A lipid droplet induction and imaging reagent and its preparation method and application
A technology of reagents and lipid droplets, which is applied in the field of lipid droplet induction and imaging reagents and its preparation, can solve the problems of poor safety, poor water solubility, and inability to specifically trace lipid droplets, and achieve good cytocompatibility, Low toxicity and good water dispersibility
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Embodiment 1
[0034] (1) Weigh 10mg of diblasonic acid phosphatide (DOPS, structural formula) figure 2 ) And dissolved in 0.5 ml of chloroform, and the nitrogen was blown up and dried in a vacuum drying box for 4 hours. After adding 1 ml of phosphate buffer oscillated water, a liposome was prepared using a probe ultrasound (163W, 4 minutes), named DOPS liposome;
[0035] (2) Fluorescent phospholipids having an NBD mark with a 0.2 ml concentration of 1 mg / ml and the head is a phosphatidyl racemin group (named NBD-PS, and the structural formula is attached. figure 2 (Solvent is chloroform), and mixed with DOPS (10 mg) dissolved in 0.5 ml of chloroform, and the nitrogen was blown out of the vacuum drying tank in a vacuum drying tank for 4 hours. After adding 1 ml of phosphate buffer hydrated dispersion, a liposome was prepared using a probe ultrasound (163W, 4 minutes), named DOPS / NBD-PS liposome (the structure was attached image 3 .
Embodiment 2
[0037] Different saturation of lipids induced and imaging liposomes:
[0038] The preparation method is the same as that of Example 1, and the DOPS used in Example 1 (2) is replaced with an equal mass of Palmyl phosphatide (POPS).
Embodiment 3
[0040] Lip drop induction and imaging liposomes of different head groups:
[0041] The preparation method is the same as that of Example 1, and the DOPS used in (2) in Example 1 is replaced by equal quality diblasceryl glycerol (DOPG), diblastin phosphatidylinol (DOPI), double Oil liponic acid (DOPA) or laminated diblactyl phosphatidylglycerol (DOCA).
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