Preparation method of autophagy-imitated immune cell supported antitumor therapeutic agent
An immune cell and anti-tumor technology, which is applied in the field of preparation of immune cell-loaded anti-tumor therapeutic agents, can solve the problems of ineffective control of irregular release of materials, poor dispersion, and low phagocytosis, and achieve good drug slow-release behavior, The effect of improving load and good migration ability
Patent Information
- Authority / Receiving Office
- CN · China
- Current Assignee / Owner
- Publication Date
- 2018-11-16
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Abstract
Description
technical field
[0001] The invention belongs to the field of nanomedicine, and in particular relates to a preparation method of immune cells imitating autophagy loaded with an anti-tumor therapeutic agent. Background technique
[0002] Live cell drug delivery has broad application prospects in biomedical engineering, materials science, pharmacy and other fields. In the past few years, live cell delivery was mainly formed by co-incubation of living cells with drug-loaded nanoparticles or drugs. For example, Jinhyang Choi et al. used mouse macrophages to load contrast diagnostic agents; Wen-Chia Huang et al. used monocyte-macrophages to load nanoparticles loaded with chemotherapeutic drugs. This loading method produces more toxicity to cells on the one hand, and on the other hand, the loading amount is relatively low.
[0003] For a long time, anti-tumor therapeutic agents are generally encapsulated with polymer materials such as liposomes and polymer nanoparticles to reduce ...
Examples
Embodiment 1
[0027] A method for preparing an autophagy-imitating immune cell-loaded anti-tumor therapeutic agent, using the following steps:
[0028] (1) A certain number of macrophages were treated with Tris-MgCl 2 The buffer was frozen and thawed several times, passed through a mini-extruder (40nm-100nm), added 0.5-1M Sucrose (final concentration 0.125-0.25M), centrifuged (800-2000g, 5-15min), took the upper layer, and centrifuged again (2000-3000g , 30~40min), remove the lower layer, and add Tris~MgCl 2 buffer (containing 0.125 ~ 0.25M sucrose) wash, and then twice H 2 O washed, collected and freeze-dried.
[0029] (2) Weigh 3-4 mg of cell membrane fragments from the freeze-dried sample in step (1) and dissolve them in PBS (1X); take 8-10 mg of Ce6, add them to the cell membrane suspension, and ultrasonically pulverize (the control power is 80-150 W, each time ultrasonic 5-10s, the total duration of ultrasound is 5-10min). After the sonication is over, take out the solution at room...