Use of pitaya ovule extract to prepare composition for delaying skin aging
A technology of skin aging and red dragon fruit, applied in the field of plant extracts, can solve problems such as enzyme decomposition, complicated process, and risk of immune rejection
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Embodiment 1
[0030] Preparation of Red Dragon Fruit Ovule Extract
[0031] Red dragon fruit, also known as dragon fruit or cactus fruit, is a plant of the genus Trigonum in the family Cactaceae. It is native to Central America and is now widely planted in Taiwan, China. The fruit of this plant is rich in dietary fiber and can stimulate gastrointestinal peristalsis, which can be used to prevent constipation.
Embodiment 2
[0035] Red dragon fruit ovule extract promotes collagen secretion
[0036] In order to test the influence of the red dragon fruit ovule extract of the present invention on the collagen production of skin cells, the present embodiment measures human skin fibroblast CCD-966SK through the red dragon fruit ovule extract described in Example 1 with a collagen secretion test Changes in collagen production after treatment. Briefly, CCD-966SK cells were divided into 2×10 4 Cells / well were seeded in 24-well plates, and each well contained 500 μL of cell culture medium. After culturing the cells at 37°C for 24 hours, the cell culture medium was removed and the cells were washed with PBS solution. Secondly, add 500 μL of 8 mg / mL red dragon fruit ovule extract and 500 μL of FBS-free cell culture medium to each well of cells (experimental group), and treat the cells with 500 μL of FBS-free cell culture medium as a blank control group . After the aforementioned two groups of cells were ...
Embodiment 3
[0039] Red dragon fruit ovule extract promotes skin fibroblast proliferation
[0040] In order to test whether the red dragon fruit ovule extract of the present invention promotes the proliferation of human skin fibroblasts, this example uses a cell proliferation test to measure the proliferation status of CCD-966SK cells after being treated with the red dragon fruit ovule extract described in Example 1. Briefly, CCD-966SK cells were seeded in 96-well plates at 3000 cells / well, and each well contained 0.1 mM non-essential amino acids, 1.5 g / L sodium bicarbonate, 1 mM sodium pyruvate, and 10% FBS MEM medium. After culturing the cells at 37°C for 2 hours, remove the medium, and treat the cells in each well in the following manner: (a) apply 100 μL of the aforementioned medium without FBS (blank control group); (b) apply 100 μL containing 20 The aforementioned culture medium with %FBS (positive control group); or (c) 100 μL of the aforementioned culture medium without FBS but ad...
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