Externally-applied dressing and preparation method and application thereof
A technology of dressing and raw material solution, applied in the medical field, can solve the problems of expensive exogenous growth factors, complex pathological mechanism, and loss of active ingredients in the gel
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Embodiment 1
[0058] Embodiment 1: the preparation of dressing
[0059] In this example, an 8% by weight solution of medical grade polyvinyl alcohol in deionized water was prepared. Independently medical chitosan is dissolved in the aqueous solution of 1% by weight of acetic acid with the concentration of 2% by weight, adds the deferoxamine solid powder of pre-calculated amount in this chitosan solution, forms chitosan solution, described Feroxamine was added in such an amount that the deferoxamine content in the final dressing was 1% by weight of the total dressing solids. The polyvinyl alcohol solution prepared above and the chitosan solution were mixed in a weight ratio of 4:6 and placed in a syringe pump. Using the electrospinning machine shown in Figure 1 of the present invention, a 0.6mm stainless steel needle is selected as the spinning nozzle and connected to a high-voltage positive electrode, and a rotating receiving plate is set at a distance of 8 cm from the needle. The voltage...
Embodiment 2
[0062] Example 2: Control dressing (dressing without deferoxamine)
[0063] In this example, the preparation steps of Example 1 were repeated to form a dressing, but the difference was that deferoxamine was not used in the raw material, and the prepared dressing was recorded as a control dressing.
Embodiment 3
[0064] Example 3: In this example, the performance of VEGF protein expression was tested using the dressings of the present invention prepared in Example 1 above with different contents of deferoxamine.
[0065] sample culture
[0066] Dressings with DFO content of 0.8, 0.9, 1.0% by weight were cut into 15x15 mm 2 The size of the square is preset at the bottom of the 6-well plate, according to 2x10 5 Seed skin fibroblasts at cell density, place at 37°C, 5% CO 2 Incubate in the incubator and replace the medium every other day. The protein in the cells was extracted on the third day of the growth of the cultured cells, with at least 3 samples in each group, and repeated 3 times.
[0067] protein extraction
[0068] The steps of protein extraction are as follows:
[0069] (1) 100 μl RIPA (Beyotime, China) and 1 μl protease inhibitor PMSF (Beyotime, China)) were added to each well of a 6-well plate, and placed on ice.
[0070] (2) Scrape the cells carefully with a cell s...
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