Method for screening cancer prevention agent or anticancer agent using morphological characteristics of luterial
A technology for anticancer agents and preventive agents, which can be used in the screening of compounds, scientific instruments, electrochemical variables of materials, etc., and can solve the problems of low efficiency of anticancer agents and long time of anticancer agents
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Embodiment 1
[0186] Example 1: Separation of Luterial
[0187]As shown in Table 5 below, Luterial was isolated from the blood of the following patients: (1) lung cancer patients, (2) pancreatic cancer patients, (3) colon cancer patients, (4) liver cancer patients, (5) prostate cancer patients, ( 6) Breast cancer patients, (7) Thyroid papillary carcinoma patients, (8) Kidney cancer patients, (9) Leukemia patients, (10) Patients with advanced cancer (stomach cancer, colorectal cancer, gallbladder cancer) and (11) Patients with stage 4 metastatic cancer (lung, prostate, breast) were identified. Blood is collected from patients confirmed to have cancer and then centrifuged to settle material in the blood. Allow the centrifuged blood to sit for 5-10 minutes, then collect the supernatant by pipetting. Subsequently, 5 μl of CD39 antibody-conjugated ferromagnetic nanoparticles or CD73 antibody-conjugated ferromagnetic nanoparticles were added to 100-200 μl of blood and incubated for 30 min, af...
Embodiment
[0190] Example: Preparation of Candidates
[0191] 100 g of the following medicinal plants were cut to fit a 2-3 liter (20- to 30-fold by volume) size container and placed in the container: sumac, forsythia, poria cocos, angelica root and kiwi fruit. Then 500-800 g (equivalent to 5-8 times the plant weight, preferably 600 g of 6 times the plant weight) of distilled water was added to the container, followed by shaking at 80° C. for about 8 hours, thereby obtaining a hot water extract. CD39 antibody-conjugated ferromagnetic nanoparticles or CD73 antibody-conjugated ferromagnetic nanoparticles were added to 100-200 μl of hot water extract and incubated for 30 minutes. Next, the mixture was maintained in a magnetic separator for 1-2 minutes to collect Luterion-bound magnetic nanoparticles, and the supernatant was discarded, followed by washing. Next, 0.033 wt % BSA (Bovine Serum Albumin) / PBS buffer was added to the Luterion-bound magnetic nanoparticles, followed by incubation ...
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