PDRN-containing whitening and freckle-removing composition and application thereof
A whitening and freckle-removing composition technology, which is applied in the field of whitening and freckle-removing compositions, can solve the problems of reducing the transmission speed of melanosomes, repeated whitening and freckle-removing effects, and inconspicuous whitening and freckle-removing effects, and achieves the repair of epidermal defense function and stable curative effect , promote skin collagen synthesis effect
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Embodiment 1
[0043] 1. Prepare PDRN (polydeoxyribonucleotide), comprising the following steps:
[0044] (1) Mix male salmon testis with 1 wt% trichloroacetic acid solution in a mass ratio of 1:4, homogenate, centrifuge at 4000 rpm for 5 min, and discard the supernatant;
[0045] (2) Add lysate to the precipitate obtained in step (1), mix well, heat in a water bath at 90°C for 15min, cool to room temperature and centrifuge at 6000rpm for 10min, and take the supernatant; the lysate contains 100mM Tris-HCl , 200mM NaCl, 5mM EDTA and 0.2wt% SDS, the pH of which is 8.0;
[0046] (3) Add an equal volume of 4°C pre-cooled isopropanol to the supernatant obtained in step (2), mix well, place it at -20°C for 30 minutes, centrifuge at 8000 rpm for 10 minutes, discard the supernatant, collect the precipitate, and Air-dry the precipitate until there is no ethanol smell to obtain PDRN.
[0047] 2. Perform gel electrophoresis on the PDRN prepared above:
[0048] Accurately weigh PDRN, add TE solution,...
Embodiment 2
[0051] 1. Preparation of PDRN (polydeoxyribonucleotide)
[0052] (1) Mix male salmon testis with 1 wt% trichloroacetic acid solution at a mass ratio of 1:10, homogenate, centrifuge at 4000 rpm for 5 min, and discard the supernatant;
[0053] (2) Add lysate to the precipitate obtained in step (1), mix well, heat in a water bath at 95°C for 10 minutes, cool to room temperature and centrifuge at 7000 rpm for 10 minutes, and take the supernatant; the lysate contains 150mM Tris-HCl , 200mM NaCl, 4mM EDTA and 0.25wt% SDS, its pH is 8.2;
[0054] (3) Add an equal volume of 4°C pre-cooled absolute ethanol to the supernatant obtained in step (2), mix well, place it at -20°C for 30min, centrifuge at 8000rpm for 10min, discard the supernatant, collect the precipitate, and Air-dry the precipitate until there is no ethanol smell to obtain PDRN.
[0055] 2. Perform gel electrophoresis on the PDRN prepared above: use gel electrophoresis to measure the molecular weight of DNA in the sample,...
Embodiment 3
[0057] 1. Preparation of PDRN (polydeoxyribonucleotide)
[0058] (1) Mix male salmon ovary with 1 wt% trichloroacetic acid solution at a mass ratio of 1:4, homogenate, centrifuge at 4000 rpm for 5 min, and discard the supernatant;
[0059] (2) Add lysate to the precipitate obtained in step (1), mix well, heat in a water bath at 70°C for 20min, cool to room temperature and centrifuge at 7000rpm for 10min, and take the supernatant; the lysate contains 100mM Tris-HCl , 150mM NaCl, 2mM EDTA and 0.15wt% SDS, the pH of which is 8.0;
[0060] (3) Add an equal volume of 4°C pre-cooled absolute ethanol to the supernatant obtained in step (2), mix well, place it at -20°C for 30min, centrifuge at 8000rpm for 10min, discard the supernatant, collect the precipitate, and Air-dry the precipitate until there is no ethanol smell to obtain PDRN.
[0061] 2. Perform gel electrophoresis on the PDRN prepared above:
[0062] The molecular weight of DNA in the sample was determined by gel electro...
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