Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Anti-cancer drug-loading nanofiber film and preparation method thereof

A technology of nanofiber membranes and anticancer drugs, which is applied in the direction of antineoplastic drugs, drug combinations, and pharmaceutical formulations, can solve the problems of heavy economic burdens on patients’ families and the country, high cost of repeated operations, and short effective time of drugs to prevent Tumor recurrence, good drug sustained-release performance, favorable effects of specific surface area

Inactive Publication Date: 2014-01-08
DONGHUA UNIV
View PDF3 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0004] 1. The cost of repeated surgery is high and the harm to the patient is great
Because cancer patients are in a state of physical and mental exhaustion after surgery, re-operation in a short period of time will bring great trauma and pain to the patient's body and mind, and the cost of repeated operations is high, which is a heavy economic burden on the patient's family and the country.
[0005] 2. Clinicians apply anti-tumor drugs on the tumor site after surgery to eliminate residual tumor cells. This method is extremely extensive and cannot be accurately dosed.
Most antineoplastic drugs have a relatively large killing effect on normal cells, so the choice of drug dosage is extremely important, otherwise the drug concentration will cause patient poisoning if the drug concentration is too large, and it will be ineffective if it is too small; Sustained release, the sudden release of the drug may cause poisoning of the patient, or the effective time of the drug is very short, and the drug concentration is far lower than its effective concentration when the tumor recurs

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0029] Weigh 0.0133g of 5-fluorouracil with a balance and dissolve it in 0.5ml of glacial acetic acid, and heat it slightly to dissolve it completely, weigh 0.66g of polylactic acid PLLA and 0.0133g of tetramethylporphine with a balance, and dissolve them in In chloroform, and seal the bottle to prevent solvent volatilization, stir on a magnetic stirrer until completely dissolved. Then add the glacial acetic acid solution of 5-fluorouracil prepared above, and continue to stir on the magnetic stirrer; after the uniformly mixed solution was left to stand for 5 hours, the bottle mouth was opened, and then 3ml of acetone was added, stirred evenly, and the instant Obtain electrospinning polymer solution. The obtained solution was electrospun with an applied voltage of 15KV, a receiving distance of 12cm, a spinning speed of 0.7ml / h, and a spinneret diameter of 0.8mm. The diameter of the obtained nanofiber is between 350nm and 1000nm.

Embodiment 2

[0031] Weigh 0.0133g of 5-fluorouracil with a balance and dissolve it in 0.5ml of glacial acetic acid, and heat it slightly to dissolve it completely, weigh 0.66g of polylactic acid PLLA and 0.0133g of tetramethylporphine with a balance, and dissolve them in In chloroform, and seal the bottle to prevent solvent volatilization, stir on a magnetic stirrer until completely dissolved. Then add the glacial acetic acid solution of 5-fluorouracil prepared above, and continue to stir on the magnetic stirrer; let the uniformly mixed solution stand for 5 hours, open the bottle mouth, then add 3ml of acetone, stir evenly, and obtain static electricity Spun polymer solution. Electrospinning was performed on the obtained solution, the applied voltage was 20KV, the receiving distance was 12cm, the spinning speed was 0.8ml / h, and the diameter of the spinneret was 0.8mm. The diameter of the obtained nanofiber is between 500nm and 1500nm.

Embodiment 3

[0033]Weigh 0.0133g of 5-fluorouracil with a balance and dissolve it in 0.5ml of glacial acetic acid, and heat it slightly to dissolve it completely, weigh 0.66g of polylactic acid PLLA and 0.0133g of tetramethylporphin with a balance, and dissolve them in 7ml In chloroform, and seal the bottle to prevent solvent volatilization, stir on a magnetic stirrer until completely dissolved. Then add the glacial acetic acid solution of 5-fluorouracil prepared above, and continue to stir on the magnetic stirrer; after the uniformly mixed solution was left to stand for 5 hours, the bottle mouth was opened, and then 3ml of acetone was added, and stirred evenly, to obtain Electrospinning polymer solutions. Electrospinning was performed on the obtained solution, the applied voltage was 15KV, the receiving distance was 12cm, the spinning speed was 0.8ml / h, and the diameter of the spinneret was 0.8mm. The diameter of the obtained nanofiber is between 400nm and 1200nm.

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

PropertyMeasurementUnit
diameteraaaaaaaaaa
diameteraaaaaaaaaa
diameteraaaaaaaaaa
Login to View More

Abstract

The invention relates to an anti-cancer drug-loading nanofiber film and a preparation method thereof. The nanofiber film is composed of a loading drug and a substrate, wherein a photosensitizer and a chemotherapeutic drug in a molar ratio of 1:(1-2) are used as the loading drug of the nanofiber film; a biodegradable high molecular material is used as the substrate of the nanofiber film; and the total drug mass is 4% of the substrate mass. The preparation method comprises the steps of: (1) adding the chemotherapeutic drug to glacial acetic acid, heating to dissolve the drug to obtain a chemotherapeutic drug solution; adding the photosensitizer and the biodegradable high molecular material into an organic solvent, uniformly stirring, and then adding the chemotherapeutic drug solution to prepare a high polymer solution; and (2) carrying out electrostatic spinning on the high polymer solution, and volatilizing the organic solvent and the glacial acetic acid to obtain the anti-cancer drug-loading nanofiber film. The anti-cancer drug-loading nanofiber film can be used as a wound dressing at an operation wound for preventing infection, stopping bleeding and promoting healing of the operation wound; and the preparation method has the advantages of simplicity in operation, low cost, good drug slow-release performance and broad application prospect.

Description

technical field [0001] The invention belongs to the field of composite nanofiber and its preparation, in particular to a nanofiber membrane loaded with anticancer drugs and its preparation method. Background technique [0002] Tumor is a common and frequently-occurring disease that seriously threatens human life. According to WHO statistics, among the 6 billion people in the world, an average of 6.9 million people die from malignant tumors each year, and 8.7 million new cases are diagnosed, and the number is still increasing year by year. At present, there are 1.8 million cancer patients in my country, and the mortality rate is the second among all causes. Therefore, governments, research institutes and pharmaceutical companies all over the world have been giving great importance and support to the research on tumor therapeutic drugs and methods. At present, the commonly used methods for clinical treatment of tumors include chemotherapy, radiotherapy and surgical resection...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Patents(China)
IPC IPC(8): A61K9/70A61K45/06A61K41/00A61K47/34A61P35/00
Inventor 陈志龙陈娜刘志强严懿嘉
Owner DONGHUA UNIV
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products