A kind of combined drug composition for anti-double hit lymphoma and application thereof
A composition and lymphoma technology, applied in the field of biomedicine, can solve the problems of lack of large-scale clinical research, low incidence, and little effect, etc., and achieve significant killing effect, inhibit growth, reduce tumor burden and infiltration degree
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Embodiment 1
[0050] Inhibitory Effect of Combined Pharmaceutical Composition on Proliferation of DHL Cell Line
[0051] Take 2×10 4 The DHL cell lines TMD8 and MCA in the logarithmic growth phase were inoculated in 96-well plates, and the control group (DMSO), different concentrations of Venetoclax groups (nm level), different concentrations of Chiauranib groups (μm level), and Venetoclax combined with Chiauranib groups were set up for 24 hours. After 48 hours, use the CCK8 kit to detect the proliferation of DHL cells in different experimental groups, and use compusyn software to make the combination index (CI) after the combination of the two drugs. CI less than 1 indicates synergy, and CI greater than 1 indicates antagonism , CI equal to 1 means that there is an additive effect, and the smaller the CI value, the stronger the synergistic effect of the two drugs on cytotoxicity. The result is as figure 1 (MCA 24h), figure 2 (TMD8 24h), image 3 (MCA48h) and Figure 4 As shown in (TMD...
Embodiment 2
[0058] Apoptosis-inducing effect of combined pharmaceutical composition on DHL cell line
[0059] Take 2×10 5 The DHL cell lines TMD8 and MCA in the logarithmic growth phase were inoculated in 24-well plates, and the control group (DMSO), different concentrations of venetoclax groups (nm level), different concentrations of Chiauranib groups (μm level), and venetoclax combined with Chiauranib groups were set up for 24 hours And 48h later, the apoptosis of DHL cells was detected by Annexin V / PI kit. The result is as Figure 5 (MCA 24h), Figure 6 (TMD8 24h), Figure 7 (MCA 48h) and Figure 8 As shown in (TMD8 48h), the histogram in the figure can be seen from the figure: the combined pharmaceutical composition involved in the present invention has an obvious effect of inducing DHL cell apoptosis, which is time- and concentration-dependent.
Embodiment 3
[0061] Verification from the animal level that the combined pharmaceutical composition has the effect of killing DHL in vivo
[0062] 1. Experimental method
[0063] 1) Construct a nude mouse tumor-bearing model using DHL cell lines
[0064] SPF-grade nude mice were purchased from Shanghai Slack, aged 4-6 weeks, half male and half male, and all operations on the mice were carried out in a sterile laminar flow room. Suspend the MCA cells in 0.2 mL medium containing 0.5% FBS (each 0.2 mL contains 5×10 6 cells), inoculated subcutaneously in the right forelimb of the mouse, until the tumor volume grew to 75-150mm 3 , the in vivo drug experiment can be started.
[0065] 2) In vivo experiment
[0066] Set up the control group (the reagent is normal saline), the Venetoclax group (20 μg / g / day), the Chiauranib group (40 μg / g / day), and the Venetoclax combined with Chiauranib group, and administer the drugs every day for two weeks, and monitor the mice every two days body weight and...
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