Immune nanometer cellulose magnetic liposome and preparation method thereof
A nanocellulose and magnetic liposome technology, applied in the field of biological nanomagnetic materials, can solve the problems of reducing antibody activity, high temperature, and difficulty in maintaining activity, and achieve the effect of good biocompatibility
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Embodiment 1
[0025] Example 1 Preparation of immune nano-cellulose magnetic liposomes using antibody precursors
[0026] (1) Put 5.0mg DSPE-PEG-NH 2 Mix with 1.0 mg of anti-EpCAM monoclonal antibody, and add 5.0 mL of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDC.HCL) at a concentration of 1.0 mg / mL In the middle of the reaction for 24 hours, the 8000-10000 molecular weight dialysis bag is dialyzed to remove the unreacted condensing agent; the antibody precursor DSPE-PEG-EpCAM is obtained after lyophilization.
[0027] (2) Prepare immune nano-cellulose magnetic liposomes by film dispersion method. Mix 10.0 mg of lecithin, 6.0 mg of cholesterol, 2.0 mg of carboxymethyl chitosan stearyl quaternary ammonium salt and 3.0 mg of oil-soluble magnetic nanoparticles in 10.0 mL of oil phase chloroform, incubate for more than 20 minutes, and put In the eggplant-shaped bottle, the lipid film is formed by rotary evaporation;
[0028] (3) Mix the formed lipid membrane with an aqueous solu...
Embodiment 2
[0029] Example 2 Preparation of Nano-cellulose Magnetic Liposome
[0030] Add lecithin 5.0mg, cholesterol 2.0mg, DSPE-PEG-NH 2 1.0 mg and 1.0 mg of oil-soluble magnetic nanoparticles were dissolved in dichloromethane; mixed as an organic phase, removed the organic solvent to form a film, and then added octadecyl quaternary ammonium salt containing carboxymethyl chitosan (concentration 0.3 mg / mL) and 5.0 mL of carboxymethyl cellulose (nanocellulose concentration 0.5 mg / mL) to hydrate the lipid membrane. The aqueous phase is 0.9% saline or a buffer solution with pH=5 to 9, Ultrasound for more than 30 minutes during hydration, and then magnetically separate more than 3 times for use.
Embodiment 3
[0031] Example 3 Preparation of immunological nano-cellulose magnetic liposomes
[0032] Take the 20% solid content and 50~100nm particle size of the aminoated nanocellulose magnetic liposome (lecithin / cholesterol / nanocellulose / DSPE-PEG-NH 2 ) Mix 1.0 mL of the solution with 1 mL of the solution containing 2.0 mg of anti-human epidermal growth factor receptor 2 (HER2) monoclonal antibody, and add 5 mg of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide The hydrochloride salt, mixed uniformly, stirred at room temperature for 48 hours, after magnetic separation and washing, the weight percentage of the magnetic beads and the monoclonal antibody contained in the prepared immunomagnetic liposome is 25:1, which can be placed in Store in a mixed solution of water and ethanol (20% by weight of ethanol). This embodiment can be extended to amino or carboxylated magnetic beads with a solid content of 0.5%-30%.
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