Ultrasonic contrast agent of uterus oviduct tract and preparation method of ultrasonic contrast agent
A technology for ultrasound contrast agents and fallopian tubes, which is applied in the field of medical contrast agents and injectable ultrasound targeting contrast agents. It can solve the problems of unsatisfactory particle size and distribution of microbubbles, complex preparation process, and complex synthesis process, etc., and achieve good clinical application. Foreground, uniform particle size distribution, and good biocompatibility
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Embodiment 1
[0047] Dissolve 48 mg of lecithin, 2.4 mg of diarachidoylphosphatidylcholine (DAPC), 500 mg of polyethylene glycol-2000, 7.2 mg of poloxamer, and 600 mg of folic acid-polyethylene glycol phospholipid in 10 mL Place the mixture in a beaker of normal saline, then place the mixture in a water bath at 50°C, and stir it magnetically for 30 minutes to obtain a uniformly mixed solution;
[0048] Will SF 6 The gas is passed into the solution, and then treated with a high-speed liquid shearing machine at 18000 rpm. At this time, the gas-encapsulated microsphere suspension is obtained. (Respectively at 13000rpm, 15000rpm, repeat the test)
Embodiment 2
[0050] Dissolve 48 mg of lecithin, 2.4 mg of diarachidoylphosphatidylcholine (DAPC), 500 mg of polyethylene glycol-2000, 7.2 mg of poloxamer, and 600 mg of folic acid-polyethylene glycol phospholipid in 10 mL Put the mixed solution in a beaker of normal saline, and then magnetically stir the mixed solution for 30 minutes in a water bath at 50°C to obtain a uniformly mixed solution; liposome suspension.
[0051] Leave the liposome suspension at room temperature for 24 hours, discard the supernatant, add an equal amount of distilled water to wash, purify 3 times, then discard the supernatant to obtain the upper layer mixture; vacuum freeze-dry the mixture Next, the liposome dry powder was obtained.
[0052] then SF 6 The gas is injected into the liposome dry powder, and then the dry powder obtained at this time is dissolved in physiological saline to obtain a stable ultrasound contrast agent with uniform particle size.
Embodiment 3
[0054] Dissolve 48 mg of lecithin, 2.4 mg of diarachidoylphosphatidylcholine (DAPC), 500 mg of polyethylene glycol-2000, 7.2 mg of poloxamer, and 600 mg of folic acid-polyethylene glycol phospholipid in 10 mL Place the mixture in a beaker of normal saline, then place the mixture in a water bath at 50°C, and stir it magnetically for 30 minutes to obtain a uniformly mixed solution;
[0055] Pass perfluoropentane into the solution, and then process it with a high-speed liquid shearing machine at 18000 rpm, at this time, a suspension of microspheres wrapped in perfluoropentane is obtained.
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