Unlock instant, AI-driven research and patent intelligence for your innovation.

PLGA (poly(lactic-co-glycolic acid) fiber-microsphere dual-drug-loaded composite scaffold and preparation method of PLGA fiber-microsphere dual-drug-loaded composite scaffold

A composite stent and dual drug-loading technology, which is applied in the fields of medical science and prosthesis, can solve problems such as complex methods, and achieve the effects of simple methods, avoiding inactivation, and high biological safety

Active Publication Date: 2016-08-24
NORTHWESTERN POLYTECHNICAL UNIV
View PDF5 Cites 17 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0007] In order to overcome the shortcomings of the complex method of preparing PLGA fiber-microsphere dual drug-loaded composite scaffold, the present invention provides a PLGA fiber-microsphere dual drug-loaded composite scaffold and its preparation method

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
  • PLGA (poly(lactic-co-glycolic acid) fiber-microsphere dual-drug-loaded composite scaffold and preparation method of PLGA fiber-microsphere dual-drug-loaded composite scaffold

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0024] Example 1: 200 mg of PLGA (100 kDa, 75 / 25) was weighed, and 50 mg of simvastatin was dissolved in a mixed solvent of dichloromethane and N,N-dimethylformamide (2:1, v / v) , sealed, left at 4°C overnight, magnetically stirred for 4h, vortexed for 10min, ultrasonicated for 30s to eliminate air bubbles, and a uniform electrospinning solution containing simvastatin was obtained; PLGA (50kDa, 50 / 50) and BMP-2 were prepared uniformly electrospray solution. The specific method is as follows: dissolve 60 mg of PLGA (50kDa, 50 / 50) in dichloromethane, seal it, let stand at 4°C overnight, stir magnetically for 4 hours, vortex for 10 minutes, and then sonicate for 45 seconds to eliminate air bubbles to obtain a PLGA solution; 2 200ug was dissolved in 4mL PBS buffer solution; 100μL of BMP-2-containing PBS solution was added to the PLGA solution, in an ice bath, ultrasonicated for 5s, stopped for 5s, and then ultrasonicated for 5s, repeated 10 times, emulsified to obtain a uniform BMP...

Embodiment 2

[0025]Example 2: 200 mg of PLGA (100 kDa, 75 / 25) was weighed, and 20 mg of lovastatin was dissolved in a mixed solvent of dichloromethane and N,N-dimethylformamide (2:1, v / v) , sealed, left standing overnight at 0°C, magnetically stirred for 5.5h, vortexed for 15min, and ultrasonicated for 45s to eliminate air bubbles to obtain a uniform electrospinning solution containing lovastatin; PLGA (55kDa, 50 / 50) and EGF were prepared into a uniform EFI solution. The specific method is as follows: Dissolve 60 mg of PLGA (55kDa, 50 / 50) in dichloromethane, seal it, let it stand overnight at 0°C, stir magnetically for 5 hours, vortex for 10 minutes, and then sonicate for 60 seconds to eliminate bubbles to obtain a PLGA solution; EGF 10ug Dissolve in 10mL of PBS buffer solution; add 200μL of EGF-containing PBS solution to PLGA solution, in ice bath condition, sonicate for 5s, stop for 5s, and then sonicate for 5s, repeat 8 times, and emulsify to obtain a uniform electrospray solution conta...

Embodiment 3

[0026] Example 3: 200 mg of PLGA (120 kDa, 75 / 25) was weighed, and 10 mg of pravastatin was dissolved in a mixed solvent of dichloromethane and N, N-dimethylformamide (2:1, v / v) , sealed, left standing overnight at 0°C, magnetically stirred for 5h, vortexed for 15min, ultrasonicated for 60s to eliminate air bubbles, and a uniform electrospinning solution containing pravastatin was obtained; PLGA (60kDa, 50 / 50) and TGF-β were prepared uniformly electrospray solution. The specific method is as follows: dissolve 60 mg of PLGA (60kDa, 50 / 50) in dichloromethane, seal it, let stand at 0°C overnight, stir magnetically for 4.5 hours, vortex for 15 minutes, and then sonicate for 30 seconds to eliminate air bubbles to obtain a PLGA solution; -β10ug was dissolved in 10mL of PBS buffer solution; 100μL of TGF-β-containing PBS solution was added to the PLGA solution, in an ice bath, ultrasonicated for 5s, stopped for 5s, and then ultrasonicated for 5s, repeated 10 times, emulsified to obtai...

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
molecular weightaaaaaaaaaa
molecular weightaaaaaaaaaa
Login to View More

Abstract

The invention discloses a PLGA (poly(lactic-co-glycolic acid) fiber-microsphere dual-drug-loaded composite scaffold and a preparation method of the PLGA fiber-microsphere dual-drug-loaded composite scaffold and aims to solve the technical problem of complexity of a conventional preparation method of the PLGA fiber-microsphere dual-drug-loaded composite scaffold. The technical scheme comprises steps as follows: an electrostatic spinning liquid containing statin drugs is prepared from PLGA fibers and the statin drugs, a homogeneous electronic injection solution is prepared from the PLGA fibers and bioactive factors in a mass ratio being (20-600,000):1, finally, the prepared electrostatic spinning liquid and the electronic injection solution are subjected to electrospinning and electronic injection simultaneously, collected scaffold materials are placed in a vacuum drying oven to be dried for 24-48 h, and the PLGA fiber-microsphere composite scaffold material loaded with the station drugs and the bioactive factors is obtained. With the adoption of an electronic injection method of an emulsion, a water-in-oil emulsion is formed, inactivation caused by direct contact of the drugs and an organic solvent is avoided, and the method is simple. Meanwhile, a surfactant and an emulsifier are not used in the preparation process, so that the bio-safety is higher.

Description

technical field [0001] The invention relates to a PLGA fiber-microsphere double drug-loaded composite support, and also relates to a preparation method of the PLGA fiber-microsphere double drug-loaded composite support. Background technique [0002] The application of controlled drug release systems has enormous commercial potential, with annual sales in the United States exceeding $1 billion. With the extensive research and application of pharmaceutical degradable polymer materials, controlled release systems are increasing. Degradable polymer gels, microspheres and nanofibers can all be used as drug carriers. In recent years, biocompatible and degradable polymer biomaterials have brought hope for tissue repair and reconstruction as new tissue engineering scaffold materials. However, the existing scaffolds for tissue repair and reconstruction have single functions, and are difficult to meet the complex needs in tissue repair and reconstruction. [0003] Electrospinning t...

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 Applications(China)
IPC IPC(8): A61L27/54A61L27/18A61L27/50
CPCA61L27/18A61L27/50A61L27/54C08L67/04
Inventor 赵雯李姣姣刘文龙靳凯翔牛银波
Owner NORTHWESTERN POLYTECHNICAL UNIV