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A kind of preparation method of drug-loaded gold nano dendrite particles

A gold nanoparticle and gold nanotechnology, which is applied in the field of preparation of drug-loaded gold nanodendrite particles, can solve the problems of gold nanomaterial temperature rise, tumor tissue killing, and no in-depth research, so as to achieve controllable release rate and increase The effect of drug loading

Active Publication Date: 2021-05-07
ZHEJIANG UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, the research on the photothermal conversion effect of gold nanomaterials mainly focuses on the photothermal effect on tumor tissue, that is, under the excitation of near-infrared light, the temperature of gold nanomaterials rises, causing large-scale killing of tumor tissues. In other fields (such as drug release field) application has not been studied in depth, and more in-depth exploration is needed
[0004] In summary, there is currently no technology that combines gold nanomaterials with photothermal conversion effects for drug delivery.

Method used

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  • A kind of preparation method of drug-loaded gold nano dendrite particles
  • A kind of preparation method of drug-loaded gold nano dendrite particles
  • A kind of preparation method of drug-loaded gold nano dendrite particles

Examples

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Embodiment 1

[0024] In this embodiment, a preparation method of drug-loaded gold nanodendritic particles comprises the following steps in sequence:

[0025] (1) Preparation of spherical gold nanoparticle seeds: Add 0.5mL of 50mM tetrachloroauric acid aqueous solution to 50mL deionized water and boil for 5 minutes, then add 1mL of 30mM sodium citrate solution for reduction, and allow the mixture to react for 15 minutes , then cooled to room temperature, centrifuged at 11000 rpm for 30 min, and then dispersed into 50 mL of deionized water to obtain spherical gold nanoparticles.

[0026] (2) Growth of gold nanodendrites: 500 μL of spherical gold nanoparticles in step (1), 8 mL of 0.2 M oleylamine methanol solution, 500 μL of 150 mM chloroauric acid ethanol solution and 30 μL of 0.3 M vitamin C methanol solution was added into the reaction bottle for reaction, and then placed on a stirring shaker for about 10 minutes to 24 hours to generate hydrophobic gold nano dendrites.

[0027] (3) Phase ...

Embodiment 2

[0030] In this embodiment, a preparation method of drug-loaded gold nanodendritic particles comprises the following steps in sequence:

[0031] (1) Preparation of spherical gold nanoparticle seeds: the 50mM tetrachloroauric acid aqueous solution of 5mL was added to 50mL deionized water and boiled for 5 minutes, then added 20mL of 30mM sodium citrate solution for reduction, and the mixture was reacted for 15 minutes, Then cool to room temperature, centrifuge at 11000 rpm for 30 min, and then disperse into 50 mL of deionized water to obtain spherical gold nanoparticles.

[0032] (2) Growth of gold nanodendrites: In step (1), 10 μL of spherical gold nanoparticle seeds, 1 mL of oleylamine methanol solution with a concentration of 0.2 M, 20 μL of chloroauric acid ethanol solution with a concentration of 150 mM and 30 μL of a concentration of 0.3 The vitamin C methanol solution of M is added into the reaction flask for reaction, and then placed on a stirring shaker for about 10 minu...

Embodiment 3

[0036] In this embodiment, a preparation method of drug-loaded gold nanodendritic particles comprises the following steps in sequence:

[0037] (1) Preparation of spherical gold nanoparticle seeds: 2mL of 50mM tetrachloroauric acid aqueous solution was added to 50mL deionized water and boiled for 5 minutes, then added 8mL of 30mM sodium citrate solution for reduction, and the mixture was reacted for 15 minutes, Then cool to room temperature, centrifuge at 11000 rpm for 30 min, and then disperse into 50 mL of deionized water to obtain spherical gold nanoparticles.

[0038] (2) Growth of gold nanodendrites: 100 μL of spherical gold nanoparticle seeds in step (1), 2 mL of oleylamine methanol solution with a concentration of 0.2 M, 100 μL of chloroauric acid ethanol solution with a concentration of 150 mM and 30 μL of a concentration of 0.3 The vitamin C methanol solution of M is added into the reaction bottle for reaction, and then placed on a stirring shaker for about 10 minutes...

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Abstract

The invention discloses a preparation method of drug-loaded gold nano dendrite particles. Specifically, gold nanoparticles are used as seeds to prepare hydrophilic gold nanodendrite particles, and then the model drug is loaded on the surface of gold nanodendrite particles to prepare a drug-loaded gold nanodendrite particle, which can be detected by near-infrared light. Or pH-regulated drug release. The drug-loaded gold nanodendrite particles of the present invention have good dispersibility, superior drug-loading performance, strong photothermal conversion effect, photothermal-induced release performance and pH-responsive release performance, and are useful in drug release, anticancer therapy, etc. The field has broad application prospects.

Description

technical field [0001] The invention belongs to the field of biomedical materials, and relates to a preparation method of drug-loaded gold nano dendrite particles. Background technique [0002] A drug carrier is a system that can be loaded with functional drugs and delivered to the lesion site or target organ (such as: tumor tissue, diseased tissue) after entering the human body. The role of the drug carrier is to provide continuous drug delivery to the lesion site or target organ in the human body, provide convenience for patients, reduce the frequency of treatment, and also reduce the impact of carrier-free drugs on other healthy tissues in the body. side effects. However, traditional drug carriers have disadvantages such as low drug loading, poor dispersion effect, and uncontrollable drug release rate. [0003] In recent years, due to the high photothermal conversion efficiency of gold nanomaterials, easy synthesis, easy characterization, easy modification, stable prope...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): A61K9/51A61K47/02A61K47/10A61K41/00A61P35/00B22F9/24B22F1/00
CPCA61K41/0052A61P35/00A61K9/5115A61K9/5146B22F9/24B22F1/145
Inventor 杨明英帅亚俊
Owner ZHEJIANG UNIV