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Fe3O4/MoO3-x-GOD-PVP nano-enzyme as well as preparation method and application thereof

A moo3-x-god-pvp, moo3-x-god technology, applied in the field of biomedical nanomaterials, can solve the problems of drug resistance of tumor cells, limited therapeutic effect, drug leakage, etc., and achieve excellent dual catalytic performance, Improve the effect, enhance the effect of efficiency

Active Publication Date: 2022-04-22
NANJING MEDICAL UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0003] At present, although many TME-responsive nanoplatforms have been established, most nanoplatforms targeting TME-responsiveness achieve tumor suppression by transporting chemotherapeutic drugs, and these platforms have some unavoidable defects.
For example, there will still be inevitable drug leakage in normal tissues, which will cause damage to normal tissues. The low drug loading of drug carriers and long-term use of chemotherapy drugs will cause drug resistance in tumor cells. Even if the dosage of drugs is increased, the treatment effect is still limited

Method used

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  • Fe3O4/MoO3-x-GOD-PVP nano-enzyme as well as preparation method and application thereof
  • Fe3O4/MoO3-x-GOD-PVP nano-enzyme as well as preparation method and application thereof
  • Fe3O4/MoO3-x-GOD-PVP nano-enzyme as well as preparation method and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0044] Step 1, 1.25g FeCl·H 2 O was dissolved in 7.75 mL of water. Under vigorous stirring, 6.25 mL of ammonia water (25%) was added to the above aqueous solution, followed by stirring in air for 10 minutes. The above mixture was added to a 50 mL stainless steel autoclave lined with polytetrafluoroethylene. Then, 5 mL of polyethyleneimine aqueous solution (108 mg / mL) was further added to the autoclave. After stirring, the reaction vessel was placed at 134° C. for 3 hours, and then the mixture was cooled to room temperature. The black precipitate was collected by magnetic separation and purified 5 times with water to remove excess reactants and by-products. Finally, the Fe 3 o 4 The nanoparticles were vacuum dried at 37°C for 24 h for further use.

[0045] Step 2, mix 2mmol molybdenum powder with 24mL ethanol. With vigorous stirring, 3 mL of H 2 o 2 (30%) was added to the above mixture. After 1 h, the mixture was transferred to a 50 mL Teflon-lined stainless steel aut...

Embodiment 2

[0050] Step 1, 1.25g FeCl·H 2 O was dissolved in 7.75 mL of water. Under vigorous stirring, 6.25 mL of ammonia water (25%) was added to the above aqueous solution, followed by stirring in air for 10 minutes. The above mixture was added to a 50 mL stainless steel autoclave lined with polytetrafluoroethylene. Then, 5 mL of polyethyleneimine aqueous solution (108 mg / mL) was further added to the autoclave. After stirring, the reaction vessel was placed at 134° C. for 3 hours, and then the mixture was cooled to room temperature. The black precipitate was collected by magnetic separation and purified 5 times with water to remove excess reactants and by-products. Finally, the Fe 3 o 4 The nanoparticles were vacuum dried at 37°C for 24 h for further use.

[0051] Step 2, mix 2mmol molybdenum powder with 24mL ethanol. With vigorous stirring, 3 mL of H 2 o 2 (30%) was added to the above mixture. After 1 h, the mixture was transferred to a 50 mL Teflon-lined stainless steel aut...

Embodiment 3

[0056] Get the Fe prepared by appropriate embodiment 1 3 o 4 / MoO 3-x -GOD-PVP nanozyme was pressed into KBr tablets, and the infrared absorption was tested using an infrared spectrometer. Such as figure 2 As shown, Fe 3 o 4 / MoO 3-x - The infrared spectra of GOD-PVP nanozyme at 1001 and 853 cm -1 The nearby peaks are attributed to Mo=O stretching vibrations and Mo-O-Mo bonds. 1123cm -1 Nearby absorption, which is attributed to the C–O stretching vibration of glucose oxidase. 1283cm -1 is the stretching vibration of the polyvinylpyrrolidone N-C bond, which proves that the Fe 3 o 4 / MoO 3-x - Composition of GOD-PVP nanozymes.

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Abstract

The invention discloses a Fe3O4 / MoO3-x-GOD-PVP (Polyvinyl Pyrrolidone) nano enzyme as well as a preparation method and application thereof. The preparation method comprises the following steps: compounding Fe3O4 nano particles and MoO3-x nano sheets, and modifying a Fe3O4 / MoO3-x nano compound by using glucose oxidase and polyvinylpyrrolidone. The Fe3O4 / MoO3-x-GOD-PVP nano-enzyme prepared by the invention has good biocompatibility, low toxicity and excellent dual catalytic performance, can generate OH in the presence of H2O2, can catalyze the decomposition of glucose, and can be applied to the catalytic treatment of tumors. In addition, the Fe3O4 / MoO3-x-GOD-PVP nano-enzyme has good photo-thermal performance, and the catalytic treatment effect can be enhanced by means of temperature rise.

Description

technical field [0001] The invention belongs to the technical field of biomedical nanomaterials, in particular to a Fe 3 o 4 / MoO 3-x -GOD-PVP nanozyme and its preparation method and application. Background technique [0002] Malignant tumors are the number one killer that threatens human life, health and safety. Recently, the morbidity and mortality of malignant tumors are increasing worldwide. The cure of malignant tumors has always been the goal pursued by biomedical researchers. The tumor microenvironment (TME) is accompanied by a series of abnormal characteristics in the process of tumor growth and deterioration, mainly reflected in: low pH value, which leads to the acidic environment of tumor tissue. The extracellular pH of tumor cells is 6.5-6.9, and the pH of intracellular lysosomes is 4.0-6.0, both of which are lower than those of normal tissues (pH 7.4). h 2 o 2 Overexpression. H in TME 2 o 2 The concentration can reach 100μmol / L, which is 100 times high...

Claims

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Application Information

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IPC IPC(8): A61K41/00A61K38/44A61K33/26A61K33/24A61K47/58A61P35/00B82Y5/00B82Y40/00
CPCA61K41/0052A61K38/443A61K33/26A61K33/24A61K47/58A61P35/00B82Y5/00B82Y40/00A61K2300/00
Inventor 吴凡程文全陈彦君米海尔妮萨古丽·麦麦提吐尔孙许如平廖晨浩姜慧君韩峰蔡政
Owner NANJING MEDICAL UNIV