Device and method for preparing and collecting lipidosome
A collection device and liposome technology, applied in chemical instruments and methods, laboratory utensils, laboratory containers, etc., can solve problems such as increased difficulty, complicated operation, and increased investment, so as to improve separation efficiency and collection Efficiency, improve preparation efficiency, reduce the effect of intermediate process
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Embodiment 1
[0035] The liposome preparation and collection device of the present embodiment such as figure 1 , image 3 , Figure 3A , Figure 4 , Figure 4A , Figure 5 , Figure 5A , Image 6 , Figure 6A , Figure 7 with Figure 7A As shown, the device includes: a signal generator 1 for sending electrical signals, and a chip 2 for preparing and collecting liposomes. In this embodiment, the signal generator and the chip for preparing and collecting liposomes are connected by conductive tape 6 . A preparation chamber 3 , a collection chamber 4 , and a waste liquid chamber 5 are made in the chip 2 for preparing and collecting liposomes. The chip 2 is composed of a base plane and a wall material layer thereon, and the wall material layer is further divided into upper and lower layers.
[0036] The preparation chamber 3 includes a base electrode 7 and an upper layer electrode 10. The middle preparation chamber 8 is between the electrodes. The electrodes are connected to the signal...
Embodiment 2
[0042] The liposome preparation and collection device of the present embodiment such as figure 1 shown.
[0043] Mix and dissolve lecithin and cholesterol in ether solvent at a mass ratio of 5:1, add fluorescent dye DiI (1,1'-dioctadecyl-3,3,3',3'-tetramethylindocarbocyanine perchlorate) to stain the organic phase Treatment, then, the organic phase is added dropwise on the base electrode 7 of the preparation chamber, then, nitrogen is blown for 5 minutes to allow the ether to evaporate, and then the chip 2 for preparing and collecting liposomes is placed in a vacuum environment for 2 hours, and the ether is allowed to evaporate. Complete evaporation, after forming a dry lipid film on the base electrode, add a solution containing 200mM glucose and 20mM Nacl to the preparation chamber of the preparation chamber 3, and then connect the signal generator 1 and the upper layer electrode 10, the base electrode through the conductive tape 6 7. Apply an electrical signal to the prepar...
Embodiment 3
[0046] The structure of the liposome preparation and collection device used in this embodiment is as follows: figure 2 As shown, its basic structure is the same as that of Example 1, except that there are four collection chambers 4 and four waste liquid chambers 5, which are connected one to one to collect giant liposomes of different particle sizes.
[0047] Mix and dissolve lecithin and cholesterol in ether solvent at a mass ratio of 5:1, add fluorescent dye DiI (1,1'-dioctadecyl-3,3,3',3'-tetramethylindocarbocyanine perchlorate) to stain the organic phase Treatment, then, the organic phase is added dropwise on the base electrode 7 of the preparation chamber, then, nitrogen is blown for 5 minutes to allow the ether to evaporate, and then the chip 2 for preparing and collecting liposomes is placed in a vacuum environment for 2 hours, and the ether is allowed to evaporate. After complete evaporation and a dry lipid film formed on the base electrode, a solution containing micr...
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