Application of aphanothece sacrum polysaccharide in preparation of medicine for treating scalds
A technology of cyanobacterial polysaccharide and Shuiqian Temple, which is applied in the field of biomedicine, can solve the problem that there is still less research on the mechanism of scald repair, and achieve the effects of reducing the production amount, slowing down the acute inflammatory response, and increasing the content.
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Embodiment 1
[0049] Example 1 Effect of Shuiqianji Spirulina Polysaccharide on Rat Scald Healing Rate
[0050] figure 2 It is the wound recovery of different treatment groups on the 15th, 17th, 19th, and 21st day. The front wound is the control wound, and the rear wound is the treatment wound. On the 15th day, under the effect of the rat's own recovery ability, the wound has basically healed. Scab, there is a certain amount of bleeding from the wound, which may be due to unnatural shedding of the scab due to scratching, scratching and other reasons. Compared with the normal saline negative control wound, the recovery effect of the other three groups was significantly better, and the recovery effect was negative control normal saline, combined drug group, silver sulfadiazine, and Shuiqiansi cyanobacteria polysaccharide. Therefore, it can be preliminarily determined that Shuiqianji cyanobacteria polysaccharide has a therapeutic effect on the recovery of scald wounds, and the therapeutic ef...
Embodiment 2
[0052] Example 2 Effect of Shuiqianji Spirulina Polysaccharide on Initial Scald Inflammation
[0053] 1. Determination of serum inflammatory factor levels
[0054] Use enzyme-linked immunosorbent assays (Enzyme linked immunosorbent assays, ELISA) to measure the levels of TNF-α and IL-1β (inflammatory factors) in serum. The kits used below are Abcam kits (ab100767 and ab46070). Operate according to the instructions, and each group 3 test samples, 2 parallel replicates for each sample.
[0055] Sample and reagent preparation: Dilute the standard, HRP, washing buffer, IL-1β antibody, TNF-α antibody and biotin-labeled secondary antibody to 1x, and use Diluent A to pretreat the sample.
[0056] IL-1β: add 100 μL standard and sample, incubate at room temperature for 2.5 hours; wash the plate with 300 μL washing buffer for each well, wash 4 times, remove as much liquid as possible each time; add 100 μL detection antibody to each well, incubate for 1 hour, gently Shake; wash the pla...
Embodiment 3
[0064] Example 3 Effect of Shuiqiansi Spirulina Polysaccharide on Type I and Type III Collagen Tissue Distribution
[0065] A. Fixative preparation (4% paraformaldehyde)
[0066] Phosphate buffer A (0.2mol / L): Take NaH 2 PO 4 2H 2 O 27.6g dissolved in ddH 2 O, set the volume to 1L.
[0067] Phosphate buffer B (0.2mol / L): take Na 2 HPO 4 12H 2 O 71.6g dissolved in ddH 2 O, set the volume to 1L.
[0068] PB solution (0.1mol / L): take buffer A and buffer B, mix them at a ratio of 19:81, adjust the pH value to 7.4, add an equal volume of ddH 2 O and 40g of paraformaldehyde powder, heat and stir at 65°C, after completely dissolving, dilute to 1L.
[0069] B. Paraffin tissue embedding (n-butanol method)
[0070] Prepare nine 50ml centrifuge tubes, mark No. 1-9, add 50% ethanol in order; ethanol: n-butanol: water (5:2:3) mixture; ethanol: n-butanol: water (10:7:3 ) mixture; ethanol: n-butanol: water (9:9:2) mixture; ethanol: n-butanol (1:3) mixture; ethanol: n-butanol (3:1...
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