Targeted ultrasonic contrast agent for enhancing ultrasonic diagnosis of carotid arteriosclerosis and preparation method thereof
A technology for ultrasound contrast agents and arteriosclerosis, which is applied in the direction of echo/ultrasound imaging agents, preparations for in vivo tests, and pharmaceutical formulations. It can solve the problems of complex preparation methods, high requirements for storage and transportation conditions, and high use costs. The method is simple and easy, the clinical dosage is reduced, and the cost is low
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Embodiment 1
[0023] Example 1: A targeted ultrasound contrast agent for enhancing ultrasound diagnosis of carotid atherosclerosis
[0024] 7 parts of hyaluronic acid, 93 parts of soybean lecithin, 40% tert-butanol solution, appropriate amount of perfluoropropane, prepared according to the following steps:
[0025] (1) Add soybean lecithin containing hyaluronic acid to a mixed solution of 8 times the weight of tert-butanol and water, homogenize at 30°C for 4 minutes under a pressure of 100MPa, and then filter and sterilize through a 220nm filter membrane to obtain an emulsion;
[0026] (2) Divide the emulsion obtained in step (1) into vials and vacuum freeze-dry to obtain freeze-dried powder, then slowly fill in perfluoropropane to 55KPa in a vacuum state, and then slowly fill in the mixed gas of perfluoropropane and nitrogen to 1 standard atmospheric pressure, then use a rubber stopper to seal the vial, and the volume ratio of perfluoropropane in the mixed gas is 50%;
[0027] (3) Use the...
Embodiment 2
[0028] Example 2: A targeted ultrasound contrast agent for enhancing ultrasound diagnosis of carotid atherosclerosis
[0029] 3 parts of hyaluronic acid, 4 parts of mannuronic acid, 93 parts of soybean lecithin, 40% tert-butanol solution, appropriate amount of perfluoropropane, prepared according to the following steps:
[0030] (1) Add soybean lecithin containing hyaluronic acid and mannuronic acid to a mixed solution of 8 times the weight of tert-butanol and water, homogenize at 30°C and 100MPa pressure for 4 minutes, then filter and sterilize through a 220nm filter membrane, get lotion;
[0031] (2) Divide the emulsion obtained in step (1) into vials and vacuum freeze-dry to obtain freeze-dried powder, then slowly fill in perfluoropropane to 55KPa in a vacuum state, and then slowly fill in the mixed gas of perfluoropropane and nitrogen to 1 atmospheric pressure, then use a rubber stopper to seal the vial, and the volume ratio of perfluoropropane in the mixed gas is 50%;
...
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