Liver organoid model-based drug hepatotoxicity evaluation method
An evaluation method and organoid technology, applied in the field of biomedicine, can solve the problems of limited practicability and long-term culture capacity, and achieve the effects of reducing the cost of new drug development, easy operation, and reducing labor costs.
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Embodiment 1
[0039] This embodiment provides a method for evaluating hepatotoxicity of chloroquine phosphate based on a liver organoid model, comprising the following steps:
[0040] 1. Establishment of mouse liver organoid model:
[0041] 1) Sample cleaning: the mouse liver tissue was washed several times with normal saline containing 1% double antibody, and the obvious fat tissue was removed.
[0042] 2) Sample cutting: Cut the tissue into small pieces of about 0.5mm^3.
[0043] 3) Tissue digestion: ①Disperse the sheared tissue in normal saline, centrifuge to remove the supernatant, add collagenase, dispase and DNaseI to the precipitate, shake and digest at 37°C for 30min, add 1% green chain double antibody The normal saline was used to stop the digestion, and the cell pellet was collected; ②Continue to add collagenase, dispase and DNaseI to the pellet, shake and digest at 37°C for 2 hours, add green chain normal saline containing 1% double antibody to stop the digestion, and let it sta...
Embodiment 2
[0052] This embodiment provides a method for evaluating the hepatotoxicity of mitoxantrone based on a liver organoid model, comprising the following steps:
[0053] 1. Establishment of mouse liver organoid model:
[0054] 1) Sample cleaning: the mouse liver tissue was washed several times with normal saline containing 1% double antibody, and the obvious fat tissue was removed.
[0055] 2) Sample cutting: Cut the tissue into small pieces of about 0.5mm^3.
[0056] 3) Tissue digestion: ①Disperse the sheared tissue in normal saline, centrifuge to remove the supernatant, add collagenase, dispase and DNaseI to the precipitate, shake and digest at 37°C for 30min, add 1% green chain double antibody The normal saline was used to stop the digestion, and the cell pellet was collected; ②Continue to add collagenase, dispase and DNaseI to the pellet, shake and digest at 37°C for 2 hours, add green chain normal saline containing 1% double antibody to stop the digestion, and let it stand P...
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