Human blood cerebrospinal fluid barrier model as well as preparation method and application thereof
A cerebrospinal fluid and barrier technology, which is applied in the field of human blood and cerebrospinal fluid barrier model and its preparation, can solve the problems of simple model structure, limited experimental research, and difficulty in reproducing the physiological function of BCSFB, and achieves high repeatability, good compatibility, and operation. simple effect
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[0038] According to a typical embodiment of the present invention, a method for preparing a human blood and cerebrospinal fluid barrier model is provided, the method comprising:
[0039]Step S1, preparing a microfluidic chip with a biocompatible material by an inversion method, and the microfluidic chip contains an upper channel and a lower channel arranged adjacently;
[0040] The biocompatible material includes polyethylene terephthalate PDMS prepolymer; or type I collagen, matrigel, GelMA, sodium alginate, fibrinogen, HAMA, HA-CA, silk fibroin, chitosan and at least one of gelatin.
[0041] The step S1 specifically includes:
[0042] Step S101, obtaining a male mold with an adjacent upper channel and a lower channel;
[0043] The length, width and height of the upper channel and the lower channel are respectively 9000-11000 μm, 800-1200 μm and 20-200 μm.
[0044] If the height of the channel is less than 20μm, the internal hydraulic impedance is too large, the sample loa...
Embodiment 1
[0066] Embodiment 1. A human blood and cerebrospinal fluid barrier model and its preparation method
[0067] (1) The microfluidic chip is fabricated by a standard soft lithography flip-molding method. First, a silicon master mold etched with a micro-channel structure is fabricated by soft lithography. Secondly, the upper and lower layers of the chip are fabricated by a reverse molding method using PDMS. Subsequently, the chip was thoroughly dusted with 3M tape, and a piece of porous polyethylene terephthalate (PET) film (film thickness 7 μm, pore diameter 0.4 μm, pore density 0.4 μm) was flatly placed between the upper and lower channels under a stereo microscope. 4×10 6 / cm 2 ), align the upper and lower channels, and use a clamp made of poly-methyl methacrylate (PMMA) for fixed assembly. Finally, fully sterilize the assembled chips for later use;
[0068] (2) The upper channel of the chip was coated with Matrigel 80 μg / mL, and the lower channel was coated with Laminin (...
Embodiment 2
[0071] In the embodiment of the present invention, the length of the chip channel is increased by 20000 μm, and other structures and steps are the same as those in Embodiment 1.
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