Preparation method of mesoporous silica in situ doped acrylic resin bone cement composite for enhancing durable release capacity of medicines

A technology of mesoporous silica and acrylic resin, applied in medical science, prosthesis, etc., can solve the problem of the influence of nanoparticle composite PMMA bone cement on drug release characteristics, and achieve enhanced sustainable release time, sustained uniform release, and voids. The effect of a large space fraction

Inactive Publication Date: 2020-02-07
NANJING DRUM TOWER HOSPITAL
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

This patented technology provides improved biodegradation/repair coatings made from certain types of porous ceramics that have excellent handling capabilities and ability to control how they react when exposed to water or other liquids. These coating layers help prevent diseases caused by harmful substances released during medical procedures such as surgery. They may include various chemical agents like antibiotics, growth factors, cytokines, chemotherapy medications, etc., making them ideal carriers for deliver these compounds into tissues.

Problems solved by technology

This patents discusses different ways how poly-(MonomethAcrylimide)-PMMA bactericidal cements were developed during orthopedics surgeries. They found that they had better osteointegral capacity compared to traditional calcium hydroxyapatite ceramics but also improved their resistance against corrosion from body fluids. Additionally, there may exist various methods such as coating the surface before inserting the prosthesive device inside the patient’ s skeleton. These techniques aimed at integrating the prosthealthymaycate interfaces with surrounding soft tissues while reducing the likelihood of infectious disease later when treatments like hip replacements.

Method used

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  • Preparation method of mesoporous silica in situ doped acrylic resin bone cement composite for enhancing durable release capacity of medicines
  • Preparation method of mesoporous silica in situ doped acrylic resin bone cement composite for enhancing durable release capacity of medicines
  • Preparation method of mesoporous silica in situ doped acrylic resin bone cement composite for enhancing durable release capacity of medicines

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Experimental program
Comparison scheme
Effect test

Embodiment 1

[0037] Mesoporous hollow spherical silica nanomaterials are in-situ doped with acrylic resin bone cement composite materials, and the specific preparation process is as follows:

[0038] (1). Preparation of hollow silica nanomaterials

[0039] Take 0.9 g of ferric chloride hydrate and add it to 30 mL of ethylene glycol, stir to dissolve, then add 4 g of anhydrous sodium acetate and 0.8 g of sodium citrate in turn, stir and mix, then transfer the liquid into the reaction kettle, at 150 After reacting at a temperature of ℃ for 10 h, the reactant was taken out, washed twice with water and ethanol and dried to obtain the synthesized ferric oxide.

[0040] Take 40 mg of prepared ferric oxide and add it to 35 mL of deionized water, then add 0.9 mL of hydrazine hydrate, sonicate for 10 min, then add 150 mL of deionized water and 30 μL of ethyl orthosilicate, mechanically Stir the reaction for 2 h, remove the supernatant and continue to add 150 mL of deionized water, 0.9 mL of hydrazine

Embodiment 2

[0049] Mesoporous rod-shaped silica nanomaterials are in-situ doped with acrylic resin bone cement composite materials, and the specific preparation process is as follows:

[0050] (1). Preparation of mesoporous rod-shaped silica nanomaterials

[0051] Add 25 g of polyvinylpyrrolidone and 250 mL of 1-pentanol into a closed round-bottomed flask, mix ultrasonically for 2 h, then add 30 mL of absolute ethanol, 7.5 mL of ultrapure water and 6 mL of 0.3 M lemon Sodium dihydrate aqueous solution, mixed well, added 7.5 mL ammonia solution with a mass fraction of 20%, 0.6 mL ethyl orthosilicate, stirred for 30 h, collected by centrifugation, washed with deionized water and ethanol and dried to obtain mesoporous Rod-shaped silica sphere nanomaterials. see image 3 It is a transmission electron microscope image of a rod-shaped silica nanomaterial, which shows that it has been successfully prepared.

[0052] (2). Preparation of aminated rod-shaped silica nanomaterials

[0053] Disperse

Embodiment 3

[0059] Mesoporous tubular silica nanomaterials are in-situ doped with acrylic resin bone cement composites, and the specific preparation process is as follows:

[0060] (1). Preparation of Mesoporous Tubular Silica Nanomaterials

[0061] Dissolve 10 g of tetraethyl orthosilicate in 7 mL of ethanol, add 75 µL of HCl solution at room temperature, and react for 35 min; dissolve 3 g of P123 in 35 mL of ethanol, then add it to the above-reacted solution, and continue to react for 35 min , vacuum filtered to the polycarbonate template, and soaked in the ethanol solution containing P123 prepared above for 3h. Subsequently, the polycarbonate template was moved into the reaction kettle and maintained at a temperature of 70° C. for 2 days, and finally the polycarbonate template was removed using dichloromethane to obtain a mesoporous tubular silica sphere nanomaterial. see Figure 4 It is a transmission electron microscope picture of the tubular silica nanomaterial, which shows that it h

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Abstract

The invention discloses a preparation method of a mesoporous silica in situ doped acrylic resin bone cement composite for enhancing durable release capacity of medicines. The preparation method comprises the steps of firstly, mixing an amino silicon dioxide nanometer material with bone cement liquid to obtain a mixture, mixing the mixture with a bone cement solidifying agent, and in the process ofa polyreaction, performing in-situ introduction of the mesoporous silica nanometer material containing medicines; and uniformly mixing a mesoporous silica material with the liquid agent, and besides,enabling amino and carboxyl in bone cement acrylic resin to form electrostatic interaction to realize uniform and stable distribution in the bone cement, and achieve the purpose of durable and uniform release of the medicines. The prepared composite is high in operability, self spaces can be used for efficiently loading the medicines, and unique 2-8-nm mesoporous bore diameter is designed to enable the medicines distributed in the deep layer of the bone cement to be slowly released to the outside of the cement, so that durable and efficient release of the medicines is realized, besides, the characteristic and the function of the bone cement can be individually improved, and the biocompatibility and the anti-infection characteristic of the bone cement can be improved.

Description

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Claims

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Application Information

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Owner NANJING DRUM TOWER HOSPITAL
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