A therapeutic liquid for treating ischemic stroke, its preparation method and application
A technology of ischemic stroke and treatment solution, which is applied in the field of treatment solution for ischemic stroke and its preparation, can solve the problem of limited treatment strategies for cerebral hypoxia, reduce infarct size, improve cell metabolism, Improving the effect of dysfunction
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[0033] Such as figure 1 and figure 2 As shown, the present invention provides a kind of preparation method of ischemic stroke treatment liquid, comprises the following specific steps:
[0034] S1: culturing Synechococcus elongatus to obtain a resuspension of Synechococcus elongatus;
[0035] S2: modifying up-converting nanoparticles (UCNPs) to obtain a suspension of up-converting nanoparticles;
[0036] S3: Mix the resuspension of Synechococcus elongatus in the step S1 with the resuspension of upconversion nanoparticles in the step S2 in a volume ratio (1-10): 1 to obtain a treatment solution.
[0037] Further, the step S1 specifically includes the following steps:
[0038] S11: Set the concentration to (1-5)×10 6 Synechococcus elongatus culture solution and BG11 medium (blue-green medium) mixed in a volume ratio of 3:(4-6) per μL, followed by a cycle of 8 hours of light and 16 hours of darkness at 25-28°C Continuous training;
[0039] S12: Increase 3-4mL of BG11 medium...
Embodiment 1
[0065] The invention provides a method for preparing an ischemic stroke treatment liquid, comprising the following specific steps:
[0066] S1: set the concentration to 1×10 6 Individual / μL Synechococcus elongatus culture solution and BG11 medium are mixed according to the volume ratio of 3:4, and continuously cultured at 25°C for 8 hours of light and 16 hours of darkness cycle;
[0067] S2: Add 3 mL of BG11 medium every 4 days to offset the amount of evaporation, and continue culturing for 10 days;
[0068] S3: Discard 50% of the culture solution in step S2 when the concentration of the culture solution is supersaturated (i.e., precipitation or bacterial film occurs), and then increase the same volume of BG11 medium to continue culturing for 20 days to obtain a mixed culture solution;
[0069] S4: Take about 7mL of the mixed culture solution, centrifuge at 4000rpm for 10 minutes, discard the supernatant, and then add 200μL of phosphate buffered saline solution with a concent...
Embodiment 2
[0077] The invention provides a method for preparing an ischemic stroke treatment liquid, comprising the following specific steps:
[0078] S1: Set the concentration to 2×10 6 Synechococcus elongatus culture solution and BG11 culture medium of each / mL were mixed according to the volume ratio of 3:5, and were continuously cultured at 26°C for 8 hours of light and 16 hours of dark cycle;
[0079] S2: Add 3 mL of BG11 medium every 5 days to offset the amount of evaporation, and continue to culture for 11 days;
[0080] S3: Discard 50% of the culture solution in step S2 when the concentration of the culture solution is supersaturated (that is, precipitation or bacterial film occurs), and then increase the same volume of BG11 medium to continue culturing for 25 days to obtain a mixed culture solution;
[0081] S4: Take about 9 mL of the mixed culture solution, centrifuge at 5000 rpm for 12 minutes, discard the supernatant, and then add 300 μL of phosphate buffered saline solution ...
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