Urine exosome extraction reagent tube and manufacturing method thereof

A production method and exosome technology, which can be applied in sterilization methods, biochemical equipment and methods, biological material sampling methods, etc., and can solve problems such as easy clogging of color columns, low exosome extraction efficiency, lipoprotein pollution, etc. problems, to achieve the effect of increasing extraction efficiency, preventing contamination, and increasing contact area

Pending Publication Date: 2022-02-22
THE SECOND XIANGYA HOSPITAL OF CENT SOUTH UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

[0005] Existing exosome techniques are time-consuming (ranging from 40min to 10 hours), and there are different degrees of contamination of extraction reagents (such as residues of precipitation reagents in the PEG precipitation method, such as residues of high-salt reagents in the column-passing method, such as magnetic In the bead adsorption method, the pollution of the magnetic bead anchor chain antibody, the pollution of the eluent EDTA), although the positive char

Method used

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  • Urine exosome extraction reagent tube and manufacturing method thereof
  • Urine exosome extraction reagent tube and manufacturing method thereof
  • Urine exosome extraction reagent tube and manufacturing method thereof

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Embodiment 1

[0030] like Figure 1-4 As shown, the present invention provides a urine exosome extraction reagent tube, comprising a cap 1, an outer tube 2 and an inner tube 3, the top surface of the outer tube 2 is threaded with the cap 1, and the inside of the outer tube 2 is sleeved with The inner tube 3, the inner wall of the inner tube 3 is provided with a nanofiber membrane 4.

[0031] Both the outer walls of the outer tube 2 and the inner tube 3 are provided with capacity scale lines, and both the outer tube 2 and the inner tube 3 are made of polycarbonate material.

[0032] The manufacturing method of the urine exosome extraction reagent tube, the manufacturing steps are as follows:

[0033] A: Dissolve PLLA with a molecular weight of 90,000 and chitosan in a ratio of 5:1 in trifluoroethanol solution to prepare a mixed solution with a concentration of 8wt%, and fully dissolve PLLA and shell at room temperature of 25-30°C polysaccharide mixture;

[0034] B: Use a 27g needle to pus...

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Abstract

The invention discloses a urine exosome extraction reagent tube and a manufacturing method, the urine exosome extraction reagent tube comprises a cap, an outer tube and an inner tube, the top end surface of the outer tube is sleeved with the cap through threads, the inner tube is sleeved with the outer tube, and the inner wall of the inner tube is provided with a nanofiber membrane. The whole reaction can be completed in a short time, and long-time waiting is not needed; by utilizing a positive and negative charge attraction principle, not only is the pollution of a separation reagent avoided, but also non-charged lipoprotein with the particle size of 50-200nm in the urine can be removed; the pore size of the positive charge porous nanofiber membrane is about 50-200nm, so that the high-purity exosome with the particle size of 50-200nm can be obtained, and the pollution of microvesicles with other particle sizes can be prevented; and the porous structure on the positive charge porous nanofiber membrane greatly increases the contact area between the membrane and a sample, and increases the extraction efficiency of the urine exosome.

Description

technical field [0001] The invention relates to the technical field of exosome extraction, in particular to a urine exosome extraction reagent tube and a production method. Background technique [0002] Exosomes were first seen in 1981. EG Trams et al. found small vesicles with a membrane structure in the supernatant of sheep erythrocytes cultured in vitro, and named them exosomes. For the role of exosomes, it was speculated that it was a way for cells to excrete waste. In 1996, GRaposo et al. found that immune cells similar to B lymphocytes also secreted antigen presenting vesicles, and the secreted exosomes could directly stimulate the anti-tumor response of effector CD4+ cells. In 2007, HValadi et al. further discovered that cells can exchange genetic material through RNA in exosomes. With more and more studies on exosomes, researchers have found that they are widely involved in various biological processes such as the body's immune response, antigen presentation, cell ...

Claims

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Application Information

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IPC IPC(8): C12M1/24C12M1/12C12M1/00D01F8/14D01F8/18D06M15/285D06M10/00D06M10/10D06M101/32D06M101/02
CPCC12M23/06C12M33/14C12M33/10C12M47/04D01F8/14D01F8/18D06M15/285D06M10/001D06M10/10D06M2101/32D06M2101/02
Inventor 沈宏伟易路
Owner THE SECOND XIANGYA HOSPITAL OF CENT SOUTH UNIV
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