Sustained release drug nanofibers and preparation method thereof

A technology of nanofibers and slow-release drugs, which is applied in the direction of pharmaceutical formulations, drug delivery, and medical preparations of non-active ingredients. It can solve problems such as unsatisfactory drugs, and achieve improved encapsulation efficiency, maintenance of biological activity, and long-term stable release. Effect

Active Publication Date: 2018-12-11
TSINGHUA UNIV
View PDF2 Cites 8 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0003] The traditional method is to coat the surface of the drug with a slow-release shell, through which the release period of the drug can be extende

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

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Sustained release drug nanofibers and preparation method thereof
  • Sustained release drug nanofibers and preparation method thereof

Examples

Experimental program
Comparison scheme
Effect test

Example Embodiment

[0045] see figure 2 , the embodiment of the present invention also provides a preparation method of the sustained-release drug nanofiber, comprising the following steps:

[0046] S100, providing the drug-loaded nano-microspheres 11;

[0047] S200, mixing the drug-loaded nano-microspheres 11 and the core layer sustained-release material in a solvent to obtain a core layer spinning solution;

[0048] S300, prepare a plurality of shell layer spinning solutions respectively, and each shell layer spinning solution includes a solution of the material of the nanofiber sustained-release layer 20;

[0049] S400, performing coaxial electrospinning on the core layer spinning solution and the plurality of shell layer spinning solutions with a coaxial spinning needle having a plurality of coaxially arranged liquid outlets , for simultaneously outputting the core layer spinning solution and the multiple shell layer spinning solutions.

[0050] The drug-loaded nano-microspheres 11 can be...

Example Embodiment

[0063] Example 1 Preparation of drug-loaded nano-microspheres 11

[0064] This example is used to prepare drug-loaded nano-microspheres 11 with two-layer nano-microsphere sustained-release layers, and the nano-microsphere sustained-release layers are respectively chitin layer and BSA layer.

[0065] Mix 80 μg of BMP-2 and 100 mg of BSA, and dissolve with 10 mL of deionized water under slight magnetic stirring to obtain a drug-loaded BSA aqueous solution;

[0066] Add 50 mg of chitin to 50 mL of 0.5wt% acetic acid solution, stir magnetically, and prepare a 1 mg / mL chitin solution;

[0067] Under the condition of magnetic stirring, a total of 40 mL of ethanol was uniformly injected into the drug-loaded BSA aqueous solution of the first step at a speed of 2 mL / h with a micro-syringe pump, and then stirred overnight;

[0068] Under the condition of magnetic stirring, 40 mL of the chitin solution prepared in the second step was injected at a constant speed of 0.5 mL / min with a mic...

Example Embodiment

[0071] Example 2 Preparation of drug-loaded nano-microspheres 11

[0072] The difference between this example and Example 1 is only that the nano-microsphere sustained-release layer of the drug-loaded nano-microsphere 11 has three layers, which are a chitin layer, a BSA layer and a chitin layer, respectively.

[0073] Mix 80 μg of BMP-2 and 100 mg of BSA, and dissolve with 10 mL of deionized water under slight magnetic stirring to obtain a drug-loaded BSA aqueous solution;

[0074] Add 50 mg of chitin to 50 mL of 0.5wt% acetic acid solution, stir magnetically, and prepare a 1 mg / mL chitin solution;

[0075] Under the condition of magnetic stirring, a total of 40 mL of ethanol was uniformly injected into the drug-loaded BSA aqueous solution of the first step at a speed of 2 mL / h with a micro-syringe pump, and then stirred overnight;

[0076]Under the condition of magnetic stirring, inject 40 mL of the chitin solution at a constant speed of 0.5 mL / min with a micro-syringe pump,...

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
Quality scoreaaaaaaaaaa
Login to view more

Abstract

The invention discloses sustained release drug nanofibers which are of a core-shell structure and comprise multiple nanofiber sustained release layers and nanofiber cores; each nanofiber core is wrapped with multiple nanofiber sustained release layers and comprises a mixed drug-loaded nanoparticle and a core layer sustained release layer; and the mixed drug-loaded nanoparticle is of the core-shellstructure and comprises an active drug and nanoparticle sustained release layers wrapping the active drug. The invention also discloses a preparation method of the sustained release drug nanofibers.

Description

technical field [0001] The invention relates to the field of biomaterials, in particular to sustained-release drug nanofibers and a preparation method thereof. Background technique [0002] Some drug treatments for diseases require a certain cycle, such as bone cell repair, periodontitis, etc. If it is directly injected into the body, the drug will be rapidly dispersed and degraded in a short period of time, such as within a day, and cannot play a long-term role in promoting recovery. Therefore, how to maintain and prolong the biological activity of the drug in the body environment is the key to the drug's real clinical effect. In order to solve the problem of high-efficiency application of drugs, drug controlled release technology can be introduced. That is, the use of biodegradable polymer materials to load drugs, quantitative and sustained release to seed cells, so that the drug can maintain activity for a long time, which is also an important factor in the evaluation o...

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
IPC IPC(8): A61K9/00A61K9/51A61K9/52A61K31/192A61K31/4164A61K31/65A61K38/18A61K47/34A61K47/36A61K47/42
CPCA61K9/0092A61K9/5161A61K9/5169A61K31/192A61K31/4164A61K31/65A61K38/1825A61K38/1841A61K38/1858A61K38/1866A61K38/1875A61K47/34A61K47/36A61K47/42
Inventor 张洪玉王毅
Owner TSINGHUA UNIV
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products