Preparation and application of antibacterial modified exosome burn wound healing-promoting biological dressing
A biological dressing and exosome technology, which is applied in drug delivery, medical science, absorbent pads, etc., can solve the problems of exosomes lack of antibacterial function and limited effect, and achieve the promotion of wound healing, good wound healing, and good air permeability Effect
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Embodiment 1
[0053] Example 1 The preparation of antibacterial modified exosome burn wound healing biological dressing sample 1 (the synthesis process is as follows Figure 5 shown)
[0054] (1) Collect the stem cell culture medium, and centrifuge the collected cell culture supernatant at 4° C. and 2000 g to remove cell debris and dead cells in the supernatant. The centrifuged supernatant was collected and filtered through a 0.22 μm filter membrane. Place the filtered culture supernatant in an ultrafiltration centrifuge tube (30KD), centrifuge at 4°C and 5000g for 20min, and collect the ultrafiltered liquid;
[0055] (2) Pass the ultrafiltration liquid collected in step (1) through the qEV-exosome separation column, and place a 15ml centrifuge tube under the column for collecting the isolated exosomes. Before extracting exosomes, rinse with 10ml of PBS, add 0.5ml of ultrafiltered cell culture supernatant, discard 3ml of waste liquid, and start collecting 2ml of exosome solution. At this ...
Embodiment 2
[0061] Example 2 Preparation of antibacterial modified exosome burn wound healing biological dressing sample 2
[0062] (1) Collect the stem cell culture medium, and centrifuge the collected cell culture supernatant at 4° C. and 2000 g to remove cell debris and dead cells in the supernatant. The centrifuged supernatant was collected and filtered through a 0.22 μm filter membrane. Place the filtered culture supernatant in an ultrafiltration centrifuge tube (30KD), centrifuge at 4°C and 5000g for 20min, and collect the ultrafiltered liquid;
[0063] (2) Pass the ultrafiltration liquid collected in step (1) through the qEV-exosome separation column, and place a 15ml centrifuge tube under the column for collecting the isolated exosomes. Before extracting exosomes, wash them with 10ml of PBS, add 0.5ml of ultrafiltered cell culture supernatant, discard 3ml of waste liquid, and start collecting 2ml of exosomes. At this time, pay attention to supplementing PBS above the column to pr...
Embodiment 3
[0068] Example 3 Preparation of antibacterial modified exosome burn wound healing biological dressing sample 3
[0069] (1) Collect the stem cell culture medium, and centrifuge the collected cell culture supernatant at 4° C. and 2000 g to remove cell debris and dead cells in the supernatant. The centrifuged supernatant was collected and filtered through a 0.22 μm filter membrane. Place the filtered culture supernatant in an ultrafiltration centrifuge tube (30KD), centrifuge at 4°C and 5000g for 20min, and collect the ultrafiltered liquid;
[0070] (2) Pass the ultrafiltration liquid collected in step (1) through the qEV-exosome separation column, and place a 15ml centrifuge tube under the column for collecting the isolated exosomes. Before extracting exosomes, rinse with 10ml of PBS, add 0.5ml of ultrafiltered cell culture supernatant, discard 3ml of waste liquid, and start collecting 2ml of exosome solution. At this time, pay attention to supplementing PBS above the column. ...
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