Preparation method and application of injectable gelatin-iodized oil homogeneous preparation for vascular embolism
A technology of vascular embolism and gelatin, which is applied in the field of preparation of injectable gelatin-iodol homogeneous preparations for vascular embolism, can solve the problems of inability to improve the loss and loss of lipiodol, incomplete tumor embolization, tumor recurrence, etc., and achieve embolism-enhancing drugs carrying effect
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[0033] Example 1
[0034] (1) Mix the medical gelatin sponge particles with sterile water, then swelling in a 50 ° C water bath to form liquid gelatin, where gelatin is 20% by weight in sterile water;
[0035] (2) The liquid gelatin obtained by step (1) is added to the autoclave with a volume ratio of 48.0% of the iodine injection of 0.1: 1, pressurized to 20 MPa, temperature control at 50 ° C, to be temperature After the pressure is stable, the holding pressure is stirred for 1 h;
[0036] (3) After the decompression, the blood vessels prepared from the autoclave can be injected into an adhesive-iodine average phase-containing agent.
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[0037] Example 2
[0038] (1) Mix the medical gelatin sponge particles with a sterile water dissolved with DOX, and then fluid gelatin in a 50 ° C water bath, wherein gelatin is 20% by weight in sterile water, and the concentration of DOX in sterile water is 10mg / ml;
[0039] (2) The liquid gelatin obtained by step (1) is added to the autoclave with a volume ratio of 48.0% of the iodine injection of 0.1: 1, pressurized to 20 MPa, temperature control at 40 ° C, to be temperature After the pressure is stable, the holding pressure is stirred for 1 h;
[0040] (3) After the decompression, the prepared hepatic artery embolization agent was collected from the autoclave.
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[0041] Example 3
[0042] (1) Mix the medical gelatin sponge particles with a sterile water dissolved with water-soluble drug Rodam, then use a 50 ° C water bath to form liquid gelatin, where gelatin is 20% by weight in sterile water, Rhodamin is not The concentration of the bacteria is 1 mg / ml;
[0043] (2) The liquid gelatin obtained by step (1) is added to the autoclave with a volume ratio of 48.0% of the iodine injection of 0.1: 1, pressurized to 20 MPa, temperature control at 40 ° C, to be temperature After the pressure is stable, the holding pressure is stirred for 1 h;
[0044] (3) After the decompression, the prepared hepatic artery embolization agent was collected from the autoclave;
[0045] (4) Dispersion of fat-soluble pharmaceutical coumarin-6 in step (3) prepared a composite embolization agent, wherein the coumarin-6 has a concentration of 1 mg / mL in the composite embolization agent.
[0046] Compared with the conventional formulation (hand mixing) of the liquid ...
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