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Preparation method of composite particle of polymer embedded hydrophilic antitumor drug

A technology of anti-tumor drugs and composite particles, which is applied in the field of preparation of polymer drug carrier drugs, can solve the problems of poor drug stability, complicated and cumbersome operations, environmental pollution, etc., and achieves high drug loading and encapsulation efficiency. Prospects, the effect of avoiding environmental pollution

Inactive Publication Date: 2015-02-11
HEBEI UNIVERSITY OF SCIENCE AND TECHNOLOGY
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0005] Composite microspheres or microcapsules embedded with hydrophilic anti-tumor drugs obtained by the above method are complex and cumbersome to operate, the drug loading and coating rate are low, the drug and the polymer drug carrier are physically mixed, and the molecular distribution of the drug is relatively low. Inhomogeneity, prone to agglomeration, poor drug stability, thus affecting the therapeutic effect
In addition, the use of organic solvents in the embedding process is likely to cause secondary damage to the human body and cause environmental pollution

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0023] Example 1: Preparation of polydiethylaminoethyl methacrylate composite particles embedded with 5-fluorouracil

[0024] Weigh 50g of ethanol and 50g of deionized water according to the ratio of 70:30, mix well, add 3.0g of PVP K30, stir until dissolved, under magnetic stirring, completely dissolve 1.5g of 5-fluorouracil in the above mixed solution to form A solution; Weigh 15g of diethylaminoethyl methacrylate, add 0.15g of BPO, stir until completely dissolved to form liquid B; transfer component A into a 250mL four-necked bottle equipped with a stirring device, a thermometer and a reflux condensing device, at room temperature Slowly add component B, stir until completely mixed to form a homogeneous solution, continue to stir and feed N 2 , put the reaction bottle in a water bath that has been raised to the specified temperature of 80°C for constant temperature reaction. The reaction system gradually becomes turbid from the initial transparent and homogeneous solution, a...

Embodiment 2

[0025] Example 2: Preparation of poly-N-isopropylacrylamide composite particles embedded with 5-fluorouracil

[0026] Weigh 50g of ethanol and 50g of deionized water according to the ratio of 50:50, mix evenly, add 4.5g of PVP K30, stir until dissolved, and completely dissolve 1.5g of 5-fluorouracil in the above mixed solution under magnetic stirring to form A solution; Weigh 15g of N-isopropylacrylamide, add 0.3g of AIBN, and stir until completely dissolved to form liquid B; transfer component A into a 250mL four-necked bottle equipped with a stirring device, a thermometer, and a reflux condensing device, at room temperature Slowly add component B, stir until completely mixed to form a homogeneous solution, continue to stir and feed N 2 , put the reaction bottle in a water bath that has been raised to the specified temperature of 70°C for constant temperature reaction. The reaction system gradually becomes turbid from the initial transparent and homogeneous solution, and fina...

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PUM

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Abstract

The invention specifically relates to a preparation method of a polymer drug carrier-loaded drug, and in particular relates to a composite particle of a polymer embedded hydrophilic antitumor drug prepared through in-situ dispersion polymerization, belonging to the cross technical field chemical engineering, pharmaceutical engineering and material engineering. The hydrophilic antitumor drug is embedded through an in-situ dispersion polymerization technology; a mixed solution of ethanol and de-ionized water serves as a dispersion medium; a monomer, the hydrophilic antitumor drug, an initiator and a dispersant are dissolved in the mixed solution to form a homogeneous solution; and a dispersion polymerization reaction is conducted to obtain the composite particle of the mono-disperse polymer embedded hydrophilic antitumor drug in micrometer size. The method disclosed by the invention, which embeds the drug in the polymer particle through one-step dispersion polymerization, is simple in preparation, and drug molecules are uniformly distributed in the polymer particle; the polymer particle is in micro-sized mono-dispersion; drug loading capacity and encapsulation efficiency of the drug are relatively high; and the preparation method has a broad application prospect in aspect of pharmaceutical preparations.

Description

technical field [0001] The present invention specifically relates to a preparation method of polymer drug carrier drug loading, in particular to the preparation of composite particles of polymer-embedded hydrophilic anti-tumor drugs by using in-situ dispersion polymerization method, which belongs to the interdisciplinary technology of chemical engineering, pharmaceutical engineering and material engineering field. Background technique [0002] The side effects of anti-tumor drugs are large. While killing tumor cells, they will cause damage to normal tissue cells in the body, reduce human immunity, and are not conducive to the recovery of tumor patients. Therefore, it is necessary to select a suitable drug carrier for anti-tumor drugs to package Buried, to eliminate or reduce the harm to the human body. [0003] Polymer materials with excellent biocompatibility are widely used in drug carriers. They not only have good processability, but also can regulate the release of drug...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): A61K47/34A61K9/14A61K45/00A61P35/00C08F120/34C08F120/54
Inventor 唐二军杜朋亚
Owner HEBEI UNIVERSITY OF SCIENCE AND TECHNOLOGY
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