CN100515506C - Core/shell type polyurethane magnetic compound microsphere, preparation method and use thereof - Google Patents
Core/shell type polyurethane magnetic compound microsphere, preparation method and use thereof Download PDFInfo
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- CN100515506C CN100515506C CNB2006101251360A CN200610125136A CN100515506C CN 100515506 C CN100515506 C CN 100515506C CN B2006101251360 A CNB2006101251360 A CN B2006101251360A CN 200610125136 A CN200610125136 A CN 200610125136A CN 100515506 C CN100515506 C CN 100515506C
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Abstract
The invention relates to a corn/case polyurethane magnetic composite micro ball, and relative preparation, wherein it uses inorganic magnetic particles as corn, uses polyurethane as case, while its diameter reaches 800micrometer; and its production comprises that: planting -NH and -NH2 groups on the surface of magnetic inorganic powder; than polymerizing into polyurethane prepolymer; forming stable oil/water suspension in the disperser solution; then polymerizing into magnetic inorganic/ polyurethane magnetic composite micro ball. The inventive micro ball has X-ray contrast, high magnetic response and low density of polyurethane macromolecule, etc. And inventive production has simple process and low cost. Said micro ball can be used to prepare vessel plunge material and drug carrier.
Description
Technical field
The present invention relates to a kind of method of solution polymerization core/shell type polyurethane magnetic compound microsphere.
Background technology
Magnetic composite microsphere combines the advantage of magnetic inorganic material and macromolecular material, have a lot of good characteristics, as have magnetic responsiveness, and under the effect of externally-applied magnetic field, can separate easily, density is hanged down suspension stability preferably in solution.The micro phase separation structure of polyurethane makes it have the biocompatibility better than other macromolecular material (comprising blood compatibility and histocompatibility), have excellent high resiliency and high strength simultaneously, and the Barium hexaferrite material there are good X ray development and good magnetic responsiveness.Combine both advantages, polyurethane magnetic compound microsphere is water insoluble, stable in properties, not biodegradation in vivo, having excellent biological compatibility and safety, good magnetic conductance tropism and targeting polarization are arranged, is a kind of potential application foreground composite that has, can be applied in cell separation, immobilized enzyme, target medicine carrier, immunoassay, particularly biomedical sectors such as interventional therapy are filled in the blood vessel inspection.
At present the preparation method of magnetic composite microsphere mainly contains coprecipitation, heteropolymerization method, electroless plating method, ultrasonic method, construction from part etc. successively.Coprecipitation is the method for preparing magnetic composite microsphere in early days, and the advantage of utilizing this legal system to be equipped with magnetic composite microsphere is that method is simple, easy operating, but the complex microsphere particle size distribution broad that makes, and particle diameter is in Nano grade and wayward, out-of-shape.Zhao Wen; introduce with electroless plating method in the paper " polystyrene magnetic microsphere electroless plating method preparation research " that Zhang Qiuyu delivered on " material protection " 2004 the 37th the 12nd phases of volume and prepared polystyrene acrylonitrile (P (St-co-AN)) for examining, Ni is the magnetic microsphere of shell.About core particle diameter 400 nanometers, thickness 10～15 nanometers of shell Ni.It is the complex microsphere of shell that this method is mainly used to prepare with the macromolecule to the nuclear magnetism material.Foreign scholar Caruso F (Magnetic core-shell particles:preparation of magnetite multilayers on polymer latexmicrospheres.Adv.Mater., 1999,11 (11): 950-953) using successively construction from part to prepare monodispersed serves as nuclear PDDA (PDADMAC) and Fe with polystyrene (PS)
3O
4Alternately the magnetic microsphere of the many shells that occur is successively assembled the polymer microsphere controllable granularity system for preparing, and is evenly big or small, magnetic particle content unanimity, but preparation technology is too complicated.The bright grade of domestic Qiu Guang people (preparation of large grain size magnetic polymer microsphere. applied chemistry, 1997,14 (5): 74-76), surperficial swelling initiator polyreaction at magnetic particle takes place on the magnetic particle surface, making particle diameter is situated between and 50～500 microns big particle diameter microsphere, but the microsphere magnetic responsiveness of this method preparation relatively a little less than, magnetic property is wayward.
Summary of the invention
The purpose of this invention is to provide a kind of polyurethane magnetic compound microsphere.
Another object of the present invention provides a kind of method of solution polymerization polyurethane magnetic compound microsphere.
This polyurethane magnetic compound microsphere has high magnetic responsiveness, and particle diameter is bigger, and density is low, and suspension stability is good, can develop good biocompatibility by X-ray;
Realize the polyurethane magnetic compound microsphere of the object of the invention, its nuclear is the inorganic magnetic microgranule, and shell is a polyurethane.
The preparation method of polyurethane magnetic compound microsphere of the present invention is at first to pass through the magnetic inorganic micropowder surface modification to about 1 micron, at its surface grafting-NH ,-NH
2Group, then in the presence of the magnetic inorganic micropowder after the modification, original position prepolymerization synthesis of polyurethane prepolymer.The reaction of synthesis of polyurethane prepolymer is from the surface of magnetic inorganic micropowder, prepolymer forms stable oil/water (O/W) suspension system in the aqueous solution that contains polyethylene of dispersing agent ketopyrrolidine (PVP K30) then, suspension polymerisation forms magnetic inorganic/polyurethane magnetic compound microsphere, at last with the microsphere Magnetic Isolation, wash alcohol repeatedly and wash, obtain clean polyurethane magnetic compound microsphere after the drying.
The concrete grammar step is:
Step 1: magnetic inorganic micropowder silane-modified
The adding volume ratio is 2.4: 100: 100 a silane coupler in exsiccant container, distilled water and dehydrated alcohol are made into mixed solution, with the mass/volume ratio is to mixed solution in to add the magnetic inorganic micropowder at 0.5: 100, ultra-sonic dispersion becomes unit for uniform suspension, this suspension transferred to be furnished with reflux condensing tube, sealing is stirred and heated to 70 ± 0.5 ℃ in the drying receptacle of mechanical agitator, isothermal reaction is more than 5 hours, leave standstill washing, solid-liquid separation, more than 5 hours, obtain the magnetic inorganic micropowder of modification 80 ± 1 ℃ of dryings;
Because the water-wet behavior of magnetic inorganic microparticle surfaces, in the easy hydroxylating of magnetic inorganic microparticle surfaces, silane coupler is hydrolyzed to silanol in aqueous solution, the hydroxyl of these silanols with in the hydroxyl generation dehydration of magnetic inorganic microparticle surfaces, the coupling agent chemisorbed is arrived at the magnetic inorganic microparticle surfaces, and this process can be used formula (1) (2) expression:
Step 2: prepolymerization
Magnetic inorganic micropowder after the surface modification that step 1 is obtained is configured to suspension by mass/volume than 1: 60～100 with organic solvent dimethylbenzene, after ultra-sonic dispersion is even, transfer in the container that agitator is housed, with-1: 1 polynary two isocyanide ester and polyvalent alcohol of adding of NCO/-OH mol ratio, the prepolymerization of sealing stirring at normal temperature obtained the xylene solution of prepolymer more than 3 hours;
Isocyanates and active hydrogen compounds reaction sequence be-NH＞-NH
2＞-OH＞H
2Following polyreaction, can take place by the order that adds reactant in O＞COOH: during prepolymerization, toluene di-iso-cyanide ester (TDI) elder generation and magnetic inorganic surface grafting-NH ,-NH
2Reaction generates the urea that contains end-NCO group and is grafted to the surface of microgranule (as reaction (3), (4)); After adding PEG, end-NCO and unreacted TDI and PEG reaction generate carbamate (as reaction (5)).
Step 3: suspension polymerisation
Press the aqueous solution of mass volume ratio configuration in 1: 100 polyethylene of dispersing agent ketopyrrolidine (PVP K30), be heated to 70 ± 1 ℃, the xylene solution of the prepolymer that dropping step 2 obtains in solution, dropping accounts for glycerol and several triethanolamine of solution 0.4% (volume), sealing was stirred the constant temperature polymerization more than 5 hours, the Magnetic Isolation complex microsphere, and washing, alcohol are washed repeatedly, drying promptly obtains clean core/shell type polyurethane magnetic compound microsphere.
Owing to be dissolved with low molecular polylols such as glycerol and triethanolamine in the solution system,, form the shell (as reaction (6)) of microsphere so crosslinked fast and chain extending reaction can take place on the surface of the microgranule that forms in prepolymerization during suspension polymerisation.
R in the reaction equation
1-NCO, R
2-NCO, R
3-NCO is the toluene di-isocyanate(TDI) end isocyanate group (NCO) polyurethanes partially polymerized with different extent of polymerizations.
Wherein, step 1 described magnetic inorganic micropowder be for can developing under X-ray, particle diameter less than or near 1 micron Barium hexaferrite (BaFe
12O
19), ferroso-ferric oxide, Conjugate ferrite (CoxFe
2-xO
4), γ-iron sesquioxide microparticle material.
The described silane coupler of step 1 is for having-NH-NH
2The silane coupler of reactive group; Described having-NH ,-NH
2The silane coupler of reactive group is N-β-aminopropyl trimethoxysilane, or aminopropyl trimethoxysilane.
The described multicomponent isocyanate of step 2 is toluene two cyanates, or methyl diphenylene diisocyanate.
The described polyvalent alcohol of step 2 is Polyethylene Glycol or polyester.
The magnetic polyurethane microsphere of the present invention's preparation is characterised in that: 1) magnetic core combines firmly with the polyurethane shell; 2) particle diameter is controlled within the specific limits; 3) density is low, and suspending stabilized performance is good, and magnetic property can be regulated by the magnetisable material content of regulating in the microsphere; 4) X-ray can develop down, and thermal stability is good, good biocompatibility.Simple, the low production cost of the preparation method of related polyurethane magnetic compound microsphere among the present invention, microspheres quality are good, are easy to suitability for industrialized production.
Magnetic inorganic micropowder silane-modified be for the polyurethane compound tense, inorganic matter can with the polyurethane strong bonded.
With polyurethane is that shell is in order to utilize the active group of polyurethane surface, to be convenient to medicine carrying and somatomedin etc.
The magnetic polyurethane microsphere of the present invention preparation can be applied in cell separation, immobilized enzyme, target medicine carrier, immunoassay, particularly biomedical sector such as blood vessel embolism interventional therapy.Be used to prepare the blood vessel embolism injectable suspensions.
Description of drawings
Fig. 1 is that the gained Barium hexaferrite is the infrared spectrogram of the polyurethane magnetic compound microsphere of nuclear in the embodiment of the invention 1.
Fig. 2 is that the gained Barium hexaferrite is the hysteresis curve of the polyurethane magnetic compound microsphere of nuclear in the embodiment of the invention 1.
Fig. 3 is that the gained Barium hexaferrite is the surface scan Electronic Speculum figure of the polyurethane magnetic compound microsphere of nuclear in the embodiment of the invention 1.
Fig. 4 is that the gained Barium hexaferrite is the cross section sem photograph of the polyurethane magnetic compound microsphere of nuclear in the embodiment of the invention 1.
The specific embodiment
Embodiment 1:
Take by weighing 2 gram BaFe
12O
19Powder joins in the mixed solution that contains 200 milliliters of dehydrated alcohol of 200 ml distilled waters, in solution, dripped 4.8 milliliters of N-β-aminopropyl trimethoxysilane (HC-792) ultra-sonic dispersion 10 minutes, transfer to be furnished with reflux condensing tube, in the dry three-neck flask of mechanical agitator, sealing is stirred and heated to 70 ℃, and washing is left standstill in isothermal reaction 5 hours, solid-liquid separation, drying is 5 hours in 80 ℃ of constant temperature air dry ovens, grinds, and gets the BaFe of modification
12O
19Powder is standby.
Take by weighing 1 BaFe of gram after the modification
12O
19Powder, joined in the dry bottle that 70 milliliters of dimethylbenzene are housed ultra-sonic dispersion 10 minutes, Dropwise 5 milliliter toluene di-isocyanate(TDI), the room temperature sealing was stirred 50 minutes, add 10 gram PEG, 1.5 the milliliter toluene di-isocyanate(TDI) stirred after 120 minutes, the xylene solution of prepolymer splashed into 2% (mass/volume) polyvinylpyrrolidone PVP K30 is housed, in the three-neck flask of 300 ml water solution of several triethanolamine, add 1.5 milliliters of chain extender glycerol, sealing is stirred and heated to 70 ℃, isothermal reaction 5h, to obtain to such an extent that product is washed 4～5 times, magnetic separates, and with the alcohol solution dipping of 50% (volume) 12 hours, drying obtained the brown microsphere.The particle diameter of microsphere is at 50～150 microns.Saturation magnetization 3.36 c.g.s. electromagnetic unit/grams (emu/g), than remanent magnetization 0.93 c.g.s. electromagnetic unit/gram (emu/g), coercivity is 306 oersteds (Oe).
Embodiment 2:
Take by weighing 1 BaFe of gram after the modification
12O
19Powder, joined in the dry bottle that 70 milliliters of dimethylbenzene are housed ultra-sonic dispersion 10 minutes, Dropwise 5 milliliter toluene di-isocyanate(TDI), the room temperature sealing was stirred 50 minutes, add 10 gram cetomacrogol 1000s, 1.5 the milliliter toluene di-isocyanate(TDI) stirred after 120 minutes, the xylene solution of prepolymer splashed into 1% (mass/volume) polyvinylpyrrolidone is housed, in the three-neck flask of 300 ml water solution of several triethanolamine, add 1.5 milliliters of chain extender glycerol, sealing is stirred and heated to 70 ℃, isothermal reaction 5 hours, to obtain to such an extent that product is washed 4～5 times, magnetic separates, and with the alcohol solution dipping of 50% (volume) 12 hours, drying obtained the brown microsphere.The particle diameter of microsphere is at 200～300 microns.
Embodiment 3:
Take by weighing 2 gram Fe
3O
4Powder joins in the mixed solution that contains 200 milliliters of dehydrated alcohol of 200 ml distilled waters, in solution, dripped 4.8 milliliters of N-β-aminopropyl trimethoxysilane ultra-sonic dispersion 10 minutes, transfer to be furnished with reflux condensing tube, in the dry three-neck flask of mechanical agitator, sealing is stirred and heated to 70 ℃, and washing is left standstill in isothermal reaction 5 hours, solid-liquid separation, drying is 5 hours in 80 ℃ of constant temperature air dry ovens, grinds, and gets the Fe of modification
3O
4Powder is standby.
Take by weighing 1 Fe of gram after the modification
3O
4Powder, joined in the dry bottle that 70 milliliters of dimethylbenzene are housed ultra-sonic dispersion 10 minutes, drip 9.5 milliliters of methyl diphenylene diisocyanates, adding hydroxyl value is 55 ± 3 milligrams of KOH/ grams, PEPA 15 grams of M=2000, the room temperature sealing was stirred after 180 minutes, the xylene solution of prepolymer splashed into 1% (mass/volume) polyvinylpyrrolidone is housed, in the three-neck flask of 300 ml water solution of several ethylenediamines, add 2 milliliters of chain extender glycerol, sealing is stirred and heated to 70 ℃, isothermal reaction 5h will obtain to such an extent that product is washed 4～5 times, and magnetic separates, with the alcohol solution dipping of 50% (volume) 12 hours, drying obtained the dark brown microsphere.Microspherulite diameter is at 300～800 microns.
Embodiment 4:
Take by weighing 2 gram CoxFe
2-xO
4Powder joins in the mixed solution that contains 200 milliliters of dehydrated alcohol of 200 ml distilled waters, in solution, dripped 4.8 milliliters of N-β-aminopropyl trimethoxysilane ultra-sonic dispersion 10 minutes, transfer to be furnished with reflux condensing tube, in the dry three-neck flask of mechanical agitator, sealing is stirred and heated to 70 ℃, isothermal reaction 5 hours.Leave standstill washing, solid-liquid separation, drying is 5 hours in 80 ℃ of constant temperature air dry ovens, grinds, and gets the CoxFe of modification
2-xO
4Powder is standby.
Take by weighing 1 CoxFe of gram after the modification
2-xO
4Powder, joined in the dry bottle that 70 milliliters of dimethylbenzene are housed ultra-sonic dispersion 10 minutes, drip 6.5 milliliters of toluene di-isocyanate(TDI)s, adding 10 gram cetomacrogol 1000 room temperature sealings stirred after 120 minutes, the xylene solution of prepolymer splashed into 1% (mass/volume) polyvinylpyrrolidone is housed, in the three-neck flask of 300 ml water solution of several triethanolamine, add 1.5 milliliters of chain extender glycerol, sealing is stirred and heated to 70 ℃, isothermal reaction 5 hours will obtain to such an extent that product is washed 4～5 times, and magnetic separates, with the alcohol solution dipping of 50% (volume) 12 hours, drying obtained the grey black microsphere.Microspherulite diameter is at 400～700 microns.
Embodiment 5:
Take by weighing 2 gram γ-Fe
2O
3Powder joins in the mixed solution that contains 200 milliliters of dehydrated alcohol of 200 ml distilled waters, in solution, dripped 4.8 milliliters of N-β-aminopropyl trimethoxysilane ultra-sonic dispersion 10 minutes, transfer to be furnished with reflux condensing tube, in the dry three-neck flask of mechanical agitator, sealing is stirred and heated to 70 ℃, and washing is left standstill in isothermal reaction 5 hours, solid-liquid separation, drying is 5 hours in 80 ℃ of constant temperature air dry ovens, grinds, and gets the γ-Fe of modification
2O
3Powder is standby.
Take by weighing the 1 γ-Fe of gram after the modification
2O
3Powder, joined in the dry bottle that 70 milliliters of dimethylbenzene are housed ultra-sonic dispersion 10 minutes, drip 6.5 milliliters of toluene di-isocyanate(TDI)s, adding 10 gram cetomacrogol 1000 room temperature sealings stirred after 120 minutes, the xylene solution of prepolymer splashed into 1% (mass/volume) polyvinylpyrrolidone is housed, in the three-neck flask of 300 ml water solution of several triethanolamine, add 1.5 milliliters of chain extender glycerol, sealing is stirred and heated to 70 ℃, isothermal reaction 5 hours will obtain to such an extent that product is washed 4～5 times, and magnetic separates, with the alcohol solution dipping of 50% (volume) 12 hours, drying obtained the bronzing microsphere.Microspherulite diameter is at 350～650 microns.
Embodiment 6:
According to will the vascular embolization caliber, sieve be got 100 milligrams of 200～300 microns Barium hexaferrite polyurethane magnetic compound microspheres, behind the sterilization, is made into suspension in 10 milliliters normal saline.Under X-ray developed monitoring, the suspension that will contain microsphere through conduit was expelled to the target area, according to blood flow direction and blood vessels caliber size restriction, the coalition external magnetic field is fixed on the target area with magnetic microsphere, play vascular embolization, the nutrition supply of blocking-up target area, the effect of treatment arteriovenous malformotion and arteriovenous aneurysm.
Embodiment 7:
Getting 100 milligrams of commercially available paclitaxels places glass drying oven to stir up to paclitaxel and all dissolve while adding human physiology saline, according to will the vascular embolization caliber, sieve is got 100 milligrams of 200～300 microns Barium hexaferrite polyurethane magnetic compound microspheres, behind the sterilization, join in the solution, replenish the mixing suspension that an amount of normal saline is configured to microsphere, paclitaxel.Left standstill 24 hours, microsphere surface has micropore to adsorb paclitaxel generation swelling easily.The microsphere that leaches after the swelling is configured to suspension in 10 milliliters normal saline, under X-ray develops monitoring, through conduit suspension is expelled to the target area, according to blood flow direction and blood vessels caliber size restriction, the coalition external magnetic field is fixed on the target area with magnetic microsphere, play the effect of vascular embolization, along with the release of paclitaxel, can strengthen simultaneously the tumor treatment effect.
When microsphere absorption cancer therapy drug,, can strengthen the effect of treatment of cancer along with the release of medicine; If microsphere absorption is analgesic, can alleviate the pain that causes because of ischemia behind the thromboembolism.
Claims (5)
1, a kind of preparation method of core/shell type polyurethane magnetic compound microsphere is characterized in that method step is:
Step 1, be to be made into mixed solution at 2.4: 100: 100 with volume ratio with silane coupler, distilled water, dehydrated alcohol, with the mass/volume ratio is to mixed solution in to add the magnetic inorganic micropowder at 0.5: 100, ultra-sonic dispersion becomes unit for uniform suspension, this suspension transferred to be furnished with reflux condensing tube, sealing is stirred and heated to 70 ± 0.5 ℃ in the drying receptacle of mechanical agitator, isothermal reaction is more than 5 hours, leave standstill washing, solid-liquid separation, 80 ± 1 ℃ of dryings more than 5 hours, obtain the magnetic inorganic micropowder of modification, described silane coupler is for having-NH-NH
2The silane coupler of reactive group;
Magnetic inorganic micropowder after step 2, the surface modification that step 1 is obtained is configured to suspension by mass/volume than 1: 60～100 with organic solvent dimethylbenzene, after ultra-sonic dispersion is even, transfer in the container that agitator is housed, add 1: 1 polynary two isocyanide ester and polyvalent alcohols of mol ratio, the prepolymerization of sealing stirring at normal temperature obtained the xylene solution of prepolymer more than 3 hours;
Step 3, press the aqueous solution of mass volume ratio 1: 100 configuration polyethylene of dispersing agent ketopyrrolidine, be heated to 70 ± 1 ℃, the xylene solution of the prepolymer that dropping step 2 obtains in solution, dropping accounts for glycerol and several triethanolamine of solution 0.4% (volume), sealing was stirred the constant temperature polymerization more than 5 hours, the Magnetic Isolation complex microsphere, and washing, alcohol are washed repeatedly, drying promptly obtains clean core/shell type polyurethane magnetic compound microsphere.
2, preparation method according to claim 1 is characterized in that step 1 described magnetic inorganic micropowder for can developing under X-ray, particle diameter is less than Barium hexaferrite, ferroso-ferric oxide, Conjugate ferrite or γ-iron sesquioxide microparticle material of 1 micron.
3. preparation method according to claim 1 is characterized in that described having-NH ,-NH
2The silane coupler of reactive group is N-β-aminopropyl trimethoxysilane, or aminopropyl trimethoxysilane.
4. preparation method according to claim 1 is characterized in that the described multicomponent isocyanate of step 2 is toluene two cyanates, or methyl diphenylene diisocyanate.
5. preparation method according to claim 1 is characterized in that the described polyvalent alcohol of step 2 is that Polyethylene Glycol or hydroxyl value are 55 ± 3 milligrams of KOH/ grams, the PEPA of M=2000.
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| CN102174195B (en) * | 2011-01-07 | 2012-09-19 | 山东轻工业学院 | Preparation method of core-shell magnetic conductive polymer microspheres and application thereof |
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| CN114410268B (en) * | 2021-12-31 | 2024-03-12 | 深圳市安品有机硅材料有限公司 | Magnetic permeability polyurethane pouring sealant and preparation method thereof |
| CN114307996B (en) * | 2022-02-25 | 2023-12-29 | 苏州海狸生物医学工程有限公司 | Preparation method of functionalized magnetic microsphere |
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