Method for inducing reverse Malangoni flow based on photo-thermal and method for delivering drug cluster cells
A photothermal induction, cell technology, applied in animal cells, vertebrate cells, tumors/cancer cells, etc., can solve the problems of inactivation, thermal damage, photodamage of biological samples, etc., and achieve the effect of avoiding damage
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[0039]The preparation method of the drug-loaded particles of the present invention preferably includes using 1 μm mesoporous silica particles to modify carboxyl groups and load the drug. The drug loaded by the drug-loaded particles of the present invention is preferably determined for the type of the cell, and when the cell is a blood cancer cell or a HeLa cell, the drug includes doxorubicin hydrochloride (DOX). In the present invention, the concentration of the drug-loaded particles is preferably 0.001 mg / ml, and the 1 μm mesoporous silica nanoparticles and DOX are preferably purchased from Xi'an Ruixi Biotechnology Co., Ltd. The method of drug loading is not particularly limited in the present invention, but preferably includes 1 ml of porous silicon spheres modified with carboxyl groups, adding 1 ml of doxorubicin hydrochloride with a concentration of 5 ng / ml, wrapping with tin foil, and placing on a shaker at room temperature for 24 hours. The drug loading method was carri...
Embodiment 1
[0043] Step 1: Preparation of droplets surrounded by silicone oil
[0044] First, drop a small amount of silicone oil (viscosity 5) on the glass substrate placed horizontally, and the silicone oil spreads rapidly on the glass surface to form an oil film with a thickness of about 5 μm. A small amount (5 μL) of aqueous solution was added dropwise to the center of the oil film. Due to the high density of the water droplets, the silicone oil was gradually discharged under the action of gravity. After the water droplet touches the glass surface, it quickly spreads on the glass surface due to the formation of a three-phase contact line. figure 1 Droplets surrounded by silicone oil are shown.
[0045] Step 2: Culture of blood cancer cells and staining of cells with live and dead dyes
[0046] Blood cancer cells were cultured in RPMIMedium 1640 basic (1X) medium supplemented with 10% fetal bovine serum (FBS) and 1% penicillin / streptomycin (Pen / strem), and placed at 37°C in 5 %CO 2...
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