure molecules. Background technique [0002] In 1961, Lerman proved that acridine is embedded in the base of DNA and proposed the DNA intercalator model for the first time. Planar aromatic fused ring structure molecules can be inserted into DNA as DNA intercalants. Deoxyribonucleic acid (DNA), as a carrier of genetic information, contains the most abundant information of organic organisms and is the target of many molecules. When the molecule is inserted into the DNA, the DNA conformation changes, or it is covalently cross-linked with the DNA strand, or the DNA is cut to hinder its replication and transcription, affect gene expression, and thus display cytotoxicity. In 1993, Pasternack et al. used a common fluorescence spectrophotometer to select appropriate excitation and emission passband widths, and used equal excitation and emission wavelengths to...

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
Patent Type & Authority Applications(China)
IPC IPC(8): G01N21/63
Inventor 李军生李姹姹杨小梅黄国霞阎柳娟
Owner GUANGXI UNIVERSITY OF TECHNOLOGY
Features
  • R&D
  • Intellectual Property
  • Life Sciences
  • Materials
  • Tech Scout
Why Patsnap Eureka
  • Unparalleled Data Quality
  • Higher Quality Content
  • 60% Fewer Hallucinations
Social media
Patsnap Eureka Blog
Learn More