Biodegradable microcapsulated ultrasonic contrast medium and its prepn process
A biodegradable, ultrasonic contrast agent technology, applied in MRI/MRI contrast agents, drug delivery, emulsion delivery, etc., can solve the problems of small harmonic enhancement multiples, troublesome clinical application, and increase the cost of diagnosis.
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Embodiment 1
[0041] At 15°C, a dichloromethane solution of 5 mg distilled water and 200 mg polylactide (PLA) with a molecular weight of 10,000 was ultrasonically emulsified for 1 minute in the presence of Span 80 to form a water-in-oil emulsion. Inject 100 ml of 1% gelatin solution in the presence of Tween 80 and emulsify for 1 minute. The resulting water-in-oil-in-water emulsion. After stirring at 1000 rpm for 5 hours, the obtained microcapsules were separated by centrifugation. Washing with distilled water for four times, finally dispersing in water, freeze-drying to obtain a microcapsule type polylactide ultrasonic contrast agent with a particle diameter of 2-8 microns and a thickness of a capsule wall of 100 nanometers.
[0042] Dogs were used as simulated animals, and the ultrasound imaging effect in vivo was measured by intravenous infusion. The results showed that PLA microcapsules had more obvious imaging effects than the commercially available ultrasound contrast agents NF FC and...
Embodiment 2
[0045] At 20°C, a dichloromethane solution of 5 mg of distilled water and 200 mg of poly(lactide-co-glycolide) (PLGA) with a molecular weight of 10,000 was ultrasonically emulsified in the presence of Span 60 for 1 min to form a water-in-oil emulsion. At a stirring speed of 15,000 rpm, inject 100 ml of 1% gelatin solution in the presence of Tween 60, and emulsify for 1 minute. Add 300ml of distilled water (dichloromethane saturated), stir for 30 minutes, and obtain microcapsules by centrifugation. Washing with distilled water three times, finally dispersing in water, freeze-drying to obtain microcapsule type poly(lactide-glycolide) copolymer ultrasonic contrast agent with particle diameter of 6-12 microns and capsule wall thickness of 100 nanometers.
[0046] Effect of microencapsulated poly(lactide-glycolide) copolymer ultrasound contrast agent on ultrasound imaging and
[0047] Example 1 is similar.
Embodiment 3
[0049] A solution of 3 mg distilled water and 200 mg poly(lactide-caprolactone) copolymer (PLC) with a molecular weight of 150,000 in dichloromethane was ultrasonically emulsified in the presence of Span 60 for 90 seconds at 18° C. to form a water-in-oil emulsion. Inject 100 ml of 5% polyvinyl alcohol solution at a stirring speed of 5000 rpm, and emulsify for 5 minutes. The obtained water-in-oil-in-water emulsion was stirred at 1000 rpm for 3 hours, and the obtained microcapsules were separated by centrifugation. Washing with distilled water three times, dispersing in water, freeze-drying to obtain a microcapsule type poly(lactide-caprolactone) copolymer ultrasonic contrast agent with a particle diameter of 6-12 microns and a capsule wall thickness of 100 nanometers.
[0050] The Ratio of Ultrasonic Development Effect of Microencapsulated Poly(lactide-caprolactone) Copolymer Ultrasound Contrast Agent
[0051] Example 1 is better.
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