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An acid-responsive fe 3 o 4 -rgo-mtx nano medicine and its preparation method and application

A nano-drug and nano-particle technology, applied in the fields of nano-drugs, drug combinations, nano-technology, etc., can solve the problems of difficult control of drug release, toxic and side effects, poor biocompatibility of nanoparticles and poor drug loading, etc. Accepts functional groups, avoids damage, is easily doped and chemically modified

Active Publication Date: 2022-03-25
JIANGSU UNIV OF TECH
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

But there are also some problems, such as Fe 3 o 4 The biocompatibility and drug loading capacity of nanoparticles and drugs are not good, and the release of drugs is difficult to control, resulting in certain toxic and side effects

Method used

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  • An acid-responsive fe  <sub>3</sub> o  <sub>4</sub> -rgo-mtx nano medicine and its preparation method and application
  • An acid-responsive fe  <sub>3</sub> o  <sub>4</sub> -rgo-mtx nano medicine and its preparation method and application
  • An acid-responsive fe  <sub>3</sub> o  <sub>4</sub> -rgo-mtx nano medicine and its preparation method and application

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0035] Weigh 1.08g FeCl in turn 3 ·6H 2 O, 3.0g sodium acetate and 1.0g PEI, measure 40mL of ethylene glycol, put it in a 50mL beaker, stir ultrasonically for 20min to make the system disperse uniformly, then add the weighed 1.0g RGO, continue ultrasonic stirring for 10min, to obtain a uniformly dispersed Mix liquids. The homogeneous mixed liquid was transferred into a 100 mL polytetrafluoroethylene reaction kettle, and the reaction was carried out at 200 °C for 10 h. After the reaction, the product was poured out, and the product was extracted by magnetic decantation, washed with deionized water three times, and washed with ethanol three times. Finally, the product was dried in a vacuum oven at 30°C to obtain dry Fe 3 O 4-RGO nanoparticles.

[0036] Weigh 60 mg of dry Fe in turn 3 O 4 -RGO nanoparticles, 12mg MTX and 20mL deionized water were placed in a beaker, and the system was uniformly dispersed by ultrasonic for 8min. Then transferred to a three-necked flask, an...

Embodiment 2

[0040] Weigh 1.08g FeCl in turn 3 ·6H 2 O, 3.0g sodium acetate and 1.0g PEI, measure 40mL of ethylene glycol, put it in a 50mL beaker, stir ultrasonically for 20min to make the system evenly dispersed, then add the weighed 2.0g RGO, continue ultrasonic stirring for 10min, to obtain a uniform dispersion of mixed liquids. The above homogeneous mixed liquid was transferred into a 100 mL polytetrafluoroethylene reaction kettle, and the reaction was carried out at 200 °C for 10 h. After the reaction, the product was poured out, and the product was extracted by magnetic decantation, washed with deionized water three times, and washed with ethanol three times. Finally, the product was dried in a vacuum oven at 30 °C to obtain dry Fe 3 O 4 -RGO nanoparticles.

[0041] Weigh 60 mg of dry Fe in turn 3 O 4 -RGO nanoparticles, 20mg MTX and 20mL deionized water were placed in a beaker, and the system was uniformly dispersed by ultrasonic for 8min. Then transferred to a three-necked...

Embodiment 3

[0044] Weigh 1.08g FeCl in turn 3 ·6H 2 O, 3.0g sodium acetate and 0.5g PEI, measure 40mL ethylene glycol, put it in a 50mL beaker, stir ultrasonically for 20min to make the system disperse uniformly, then add the weighed 1.0g RGO, continue ultrasonic stirring for 10min, to obtain a uniform dispersion of mixed liquids. The above homogeneous mixed liquid was transferred into a 100 mL polytetrafluoroethylene reaction kettle, and reacted at 190 °C for 8 h. After the reaction, the product was poured out, and the product was extracted by magnetic decantation, washed with deionized water three times, and washed with ethanol three times. Finally, the product was dried in a vacuum oven at 30 °C to obtain dry Fe 3 O 4 -RGO nanoparticles.

[0045] Weigh 60 mg of dry Fe in turn 3 O 4 -RGO, 12 mg MTX and 20 mL of deionized water were placed in a beaker, and the system was uniformly dispersed by ultrasonic for 8 min. Then transferred to a three-necked flask, and reacted at 25°C in ...

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Abstract

The invention belongs to the technical field of material preparation and nano-medicine, in particular to an acid-responsive Fe 3 o 4 ‑RGO‑MTX nanomedicine and its preparation method and application. The nanomedicine includes Fe 3 o 4 ‑RGO carrier and methotrexate loaded on Fe 3 o 4 On the surface of nanoparticles and RGO sheets; the Fe 3 o 4 The drug-loading rate of ‑RGO carrier is 84%-99%, and the drug-loading amount is 13%-23%. The invention also provides an acid response type Fe 3 o 4 ‑RGO‑MTX nanomedicine preparation method. Fe prepared by the present invention 3 o 4 ‑RGO nanoparticles, as the carrier of MTX, have magnetic targeting effect and improve the biological affinity of the carrier; the unique single-atom thickness and two-dimensional planar structure of RGO can greatly improve the drug loading and sustained release of the anticancer drug MTX Effect, improve drug efficacy and bioavailability.

Description

technical field [0001] The invention belongs to the technical field of material preparation and nano-medicine, and in particular relates to an acid-responsive Fe 3 O 4 -RGO-MTX nanomedicine and its preparation method and application. Background technique [0002] Tumor is a worldwide problem that threatens human life and health. Clinical non-surgical treatments for malignant tumors, including radiotherapy and chemotherapy, all aim to kill tumor cells. The biggest deficiency is the lack of specificity for tumor cells. [0003] Methotrexate (MTX) is one of the well-known antineoplastic drugs for the treatment of liver, breast, skin, lung and other malignancies. Unfortunately, MTX has a very short plasma half-life and high efflux rate compared to the influx rate, requiring high doses of MTX for treatment. Moreover, the drug dose actually applied to the organism does not completely reach the tumor site, but spreads throughout the body, thereby causing toxic and side effects t...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): A61K41/00A61K9/14A61K31/519A61K47/02A61K47/04A61P35/00B82Y5/00B82Y30/00B82Y40/00
CPCA61K41/00A61K31/519A61K47/02A61K9/143A61P35/00
Inventor 吴娟胡月童霏朱炳龙秦恒飞程庆霖刘维桥
Owner JIANGSU UNIV OF TECH