CN1092426A - Terminal estergroup silicagel high-effect hydrophobic chromatographic stuffing and synthetic method - Google Patents
Terminal estergroup silicagel high-effect hydrophobic chromatographic stuffing and synthetic method Download PDFInfo
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- CN1092426A CN1092426A CN 93103028 CN93103028A CN1092426A CN 1092426 A CN1092426 A CN 1092426A CN 93103028 CN93103028 CN 93103028 CN 93103028 A CN93103028 A CN 93103028A CN 1092426 A CN1092426 A CN 1092426A
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Abstract
The present invention discloses a class silica matrix organic compound and a synthetic method thereof, particularly a class end ester group HPHIC filler and a synthetic method thereof.The structure of HPHIC of the present invention filler is a silica gel
Description
The present invention relates to a class silica matrix organic compound and a synthetic method thereof, particularly the filler and the synthetic method thereof of the efficient hydrophobic interaction chromatography of a class end ester group.
Hydrophobic interaction chromatograph (Hydrophobic Interaction Chromatography is called for short hydrophobic chromatography) is the proteinic a kind of liquid-phase chromatography method of separation and purification that the seventies grows up.It has need not be poisonous and expensive organic solvents make the little and separation selectivity of protein active loss behind moving phase, the purifying and can wait advantage well, thereby obtained development rapidly.Now become an important means in Bio-engineering Products aftertreatment, the pharmaceutical grade protein separation and purification.
Early stage hydrophobic chromatographic stuffing utilizes agarose, dextran etc. to make for matrix organic group on its surface bond.Had again afterwards alkyl such as phenyl and butyl were bonded on the hydrophilic polymer matrix to obtain semirigid hydrophobic chromatographic stuffing.Latter's separation performance is better, but bad mechanical property is not high pressure resistant, can not be used for high performance liquid chromatography, so velocity of separation is slow.At present best hydrophobic chromatography post is that TOYO SOTA company by Japan produces, and the commodity that the bonding phenyl obtains on hydrophilic polymer matrix are called TSK pheny1-5pw type hydrophobic chromatographic stuffing.But using behind the each sample introduction of this pillar all will be with the regeneration of NaOH solution, process complexity.And because of hydrophobicity is too strong, some albumen does not go out the peak, and withstand voltage properties is also relatively poor.
It is that the HPHIC filler (High perform-ance Hydrophobic Interaction Chromatography, HPHIC is called for short the HPHIC) of matrix generally is to use suitable aglucon on the reactive behavior bonding of silicon hydroxyl on silica gel surface and make with silica gel that the eighties has occurred mid-term.The hydrophobic chromatographic stuffing that wherein report is maximum, effect is preferably the polyethylene glycols aglucon, its aglucon is-(CH
2CH
2O)
n-R(R=H, methyl, ethyl, phenyl).This class filler good mechanical property, high pressure resistant, can be used for high performance liquid chromatography, but the poor performance of resisting high-concentration guanidine hydrochloride solution, resolution is general.Therefore in the aftertreatment of Bio-engineering Products, be restricted.
The present invention is on the basis of the silica matrix compound that adopts the multiple different structure of multiple synthetic method synthetic, the compound kind and the synthetic method that can be used as the HPHIC filler have therefrom been filtered out, with the aftertreatment of satisfying Bio-engineering Products and the needs of scientific effort.This compounds, when the liquid chromatography stuffing, high pressure resistant, anti-Guanidinium hydrochloride, good, the easy regeneration of separation performance, protein active rate of recovery height, hydrophobicity are suitable, are applicable to the aftertreatment of Bio-engineering Products, and performance is better than existing product.
The objective of the invention is to adopt a kind of new synthetic method and technology, synthesized the compound of a class novel silica gel matrix.This compounds can be used for high performance liquid chromatography, as the HPHIC filler of isolated protein.
The object of the present invention is achieved like this:
The present invention is on silica matrix, adopts the method for multistep bonding to obtain the silica matrix compound that a class end group is an ester group.Its structure is silica gel ≡
。Such material is a well behaved HPHIC filler.
Synthetic method of the present invention is that macroporous silica gel with γ-glycidyl ether propyl group-Trimethoxy silane reaction, makes the silica gel that contains epoxy group(ing) then earlier through cleanup acid treatment.Epoxy group(ing) silica gel is respectively the compound reaction of hydroxyl and ester group again with two end group, to obtain the product of band edge ester group; Also can allow contain epoxy group(ing) silica gel earlier with a diol reaction, and then allow this product further with acid anhydrides or acyl chloride reaction, obtain end ester group silica matrix of the present invention HPHIC filler.
Concrete synthesis step of the present invention is as follows:
1, the cleanup acid treatment of silica gel and activation:
(add an amount of nitric acid or hydrochloric acid soln among the aperture 30nm～100nm) to macroporous silica gel, ultrasonic in ultrasonator, vacuumized simultaneously 1～5 minute, and be adsorbed on the solution displacement that the lip-deep gas of silica gel reacted to remove the gas that retains in the silica gel pore as much as possible, to make as far as possible.Refluxed 2～5 hours, become the silanol base to remove the various impurity that remain in the silica gel surface to greatest extent and the silicon ehter bond is destroyed, filter with the glass sand core funnel, it is constant to be washed till pH value with distilled water, 130～200 ℃ of oven dry down, the silica gel that activity is good is placed in the moisture eliminator to be preserved.
2, the preparation of epoxy group(ing) silica gel:
γ-glycidyl ether propyl group-Trimethoxy silane the aqueous solution that in the activated silica gel that cleanup acid treatment is crossed, adds an amount of 3-15%, after ultrasonic and the processing of bleeding, transferring pH value is 4～7, heated and stirred is 0.5～1 hour in 80～110 ℃ heating bath.Filter with sand core funnel then, wash with water, wash with methyl alcohol again, be placed in the vacuum drier dry 48 hours.
This reaction is:
3, the preparation (I) of end ester group silica matrix HPHIC filler:
The epoxy group(ing) silica gel that second step made and the binary alcohol esters of carboxylic acid (
) under boron trifluoride catalysis, in the solution of no reactive hydrogen solvent, react.Reactant is done the ultrasonic processing that vacuumizes earlier, and heated and stirred is 0.5～1 hour in 80～120 ℃ of oil baths, adds an amount of 2～6mol/L NaOH solution after reaction is finished and destroys boron trifluoride, filters then, and water, methanol wash are drained.Products therefrom is the ester group compound of a class silica matrix of the present invention, i.e. ester group HPHIC filler.
R=alkyl wherein, phenyl,
; R
1=phenyl, alkyl, substituted-phenyl
R and R
1The structures shape of two groups the hydrophobicity of filler, stratographic selectivity and resolution are also played crucial effects.
4, the preparation (II) of end ester group silica matrix HPHIC filler:
The silica matrix ester group compound can also be synthetic with another kind of method.
The epoxy group(ing) silica gel that second step made reacts with α, ω dibasic alcohol or poly-dihydric alcohol earlier, obtain a silica matrix compound that contains terminal hydroxy group, this compound is under the alkaline organic catalysis of no reactive hydrogens such as tertiary amine, with acid anhydrides or acyl chloride reaction, obtain holding the silica matrix compound of ester group, ester group promptly of the present invention HPHIC filler.
(A) reaction of epoxy group(ing) silica gel and dibasic alcohol.
The reaction conditions of epoxy group(ing) silica gel and dibasic alcohol or poly-dihydric alcohol and aftertreatment are all with the 3rd step.
（m＝1，2，3，n＝1～40）
(B) preparation of ester group HPHIC filler
The reaction product of above-mentioned epoxy group(ing) silica gel and dibasic alcohol or poly-dihydric alcohol under the alkaline organic catalysis of tertiary amine or other no reactive hydrogens, obtains the silica matrix ester group compound with acid anhydrides or acyl chloride reaction, i.e. ester group HPHIC filler.Difference was when acid anhydrides and acyl chlorides were made reaction reagent, and acid anhydrides will be heated to 60～120 ℃, and acyl chlorides needn't heat.The proton that the alkaline organic of tertiary amine or other no reactive hydrogens can acceptable response be emitted promotes reaction.Reaction can be made solvent with inertia reagent such as benzene, but also double as solvent of some tertiary amine itself.Reaction mixture should vacuumize processing through ultrasonic.Reaction is finished after-filtration and is gone out product, uses methyl alcohol, water, methanol wash in turn, drains vacuum-drying.Product should be kept at cool place, dry place.
R wherein
1=phenyl, substituted-phenyl, alkyl
R
1Structure all influential to hydrophobicity, selectivity, the erosion resistance of filler.
Advantage of the present invention is to adopt new synthesis route and processing method, has synthesized class novel cpd-silica matrix ester group compound.This compounds can be used as the HPHIC filler, and excellent property.
Because one of reactant is the solid silicone that contains a large amount of apertures in this synthetic route, is reflected at the solid-liquid two-phase interface and carries out.In order to impel the gas in the aperture to discharge, make the abundant and uniform contact of reaction solution and silica gel all surface, so in per step building-up reactions, treatment step ultrasonic and that vacuumize is simultaneously arranged all.
End ester group silica matrix compound of the present invention owing to connect an ester group on end group, is compared with original terminal hydroxy group, terminal methyl, end phenyl filler, and hydrophobicity changes to some extent.Be improved aspect the corrodibility of separation performance, anti-guanidine hydrochloride solution.Overcome the not disadvantage of anti-guanidine hydrochloride solution of terminal hydroxy group hydrophobic chromatographic stuffing, improved separation performance and improved peak capacity.Contrast Fig. 1 and Fig. 2 can see that the filler of this product obviously is better than the hydrophobic chromatographic stuffing of original terminal hydroxy group.
Filler good mechanical property of the present invention, withstand voltage＞60MPa, can be used for high performance liquid chromatography, improved separation and analysis speed greatly.Protein-active rate of recovery height, in the time of 4 ℃, the activity recovery of N,O-Diacetylmuramidase and αDian Fenmei＞90%.Separate favorable reproducibility, can be widely used in the separating of albumen, enzyme and Bio-engineering Products (Fig. 1, Fig. 3～Fig. 6).
The filler long service life, the filler after using 1500 hours under the PH=7 situation, after cleaning, separation performance is not seen change.
Filler is easy to regeneration, is renewable complete as long as wash with 10 times of rare salts solutions with upper volume (being the B elutriant in the hydrophobic chromatography).Not resembling will be with the regeneration of NaOH solution behind each sample introduction some commodity post.
Some albumen does not go out the peak on some commodity post.And filler of the present invention does not have this bad phenomenon.
The guanidine hydrochloride solution crude product of Bio-engineering Products can directly be gone up sample.In step separation, reach purifying, removed the purpose of Guanidinium hydrochloride, finished the work that needs several steps finish in the past.
Fig. 1 protein and the enzyme separation graph on the filler of ester group HPHIC
1, the stainless steel column of chromatographic column: 4.1 * 100mm, silica gel aperture 50nm, 2, elutriant: A, 3mol/L(NH
4)
2SO
4+ 0.01mol/LKH
2PO
4, PH7; B, 0.01mol/LKH
2PO
4, PH7; 3, flow velocity: 1ml/min; 4, gradient time 0～100%B is 20 minutes; Ultraviolet detection wavelength 280nm; 5, protein sample: cytochrome C (1), myohaemoglobin (2), conalbumin (3), N,O-Diacetylmuramidase (4), αDian Fenmei (5), ferritin (6), Regular Insulin (7).
Fig. 2 protein and enzyme separating on the filler of terminal hydroxy group HPHIC
The stainless steel column of 1 chromatographic column: 4 * 150mm
2 filling-material structures are:
The same Fig. 1 of 3 chromatographic conditions
4 protein samples: cytochrome C (1), myohaemoglobin (2), conalbumin (3), N,O-Diacetylmuramidase (4), αDian Fenmei (5), Regular Insulin (6)
Fig. 3 enzyme and the albumen separation graph on the post of ester group polyoxyethylene glycol spacerarm type HPHIC.
The stainless steel column of 1 chromatographic column: 4.1 * 150mm, silica gel aperture 30nm.
2 chromatographic conditions and protein sample: same Fig. 1
Fig. 4 enzyme and the albumen separation graph on the post of end ester group polytetramethylene glycol spacerarm type HPHIC
The stainless steel column of 1 chromatographic column: 4 * 100mm;
The same Fig. 1 of 2 chromatographic conditions and protein sample
The color atlas of Fig. 5 genetically engineered human interferon gamma
The stainless steel column of 1 chromatographic column: 4 * 150mm
2 fillers are ester group polyoxyethylene glycol aglucon hydrophobic chromatographic stuffing
3 samples: the 7M Guanidinium hydrochloride crude product of genetic engineering interferon γ
The color atlas of Fig. 6 genetically engineered interleukin 8 quality 2
The same Fig. 5 of 1 chromatographic column and filler
2 samples: the 7M guanidine hydrochloride solution of engineered interleukin 8 quality 2
The preparation of example (one) phenylformic acid polyoxyethylene glycol ester group HPHIC filler
1, the pickling of silica gel: add 100ml 6mol/L hydrochloric acid in the 10 gram macroporous silica gels, vibration vacuumizes simultaneously and handled 2～5 minutes in ultrasonator, refluxed then 4 hours, filter with the glass sand core funnel, it is constant to be washed till pH value with distilled water, 130～180 ℃ of oven dry down, be placed in the moisture eliminator and preserve
2, the preparation of epoxy group(ing) silica gel:
In the silica gel that 10 gram cleanup acid treatment are crossed, γ-glycidyl ether propyl group-Trimethoxy silane the aqueous solution that adds 70ml 5～10% is transferred pH value to 5.8, ultransonic vacuumizing simultaneously 2～5 minutes on ultrasonator, heating and stirring 0.5 to 1 hour in 80～110 ℃ of oil baths is filtered then.Wash with water earlier, wash with methyl alcohol again; Be placed on dried for standby in the vacuum drier.
3, the reaction of epoxy group(ing) silica gel and phenylformic acid macrogol ester:
Add the poly-ethanol 400 benzoic ether solution of the 1.4-dioxane of 60ml 2～5% in the 10 gram epoxy group(ing) silica gel, add boron trifluoride ether solution 5ml again.Ultrasonicly vacuumize processing, then 80～110 ℃ of heated and stirred 0.5～1 hour.Add 4mol/L NaH 10ml after reaction is finished, stirred 2 minutes.Filter, use methyl alcohol, water, methanol wash successively.Drain solvent, vacuum-drying promptly gets the new and effective hydrophobic chromatographic stuffing of the present invention.
The preparation of example (two) phenylformic acid polytetramethylene glycol ester group HPHIC filler
The preparation of the pickling of 1 silica gel and epoxy group(ing) silica gel: with example ()
Add 1 of 60ml 2～5% polytetramethylene glycols (M ≈ 800) in the 2 epoxy group(ing) silica gel, the 4-dioxane solution adds the 5ml boron trifluoride ether solution again.Ultrasonic, vacuumized two minutes.80～110 ℃ of heated and stirred 0.5～1 hour.After having reacted, add 4mol/L NaOH 10ml, stirred 2 minutes.Filter, use methyl alcohol, water, methanol wash successively.Drain solvent, vacuum-drying.
3, the preparation of phenylformic acid polytetramethylene glycol ester group HPHIC filler:
Add the 60ml anhydrous triethylamine in the product in above-mentioned the 2nd step of 10 grams, 2 gram benzoyl oxides, ultrasonic, vacuumized two minutes.Refluxed 0.5～1 hour.Filter, use methyl alcohol, water, methanol wash successively.Drain solvent, vacuum-drying.
The preparation of example (three) acetate groups polyoxyethylene glycol 800 spacerarm HPHIC fillers
The preparation of the pickling of 1 silica gel and epoxy group(ing) silica gel is with example ()
The reaction of 2 epoxy group(ing) silica gel and polyoxyethylene glycol 800:
Add 1 of 60ml 2～5% polyoxyethylene glycol 800 in the 10 gram epoxy group(ing) silica gel, the 4-dioxane solution adds the 5ml boron trifluoride ether solution again.Ultrasonic, vacuumized two minutes.80～110 ℃ of heated and stirred 0.5～1 hour.Reacted the back and added 4mol/L NaOH 10ml, stirred 2 minutes.Filter, use methyl alcohol, water, methanol wash successively.Drain solvent, vacuum-drying.
3, the preparation of acetate groups polyoxyethylene glycol 800 spacerarm HPHIC fillers
The above-mentioned product of 10 grams adds the 60ml pyridine, drips 2～5ml Acetyl Chloride 98Min., after dripping off, and ultrasonic two minutes.At room temperature placed 1～3 hour, and filtered, wash with methyl alcohol, water, methyl alcohol successively, drain solvent, vacuum-drying gets product.
Claims (5)
1, end ester group silica matrix HPHIC filler, it is characterized in that this filler be on the silica gel bonding end group organic ligand that is ester group as the HPHIC filler, its chemical structure of general formula is:
R=alkyl wherein, phenyl ,-[CH
2(CH
2)
mO]
n-,-(CH
2CHO)
n-, (m=1,2,3, n=1～40); R
1=phenyl, alkyl, substituted-phenyl.
2, the synthetic method of end ester group silica matrix HPHIC filler, it is characterized in that: silica matrix compound that contains the terminal hydroxy group organic group and organic acid anhydride or acyl chloride reaction obtain holding ester group silica matrix HPHIC filler, and its feature contains the silica gel and the ester compound that contains the dibasic alcohol of terminal hydroxy group that end group is the organic group of epoxy group(ing) in addition
Reaction obtains holding ester group silica matrix HPHIC filler.
3, the synthetic method of end ester group silica matrix according to claim 2 HPHIC filler, when it is characterized in that acyl chlorides is reaction reagent in the presence of the alkaline organic of no reactive hydrogens such as tertiary amine pyridine, normal temperature is reaction down, and acid anhydrides will be heated to 60～120 ℃ of reactions 0.5～2 hour during for reaction reagent.
4, the synthetic method of end ester group silica matrix according to claim 2 HPHIC filler, it is characterized in that containing the reaction of the ester compound of the silica gel of epoxy group(ing) and dibasic alcohol, need under boron trifluoride catalysis, 80～120 ℃ were reacted 0.5～2 hour in the solvent of no reactive hydrogen.
5, the synthetic method of end ester group silica matrix according to claim 2 HPHIC filler is characterized in that reactant in each step reaction is with vacuumizing and supersound process 1～5 minute.
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN93103028A CN1041461C (en) | 1993-03-12 | 1993-03-12 | Terminal estergroup silicagel high-effect hydrophobic chromatographic stuffing and synthesis |
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN93103028A CN1041461C (en) | 1993-03-12 | 1993-03-12 | Terminal estergroup silicagel high-effect hydrophobic chromatographic stuffing and synthesis |
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| Publication Number | Publication Date |
|---|---|
| CN1092426A true CN1092426A (en) | 1994-09-21 |
| CN1041461C CN1041461C (en) | 1998-12-30 |
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Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1116933C (en) * | 1999-08-04 | 2003-08-06 | 中国科学院化学研究所 | Ester-type efficient liquid-phase chromatographic reverse filler and its preparing process |
| CN102876645A (en) * | 2012-10-26 | 2013-01-16 | 西北大学 | Double-function chromatographic medium assisted lysozyme in-vitro renaturation method |
| CN104043436A (en) * | 2013-03-15 | 2014-09-17 | 戴安公司 | Epoxy chemistry derived materials as reversed-phase and hydrophobic interaction chromatography media, method for their synthesis and use |
| US9329158B2 (en) | 2013-03-15 | 2016-05-03 | Dionex Corporation | Epoxy chemistry derived materials as mixed mode chromatography media, method for their synthesis and use |
| CN105618013A (en) * | 2014-11-24 | 2016-06-01 | 中国科学院大连化学物理研究所 | Method for preparing agglutinin high-performance affinity chromatography material by taking silica gel as substrate |
| CN115634675A (en) * | 2022-10-27 | 2023-01-24 | 青岛邦凯高新技术材料有限公司 | Electronic-grade industrial silicon dioxide base material chromatographic filler, and preparation method and application thereof |
-
1993
- 1993-03-12 CN CN93103028A patent/CN1041461C/en not_active Expired - Fee Related
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1116933C (en) * | 1999-08-04 | 2003-08-06 | 中国科学院化学研究所 | Ester-type efficient liquid-phase chromatographic reverse filler and its preparing process |
| CN102876645A (en) * | 2012-10-26 | 2013-01-16 | 西北大学 | Double-function chromatographic medium assisted lysozyme in-vitro renaturation method |
| CN104043436A (en) * | 2013-03-15 | 2014-09-17 | 戴安公司 | Epoxy chemistry derived materials as reversed-phase and hydrophobic interaction chromatography media, method for their synthesis and use |
| US9216403B2 (en) | 2013-03-15 | 2015-12-22 | Dionex Corporation | Epoxy chemistry derived materials as reversed-phase and hydrophobic interaction chromatography media, method for their synthesis and use |
| US9329158B2 (en) | 2013-03-15 | 2016-05-03 | Dionex Corporation | Epoxy chemistry derived materials as mixed mode chromatography media, method for their synthesis and use |
| CN105618013A (en) * | 2014-11-24 | 2016-06-01 | 中国科学院大连化学物理研究所 | Method for preparing agglutinin high-performance affinity chromatography material by taking silica gel as substrate |
| CN105618013B (en) * | 2014-11-24 | 2017-12-15 | 中国科学院大连化学物理研究所 | A kind of preparation method using silica gel as the agglutinin high-effective affinity chromatography material of matrix |
| CN115634675A (en) * | 2022-10-27 | 2023-01-24 | 青岛邦凯高新技术材料有限公司 | Electronic-grade industrial silicon dioxide base material chromatographic filler, and preparation method and application thereof |
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| Publication number | Publication date |
|---|---|
| CN1041461C (en) | 1998-12-30 |
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