Hydrogel embedded with chloroquine drugs as well as preparation method and application of hydrogel
A hydrogel and chloroquine technology, applied in the field of hydrogel embedded with chloroquine drugs and its preparation, can solve the problems of low efficiency, serious time-consuming, complicated loading process, etc., and achieve high yield and rapid response , reproducible effect
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Embodiment 1~3
[0045] Prepare a pure milk sample with a hydroxychloroquine concentration of 6 / 8 / 10 (mg / mL) (the dry matter in the milk is about 30 mg / mL, the same below), homogenize at a homogenization speed of 5000 r / min, and control the constant temperature Treat at 40°C for 10 minutes, cool to room temperature and then centrifuge, centrifugation conditions: 500 r / min, 10min. After the centrifugation was completed, the sample supernatant was carefully removed, and the precipitate was placed in a -80°C refrigerator and monitored in real time with a thermometer until the temperature dropped rapidly to 4°C and kept at a constant temperature for 30 minutes to obtain the prepared hydrogel.
Embodiment 4
[0052] Take 100 mL of pure milk, add 1g of hydroxychloroquine, put it in a 250mL beaker for homogenization, respectively carry out homogenization at a homogenization speed of 5000r / min, treat at a controlled constant temperature of 40°C for 10 minutes, cool to room temperature and use Nano- ZS dynamic light scattering instrument was used for characterization and then centrifuged. Centrifugal conditions: 500 r / min, 10min. After the centrifugation was completed, the supernatant of the sample was carefully removed, and the precipitate was placed in a -80°C refrigerator and monitored in real time with a thermometer until the temperature dropped rapidly to 4°C and kept at a constant temperature for 30 minutes to obtain the required milk hydrogel loaded with hydroxychloroquine.
Embodiment 5~7
[0059] Draw 100 mL of pure milk, add 1 g of hydroxychloroquine and place it in a 250 mL beaker for homogenization. Select the optimal rotation speed of 5000r / min, and then conduct centrifugation after treatment in a water bath at 40°C for 10 minutes. Centrifugation conditions: 500g, 10min. After the centrifugation was completed, the sample supernatant was carefully sucked off, and the watery precipitate was quickly placed in a -20°C refrigerator and monitored in real time with a thermometer until the temperature dropped rapidly to 4, 10, and 25°C, then taken out, and then characterized by a scanning electron microscope after standing for 30 minutes. Scanning electron microscope results such as Figure 4 . Comparing the conditions of different rapid drop temperatures, it can be found that different rapid drop temperatures play a key role in the formation of hydrogels. A stable hydrogel structure cannot be formed at a temperature of 25°C. A basic hydrogel network structure was...
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