A living cell drug delivery system based on macrophages, its preparation method and application
A technology of macrophages and drug-carrying systems, which is applied in the direction of cell culture active agents, biochemical equipment and methods, and pharmaceutical formulations. The effect of maintaining stability and maintaining activity
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preparation Embodiment 1
[0052] In this example, a living cell drug delivery system based on M2 macrophages was obtained by inducing reassembly of macrophages in vitro. Specifically, the preparation method of the living cell drug delivery system based on M2 type macrophages comprises the following steps:
[0053] (1) Synthesis of dimyristoylphosphatidylethanolamine-pegylated maytansine-4 and dimyristoylphosphatidylethanolamine-pegylated bee venom polypeptide propeptide
[0054] 1) Synthesis of Disulfide-Linked Dimyristoyl Phosphatidylethanolamine-PEGylated Maytansine-4
[0055] Disulfide-linked dimyristoylphosphatidylethanolamine-PEGylated maytansine-4 was synthesized in two steps: ① 3-(2-pyridyldimercapto)propionic acid N-hydroxysuccinimidyl ester-maytansine For the synthetic route of prime-4, see figure 2 (A). The specific steps are as follows: weigh maytansine-4 (19.5 mg, 0.025 mmol, purchased from Suzhou Borui Biological Co., Ltd.) and dissolve it in 1 mL of methanol solution, weigh 3-(2-pyrid...
preparation Embodiment 2
[0084] In this example, a living cell drug delivery system based on M1 macrophages was obtained by inducing macrophages in vitro. Specifically, the preparation method of the living cell drug delivery system based on M1 type macrophages includes the following steps: (1) Separation and purification of mouse bone marrow-derived macrophages
[0085] 1) Take mouse bone marrow cells (Balb / c-nu nude mice (purchased from Shanghai Experimental Animal Center, Chinese Academy of Sciences)), and culture them in RPMI 1640 (Gibco) medium containing 10% fetal bovine serum (Gibco). Add recombinant mouse macrophage colony-stimulating factor (M-CSF, purchased from Sigma, with a final concentration of 20ng / mL) and LPS (20ng / mL) in the culture medium, and place on a low-adhesion plate (purchased from Corning ), 37°C, 5% CO 2 After culturing for 5 days, adherent cells were obtained.
[0086] 2) Replace the medium of M1 macrophages, and add dimyristoylphosphatidylethanolamine (DMPE)-pegylated may...
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