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Preparation process of macroporous sodium polyacrylate embolization microspheres

A technology of sodium polyacrylate and embolization microspheres, which is applied in the field of medical devices, can solve problems such as irregular shape, poor conductivity, and uneven cross-linking, achieve good ion exchange kinetics, improve drug loading capacity, and polymerize uniform effect

Pending Publication Date: 2022-05-13
苏州森康微球医疗科技有限公司
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Some of these microspheres are irregular in shape and non-uniform in size, which can lead to side effects such as drift, blockage of blood vessels, and misembolization during interventional procedures, and cause damage to normal tissues.
Although some microspheres have a smooth surface, regular shape, and relatively uniform size, the microspheres have poor elasticity and stretchability, and poor conductivity. incomplete embolization
There are also microspheres that cannot bind chemotherapy drugs or have low drug loading, or the loaded drugs cannot be released slowly in blood vessels.
[0004] The currently published invention patents and commercially available embolic microsphere products are mainly gel-type products. The gel-type embolic microspheres have the problem of small micropores, which leads to the fact that when the drug is loaded, the chemotherapeutic drugs for middle molecules are mostly in the microspheres. The drug is loaded on the surface of spherical particles, and the drug loading is low
Moreover, when the gel-type microspheres are polymerized, heat will be released at the moment of chain growth, which will lead to a sharp rise in temperature and sudden polymerization, so there will be uneven cross-linking

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0032] A kind of preparation technology of macroporous sodium polyacrylate embolization microsphere, comprises the following steps:

[0033] Add 0.6kg of dispersant to 50kg of water, stir evenly, and keep warm at 50°C for 3 hours to obtain a continuous phase. The dispersant is obtained by mixing gelatin and lignin at a mass ratio of 2:1;

[0034] 50kg step Gained continuous phase is added in the reactor, with 8kg propylene glycol dimethacrylate, 1.6kgN, N-methylenebisacrylamide, 0.4kg allyl trimeric isocyanate, 4kg benzene and 0.15kg benzyl peroxide Acyl mixed evenly, added to the reaction kettle, at the speed of 105r / min, the temperature was raised to 65°C, stirred and reacted for 8 hours, and the polymer was obtained;

[0035] will step The obtained polymer was filtered, washed with hot water, and the porogen was removed by distillation to obtain spheres, which were transferred to a chromatography column, rinsed with ethanol, washed with deionized water, and sieved...

Embodiment 2

[0039] A kind of preparation technology of macroporous sodium polyacrylate embolization microsphere, comprises the following steps:

[0040] Add 0.5kg of dispersant to 50kg of water, stir and dissolve evenly, keep warm at 70°C for 5 hours to obtain a continuous phase, and set aside, the dispersant is polyvinyl alcohol;

[0041] 50kg step The resulting continuous phase was added to the reactor, and 8.5kg of glucose trimethacrylate, 0.7kg of diethylene glycol divinyl ether, 0.8kg of ethylene glycol dimethacrylate, 7kg of toluene and 0.15kg of azobisiso Mix butyronitrile evenly, add it into the reaction kettle, heat up to 70°C at a speed of 140r / min, stir and react for 8 hours, and obtain a polymer;

[0042] will step The obtained polymer was filtered, washed with hot water, and the porogen was removed by distillation to obtain spheres, which were transferred to a chromatography column, rinsed with ethanol, washed with deionized water, and sieved to obtain macroporous p...

Embodiment 3

[0046] A kind of preparation technology of macroporous sodium polyacrylate embolization microsphere, comprises the following steps:

[0047] Add 0.6kg of dispersant to 50kg of water, stir and dissolve evenly, keep warm at 60°C for 5 hours to obtain a continuous phase, and set aside, the dispersant is polyvinyl alcohol;

[0048] 50kg step Gained continuous phase is added in the reactor, butyl acrylate 3kg, glycidyl acrylate 6.3kg, allyl acrylate 0.7kg, toluene 4kg, benzoyl peroxide 0.1kg are mixed uniformly, join in the reactor, at 110r Under the rotating speed of / min, the temperature was raised to 65°C, and the polymer was stirred and polymerized for 10 hours to obtain the polymer;

[0049] will step The obtained polymer was filtered, washed with hot water, and the porogen was removed by distillation to obtain spheres, which were transferred to a chromatography column, rinsed with ethanol, washed with deionized water, and sieved to obtain macroporous polyacrylate M...

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Abstract

The invention discloses a preparation process of macroporous sodium polyacrylate embolism microspheres, and relates to the technical field of medical instruments, the macroporous sodium polyacrylate embolism microspheres are subjected to suspension polymerization by taking a dispersing agent and water as continuous phases and taking a monomer acrylate compound, a cross-linking agent polyolefine compound, a pore-foaming agent and an initiator as dispersion phases, and the macroporous sodium polyacrylate embolism microspheres are obtained. And carrying out a hydrolysis process to obtain the macroporous sodium polyacrylate embolization microspheres. The prepared macroporous sodium polyacrylate embolization microspheres have high elasticity and large drug loading capacity. According to the invention, a suspension polymerization process is adopted for the first time, and the obtained macroporous microspheres have better intragranular microporous channels, are convenient for intragranular diffusion of molecules, have better ion exchange kinetics performance, are more suitable for medium-molecular chemotherapeutic drugs to quickly enter the microporous channels and exchange of functional groups, and greatly improve the drug loading capacity; the macroporous microspheres are more uniform in polymerization, and have higher strength and better elasticity compared with the macroporous microspheres.

Description

technical field [0001] The invention relates to the technical field of medical devices, in particular to a preparation process of macroporous sodium polyacrylate embolization microspheres. Background technique [0002] Interventional therapy is a new discipline developed in recent years, and it has been listed as the three pillar clinical disciplines together with traditional internal medicine and surgery. Embolization therapy is an important part of interventional therapy. Embolization therapy has been used in arteriovenous malformations, tumors with enlarged blood vessels, uterine fibroids, uterine fibroids, and blood supply by blocking blood vessels, malformed blood vessels, or bleeding blood vessels. Abundant tumors and other aspects have achieved good curative effect, and has broad application prospects. [0003] The key to transcatheter embolization (TACA for short) is to choose the appropriate embolic agent. At present, the most widely used clinically is the microsp...

Claims

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Application Information

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IPC IPC(8): A61L24/10A61L24/04A61L24/06A61L24/08
CPCA61L24/06A61L24/104A61L24/08A61L24/04A61L24/001A61L24/0015A61L24/0036A61L2300/232A61L2300/416A61L2300/602A61L2300/622A61L2430/36
Inventor 林炳旺郑飞邢雪奎
Owner 苏州森康微球医疗科技有限公司
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