Use of plateau Rhododendron extract for protection against UV damage and sports care
An extract, ultraviolet technology, applied in the field of daily chemical industry, can solve problems such as deficiency, achieve the effects of alleviating inflammation, protecting against ultraviolet radiation damage, and improving local microcirculation
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Embodiment 1
[0054] Example 1 In vitro safety of rhododendron extract
[0055] 1.1. Experimental materials
[0056] Rhododendron japonica extract, DMEM cell culture medium, PBS buffer, skin fibroblast L929, skin stratum corneum cells HaCaT, MTT, 96-well plate
[0057] 1.2. Experimental Instruments
[0058] Stereo Microscope, Microplate Reader
[0059] 1.3. Experimental steps
[0060] The cells (skin fibroblasts L929 and skin stratum corneum cells HaCaT) were planted in 96-well plates respectively, and when the cell plating degree reached 60-70%, the medium was removed and replaced with the medium containing and not containing Rhododendron japonica extract. Fresh medium, continue to cultivate for 24 hours, then remove the medium and replace it with medium containing 0.5mg / ml MTT, after 4 hours of culture, use a microplate reader to detect the absorbance at 490nm, and process the results to make a histogram.
[0061] 1.4. Statistical Analysis
[0062] t-test test, (n=6, mean ± SD, *P<0....
Embodiment 2
[0067] Example 2 In vitro UV protection of rhododendron extract
[0068] 1.1. Experimental materials
[0069] Rhododendron extract, DMEM cell culture medium, PBS buffer, skin fibroblast L929, skin stratum corneum cells HaCaT, MTT, 96-well plate, 6-well plate, COX-2 antibody, p62 antibody, LC3-I / LC3 -II antibody, GADPH antibody.
[0070] 1.2. Experimental Instruments
[0071] Stereo microscope, microplate reader, UV-Crosslinker ultraviolet radiation instrument, protein electrophoresis instrument
[0072] 1.3. Experimental steps
[0073] 2.3.1 MTT of Rhododendron extract in vitro UV protection
[0074] The cells (skin fibroblasts L929 and skin stratum corneum cells HaCaT) were planted in 96-well plates respectively, and when the cell plating degree reached 60-70%, the medium was removed and replaced with the medium containing and not containing Rhododendron japonica extract. Fresh culture medium, remove the medium after continuing to cultivate for 8 hours, and irradiate UVB...
Embodiment 3
[0090] Example 3 Radix Rhododendron extract in vivo UV protection
[0091] 1.1. Experimental animals
[0092] C57 / BL6 mice
[0093] 1.2. Experimental materials
[0094] Cream base, cream containing Rhododendron extract (Dj-C), depilatory cream, tinfoil
[0095] 1.3. Experimental Instruments
[0096] Stereo microscope, UV-Crosslinker ultraviolet radiation instrument, protein electrophoresis instrument, electric clipper
[0097] 1.4. Experimental steps
[0098] The mice were randomly divided into 4 groups, namely the blank control group (Con), the ultraviolet model group (M), the ointment base group (Blank-C), and the ointment group containing Rhododendron japonica extract (Dj-C). After the mice were anesthetized, the hair on the back of the mouse was pushed off with an electric clipper, and the remaining stubble was removed with a depilatory cream. Figure 12 Schematic diagram of mouse ultraviolet modeling and treatment methods, according to Figure 12 Apply Blank-C and ...
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