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Preparation method of macromolecular laminar drug-loaded hydrogel with controllable drug distribution

A technology for polymer layer and drug preparation, which can be used in the fields of polymer compound inactive ingredients, drug delivery, and pharmaceutical formulations, etc., and can solve the problems of low drug concentration, complicated process, and long time consumption.

Active Publication Date: 2017-01-25
SICHUAN UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, the traditional smart hydrogel drug sustained release system has many shortcomings: because it is generally a hydrophilic homogeneous system, the release behavior of the loaded drug is mostly nonlinear. The drug concentration is often low, and the therapeutic effect cannot be achieved; the preparation form is relatively single, and it is difficult to flexibly and effectively control the dosage and administration plan, and cannot meet the complex drug release requirements
[0005] Although the above studies can overcome the problem of single drug delivery scheme of traditional homogeneous hydrogel drug-loaded materials, the preparation method is too cumbersome, and the layer structure of drug-loaded materials needs to be constructed layer by layer. The process of drying or curing crosslinking is complex and time-consuming, which cannot meet the needs of large-scale industrial production; and due to the limitation of its preparation process, the thickness and layer structure of the material single layer cannot be flexibly adjusted, and it is difficult to meet the needs of different drugs. release demand

Method used

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  • Preparation method of macromolecular laminar drug-loaded hydrogel with controllable drug distribution
  • Preparation method of macromolecular laminar drug-loaded hydrogel with controllable drug distribution

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0045] Example 1 (drug-loaded layer A and barrier layer B)

[0046] In the first step, sodium alginate and water are 10%:90% by weight, calcium carbonate-gluconolactone system (a sodium alginate cross-linking agent, wherein the molar ratio of calcium carbonate and gluconolactone is 1:2) According to 15% of the weight of sodium alginate, the drug methylene blue is prepared according to the total weight of sodium alginate and water 10%, and the polyanion polymer blend solution A is obtained by degassing and stirring with a vacuum defoaming mixer.

[0047] Chitosan and water are mixed according to the weight percentage of 10%: 90%, and genipin (which is chitosan crosslinking agent) is prepared according to 10% of the mass of chitosan, and the vacuum defoaming mixer is degassed and stirred evenly to obtain poly Cationic polymer blend solution B.

[0048] In the second step, the above-mentioned uniformly mixed sodium alginate drug-loaded blend solution (polyanionic polymer blend s...

Embodiment 2

[0052] Example 2 (drug-loaded layer A and barrier layer B)

[0053] In the first step, the weight percentage of sodium alginate and water is 10%: 90%, calcium sulfate (as a sodium alginate cross-linking agent) is 20% of the weight of sodium alginate, and the drug ibuprofen is calculated by the total weight of sodium alginate and water. The weight is 10% for batching, and the vacuum defoaming mixer is degassed and stirred to obtain a polyanionic polymer drug-loaded blend solution A.

[0054] Chitosan and water are mixed according to the weight percentage of 10%: 90%, and genipin (which is chitosan crosslinking agent) is prepared according to 10% of the mass of chitosan, and the vacuum defoaming mixer is degassed and stirred evenly to obtain poly Cationic polymer blend solution B.

[0055] In the second step, the above-mentioned uniformly mixed sodium alginate blend solution (polyanionic polymer drug-loaded blend solution A) and chitosan blend solution (polycation polymer blend...

Embodiment 3

[0059] Example 3 (drug-loaded layer A and barrier layer B)

[0060] In the first step, the weight percentage of hyaluronic acid and water is 30%: 70%, glutaraldehyde (as a hyaluronic acid crosslinking agent) is 5% of the weight of hyaluronic acid, and the drug ibuprofen is mixed with hyaluronic acid and water. The total weight is 30% for batching, and the polyanionic polymer blend solution A is obtained by degassing and stirring with a vacuum defoaming mixer.

[0061] Mix gelatin and water at a weight percentage of 20%:80%, glutaraldehyde (gelatin cross-linking agent) according to 2% of the gelatin mass, and degass and stir with a vacuum defoaming mixer to obtain a polycationic polymer blend solution b.

[0062] In the second step, the above-mentioned homogeneously mixed hyaluronic acid blend solution (polyanionic polymer blend solution A) and gelatin blend solution (polycation polymer blend solution B) are respectively stirred by an extruder at 25°C extruded, and stacked to...

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Abstract

The invention discloses a preparation method of macromolecular laminar drug-loaded hydrogel with controllable drug distribution. The preparation method mainly includes steps of performing multiple times of laminar superimposition on polyanion macromolecular blended solution A with appropriate proportion and composition and polycation macromolecular blended solution B with appropriate proportion and composition through a microlayer co-extrusion device, and sealing and placing to allow the solution A and the solution B to crosslink slowly and completely to realize structuring of drug-loaded macromolecular polyelectrolyte so as to prepare a macromolecular hydrogel drug loading system with flexible and controllable drug form distribution and drug release performance and with an alternative multilayered structure to meet different drug release demands. Compared with a traditional method using layer-by-layer superposition to prepare the macromolecular laminar drug-loaded hydrogel, the method has the advantages that the method is a continuous production method and beneficial to the improving of production efficiency; the method is simple in process, the product quality indexes of different batches of produces are stable, and the method is capable of achieving large-scale industrial production, wide in application range and promising in industrialization and market prospect.

Description

technical field [0001] The present invention relates to a preparation method of a polymer layered drug-loaded hydrogel, and more specifically relates to a solution co-extrusion preparation preparation with controllable drug distribution, customizable material structure, designable performance, and continuous production. The invention relates to a polymer layered drug-loaded hydrogel method with flexible and variable drug release behavior, which belongs to the technical field of functional composite materials. Background technique [0002] Smart hydrogel is a kind of hydrogel that can respond to external stimuli, that is, when the external temperature, pH, light, magnetic field, ion concentration, electric field, pressure, biomolecules and other factors change, its morphological structure or properties also change. of change. This responsive property makes smart hydrogels play an important role in the preparation of environment-responsive drug sustained-release materials, an...

Claims

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Application Information

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IPC IPC(8): A61K9/06A61K47/36A61K47/42A61K47/34A61K47/38A61K31/5415A61K31/192A61K31/522A61K31/196A61K31/167
CPCA61K9/0002A61K9/06A61K31/167A61K31/192A61K31/196A61K31/522A61K31/5415A61K47/34A61K47/36A61K47/38A61K47/42
Inventor 陈蓉郭少云刘桂廷
Owner SICHUAN UNIV
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