Screening method of early-stage liver cancer diagnosis markers for people with liver cirrhosis and hepatitis
A diagnostic marker and early liver cancer technology, applied in the field of clinical medical diagnosis, can solve problems affecting the cure rate and prognosis of liver cancer, and achieve high accuracy
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Embodiment 1
[0034]Example 1. Screening of Early Diagnosis Markers of Hepatitis Hepatoma.
[0035]Studies: This study included 24 patients with plasma samples and 26 patients with primary liver cancer patients, and all plasma samples were placed in the -80 ° C refrigerator. When the plasma sample was taken out, after the sample pre-treatment, the metabolic analysis of the high-performance liquid chromatography spectrophotographic system was used, and the secondary mass spectrum was compared to the standard database, and the compound has been obtained by related software to obtain a compound name. And the raw data of the peak area. The compounds in the original data were then matched by the inline metabolic analysis platform MetaboAnalyst, and the non-metabolite component was filtered, and all sample original metabolite content matrices were finally obtained.
[0036]Import the original metabolite content matrix into SIMCA-P software for different metabolites: Application of orthogonal matrix least squ...
Embodiment 2
[0044]Example 2 Screening of early diagnostic markers in cirrhosis populations.
[0045]Studies: This study included 28 cases of liver-hardened population plasma samples and blood samples of patients with primitive liver cancer, and all plasma samples were centrifuged in the -80 ° C refrigerator. When the plasma sample was taken out, after the sample pre-treatment, the metabolic analysis of the high-performance liquid chromatography spectrophotographic system was used, and the secondary mass spectrum was compared to the standard database, and the compound has been obtained by related software to obtain a compound name. And the raw data of the peak area. The compounds in the original data were then matched by the inline metabolic analysis platform MetaboAnalyst, and the non-metabolite component was filtered, and all sample original metabolite content matrices were finally obtained.
[0046]Import the original metabolite matrix into SIMCA-P software for different metabolites for differentia...
Embodiment 3
[0053]Embodiment 3, specifically, step S1 also includes the following steps:
[0054]S11, sample collection, use anti-coagulation tube to acquire target venous blood, acquire the supernatant as plasma sample by centrifugation. Specifically, 1 ml of hepatocheese, hepatitis, liver cancer patients were used, respectively, and gently reverse the collection tube, and the blood was mixed, and the low temperature was low-speed for 8 minutes (within 1 h after blood sample collection), take the supernatant As a plasma sample.
[0055]S12, the sample preoperative treatment, the sample obtained by step S11 is mixed with the experimental solvent and centrifuged, and the supernatant is obtained. Specifically, 60 μl of plasma was mixed with 300 to 350 μL of acetonitrile tweet 50s, and the protein was centrifuged at a centrifugal force 18800 g of the centrifugal force at 3 ° C. Take 140 μL of the supernatant freeze drying, and analyzed in positive spray ionization and negative electrospray ionization (E...
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