Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Sunscreen molecule, application and sunscreen cream

A technology for sunscreen and sunscreen ingredients, applied in the fields of sunscreen molecules and applications and sunscreens, can solve problems such as skin allergies and human body absorption, and achieve the effects of enhancing light-absorbing ability, strong light-absorbing ability, and accelerating the conversion of light energy into heat energy.

Inactive Publication Date: 2019-06-14
DALIAN INST OF CHEM PHYSICS CHINESE ACAD OF SCI
View PDF3 Cites 2 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The high SPF value of current sunscreens is mostly at the expense of high concentrations of effective sunscreen ingredients, such high concentrations of sunscreen ingredients may cause skin allergies or be absorbed by the body

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
  • Sunscreen molecule, application and sunscreen cream
  • Sunscreen molecule, application and sunscreen cream
  • Sunscreen molecule, application and sunscreen cream

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0021] Embodiment 1 (synthesis of sunscreen molecule):

[0022] Such as figure 2 As shown, the structure of the sunscreen molecule adopted in the embodiment is represented by the code MS. In a 100ml single-necked flask, add 500mg sinapic acid, 10ml anhydrous methanol, and two drops of concentrated sulfuric acid with a mass concentration of 98%. The mixture was refluxed at a temperature of 65° for 12 hours. After cooling to room temperature, the reaction mixture was evaporated to dryness with a rotary evaporator, and the residue was dissolved in 50 ml of ethyl acetate, washed 3 times with saturated sodium bicarbonate solution, and then dried over anhydrous sodium sulfate. , and the target product MS was separated by column chromatography. NMR 1 H spectrum and 13 The C spectrum proves that the molecular structure is indeed MS.

Embodiment 2

[0023] Embodiment 2 (preparation of sunscreen cream measures SPF value and compares the sunscreen effect of commercial sunscreen molecules):

[0024] The synthetic sunscreen molecule MS and homosalate (homosalate) were blended into the commercially available cream, the mass fraction of the molecule was 10%, and stirred with a magnetic stirrer for 24 hours under the condition of avoiding light. After stirring evenly, apply the cream mixture to a quartz glass plate (4*4cm) with a layer of 3M adhesive tape, and the amount of application is 2mg / cm 2 . After half an hour of drying in the dark, use a SHIMADZ UV-2600 ultraviolet-visible absorption spectrometer with a 60mm integrating sphere to measure the absorption spectrum. The absorption spectrum is as follows image 3 As shown, the calculated SPF value of the sunscreen cream containing MS sunscreen molecules is 11, and the SPF value of the sunscreen cream containing homosalate is 3.2.

Embodiment 3

[0025] Embodiment 3 (sunscreen molecule transient absorption experiment):

[0026] The synthesized sunscreen molecule MS was dissolved in methanol solution with a mass fraction of 10%, and its absorbance was measured as 1 with a 1mm thick quartz cuvette. Then femtosecond transient absorption spectroscopy was performed to measure the excited state decay process. The excitation wavelength is 320nm, and the detection wavelength is 400-800nm. The excited state decay curve was measured as Figure 4 shown. After fitting, its excited state lifetime is less than 2ps, that is, the molecule can convert absorbed light energy into heat energy within 2ps.

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 novel efficient UVB sunscreen molecule based on modification of a natural sunscreen molecule, and relates to preparation of the efficient UVB sunscreen molecule. A sunscreenmolecule sinapic acid structure naturally existing in plants is modified, the light absorption band of the sunscreen molecule sinapic acid structure is changed, the light absorption capacity is enhanced, meanwhile, the speed of converting light energy into heat energy is increased, and the sunscreen molecule is excellent in performance.

Description

technical field [0001] The invention relates to the field of cosmetics, in particular to a sunscreen molecule and its application and sunscreen. Background technique [0002] With the development of social economy and the affluence of people's life, the demand for traveling is increasing; at the same time, sunbathing is becoming more and more popular, which increases the chance of being exposed to ultraviolet light. Ultraviolet rays in sunlight can be divided into UVC band (200-275nm), UVB band (275-320nm), UVA band (320-400nm), almost all of the UVC band light in sunlight is absorbed by the ozone layer; most of the UVB band light Absorbed by the ozone layer, less than 2% can reach the surface of the earth. It will be particularly strong in summer and afternoon. UVB ultraviolet rays have erythema effect on the human body. Reacts with DNA, damaging DNA and causing skin cancer. The UVA band is the band with the highest content in ultraviolet rays. At the same time, the ultra...

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): C07C69/734C07C67/08A61K8/37A61Q17/04
Inventor 韩克利赵西罗健刘燕羊送球
Owner DALIAN INST OF CHEM PHYSICS CHINESE ACAD OF SCI
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com