CN107875453A - Carry preparation method of Types of Medicine electrostatic spinning guide tissue regeneration film and products thereof and application - Google Patents

Carry preparation method of Types of Medicine electrostatic spinning guide tissue regeneration film and products thereof and application Download PDF

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Publication number
CN107875453A
CN107875453A CN201711098475.9A CN201711098475A CN107875453A CN 107875453 A CN107875453 A CN 107875453A CN 201711098475 A CN201711098475 A CN 201711098475A CN 107875453 A CN107875453 A CN 107875453A
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China
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hnts
pmb
preparation
tissue regeneration
medicine
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CN201711098475.9A
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Inventor
何丹农
祝闪闪
周涓
王萍
金彩虹
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Shanghai National Engineering Research Center for Nanotechnology Co Ltd
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Shanghai National Engineering Research Center for Nanotechnology Co Ltd
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Priority to CN201711098475.9A priority Critical patent/CN107875453A/en
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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L27/00Materials for grafts or prostheses or for coating grafts or prostheses
    • A61L27/50Materials characterised by their function or physical properties, e.g. injectable or lubricating compositions, shape-memory materials, surface modified materials
    • A61L27/54Biologically active materials, e.g. therapeutic substances
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L27/00Materials for grafts or prostheses or for coating grafts or prostheses
    • A61L27/02Inorganic materials
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L27/00Materials for grafts or prostheses or for coating grafts or prostheses
    • A61L27/14Macromolecular materials
    • A61L27/18Macromolecular materials obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L27/00Materials for grafts or prostheses or for coating grafts or prostheses
    • A61L27/14Macromolecular materials
    • A61L27/22Polypeptides or derivatives thereof, e.g. degradation products
    • A61L27/222Gelatin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L27/00Materials for grafts or prostheses or for coating grafts or prostheses
    • A61L27/50Materials characterised by their function or physical properties, e.g. injectable or lubricating compositions, shape-memory materials, surface modified materials
    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01DMECHANICAL METHODS OR APPARATUS IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS
    • D01D5/00Formation of filaments, threads, or the like
    • D01D5/0007Electro-spinning
    • D01D5/0015Electro-spinning characterised by the initial state of the material
    • DTEXTILES; PAPER
    • D04BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04HMAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
    • D04H1/00Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
    • D04H1/70Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres characterised by the method of forming fleeces or layers, e.g. reorientation of fibres
    • D04H1/72Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres characterised by the method of forming fleeces or layers, e.g. reorientation of fibres the fibres being randomly arranged
    • D04H1/728Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres characterised by the method of forming fleeces or layers, e.g. reorientation of fibres the fibres being randomly arranged by electro-spinning
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L2300/00Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices
    • A61L2300/20Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices containing or releasing organic materials
    • A61L2300/252Polypeptides, proteins, e.g. glycoproteins, lipoproteins, cytokines
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L2300/00Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices
    • A61L2300/40Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices characterised by a specific therapeutic activity or mode of action
    • A61L2300/404Biocides, antimicrobial agents, antiseptic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L2430/00Materials or treatment for tissue regeneration
    • A61L2430/02Materials or treatment for tissue regeneration for reconstruction of bones; weight-bearing implants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L2430/00Materials or treatment for tissue regeneration
    • A61L2430/12Materials or treatment for tissue regeneration for dental implants or prostheses

Abstract

The present invention relates to preparation method for carrying Types of Medicine electrostatic spinning guide tissue regeneration film and products thereof and application, including carry medicine HNTs preparation and the preparation of Static Spinning medicament-carrying composite nano-fiber membrane.The present invention loads cancer therapy drug, the phenomenon of burst release that simple medicine can be avoided to occur with high polymer mixing Static Spinning using the HNTs with hollow structure as pharmaceutical carrier so that the multiple guide tissue regeneration film of the Static Spinning of preparation has good therapeutic effect;The inorganic HNTs of doping can improve the mechanical property of composite cellulosic membrane in Static Spinning polymer nanofiber of the present invention, and with good biocompatibility, degradability and promote bone uptake etc., be advantageous to medicament-carrying nano-fiber and be applied to environment inside complexity as functional organizations engineering scaffold material;It is green and raw material HNTs is a kind of cheap natural nano pipe of well-crystallized, and guide tissue regeneration film preparation method technique is simple, it is workable, it further can meet to produce and apply.

Description

Carry preparation method of Types of Medicine electrostatic spinning guide tissue regeneration film and products thereof and application
Technical field
The present invention relates to a kind of preparation method for carrying Types of Medicine electrostatic spinning guide tissue regeneration film and products thereof and application.Tool Body is using the poly- of tool degradability and good biocompatibility(Racemic lactic acid-co- caprolactones)With gelatin as matrix material Material, using galapectite as pharmaceutical carrier, a kind of composite nano-fiber membrane with antibacterial effect is prepared by electrostatic spinning technique.This Invention belongs to nano biological medical material field.
Background technology
The problem of periodontium and bone tissue defect are common in clinic, guided tissue regeneration are that treatment Cranial defect is most general Time one of means, improve the performance of guide tissue regeneration film, prepare new guide tissue regeneration film and periodontal and bone are repaiied Multiple regeneration is of great importance.The preparation of guide tissue regeneration (Guided Tissue Regeneration, GTR) membrane material is group Knit one of core technology of engineering research.Cell has preferably adhesion special on the fiber of the diameter (nanoscale) less than itself Property, therefore, the porous three-dimensional cytoskeleton prepared using electrostatic spinning is capable of the structure of preferably bionical natural extracellular matrix Feature, it is expected to turn into preferable guide tissue regeneration film material.
Macromolecule with biocompatibility particularly natural polymer such as collagen, chitosan, fibroin albumen etc. are by quiet Fibrofelt obtained by Electrospun has the characteristics that porosity is high, aperture is adjustable, structure-biological compatibility is good, in guiding tissue again Filming Material Field has broad application prospects.Gelatin(GE)It is to be prepared by the collagen hydrolysate in animal body, has Good biocompatibility, degradability and low immunogenicity.But its degradation speed is fast, early stage is easily caused to be collapsed in vivo Fall into, mechanical property deficiency.So in order to improve its mechanical property and degradation speed, typically using compound other polymers.It is poly-(Disappear Revolve lactic acid-co- caprolactones)(P(DLLA-co-CL))It is a kind of there is good biocompatibility and biodegradable high score Sub- polymer, its electrospinning fibre support can be applied to intravascular tissue engineering field, have good toughness.
Halloysite nanotubes (HNTs) are a kind of middle empty nanotubes of natural aluminosilicate hydrochlorate, cheap, are had necessarily The features such as draw ratio, big natural nano space and inner chamber load volume.Due to its stable structure, excellent mechanical property, heat Stability and biocompatibility, it is widely used at present among the developmental research of high polymer composite nano material.For passing The polymer nanofiber mechanical strength of system is low, the pharmaceutical dosage form such as common nano particle, liposome, micella and some electrostatic Spinning nano fibre carries pharmaceutically dosage form and phenomenon of burst release be present, and the problems such as nanotube medicine-carried system non-device, the present invention is by adopting The method being combined after carrying medicine with nanotube with electrostatic spinning technique, is prepared for medicament-carried nano pipe/polymer composite fiber film, So as to realize the release of permanent insoluble drug release and high drug concentration, novel antibacterial guide tissue regeneration film material can be used as.
The content of the invention
For overcome the deficiencies in the prior art, the present invention relates to a kind of preparation for carrying Types of Medicine electrostatic spinning guide tissue regeneration film Method and products thereof and application.Galapectite load antimicrobial DP finish polymyxins b is used first(PMB)(PMB/HNTs), then will PMB/HNTs, GE, P (DLLA-co-CL) are dissolved in hexafluoroisopropanol with certain proportioning(HFIP)In, pass through electrostatic spinning skill Art equipment is prepared PMB/HNTs/GE/ P (DLLA-co-CL) load medicines under certain voltage, reception distance, solution flow rate and answered Close nano fibrous membrane.The hybrid composite nano fiber system has among organizational project and regenerative medicine field It is widely applied prospect.
For purpose as realization, in the inventive solutions, one kind carries Types of Medicine electrostatic spinning guide tissue regeneration The preparation method of film, with natural nano pipe galapectite(HNTs)For raw material, contained medicine is polymyxins b(PMB), including it is following Step:
(1)Carry medicine HNTs preparation
Take a certain amount of addition PMB to be dissolved in pure water and stir 20min, add a certain amount of HNTs solution, ultrasonic disperse afterwards 40min so that galapectite(HNTs)In the fully dispersed solution to PMB;PMB and HNTs mixed solutions are placed in vacuum drying chamber, Vacuumized under conditions of 0.05, up to liquid surface, there is no bubble appearance;After vacuum drying chamber is taken out, after stirring 5min It is repeated once and vacuumizes, drive away the bubble of residual in HNTs internal cavities, makes the more PMB inside entered;In 3000rpm Under conditions of centrifugation take out supernatant it is stand-by, clean precipitation with ultra-pure water, will load medicinal powder end under conditions of 50 DEG C drying 24h, It is stand-by with using screen filtration after agate mortar mill-drying powder again;
(2)The preparation of Static Spinning medicament-carrying composite nano-fiber membrane
PMB/the HNTs that will necessarily match, gather(Racemic lactic acid-co- caprolactones)(P(DLLA-co-CL))And gelatin(GE)Add Hexafluoroisopropanol(HFIP)In, be made into mass concentration 8-10% solution, stir at room temperature obtain after 6 ~ 12h one it is homogeneous molten Liquid, resulting solution is loaded in a 10 mL glass syringes, in the KV of spinning voltage 10 ~ 13, spinning receive distance for 12 ~ 15 cm, under the conditions of solution flow rate is 0.4 ~ 0.5 mL/h, PMB/HNTs/ gelatin/P is obtained by electrospinning device (DLLA-co-CL) composite nano-fiber membrane, gained film is put into vacuum drying oven after spinning be dried overnight at room temperature it is standby With.
Described galapectite is 100-300nm.
Described medicine is antimicrobial DP finish polymyxins b.
The present invention provides a kind of load Types of Medicine electrostatic spinning guide tissue regeneration film, is prepared into according to any of the above-described methods described Arrive, the inorganic doping material part of guide tissue regeneration film is galapectite, and organic material part is poly-(Racemic lactic acid-co- is in oneself Ester)(P(DLLA-co-CL))And gelatin(GE).
The present invention provides a kind of load Types of Medicine electrostatic spinning guide tissue regeneration film answering in the reparative regeneration of periodontal and bone With.
The advantage of the invention is that:
(1)The present invention loads cancer therapy drug using the HNTs with hollow structure as pharmaceutical carrier, can avoid simple medicine The phenomenon of burst release that thing occurs with high polymer mixing Static Spinning so that the multiple guide tissue regeneration film of the Static Spinning of preparation has good Therapeutic effect;
(2)Mechanical property of the inorganic HNTs of doping with composite cellulosic membrane can be improved in Static Spinning polymer nanofiber of the present invention Can, and with good biocompatibility, degradability and promote bone uptake performance, be advantageous to medicament-carrying nano-fiber as function Type tissue engineering bracket material is applied to environment inside complexity;
(3)Raw material HNTs in the present invention is a kind of cheap natural nano pipe of well-crystallized, green, and guiding group It is simple to knit regeneration membrane preparation method technique, it is workable, it further can meet to produce and apply.
Embodiment
Technical scheme is further described below by way of specific embodiment.Following embodiment is to this The further explanation of invention, and do not limit the scope of the invention.
Embodiment 1
1. carry medicine HNTs preparation
Take a certain amount of addition PMB to be dissolved in pure water and stir 20min, add a certain amount of HNTs solution, ultrasonic disperse afterwards 40min so that in the fully dispersed solution to PMB of HNTs so that HNTs and PMB concentration ratio is 1:2.PMB and HNTs is mixed Solution is placed in vacuum drying chamber, is vacuumized under conditions of 0.05, and up to liquid surface, there is no bubble appearance.From vacuum drying After case is taken out, it is repeated once and vacuumizes after stirring 5min, drive away the bubble of residual in HNTs internal cavities, make entering for more PMB The inside entered.Centrifugation taking-up supernatant is stand-by under conditions of 3000rpm, and precipitation is cleaned with ultra-pure water.Medicinal powder end will be carried to exist 24h is dried under conditions of 50 DEG C.It is stand-by with using screen filtration after agate mortar mill-drying powder again.
2. the preparation of Static Spinning medicament-carrying composite nano-fiber membrane
Certain 0g PMB/HNTs, 0.23g GE and 0.46 g P (DLLA-co-CL) are added in 7.53g HFIP, are made into molten Liquid, a homogeneous solution is obtained after stirring 6 ~ 12h at room temperature.Resulting solution is loaded in a 10 mL glass syringes, The KV of spinning voltage 10 ~ 13, it is 12 ~ 15 cm that spinning, which receives distance, under the conditions of solution flow rate is 0.4 ~ 0.5 mL/h, is passed through Electrospinning device obtains PMB/HNTs/ gelatin/P (DLLA-co-CL) composite nano-fiber membrane, by gained film after spinning Be put into vacuum drying oven be dried overnight at room temperature it is standby.
Embodiment 2
1. carry medicine HNTs preparation
Take a certain amount of addition PMB to be dissolved in pure water and stir 20min, add a certain amount of HNTs solution, ultrasonic disperse afterwards 40min so that in the fully dispersed solution to PMB of HNTs so that HNTs and PMB concentration ratio is 1:2.PMB and HNTs is mixed Solution is placed in vacuum drying chamber, is vacuumized under conditions of 0.05, and up to liquid surface, there is no bubble appearance.From vacuum drying After case is taken out, it is repeated once and vacuumizes after stirring 5min, drive away the bubble of residual in HNTs internal cavities, make entering for more PMB The inside entered.Centrifugation taking-up supernatant is stand-by under conditions of 3000rpm, and precipitation is cleaned with ultra-pure water.Medicinal powder end will be carried to exist 24h is dried under conditions of 50 DEG C.It is stand-by with using screen filtration after agate mortar mill-drying powder again.
2. the preparation of Static Spinning medicament-carrying composite nano-fiber membrane
Certain 0.145g PMB/HNTs, 0.23g GE and 0.46 g P (DLLA-co-CL) are added in 9.82g HFIP, matched somebody with somebody Into solution, a homogeneous solution is obtained after stirring 6 ~ 12h at room temperature.Resulting solution is loaded into a 10 mL glass syringes Interior, in the KV of spinning voltage 10 ~ 13, it is 12 ~ 15 cm that spinning, which receives distance, under the conditions of solution flow rate is 0.4 ~ 0.5 mL/h, PMB/HNTs/ gelatin/P (DLLA-co-CL) composite nano-fiber membrane is obtained by electrospinning device, by institute after spinning Film be put into vacuum drying oven be dried overnight at room temperature it is standby.
Embodiment 3
1. carry medicine HNTs preparation
Take a certain amount of addition PMB to be dissolved in pure water and stir 20min, add a certain amount of HNTs solution, ultrasonic disperse afterwards 40min so that in the fully dispersed solution to PMB of HNTs so that HNTs and PMB concentration ratio is 1:2.PMB and HNTs is mixed Solution is placed in vacuum drying chamber, is vacuumized under conditions of 0.05, and up to liquid surface, there is no bubble appearance.From vacuum drying After case is taken out, it is repeated once and vacuumizes after stirring 5min, drive away the bubble of residual in HNTs internal cavities, make entering for more PMB The inside entered.Centrifugation taking-up supernatant is stand-by under conditions of 3000rpm, and precipitation is cleaned with ultra-pure water.Medicinal powder end will be carried to exist 24h is dried under conditions of 50 DEG C.It is stand-by with using screen filtration after agate mortar mill-drying powder again.
2. the preparation of Static Spinning medicament-carrying composite nano-fiber membrane
Certain 0.661g PMB/HNTs, 0.23g GE and 0.46 g P (DLLA-co-CL) are added in 14.07g HFIP, matched somebody with somebody Into solution, a homogeneous solution is obtained after stirring 6 ~ 12h at room temperature.Resulting solution is loaded into a 10 mL glass syringes Interior, in the KV of spinning voltage 10 ~ 13, it is 12 ~ 15 cm that spinning, which receives distance, under the conditions of solution flow rate is 0.4 ~ 0.5 mL/h, PMB/HNTs/ gelatin/P (DLLA-co-CL) composite nano-fiber membrane is obtained by electrospinning device, by institute after spinning Film be put into vacuum drying oven be dried overnight at room temperature it is standby.
Embodiment 4
1. carry medicine HNTs preparation
Take a certain amount of addition PMB to be dissolved in pure water and stir 20min, add a certain amount of HNTs solution, ultrasonic disperse afterwards 40min so that in the fully dispersed solution to PMB of HNTs so that HNTs and PMB concentration ratio is 1:1.PMB and HNTs is mixed Solution is placed in vacuum drying chamber, is vacuumized under conditions of 0.05, and up to liquid surface, there is no bubble appearance.From vacuum drying After case is taken out, it is repeated once and vacuumizes after stirring 5min, drive away the bubble of residual in HNTs internal cavities, make entering for more PMB The inside entered.Centrifugation taking-up supernatant is stand-by under conditions of 3000rpm, and precipitation is cleaned with ultra-pure water.Medicinal powder end will be carried to exist 24h is dried under conditions of 50 DEG C.It is stand-by with using screen filtration after agate mortar mill-drying powder again.
2. the preparation of Static Spinning medicament-carrying composite nano-fiber membrane
Certain 0.145g PMB/HNTs, 0.23g GE and 0.46 g P (DLLA-co-CL) are added in 9.82g HFIP, matched somebody with somebody Into solution, a homogeneous solution is obtained after stirring 6 ~ 12h at room temperature.Resulting solution is loaded into a 10 mL glass syringes Interior, in the KV of spinning voltage 10 ~ 13, it is 12 ~ 15 cm that spinning, which receives distance, under the conditions of solution flow rate is 0.4 ~ 0.5 mL/h, PMB/HNTs/ gelatin/P (DLLA-co-CL) composite nano-fiber membrane is obtained by electrospinning device, by institute after spinning Film be put into vacuum drying oven be dried overnight at room temperature it is standby.

Claims (4)

1. a kind of preparation method for carrying Types of Medicine electrostatic spinning guide tissue regeneration film, it is characterised in that with natural nano pipe angstrom Lip river Stone(HNTs)For raw material, contained medicine is polymyxins b(PMB), comprise the following steps:
(1)Carry medicine HNTs preparation
Take a certain amount of PMB to be dissolved in pure water and stir 20min, add a certain amount of HNTs solution afterwards, ultrasonic disperse 40min, So that in the fully dispersed solution to PMB of HNTs;PMB and HNTs mixed solutions are placed in vacuum drying chamber, under conditions of 0.05 Vacuumize, up to liquid surface, there is no bubble appearance;After vacuum drying chamber is taken out, it is repeated once and is taken out very after stirring 5min Sky, drive away the bubble of residual in HNTs internal cavities, more PMB is entered inside;Centrifuge and take out under conditions of 3000rpm Supernatant is stand-by, and precipitation is cleaned with ultra-pure water, will carry medicinal powder end and 24h is dried under conditions of 50 DEG C, ground with agate mortar dry Use screen filtration after dry powder again, obtained PMB/HNTs is stand-by;
(2)The preparation of Static Spinning medicament-carrying composite nano-fiber membrane
PMB/the HNTs that will necessarily match, gelatin(GE)With it is poly-(Racemic lactic acid-co- caprolactones)(P(DLLA-co-CL))Add In HFIP, mass concentration 8-10% solution is made into, a homogeneous solution is obtained after stirring 6 ~ 12h at room temperature, by resulting solution Load in a 10 mL glass syringes, in the KV of spinning voltage 10 ~ 13, it is 12 ~ 15 cm that spinning, which receives distance, solution flow rate Under the conditions of 0.4 ~ 0.5 mL/h, PMB/HNTs/ gelatin/P (DLLA-co-CL) is compound is obtained by electrospinning device and received Rice tunica fibrosa, gained film is put into vacuum drying oven after spinning be dried overnight at room temperature it is standby.
A kind of 2. load Types of Medicine electrostatic spinning guide tissue regeneration film according to claim 1 and preparation method thereof, it is characterised in that Described HNTs is 100-300nm.
3. one kind carries Types of Medicine electrostatic spinning guide tissue regeneration film, it is characterised in that according to any methods described of claim 1 or 2 It is prepared, the inorganic doping material part of guide tissue regeneration film is HNTs, and organic material part is poly-(Racemic lactic acid-co- Caprolactone)(P(DLLA-co-CL))And gelatin(GE).
4. Types of Medicine electrostatic spinning guide tissue regeneration film answering in the reparative regeneration of periodontal and bone is carried according to claim 3 With.
CN201711098475.9A 2017-11-09 2017-11-09 Carry preparation method of Types of Medicine electrostatic spinning guide tissue regeneration film and products thereof and application Pending CN107875453A (en)

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CN109675102A (en) * 2018-11-22 2019-04-26 宋建康 Load the guide tissue regeneration film and preparation method thereof of gelatin micro-nano ball
CN109825955A (en) * 2019-02-03 2019-05-31 南通纺织丝绸产业技术研究院 A kind of hypo-allergenic adult paper diaper of antibacterial and preparation method thereof
CN111249526A (en) * 2020-01-20 2020-06-09 重庆大学 Electrostatic spinning stent with effects of treating melanoma and repairing damaged tissues and preparation method thereof
CN112206342A (en) * 2020-09-27 2021-01-12 广东泰宝医疗科技股份有限公司 Alginate composite dressing and preparation method thereof

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Application publication date: 20180406