Magnetic resonance imaging nano contrast agent and its preparation method and application
A magnetic resonance imaging and nano-contrast agent technology, applied in the field of contrast agents, can solve problems such as difficult excretion, interference, and easy aggregation, and achieve the effects of guaranteed application range, excellent magnetic resonance imaging imaging effect, and easy metabolism and excretion
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[0030] The invention provides a method for preparing a magnetic resonance imaging nano-contrast agent, the preparation method comprising:
[0031] 1) Mix the iron source, citrate, and water and adjust the pH to acidity, then add urea and heat to reflux to obtain Fe 2 o 3 super nanoparticle Fe 2 o 3 SPs;
[0032] 2) Fe 2 o 3 SPs and bovine serum albumin (BSA) were contacted in solution to obtain magnetic resonance imaging nano-contrast agent.
[0033] In step 1) of the above preparation method, the amount of each material can be selected within a wide range, but in order to further improve the imaging effect of the prepared contrast agent, preferably, in step 1), iron source, citrate , water, urea dosage ratio is 1.6×10 -4 mol: 3.0×10 -4 -4.0×10 -4 mol: 80-150mL: 3×10 -4 mol-5×10 -4 mol.
[0034] In step 1) of the above-mentioned preparation method, the conditions of thermal reflux treatment can be selected in a wide range, but in order to further improve Fe 2 o ...
Embodiment 1
[0045] 1) Fe 2 o 3 Preparation and purification of super nanoparticles (SPs):
[0046] Under the condition of constant stirring, add 3.4×10 -4 mol trisodium citrate, 1.6×10 -4 mol ferric chloride hexahydrate, use 0.1mol L -1 sodium hydroxide to adjust the pH to 6, fully shake, mix well and add 4×10 -4 mol urea, boiled and refluxed at 120°C for 24h. After the reaction was completed, the solution was cooled to 25° C., and samples were collected. Take 1mL of the Fe prepared above 2 o 3 Add 3 mL of isopropanol to the SPs stock solution, mix well, centrifuge at 10,000 rpm for 10 min, discard the supernatant, and redisperse the obtained precipitate into water or freeze-dry it for later use.
[0047] 2) BSA-modified Fe 2 o 3 Preparation and purification of SPs:
[0048] to the purified Fe 2 o 3 Add BSA solution (the mass ratio of Fe and BSA is 1:1, the solvent in BSA solution is water, Fe 2 o 3 The ratio of SPs precipitation to BSA solution is 1mg: 1mL), re-dispers...
Embodiment 2
[0050] Under the condition of constant stirring, add 3.0×10 -4 mol trisodium citrate, 1.6×10 -4 mol ferric chloride hexahydrate, use 0.1mol L -1 sodium hydroxide to adjust the pH to 5.5, fully shake, mix well and add 3×10 -4 mol urea, boiled and refluxed at 110°C for 30h. After the reaction was completed, the solution was cooled to 25° C., and samples were collected. Take 1mL of the Fe prepared above 2 o 3 Add 3 mL of isopropanol to the SPs stock solution, mix well, centrifuge at 10,000 rpm for 10 min, discard the supernatant, and redisperse the obtained precipitate into water or freeze-dry it for later use.
[0051] 2) BSA-modified Fe 2 o 3 Preparation and purification of SPs:
[0052] to the purified Fe 2 o 3 BSA solution was added to the SPs precipitation (the mass ratio of Fe to BSA was 1: 0.8, the solvent in the BSA solution was water, Fe 2 o 3 The ratio of SPs precipitation to BSA solution is 1mg: 1mL), re-disperse; after mixing evenly, put it on a shaker...
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