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Full liquid phase organ chip and preparation method thereof

An organ chip and liquid phase technology, applied in the field of biochip and its preparation, can solve the problems of complex system, inability to simulate dynamic changes of human tissue, difficulty in changing structure, etc., and achieve universality, convenient and fast detection, and mild preparation conditions Effect

Active Publication Date: 2020-01-14
SOUTHEAST UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

In addition, some tests, such as cell sequencing, need to take samples from the inside of the chip, so the organ chip needs to integrate sampling flow channels and interfaces, which makes the whole system very complicated, which greatly restricts the development of the organ chip
In addition, the current organ chip is difficult to change its structure after construction, which makes it unable to simulate the dynamic changes of human tissue, and in some cases cannot achieve bionic functions well.

Method used

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  • Full liquid phase organ chip and preparation method thereof
  • Full liquid phase organ chip and preparation method thereof
  • Full liquid phase organ chip and preparation method thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0034] In this example, the process of preparing the all-liquid-phase organ chip is as follows: figure 1 As shown, it specifically includes the following steps:

[0035] (1) Preparation of surface-modified double bond glass

[0036] Add 30 μL of 3-(methacryloyloxy)propyltrimethoxysilane solution to the overlapped gap between the two pretreated hydroxy glasses, so that the solution completely infiltrates the surface between the overlapped glass slides while ensuring that no bubbles are generated, and react for 1 hour , washed with water and ethanol for several times, and dried to obtain a glass slide with surface-modified double bonds;

[0037] The mass concentration of 3-(methacryloyloxy)propyltrimethoxysilane in the 3-(methacryloyloxy)propyltrimethoxysilane solution is 20 wt%, and the solvent is ethanol.

[0038] (2) Preparation of polymer layer porous membrane

[0039] Prepare the prepolymer mixture: the prepolymer mixture solution includes the following components by vol...

Embodiment 2

[0051] (1) Preparation of substrates with surface-modified double bonds

[0052] This step is basically the same as in Example 1, except that the mass concentration of 3-(methacryloyloxy)propyltrimethoxysilane in the 3-(methacryloyloxy)propyltrimethoxysilane solution is 10 wt%. The solvent is ethanol.

[0053] Wherein, the substrate is plastic, and the plastic substrate is pretreated with oxygen plasma to make it hydrophilic, and then the same steps as in Example 1 are used to modify the substrate.

[0054] (2) Preparation of polymer layer porous membrane

[0055] This step prepares polymer layer porous film and embodiment 1 is substantially the same, and difference is: wherein prepolymer mixture solution comprises 15vol% HEMA (monomer), 6vol% EDMA (crosslinking agent), 50vol% cyclohexanol ( Porogen), 29vol% n-decyl alcohol (porogen), and benzoin dimethyl ether (DMPA) as photoinitiator, the addition of photoinitiator accounted for the concentration of the mixture is 0.5mg / mL...

Embodiment 3

[0065] (1) Preparation of surface-modified double bond glass

[0066] This step is basically the same as Example 1, except that the mass concentration of 3-(methacryloyloxy)propyltrimethoxysilane in the 3-(methacryloyloxy)propyltrimethoxysilane solution is 25 wt%. The solvent is ethanol.

[0067] (2) Preparation of polymer layer porous membrane

[0068] This step prepares polymer layer porous membrane and embodiment 1 is substantially the same, and difference is: wherein prepolymer mixture solution comprises 16vol% HEMA (monomer), 4vol% EDMA (crosslinking agent), 40vol% cyclohexanol ( Porogen), 40vol% n-decyl alcohol (porogen), and with benzoin dimethyl ether (DMPA) as photoinitiator, the addition of photoinitiator accounted for the concentration of the mixture is 4mg / mL;

[0069] (3) Preparation of porous membrane with hydrophobic polymer layer

[0070] In a fume hood environment, respectively add 40 mL of dichloromethane (DCM), 80 μL of 4-pentynoic acid and 100 μL of N, N...

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Abstract

The invention discloses a full liquid phase organ chip and a preparation method thereof. The full liquid phase organ chip comprises a super hydrophobic porous membrane with a hydrophilic channel, theporous membrane is sealed in an oil phase, the hydrophilic channel is provided with a fluid inlet and a fluid outlet, and the fluid inlet and the fluid outlet communicate with the hydrophilic channel;the polymer layer porous membrane is placed in a functional modification solution to obtain a hydrophobic polymer layer porous membrane; hydrophilic patterns are treated on the hydrophobic polymer layer porous membrane; then, polymer surface superhydrophobic treatment is carried out on the surface of the porous membrane with the hydrophilic channel; and then the hydrophilic channel on the surfaceof the porous membrane is wetted and sealed in the oil phase, and an inlet and an outlet which communicate with the hydrophilic channel are formed. According to the full liquid phase organ chip and the preparation method thereof, the preparation conditions are mild, the whole liquid phase organ chip can be constructed by constructing cell patterned culture on a prepared substrate, and the in-situdetection and sampling of all micro environments in the organ chip can be realized, and the spatial editing of the function and geometric layout of a fluid device can be realized as required.

Description

technical field [0001] The invention relates to the field of biochips and preparation methods thereof, in particular to an all-liquid phase organ chip and a preparation method thereof. Background technique [0002] New drug research and development is a time-consuming and huge investment industry. At present, the average research and development cost of a new drug is about 1 billion US dollars, and it takes an average of 10 years, making the development of new drugs extremely difficult. At present, 90% of drugs that have passed cell experiments and animal experiments in drug screening will be rejected in the clinical testing stage. The main reason is that there are large differences between cell experiments and animal models and human models, so the development is closer to the human body Model drug testing platform is extremely important. In recent years, with the rapid development of biotechnology and information technology, organ-on-a-chip has become a distinctive and d...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C12M3/06C12M1/00C08F220/20C08F222/14C08J9/26
CPCC12M21/08C12M25/04C12M23/16C08F220/20C08J9/26
Inventor 顾忠泽杜鑫李玉雯
Owner SOUTHEAST UNIV
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