IL-6 in brain-derived small vesicles (NDSEV) as marker for diagnosing and/or treating subarachnoid hemorrhage
A subarachnoid space, IL-6 technology, applied in the field of markers for diagnosis and/or treatment of subarachnoid hemorrhage, can solve problems such as potential ideal biomarkers for the process of pathological changes in patients with SAH that are not found.
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Embodiment 1
[0030] Example 1, IL-6NDSEV extraction and identification
[0031] 1. Ethics: All patients came from the Neurosurgery Department of the First Affiliated Hospital of Wannan Medical College, and were conducted in accordance with the Declaration of Helsinki. Before inclusion in the study, patients or guardians signed an informed consent. The experiment was approved by the Hospital Ethics Committee.
[0032] 2. Experimental design: In this study, aSAH patients admitted from May 2016 to March 2017 were included. Within 24 hours after the onset of SAH, 117 plasma samples were collected from a total of 224 SAH patients. The mean age standard deviation was 59.91±9.65 years (40-83 years); there were 72 females and 45 males. Exclusion criteria: admission after 72 hours after hemorrhage; non-aneurysmal SAH; patients with liver, kidney, heart or pulmonary insufficiency or infectious diseases; poor prognosis on admission, without any intervention. And age-matched healthy people in fast...
Embodiment 2
[0050] Example 2, IL-6NDSEV as a marker for diagnosis and / or treatment of subarachnoid hemorrhage
[0051] 1. ELISA test, using a specific ELISA kit to detect IL-6 (E-EL-H0102c, Elabscience, Wuhan Yilairite Biotechnology Co., Ltd.) and exosome marker CD81 (CSB-EL004960HU, Cusabio, Wuhan Huamei Bioengineering Co., Ltd.) concentration was quantified. Steps: ① Prepare the standard solution according to the instructions, and then add it to the first two rows of wells, and perform repeated quality control, with two wells for each concentration. Both standard solution and sample solution are 100 μl per well, cover the 96-well plate, and incubate at 37°C for 90 minutes. ② Pour off and dry the liquid in the plate, add 100 μl of biotin-labeled antibody to each well, mix by pipetting, then cover the 96-well plate, and incubate at 37°C for 30 minutes. ③ Shake off the liquid in the plate, add 350 μl of washing solution each, rinse for 2 minutes, pour out and dry the liquid in the plate....
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