Method for detecting activation of microencapsulated cells
A technology of cell activity and detection method, which is applied in the detection field of characterizing the activity of microencapsulated cells by energy charge calculation, can solve the problems of inapplicability, the detection result is lower than the actual value, and the stability of adenylate is affected, and the detection method can be achieved. Stable and reliable results
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Embodiment 1
[0020] A detection method for characterizing the activity of microencapsulated cells by energy charge
[0021] 1) Sample preparation:
[0022] A: Lysis solution: 50mM HEPES, (PH7.4), 50mAU / ml proteinase k, preheated in a 50°C water bath.
[0023] B: collect APA microencapsulated cultured Hepg2 cells, filter out the culture medium, wash with pre-cooled PBS until the wash solution is colorless, and then filter and dry the liquid. A 1ml syringe was ground to aspirate to break the capsule. After microcapsule membranes were completely damaged under the microscope, add preheated lysate, incubate in a 50°C water bath for 30 minutes, and shake at intervals of 5 minutes. Transfer the reaction system to an 80°C water bath to continue the reaction for 15 minutes, and collect the supernatant by filtration;
[0024] 2) Separation and quantification of adenylic acid:
[0025] The content of adenylic acid in the extracted samples was separated by high performance liquid chromatography. ...
Embodiment 2
[0028] A detection method for characterizing the activity of microencapsulated cells by energy charge
[0029] 1) Sample preparation:
[0030] A: Lysis solution: 50mM HEPES, (PH7.4), 50mAU / ml proteinase k, preheated in a 50°C water bath.
[0031] B: collect monomethoxypolyethylene glycol polylactic acid (PELA) microencapsulated cultured microbial cells S.cerevisiae, filter out the culture medium, wash with pre-cooled PBS until the washing liquid is colorless, filter the liquid and add the preheated lysate, Incubate in a water bath at 50°C for 30 minutes, shaking at intervals of 5 minutes. Transfer the reaction system to an 80°C water bath to continue the reaction for 15 minutes, and collect the supernatant by filtration;
[0032] 2) Separation and quantification of adenylic acid:
[0033] The content of adenylic acid in the extracted samples was separated by high performance liquid chromatography. Determination conditions are UV detector, wavelength 260nm, C18 reverse phas...
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