Application of puerarin hydrogel in drug for treating myocardial infarction
A technology of myocardial infarction and puerarin, applied in the field of puerarin small-molecule hydrogel, can solve problems such as insufficient retention, cell survival, and insufficient number of myocardial cells, and achieve the effect of promoting effect, promoting repair, and good anti-peroxidation effect
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Embodiment 1
[0033] Embodiment 1: the preparation of puerarin hydrogel
[0034] Weigh puerarin, add PBS (phosphate buffered saline), so that the concentration of puerarin in PBS is 2%wt, 4%wt, 6%wt, and heat it to 80°C-100°C with an alcohol lamp to completely dissolve the puerarin After naturally cooling to room temperature for 5 minutes, a jelly-like puerarin hydrogel can be formed.
Embodiment 2
[0035] Example 2: Effects of Puerarin Hydrogel on the Survival and Proliferation of Cardiomyocytes and Cardiac Fibroblasts
[0036] 1) Put puerarin hydrogels of different concentrations (2%, 4% and 6%) in a 96-well plate, add cells to the wells, and set the cell density to 5×10 4 / ml, no hydrogel was used as the control group, and different concentrations of puerarin hydrogels without cells were used as blank wells;
[0037] 2) When the measurement time comes, use a pipette to suck out the original medium, wash it twice with PBS, and add 10 μl of the solution in the CCK-8 kit to each well with a pipette gun;
[0038] 3) Place the 96-well plate in a 37°C, 5% carbon dioxide incubator and incubate for 4 hours;
[0039] 4) Take out the 96-well plate from the incubator, place it on a horizontal shaker, and shake it slowly for 10 minutes;
[0040] 5) Use a microplate reader to set the wavelength to 450 nm for absorbance measurement.
[0041] For experimental results, see figur...
Embodiment 3
[0042] Embodiment 3: Puerarin hydrogel to H 2 o 2 Influence of SOD activity and MDA content in induced MSCs cells
[0043] In this experiment, H 2 o 2 As an exogenous ROS mimicking the peroxidative environment after myocardial infarction in vivo, H 2 o 2 The concentration is 100μmol / L, intervene for 1h; experimental group: normal MSCs culture group, H 2 o 2 Intervention group, H 2 o 2 +2%PG (puerarin hydrogel) group, H 2 o 2+4% PG group, H 2 o 2 +6%PG group; intracellular superoxide dismutase (SOD) activity and intracellular malondialdehyde (MDA) content were detected according to the detection instructions.
[0044] For experimental results, see figure 2 , compared with the normal group, H 2 o 2 After induction for 1 h, the SOD activity and MDA content of MSCs were significantly increased (p2 o 2 The level of oxidative stress caused by H 2 o 2 Compared with two groups, 2%, 4% and 6% puerarin hydrogels could significantly reduce intracellular SOD activity...
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