Tumor cell nanogold vesicle and preparation method and application thereof, and tumor cell immune nanogold vesicle and preparation method and application thereof
A tumor cell and nano-gold technology, applied in the field of anti-tumor drugs and carriers, can solve the problems of potential safety hazards, weak killing effect, inability to effectively inhibit tumor metastasis and recurrence, etc., and achieve inhibition of recurrence, low toxicity and side effects in the body, and elimination of invasion sexual effect
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Embodiment 1
[0038] Example 1: Preparation of tumor cell nano-gold vesicles
[0039]The specific synthesis steps are as follows: add chloroauric acid solution (0.5mM) to the B16F10 cells grown to 80% and starve and mix evenly, place at 37 ° C, 5% CO 2 Cultivate in a culture environment for 4 days, then suck out the supernatant, centrifuge at 600g for 10 minutes to remove cell debris, repeat twice, collect the supernatant at 10,000g, centrifuge for 30 minutes to collect and purify the gold nanovesicles, and centrifuge the supernatant twice The second time, the collected pellets were combined and resuspended, washed with 1 ml of phosphate buffer at 600 g and centrifuged at a low speed for 10 minutes, and the supernatant was the tumor cell gold nanovesicles.
[0040] The shape of nanoparticles was observed by optical microscope and transmission electron microscope. It can be seen that the gold nanovesicles exocytized by tumor cells are purple-red. figure 1 The gold nanovesicles showing exocy...
Embodiment 2
[0043] Embodiment 2: Preparation of nano gold vesicles with immune function
[0044] The specific operation steps for the preparation of nano-gold vesicles are as follows: add 20 micrograms of tumor cell gold nano-vesicles prepared in Example 1 to the blank medium of dendritic cells DC2.4 grown to 80%, incubate for 6 hours and then replace For a new blank medium, irradiate under 8W UV light for 1 hour, then incubate at 37°C, 5% CO 2 Continue to culture in the environment. After 24 hours, collect the supernatant, 600g, 10 minutes of low-speed centrifugation to remove cell debris, repeat twice, and then 13000g of supernatant, 30 minutes of high-speed centrifugation to collect purified gold nanovesicles, supernatant repeated centrifugation Twice, the combined precipitates were resuspended in 250 microliters of phosphate buffer, washed by centrifugation at 600g for 10 minutes to obtain gold nanovesicles with immune function after being treated by immune cells.
[0045] Through th...
Embodiment 3
[0049] Example 3: Study on the in vitro photothermal conversion effect of nano-gold vesicles
[0050] In order to investigate the light-to-heat conversion ability of immune gold nanovesicles, we conducted a light-heating experiment on gold nanovesicles with an Au concentration of 100ug / mL. The specific steps are: set the power to 2W / cm 2 The near-infrared light (NIR) directly irradiates the nano-gold vesicle solution, and an infrared camera is used to monitor the temperature change of the solution within 3 minutes. The results are shown in Figure 8, which shows that the nano-gold vesicles have good light-to-heat conversion ability. Figure 8(A) is the infrared photo of the photothermal conversion of the immune nano-gold vesicles; Figure 8(B) is the corresponding temperature rise curve of the immune nano-gold vesicles. The thermal killing temperature can realize the killing effect of light and heat on tumor cells.
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