Application of aloe extract in preparation of medicine for preventing and treating porcine epidemic diarrhea
A porcine epidemic diarrhea and aloe vera extract technology, applied in the field of biotechnology applications, can solve the problems of cumbersome preparation steps, complex ingredients, single ingredients, etc., and achieve the effect of single and simple ingredients, wide range of raw materials, and no toxic and side effects
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Embodiment 1
[0034] Example 1 Aloe extract to Vero cytotoxicity test and the test of inhibiting the proliferation of PEDV in Vero cells
[0035] 1.1 Aloe Vera Extract (AE) To Vero Cytotoxicity Detection Test
[0036] Inoculate 6 × 10 in a 96-well plate 5 Cells / mL cell suspension (100 μL / well), leave a column without inoculating cells. At 37°C, 5% CO 2 cultured until the cells were fully confluent. The culture medium was sucked off, washed 3 times with PBS, the aloe extract was diluted with DMEM to different concentrations, added to a 96-well plate (100 μL / well), and each dilution concentration was replicated 8 times. At 37°C, 5% CO 2 After culturing for 24h and 48h under certain conditions, the drug solution was sucked off, washed 3 times with PBS, and 10% CCK-8 solution was prepared in DMEM and added to a 96-well plate (100 μL / well). 2 Incubate for 1 h under the conditions, measure the absorbance (λ=450nm) with a microplate reader, and calculate the cell viability after 24 h and 48 h...
Embodiment 2
[0069] Example 2 Aloe extract to IPEC-J2 cytotoxicity test and the test of inhibiting the proliferation of PEDV in IPEC-J2 cells
[0070] 2.1 Aloe extract (AE) to IPEC-J2 cytotoxicity detection test
[0071] Inoculate 6 × 10 in a 96-well plate 5 Cells / mL cell suspension (100 μL / well), leave a column without inoculating cells. At 37°C, 5% CO 2 cultured until the cells were fully confluent. The culture medium was aspirated, washed 3 times with PBS, and the drug to be tested (aloe extract (AE)) was diluted with DMEM to different concentrations, added to a 96-well plate (100 μL / well), and each dilution concentration was replicated 8 times. After culturing at 37°C and 5% CO2 for 24h and 48h, the drug solution was sucked off, washed 3 times with PBS, and 10% CCK-8 solution was prepared in DMEM and added to a 96-well plate (100 μL / well). CO 2 Incubate for 1 h under the conditions, measure the absorbance (λ=450nm) with a microplate reader, and calculate the cell viability after 2...
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