Preparation and application of a nano-immune preparation based on porous calcium carbonate
A technology of porous calcium carbonate and immune preparations, which can be applied to medical preparations without active ingredients, medical preparations containing active ingredients, and active ingredients of aluminum/calcium/magnesium, etc. Failure, limited immune response, etc., to achieve high immune activation efficiency, eliminate small lesions, and improve the efficiency of immunotherapy
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Embodiment 1
[0030] Example 1 is based on the preparation of porous calcium carbonate nano-formulations
[0031] (1) Synthesis of porous CaCO by gas diffusion reaction 3 Nanoparticles: 220 mg CaCl 2 · H 2 O and 8 g NH 4 HCO 3 CaCO obtained after simultaneously placing in a vacuum drying chamber at a control temperature of 25 ° C and keeping the entire system in a vacuum environment for 24 hours 3 The nanoparticles are separated by centrifugation at 12,000 rpm. CaCO will then be in absolute ethanol 3 The hole is loaded with IDOi to get CaCO 3 @IDOi (abbreviated as CaI).
[0032] (2) Modify the above nanoparticles with liposomes. First, an ethanol solution of 20 mg of CaI is mixed with 2 mg of DOPA. DPC, cholesterol and DSPE-PEG are then added to the above solution in a 4:4:2M ratio, the solvent is dried with a rotary evaporator, and the resulting nanoparticles are dissolved in an aqueous solution for further use. The obtained nanoparticles are then stirred with 200 mg PEI to prepare CaCO 3 @IDO...
Embodiment 2
[0036] Example 2 mouse molding experiment
[0037] 2.1 In vivo testing
[0038]Female Balb / c mice were selected as the research object, and a tumor-bearing mouse model was prepared by subcutaneous injection of mouse breast cancer cells, and the tumor was grown to 50 mm 3 Start the administration. The dosing groups were CaIPC (experimental group), LIPC, and normal saline. Tumor-bearing mice are administered intravenously, and tumor volume and weighing are measured every other day during the experimental cycle. The experimental results show that the CaIPC-treated mouse tumor growth rate in Example 1 is the slowest, indicating that the present invention can effectively inhibit tumor growth in a mouse model. Conversely, compared with the saline group, the LIPC group showed not very good tumor suppression effect, the results show that only the group treated with the present invention showed the optimal tumor treatment effect. Body weight is an important parameter to assess the systemic...
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