Stem-cell biological preparation, and preparation method and application thereof
A technology of biological preparations and stem cells, applied in the field of biomedicine, can solve problems such as unsatisfactory treatment effects, achieve the effects of promoting tissue regeneration, improving liver damage, and good therapeutic effects
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[0060] The invention provides a method for preparing a stem cell biological preparation, comprising the following steps:
[0061] a) Liver stem cells, peripheral blood stem cells, albumin and a solvent are mixed to obtain a stem cell biological preparation.
[0062] In the preparation method provided by the present invention, stem cell biological preparations can be obtained by directly mixing hepatic stem cells, peripheral blood stem cells, albumin and a solvent, and the process is specifically as follows:
[0063] a1), mixing albumin with a solvent to obtain an albumin solution;
[0064]a2), liver stem cells, peripheral blood stem cells and the albumin solution are mixed to obtain a stem cell biological preparation.
[0065] In the above preparation method provided by the present invention, albumin and a solvent are first mixed to obtain an albumin solution. Wherein, the solvent is preferably physiological saline.
[0066] After the albumin solution is prepared, the album...
Embodiment 1
[0088] Obtain liver stem cells
[0089] The liver tissue was washed several times with PBS, chopped and digested with trypsin solution (trypsin content: 0.25g / 100mL), overnight at 4°C, and taken out the next day at 37°C for 5-10 minutes of further digestion. After digestion, suck out the cell suspension, add type II collagenase solution (type II collagenase content is 0.25g / 100mL) to the remaining tissue, mix well, seal, and digest at 37°C for 10min. The digested tissue was filtered with a 200-mesh sieve, and the filtered cell suspension was centrifuged at 270 g for 5 min. After centrifugation, discard the upper liquid, and wash the lower cell pellet with PBS twice.
[0090] Use the DMEM high-glucose medium (Gibco company, lot number 12100046.) containing 15% (volume percent concentration) FBS to resuspend the cell pellet obtained above, with 1 × 10 6 cells / mL were inoculated into culture flasks. Gently shake the culture flask back and forth to distribute the cell suspensio...
Embodiment 2
[0094] Obtain peripheral blood stem cells
[0095] 1) Separation of peripheral blood mononuclear cells:
[0096] Peripheral blood and normal saline were mixed at a volume ratio of 1:1, and the mixed solution was pipetted, and then centrifuged with Ficoll separation solution (Fresenius Company, batch number: 12BS15) with a density of 1.073 g / mL. The centrifugal force of separation is 700g, and the time of centrifugal separation is 20min. After centrifugation, the buffy coat cells in the middle of the centrifugation product were taken, which were peripheral blood mononuclear cells (MNCs).
[0097] 2) Culture and expansion of peripheral blood stem cells:
[0098] After the peripheral blood mononuclear cells obtained above were counted, they were mixed with DMEM high-glucose medium (Gibco company, batch number: 12100046) containing 10% (volume percentage) FBS to obtain a cell density of 3 × 10 5 cells / mL of cell suspension, inoculate 10 mL of cell suspension into a 10 cm plate,...
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