Non-invasive body immunity function change monitoring method and application thereof
An immune, non-invasive technology, applied in the direction of chemical reaction of materials, material analysis and biological testing by observing the impact on chemical indicators, can solve the problem of detection materials and reagents, high cost, detection Long cycle and other problems, to achieve the effect of no security risk, low cost and convenient implementation
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Embodiment 1
[0030] Immunocompromised mouse model and monitoring of glucose concentration in urine
[0031] Methods: Immediately after the beginning of the experiment, the model was established, and the immunocompromised mouse model was established. The mice in the model group (number of mice n=4) were intraperitoneally injected with cyclophosphamide 150 mg / kg to prepare the immunocompromised model. time, for four consecutive weeks; the normal group was modeled, and the mice in the normal group (number of mice n=7) were intraperitoneally injected with distilled water of the same volume; After 24 hours of urine, they were killed by dislocation of the cervical spine. The immune indicators were detected by conventional methods, and the relative concentration of glucose in urine samples was detected by NMR method.
[0032] Results: The modeling results of the immunocompromised mouse model and the normal group are shown in Table 1. figure 1 and Figure 2a ~ 2f shown. Among them, the comparis...
Embodiment 2
[0043] Immunoenhanced Mouse Model and Monitoring of Urine Glucose Concentration
[0044]Method: Modeling was started at the beginning of the experiment. The normal aged mice group (O group) and the normal aged mice gavage lentinan group (OA group), 7 mice in each group; 40mg / kg·day, gavage volume of 0.1mL / 10g, gavage once a day, continuous gavage for 30d; O group and OA group of mice normal intake and drinking water; after four weeks, the metabolism cage was collected 24h urine, the day before the end of the experiment, Then they were killed by dislocation of the cervical vertebrae, and the immune indexes were detected by conventional methods, and the relative concentration of glucose was detected by NMR method.
[0045] Results: The modeling test results of mice in group O and OA are shown in Table 3 to Table 5.
[0046] Table 3 Organ Index
[0047]
[0048]
[0049] Note: Compared with group O, △ P<0.05.
[0050] Table 4 Immune function index
[0051]
[0052] ...
Embodiment 3
[0063] Method: A subject collected 15ml of morning urine during the cold period, and collected 15ml of morning urine after the cold, which were marked as G1 and G2 respectively; 10ml of G1 and G2 urine samples were taken respectively, and centrifuged in a high-speed centrifuge at 5000g for 10min at 4°C , get supernatant 0.5ml, use the sulfuric acid phenol colorimetric method with pure glucose as reference substance, detect the glucose content in the supernatant.
[0064] Results: During the cold period, the glucose concentration in the urine sample G1 was 1.08 mg / ml, and the glucose concentration in the urine sample G2 after the cold was 0.78 mg / ml, and the glucose concentration decreased by 27.8%.
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