Polypeptide repair liquid
A technology for repairing liquid and polypeptide, applied in the field of polypeptide repairing liquid, can solve problems such as toxic and side effects, and achieve the effects of reducing toxic and side effects, reducing the dosage, and preventing excessive oxidation.
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Embodiment 1
[0036] Preparation of Example 1 Polypeptide Repair Solution
[0037] (1) Preparation of pearl hydrolyzed active peptide solution by enzymatic hydrolysis
[0038] Pearls (from Pinctada martensii) from marine culture in the Beibu Gulf are ground into fine powders of 200-270 mesh, then added with distilled water, stirred to make an aqueous solution containing 50-60% (g / v) of pearl powder, and then the pearls Heat the powder aqueous solution and keep it at 45-58°C, add neutral protease (40000-50000U / G) and compound protease (10000-20000U / G) with pearl powder weight 1‰-5‰, and keep stirring for 4-5 hours Filter out the solid matter to obtain the enzymolyzed pearl hydrolyzed active polypeptide solution, then put the enzymatically hydrolyzed pearl hydrolyzed active polypeptide solution into a distillation dish, heat to 95-100°C for 5-15 minutes, and finally collect Distillate.
[0039] (2) Prepare Bingtangcao lavender extract
[0040] Purchasing the petals of high-quality, non-rot...
Embodiment 2
[0049] The bacteriostasis effect comparison of each component of embodiment 2 polypeptide repair liquid
[0050] Because the peptide repair solution contains nano-silver, lavender rock sugar grass extract and other ingredients, we first carried out a preliminary evaluation of the antibacterial activity of these ingredients. The 12 wells in each row of the 96-well plate are numbered 1 to 12 respectively. Well 1 is a blank control, well 2 is a negative control, wells 3 and 4 are positive drug control wells with different concentrations, and wells 5-7 are peptides. Repair liquid stock solution, 50% dilution of the stock solution, and 10% dilution of the stock solution. Wells 8 to 12 are pearl hydrolyzate, lavender rock sugar grass extract, nano silver, gourd tea extract, and Prunella vulgaris extract. Their respective concentrations are the same as those in the polypeptide repair solution. The total volume after dilution in the culture medium is 100 μl, and then 100 μl of culture...
Embodiment 3
[0052] Example 3 The detection of the inhibitory activity of the polypeptide repair solution to 8 strains to be tested
[0053] (1) Using the double dilution method, the peptide repair solution was treated with Pseudomonas aeruginosa, Staphylococcus epidermidis, Klebsiella pneumoniae, Staphylococcus aureus, Propionibacterium acnes, Actinomyces viscosus, Porphyromonas gingivalis Bacteria and 8 strains of Acinetobacter baumannii were serially diluted (after the strains were resuscitated and activated, a single clone was picked and inoculated in the corresponding medium, and when the OD600 value of the bacterial solution reached 0.2-0.4, the 1:100 (v / v) dilution to prepare the inoculum solution), a total of 8 concentrations: 100% stock solution, 50% stock solution, 40% stock solution, 30% stock solution, 20% stock solution, 10% stock solution, 5% stock solution and 2.5% stock solution.
[0054] (2) Use a pipette gun to add 100 μl each of the prepared double-diluted 8 concentrati...
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