CN100374453C - 2-18F-2-deoxidized-D-glucose synthesis process - Google Patents
2-18F-2-deoxidized-D-glucose synthesis process Download PDFInfo
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- CN100374453C CN100374453C CNB2005101013279A CN200510101327A CN100374453C CN 100374453 C CN100374453 C CN 100374453C CN B2005101013279 A CNB2005101013279 A CN B2005101013279A CN 200510101327 A CN200510101327 A CN 200510101327A CN 100374453 C CN100374453 C CN 100374453C
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Abstract
The present invention relates to the field of PET (positron emission tomography) application, particularly to a synthesis technique for a common radioactive drug 2-18F-2-deoxidized-D-glucose (18F-FDG) in the PET technique. The synthesis technique for the common radioactive drug 2-18F-2-deoxidized-D-glucose (18F-FDG) of the present invention comprises the procedures of trapping a nucleophilic fluorination agent 18F on a column, preparing nucleophilic substitution reaction, nucleophilic fluorination reaction, trapping fluorination intermediate on the column, solid phase basic hydrolysis on the column, neutralization on the column and isolation purification. The synthesis technique of the present invention can be used in the existing main devices, such as TRACERlab FXF-N, TRACERlab Fx FDG and other 18F-FDG automation synthetic systems. Compared with the existing process of the devices, the 18F-FDG synthesis technique is simpler and faster and has higher efficiency, higher stability and higher purity. The synthesis technique of the present invention can also be used for producing novel 18F-FDG synthesis modules.
Description
Technical field
The present invention relates to the Application Areas of PET (Positron Emission Tomography, positron emission tomography), be specifically related to radiopharmaceuticals 2-the most frequently used in the PET technology
18The F-2-DDG (
18F-FDG) synthesis technique.
Background technology
PET (Positron Emission Tomography, positron emission tomography) be to utilize photon collimation principle and r flash detection technology, at the photon of external detection annihilation radiation that tracer agent produces, the information of collection demonstrates the faultage image of target organ and provides quantitative physiological parameter after by Computer Processing.PET has become very important diagnostic tool in the clinical position at present, especially aspect the early diagnosis and brain function imaging of cancer, has irreplaceable effect for malignant tumour, cardiovascular disorder, nervous system disorders early diagnosis, early treatment, observation of curative effect and Clinical Follow-up etc.
The PET video picture must have the positron emission radioactive tracer, and its image quality, clinical examination project depend on positron emitting tracer quality and kind.2-
18F-2-DDG (2-Deoxy-2-
18F-Fluoro-D-Glucose,
18F-FDG) for having
18The radiolabeled medicine of F is the most frequently used PET radiopharmaceuticals (also claiming developer), has been widely used in the PET video picture research of tumour, cardiovascular disorder and neuropsychiatric disease.Along with the continuous development of PET technology,
18The demand of F-FDG constantly increases, so, efficient, simple, synthetic fast
18Development PET molecular image is learned a skill F-FDG and clinical position is extremely important.
18The composition principle of F-FDG mainly contains two kinds of electrophilic substitution method and nucleophilic substitution methods.The nucleophilic substitution method is because nucleophilic reagent
18F-is easy to get, and particularly can obtain the carrier free of putting of height productive rate
18F-FDG becomes at present
18The main synthetic method of F-FDG.The nucleophilic substitution method comprises that nucleophilic fluoridizes and the hydrolysis two-step reaction.Nucleophilic is fluoridized and is comprised liquid-phase fluorination process [reference 5,9] with at post solid phase fluorination method [reference 10], liquid-phase fluorination process is phase transfer catalysis process (as amino-polyether phase-transfer catalyst K222) particularly, extremely people's favor because combined coefficient is high, but fluoridation must keep definitely anhydrous.Recently, fluoridation can take place in the application of ionic-liquid catalyst [reference 11,12] in the presence of less water, and simplify synthesis step and shortened generated time, but
18The radiochemicsl purity of F-FDG and synthetic yield await further raising.Hydrolysis reaction is divided into acid (hydrochloric acid) hydrolysis [reference 5,7,8] and two kinds of methods of alkali (sodium hydroxide) hydrolysis [ reference 1,2,3,4,14] again.Liquid phase alkali (sodium hydroxide) hydrolysis method is owing to can carry out in room temperature, and the reaction times is short, and can obtain putting of height productive rate
18F-FDG becomes
18The prefered method of F-FDG automatic production.But it is a certain amount of that the liquid phase alkali hydrolysis method may produce
18F-FDG enantiomorph 2-
18F-2-deoxidation-D-seminose (
18F-FDM).In recent years, be applied in post sodium hydroxide hydrolysis method
18F-FDG synthesizes [reference 13,15,16,1], and this method promptly uses high concentration alkali solution to carry out in the post hydrolysis, also is difficult to find
18F-FDM, thereby cause people's great attention, but separation and purification still bothers.
Because the positron radioactivity nucleic transformation period is short, radioactive activity is stronger, so simple manual markings is difficult to finish, must adopt the chemosynthesis system for this reason.The positron radioactivity isotope labeling that positron emitting tracer chemosynthesis system produces medical cyclotron to some chemical substrates, thereby form positron emitting tracer.
At present both at home and abroad for
18F-FDG high-yield quick rate synthetic typical case maturation process mainly is divided into two big classes: (1) liquid-phase fluorination+alkali hydrolysis method, it is represented as the TRACERlab F of General Electric Apparatus Co.(U.S.A.) (medical system portion)
XFDG automatization synthesis system
18The F-FDG synthesis module; (2) liquid-phase fluorination+at post solid phase alkali hydrolysis method, it is represented as the TRACERlab M of General Electric Apparatus Co.(U.S.A.) (medical system portion)
XFDG automatization synthesis system
18The F-FDG synthesis module.The TRACERlab system is the earliest by the development of Belgian Coincidence Technologies company, is the device of the synthetic FDG that generally acknowledges of industry, and this synthesizer is used in combination with magnetic resonance acceleator, can produce the FDG finished product.Coincidence company is purchased by General Electric Apparatus Co.(U.S.A.) (GE company) August calendar year 2001, and continues the radiopharmaceutical synthesis system that exploitation PET imaging is used.According to the clinical application angle, GE company
18F-FDG chemosynthesis system is divided into two types: (1) tailored version: TRACERlab F
XFDG, TRACERlab M
XFDG etc.; (2) multi-usage type: TRACELAB FX
F-N, TRACELAB FX
F-EDeng.
With TRACERlab F
XFDG's
18The F-FDG synthesis module is an example, and the main synthesis technique flow process of liquid-phase fluorination+alkali hydrolysis method is as follows: the negatively charged ion pillar captures accelerator-produced
18F
-, with containing phase-transfer catalyst Kryptofix 2.2.2 (K222) and K
2CO
3The acetonitrile solution wash-out
18F is to the fluoridation bottle, and the logical He heating of decompression dewaters in the sealed reaction bottle; Add the precursor solution that is dissolved in acetonitrile, about 5 minutes of 85 ℃ of left and right sides fluoridations, logical He decompression added the heat extraction acetonitrile; Add water 2mL, 90 ℃ of insulations were cooled to 35 ℃ after 50 seconds, added 1mL 1mol/L NaOH solution 1mL, were incubated about 2 minutes; (contain PS-H through integrated post
+, PS-HCO
3, Al
2O
3With the HR-P post) separation and purification (PS: polystyrene),
18The F-FDG injection liquid.TRACERlab F
XThe FDG synthesis system adopts sealed reaction bottle and controlledly synthesis program software, adopts the decompression heating to dewater before the fluoridation, does not need to prolong the He gas transmission time, and building-up process is controlled at any time, and
18Putting of F-FDG productive rate stable (do not proofread and correct putting productive rate and generally can reach 60%),
18Almost there is not unevaporated acetonitrile in the F-FDG injection liquid.But this synthesis technique also has following deficiency: (1) particularly need buy the complete separation and purification post of import high price owing to need to buy complete raw material test kit, and production cost costs an arm and a leg.(2) accelerator-produced containing
18F
-Target water need transfer to a tapered bottle earlier, transfers to Sep-Pak QMA pillar, causes a small amount of
18F
-Radioactivity loss, and increased total synthetic time, and be not easy to observe that the QMA pillar captures
18F
-Activity.(3) always the synthetic time is longer, is about 28 minutes.
With TRACERlab M
XFDG's
18F-FDG synthesis module [reference 2] is an example, liquid-phase fluorination+as follows in the main synthesis technique flow process of post solid phase alkali hydrolysis method: the negatively charged ion pillar captures accelerator-produced
18Behind the F, with containing phase-transfer catalyst Kryptofix 2.2.2. (K222) and K
2CO
3The acetonitrile solution wash-out
18F
-To the fluoridation bottle, in reaction flask, add the logical N of acetonitrile
2Azeotropic water removing, triplicate; Add the precursor solution that is dissolved in acetonitrile, about 5 minutes of 85 ℃ of left and right sides fluoridations; Need not remove acetonitrile, directly add water 26～30mL, mixing solutions is by Sep Pak Plus
tC18 pillar (Waters company) with 10mL water wash pillar, repeats N 2～4 times
2Dry up; Add the about 0.8mL of 2mol/L NaOH solution in pillar, room temperature kept 2 minutes; Use the water wash pillar, leacheate in citrate buffer solution and hydrochloric acid and after, through Sep PakAl
2O
3Neutral pillar and Sep Pak Plus
tThe little column purification of C18,
18The F-FDG injection liquid.This synthesis system has been simplified hydrolytic process, does not need heating evaporation to remove acetonitrile after the hydrolysis, can obtain high enantiomeric purity and high putting productive rate
18F-FDG, but still have following shortcoming: need repeatedly to add the logical N of acetonitrile before (1) fluoridation
2Azeotropic water removing.(2) fluorinated intermediates needs with after big water gaging (greater than 25mL) mixes, by Sep Pak Plus
tThe C18 pillar captures fluorinated intermediates, and with big water gaging (greater than 20mL) drip washing, so that remove acetonitrile, toxicant K222 and unreacted
18F
-Thereby, cause a certain amount of fluorinated intermediates loss, can not remove toxicant K222 fully, and bring trouble to operation, increased generated time.(3) do not use cationic exchange coloum (H
+Type) remove toxicant K222, the gained injection liquid may contain micro-K222.(4) generated time is still longer, about 23 minutes of the shortest also need.(5) owing to need to buy complete raw material test kit and synthetic cage plate, production cost costs an arm and a leg.
TRACERlab FX
F-NBe a kind of production
18F mark (nucleophilic) tracer product simple and high-efficiency automatic system.This system will by phase-transfer catalyst
18F is converted into organic double compound, reacts with substrate then.System can carry out the reactor evaporate to dryness automatically, operates in 30 ℃ to 200 ℃ temperature range then, adopts integrated preparation radioactivity/ultraviolet-highly effective liquid phase chromatographic system to carry out purifying.For product separation from radioactivity/ultraviolet-high performance liquid chromatography solvent, a Solid-Phase Extraction system is gone in this System integration.At last, effect product sterilization is filtered the solution that just can obtain injection.This system is by application software, and all steps are easy to sequencing.By adjusting schedule of operation, native system can be produced multiple
18Therefore the positron radioactivity tracer agent of F mark is with a wide range of applications.Synthetic with respect to being exclusively used in automatization
18The TRACERlab F of F-FDG
XThe FDG synthesis system, TRACERlab FX
F-NThe technical process of automatization synthesis system and TRACERlab F
XThe FDG synthesis system is similar, has only increased HPLC separation and purification system.
Summary of the invention
The object of the present invention is to provide a kind of 2-
18The F-2-DDG (
18F-FDG) synthesis technique is liquid-phase fluorination+at post solid phase alkali hydrolysis method, can be applicable to existing main flow equipment such as TRACERlab FX
F-N, TRACERlab F
XFDG and other
18In the F-FDG automatization synthesis system, with respect to the existing technology of aforesaid device, this synthesis technique is a kind of more simple and easy, quick, efficient, high stability, highly purified 18F-FDG synthesis technique.Synthesis technique of the present invention also can be used for making novel
18The F-FDG synthesis module.
2-of the present invention
18The F-2-DDG (
18F-FDG) synthesis technique may further comprise the steps:
(a) nucleophilic fluorination reagent
18F
-Capture at post: pass through by medical cyclotron
18O (p, n)
18The F nuclear reaction is produced
18F
-Target water, under the rare gas element transmission, process places QMA (tetramethyl-amine) the negatively charged ion pillar of radioactivity seeker,
18F
-Be trapped on the post, reclaim
18O
-Water;
(b) preparation of nucleophilic substitution reaction: under vacuum condition, the aprotic solvent that contains phase-transfer catalyst will
18F
-Wash-out is gone in the sealed reaction bottle, heating mixing solutions to 60～95 ℃, reduction vaporization, obtain the exsiccant phase-transfer catalyst-
18F
-Mixture;
(c) nucleophilic fluoridation: under the rare gas element effect, the precursor mannose triflate solution that is dissolved in aprotic solvent is pressed into described in the step b in the reaction flask, 80～90 ℃ of reacting by heating 5～10 minutes, decompression, cooling;
(d) capturing at post of fluorinated intermediates: under the rare gas element effect, water is pressed in the reaction flask, mixes with fluorinated intermediates, and mixture is by C18 pillar (carbon 18 pillars), and fluorinated intermediates is trapped on the post, dries up pillar with rare gas element;
(e) in the basic hydrolysis of post solid phase: alkaline solution is loaded onto in the C18 pillar, room temperature hydrolysis 2-3 minute;
(f) in post neutralization and separation and purification: with water wash C18 pillar, eluant is successively by C18 pillar, AG50w-X8 pillar, Al
2O
3Neutral pillar and the aseptic filter membrane of separating collected eluant, gets neutral
18The F-FDG injection liquid.
In the synthesis technique of the present invention, described rare gas element is preferably He gas.
In the synthesis technique of the present invention, described phase-transfer catalyst is preferably amino-polyether phase-transfer catalyst Kryptofix 2.2.2., perhaps tetra-n-butyl ammonium salt, and as tetra-n-butyl bicarbonate of ammonia, i.e. (n-Bu)
4NHCO
3Kryptofix2.2.2. be 4,7,13,16,21,24-six oxa-s-1, (Kryptofix2.2.2 K222), can select German Merck company product for use to 10-diazabicyclo [8,8,8] 26 carbon alkane; Common and the K of K222
+Shared, K
+The source can select K for use
2CO
3
In the synthesis technique of the present invention, described aprotic solvent is preferably acetonitrile, DMSO (methyl-sulphoxide) or DMF (dimethyl formamide).
The optimization of steps d: described C18 pillar is 1 to 2 C18 pillar of banded successively.
The processing of waste liquid in the steps d: transfer to AG50w-X8 pillar and Al through the effusive liquid of C18 pillar
2O
3The neutral pillar that separates captures phase-transfer catalyst, free F respectively, reclaims waste liquid.
Among the step e, described alkaline solution is NaOH solution or KOH solution.
The optimization of step f: described C18 pillar is 1 to 2 C18 pillar of banded successively.
Among the step f, described AG50w-X8 pillar prepares as follows: smash sky C18 pillar or Al
2O
3The neutral pillar that separates discards weighting agent in the post, and pillar is invaded earlier after bubble sterilizes in 75% ethanol for disinfection, discards thimerosal, invades bubble again in sterilized water, discards sterilized water, dries.After alcohol disinfecting and sterile water wash, load H
+Type AG50w-X8 resin gets the AG50w-X8 pillar.The AG50w-X8 resin is that sulfonic group is connected a kind of strong cation-exchanging resin on the SDVB multipolymer.
In the synthesis technique of the present invention, described QMA negatively charged ion pillar is a Sep Pak QMA negatively charged ion pillar, and described C18 pillar is Sep Pak C18 pillar or Sep Pak plus C18 pillar, described Al
2O
3Neutral separation pillar is Sep Pak Al
2O
3The neutral pillar that separates.Sep-Pak is the reputable brand of U.S. Waters company, Sep Pak QMA anion column, Sep Pak C18 pillar or Sep Pak plus C18 pillar, Sep PakAl
2O
3Neutral separation pillar is the product of Waters company (http://www.waters.com).
Of the present invention
18The synthesis technique of F-FDG has the following advantages:
(1) is applicable to existing main flow equipment such as TRACERlab FX
F-N, TRACERlab F
XFDG and other
18F-FDG automatization synthesis system had both reached the product quality level of external synthesis technique gained, had improved existing technology again, had overcome its limitation, and building-up process is controlled, putting productive rate height, and combined coefficient is stable, the chemical purity height.
(2) adopt existing TRACERlab FX
F-NDuring synthesis technique, magnetic resonance acceleator need be produced
18F
-Target water transfers to TRACERlab FX earlier
F-NA tapered bottle in the synthesis system transfers in the Sep-Pak QMA negatively charged ion pillar; Synthesis technique of the present invention is produced magnetic resonance acceleator
18F
-Target water directly transfers to the Sep-Pak QMA negatively charged ion pillar that places in the radioactivity seeker, has reduced
18F
-Total synthetic time has been shortened in radioactive loss, simplifies the operation course, and is convenient to observe that the QMA pillar captures
18F
-Activity.
(3) existing TRACERlab FX
F-NSynthesis technique needs the heating preset time with the acetonitrile equal solvent in the evaporative removal fluorinated intermediates after fluoridation; Synthesis technique of the present invention adopts at post solid phase alkali hydrolysis method, do not need the step of solvent in the evaporative removal fluorinated intermediates, but adopt less water and fluorinated intermediates to mix the back by the C18 pillar, pillar is after rare gas elementes such as He gas dry up, remove aprotic solvents such as acetonitrile, can reduce the loss of fluorinated intermediates, simplify synthesis technique, reduce generated time.
(4) existing TRACERlab FX
F-NSynthesis technique is that resultant is transferred in the flask that fills the sterilized water that is multiple times than resultant volume (resultant peak value volume 10 times) to the Solid-Phase Extraction purifying step of resultant, then this solution is pressed the solid-phase extraction column that fills C-18; Synthesis technique of the present invention adopts self-control AG50w-X8 pillar, and commercial Sep Pak Plus C18 pillar and Sep Pak Al
2O
3The separation and purification method of neutral pillar replaces the method with a large amount of water wash C18 pillars, can remove free equally
18F
-With phase-transfer catalysts (toxicant) such as K222, K222 content in the injection liquid can be dropped to the degree that survey does not go out.
(5) existing TRACERlab F
XThe FDG synthesis technique adopts integrated post (to contain PS-H
+, PS-HCO
3, Al
2O
3With the HR-P post) separation and purification, need to buy complete separation and purification post, make
18Production and the maintenance cost of F-FDG are high, are unfavorable for clinical application; The separation pillar that synthesis technique utilization of the present invention is more cheap, as make AG50w-X8 pillar and commercialization C18 pillar and the neutral pillar of Al2O3 by oneself, replace complete separation and purification post, through pillar directly neutralize with separation and purification after, just can obtain high yield and highly purified
18The F-FDG injection liquid, production cost reduces, and changes conveniently.The AG50w-X8 pillar is used to remove phase-transfer catalysts such as K222 or tetra-n-butyl ammonium salt, Al
2O
3Neutral pillar is used to remove unreacted
18F
-, the C18 pillar is used to remove the not fluorinated intermediates and the precursor of complete hydrolysis.The basic hydrolysis product does not need with hydrochloric acid and contains the neutralization of AG11A8 post, the elutriant of Sep Pak C18 pillar after basic hydrolysis, and available self-control AG50w-X8 pillar is neutralized into neutrality (pH 6～7).
(6) synthesis technique of the present invention adopts at post solid phase alkali hydrolysis method, can improve
18The enantiomeric purity of F-FDG is higher than existing liquid phase alkali hydrolysis method.
(7) compare with the liquid phase alkali hydrolysis method, synthesis technique of the present invention adopts in basic hydrolysis of post solid phase and pillar separation and purification method, promptly at the incorporate synthesis technique of post hydrolysis, neutralization and separation and purification, simplified synthesis technique, shorten generated time, total synthetic time can shorten to below 20 minutes, and the shortest generated time is about 16 minutes.
(8) synthesis technique of the present invention, through compound experiment statistics more than 10 times,
18F-FDG does not proofread and correct putting productive rate greater than 60%, is up to 75%, and radiochemicsl purity is greater than 99%, and chemical purity and other quality control indexs all meet the radiopharmaceuticals specification of quality, can be used for animal and human's body PET video picture research.
Description of drawings
Fig. 1 is TRACERlab FX
F-NThe process flow diagram of automatization synthesis system.
Fig. 2 is 2-of the present invention
18The F-2-DDG (
18F-FDG) synthesis technique schematic flow sheet.
Fig. 3 is
18The chemical synthesis route figure of F-FDG, among the figure, 1 is the precursor mannose triflate, 2 be the precursor mannose triflate with
18F
-Nucleophilic substitution reaction takes place generate fluorinated intermediates.
Fig. 4 is what obtain with synthesis technique of the present invention
18The HPLC of F-FDG analyzes the chromatography collection of illustrative plates, after A is purifying
18F-FDG radiochromatograph collection of illustrative plates, B are standard substance
19F-FDG specific refractory power chromatography collection of illustrative plates, C are solvent specific refractory power chromatography collection of illustrative plates.
Embodiment
The invention will be further described below in conjunction with drawings and Examples.
Embodiment: synthesis technique of the present invention is applied to existing TRACERlab FX
F-NThe automatization synthesis system
1 materials and methods
1.1 instrument and reagent
PET trace magnetic resonance acceleator and Tracerlab FX
F-NThe automatization synthesis system, U.S. GE company (http://www.gehealthcare.com) product; LC-10AT HPLC analytical system, Japanese Shimadzu company product is furnished with LB 508 type radioactivity flow probes, German EG﹠amp; G company product; The CS-9301PC TLC-scanner, Japanese Shimadzu company product; The γ calculating instrument, Shanghai nuclear research institute product; CRC-15R type activity meter, U.S. CAPINTEC company product.Acetonitrile, Aldrich company product; 4,7,13,16,21,24-six oxa-s-1,10-diazabicyclo [8,8,8] 26 carbon alkane (Kryptofix2.2.2, K222), German Merck company product; 1,3,4,6-four-O-ethanoyl-2-O-trifyl-β-D-mannopyranose (abbreviation mannose triflate) and standard substance 2-19F-2-DDG, Sigma company product; Sep Pak QMA, Sep Pak Plus C18, Sep Pak Plus tC18 and Sep Pak Al
2O
3Neutral pillar, U.S. Waters company product; Self-control AG50w-X8 pillar: smash sky C18 pillar or Al
2O
3The neutral pillar that separates discards weighting agent in the post, and pillar discards thimerosal after being immersed in earlier and sterilizing in 75% ethanol for disinfection, is immersed in the sterilized water again, discards sterilized water, dries, and after alcohol disinfecting and sterilized water processing, loads AG50w-X8 resin (H
+Type, Bio-Rad company product), get the AG50w-X8 pillar; Silica gel 60 thin-layer chromatography aluminium sheets, German Merck company product; Other reagent are homemade analytical pure.
1.2 synthetic route
Employing is synthetic in the automatization of post hydrolysis method
18F-FDG.Synthetic route as shown in Figure 3; with mannose triflate 1 is precursor; with 18F-nucleophilic substitution reaction taking place generates 1; 3,4,6-four-O-ethanoyl-2-18F-β-D-mannopyranose 2; this intermediate is not purified; do not need evaporating solvent, directly be captured in the Sep Pak Plus C18 pillar, add less water drip washing and remove acetonitrile.In Sep Pak Plus C18 pillar, add the hydrolysis of NaOH (or KOH) solution.Hydrolysate is through self-control AG50w-X8 pillar, Sep Pak Al
2O
3Neutral pillar and the little column separating purification of Sep Pak Plus C18,
18The F-FDG injection liquid.
1.3 full-automatic synthesis system
As shown in Figure 1, TRACERlab FX
F-NThe technical process of automatization synthesis system mainly comprises:
18Parts such as F separates, fluoridizes, basic hydrolysis and HPLC separation and purification.This system comprises gas delivery system (He gas, air) 33, heat exchanger 29, vacuum pump 30, Dewar (Dewar) bottle 31, cold-trap 32, vacuum pump 30 is connected with heat exchanger 29 with vacuum jacketed flask 31 respectively, vacuum jacketed flask 31 is placed in the cold-trap 32, also has sealed reaction bottle 10, reservoir 1～9 and 11 and 12, receiving bottle 13～17, refuse bottle 18, valve V1～V31, QMA tube 19, Al
2O
3Post 20, HPLC system (moving phase, injection annulus, HPLC pump 21, C18 separator column 22, radioactivity seeker 23, ultraviolet detector 24, cold air system 25, magnetic stirring system 26, piping system, C18 post 27, sterilizing filter 28 and computer control system etc.Utilize TRACERlab FX
F-NSoftware package can be edited multiple PET medicine automatization synthesis program parameter, as reaction times, temperature of reaction, valve open or close etc., also can manually control in the automatization building-up process.The more detailed description document 18:TRACERlab FX that sees reference
F-NSystem operation handbook (revised edition) chapter 3.TRACERlab F
XIt is synthetic that the FDG synthesis system is exclusively used in automatization
18F-FDG, its process flow sheet and function and TRACERlab FX
F-NThe automatization synthesis system is similar, but does not have HPLC separation and purification system and reservoir (7～9).
As shown in Figure 2,2-of the present invention
18The F-2-DDG (
18F-FDG) the synthesis technique flow process mainly comprises
18F
-Separate, fluoridize, in parts such as basic hydrolysis of post solid phase and column separating purifications.This synthesis system comprises gas delivery system 15, heat exchanger 7, vacuum pump 8, Dewar (Dewar) bottle 9, cold-trap 17, vacuum pump 8 is connected with heat exchanger 7 with vacuum jacketed flask 9 respectively, vacuum jacketed flask 9 is placed in the cold-trap 17, also have Sep Pak QMA pillar 19, radioactivity probe 15, reaction flask 10, reservoir 1～6, receiving bottle 14 and 16 and 18, refuse bottle 27, controllable valve V1～V6, V10, V11, V13～V16, V19, V20, V22～V25, C18 separator column 20, self-control AG50w-X8 pillar 21, Al
2O
3Neutral pillar 22, cold air system 23, magnetic stirring system 24, piping system, sterilizing filter 25, aseptic filter membrane 26 and computer control system etc.
1.4 full-automatic synthetic preceding preparation
At TRACERlab FX
F-NThe software package inediting
18F-FDG automatization synthesis program.As shown in Figure 2, outwell the waste liquid in the cold-trap 17, in Dewar (Dewar) bottle 9, add liquid nitrogen.Open vacuum pump 8, open air pressure switch and rare gas element switch in the gas delivery system 15.Sterilizing filter 25 is installed on the venting port of 1 and No. 2 bottle.0.22 μ m aseptic filter membrane 26 and aseptic syringe needle is installed on the product delivery line, and syringe needle is inserted in the aseptic vacuum receiving bottle 18 of diaphragm seal, and receiving bottle 18 connects an aseptic exhaust syringe needle in addition.Between V10 and V11, connect
18F
-Negatively charged ion trapping column (SepPak QMA pillar 19), this pillar place radioactivity probe 15.Directly connect the pipeline between V14 and the V15, and between V14 and V15, connect Sep Pak plus C18 pillar 20, self-control AG50w-X8 pillar 21 and Sep Pak Al
2O
3The neutral pillar 22 that separates.Add reagent in the post hydrolysis method by following standard: in headpin, add the 1.5mL acetonitrile solution, include 15mg phase-transfer catalyst amino-polyether K222 (or tetra-n-butyl carbonic acid (hydrogen) ammonium) and 3mg K
2CO
3, add the acetonitrile solution (1mL) that contains 20mg precursor mannose triflate in No. 3 bottles, add 5～10mL water in No. 4 bottles, add the 0.8mL2mol/L sodium hydroxide solution in the kingpin, add 10mL water in No. 6 bottles.Close the hot cell protective door.
1.5 in post solid phase hydrolysis method
From TRACERlab FX
F-NSelect editor's solid phase hydrolysis method automatization synthetic in the menu of software
18The program of F-FDG is pressed " start " button, finishes under computer control
18The F-FDG automatization is put and is combined to, and the synthesis technique flow process is seen Fig. 2.
A) nucleophilic fluorination reagent
18F
-Capture at post.Pass through by magnetic resonance acceleator
18O (p, n)
18The F nuclear reaction is produced
18F
-, under the transmission of He gas, process places the Sep-Pak QMA negatively charged ion pillar 19 of radioactivity seeker,
18F
-Be trapped on the post,
18O
-Water is collected in the receiving bottle 16.
B) preparation of nucleophilic substitution reaction.Under vacuum pump 8 effects, contain K in the headpin
2CO
3And the acetonitrile solution of K222 (or tetra-n-butyl carbonic acid (hydrogen) ammonium) will
18The F-F-wash-out is gone in the sealed reaction bottle 10, heating mixing solutions to 60～95 ℃, evaporated under reduced pressure, obtain exsiccant [K/K222]+
18F
-(or (n-Bu) 4N+
18F
-) mixture, waste liquid is absorbed by the cold-trap 17 that places liquid nitrogen.
C) nucleophilic fluoridation.Under the effect of He gas, the precursor mannose triflate acetonitrile solution in No. 3 bottles is pressed in the reaction flask 10,80～90 ℃ of reacting by heating 5～10 minutes.After fluoridation is finished, decompression, cooling.
D) fluorinated intermediates captures at post.Under the effect of He air-flow, water is added in the reaction flask 10 in No. 4 bottles, after fluorinated intermediates is mixed, is transferred to 2 Sep Pak of banded plus C18 pillar 20, AG50w-X8 pillar 21 and Sep PakAl successively
2O
3The neutral pillar 22 that separates captures fluorinated intermediates, K222 (or tetra-n-butyl ammonium salt), free F-respectively, contains the acetonitrile waste collection in refuse bottle 27, and pillar dries up with He.
E) in the basic hydrolysis of post solid phase.Basic hydrolysis is adopted and is carried out in the post hydrolysis method, does not need the hydrochloric acid neutralization, does not also need to contain separation of AG11A8 post and neutralization.NaOH in the kingpin (or KOH) solution is pressed in the reaction flask 10, and is loaded into Sep Pak C18 pillar 20, about 2 minutes of hydrolysis time.
F) in post neutralization and separation and purification.Water in No. 6 bottles is pressed in the reaction flask 10, product after drip washing successively by 2 C18 pillars 20, self-control AG50w-X8 pillar 21 and Sep Pak Al
2O
3The neutral pillar 22 that separates is collected in the product receiving bottle 14.At last, under the effect of He atmospheric pressure, product solution reaches in the sterile product bottle 18 after aseptic filter membrane 26 is handled in the bottle 14,
18The F-FDG injection liquid.
In the present embodiment, step D and step F all adopt 2 Sep Pak plus C18 pillars, also can only adopt 1 Sep Pak plus C18 pillar in the actual process.
1.6 the quality test of product
With the pH value of accurate pH test paper mensuration injection liquid, estimate its color and clarity.
Get instant preparation
18The F-FDG injection liquid is with the activity value of activity meter mensuration different time points, with semilog graphing method estimation transformation period and nuclear purity.
With the chemical purity and the radiochemical purity of radioactivity HPLC systems measurement injection liquid, the HPLC analysis condition: C18 analytical column, moving phase are 60% acetonitrile solution that contains 0.005mol/LKF, and flow velocity is 1mL/ minute, and detector is a RI-detector.
The TLC method: silica gel aluminium sheet, developping agent are 95% acetonitrile solution [reference 5]; K222 adopts TLC chromatography and iodine vapor determination of color, and developping agent is a methyl alcohol: ammoniacal liquor=9: 1 (volume ratio) [reference 6]; Enantiomeric purity adopts the TLC method to measure, and silica-gel plate is through the 10%NaH2PO4 solution-treated, and developping agent is 95% acetonitrile solution [reference 17].
At room temperature, measure the radiochemicsl purity of injection liquid different time in 8 hours, observe its stability.
Carry out sterility test, bacterial endotoxin inspection and undue toxicity inspection with reference to two described methods of appendix of Pharmacopoeia of People's Republic of China version in 2000.
2 results
2.1 putting of 18F-FDG is combined to
At the post alkali hydrolysis method, do not need after in the sealed reaction bottle, finishing fluoridation evaporation to desolventize acetonitrile, but adopt SepPak C18 pillar to capture fluorinated intermediates, clean with less water (about 8mL), the He air-blowing is done, and gets final product the Ex-all acetonitrile, and this moment, C18 pillar collection efficiency reached the highest (about 99%).This post lower end connects self-control AG50w-X8 pillar, the neutral pillar of Sep Pak Al2O3 and the little column separating purification of Sep Pak Plus C18, is respectively applied for to remove K222 (or tetra-n-butyl ammonium salt), unreacted 18F-and the not fluorinated intermediates and the precursor of complete hydrolysis.Hydrolysate does not need hydrochloric acid and contains the neutralization of A G 11 A8 posts, and 0.8mL 2mol/L NaOH (or KOH) solution can be directly by homemade AG50w-X8 pillar neutralization, and solution just in time becomes neutral (pH 6～7).We find that 3mL 1mol/L NaOH solution or Sep Pak C18 pillar load 0.8mL2mol/L NaOH solution, and all available homemade AG50w-X8 pillar is neutralized into neutrality (pH 6～7).In addition, self-control Sep Pak AG50w-X8 pillar can be neutralized to neutrality with 1mL 1mol/L NaOH (or KOH) solution.Best fluoridation condition: 85 ℃ of reacting by heating 5 minutes; At the post optimum hydrolysising condition be: in the Sep Pak C18 pillar that captures fluorinated intermediates, load 2mol/LNaOH (or KOH) solution 0.8mL, room temperature water was terminated an agreement 2 minutes.This method
18The total synthetic time of F-FDG, the shortest time was about 16 minutes less than 20 minutes, did not proofread and correct putting productive rate greater than 60%, was up to 75%.
2.2
18The quality test result of F-FDG
18The F-FDG injection liquid is colourless or pale yellow solution, and the pH value is about 7.0.Radioactive concentration is greater than 2220MBq/mL, and specific activity is not less than 3.7 * 1010Bq/mmol.Measure with the time disintegration method
18The F transformation period is about 110 minutes, and radionuclide purity is greater than 99%.Measure with analysis mode radioactivity HPLC method
18The radiochemical purity of F-FDG injection liquid and chemical purity, typical HPLC analyzes the chromatography collection of illustrative plates and is shown in Fig. 4.
18The F-FDG injection liquid is found two peaks on the radiochromatograph collection of illustrative plates, only find a solvent peak on ultraviolet chromatography collection of illustrative plates; At standard substance
19Find two peaks on the F-FDG ultraviolet chromatography collection of illustrative plates: solvent peak and standard substance
19The F-FDG peak.The accurate product of first peak and ultraviolet chromatography collection of illustrative plates subscript on the radiochromatograph collection of illustrative plates
19The retention time unanimity of F-FDG, retention time is about t
R=3.6 minutes, this peak should be
18F-FDG.Second peak is on the radiochromatograph collection of illustrative plates
18F
-, the chromatographic peak of intermediate is very little, and almost all hydrolysis of intermediate are described.The TLC method is measured
18The F-FDG radiochemical purity, only find initial point (
18F
-) and the Rf=0.6 place (
18F-FDG) radioactivity is arranged, but the initial point radioactivity is very low.Measure through HPLC and TLC method,
18The radiochemical purity of F-FDG is greater than 99%, and chemical purity is about 100%, measures with the TLC method and do not find to contain in the injection liquid K222.Cold synthetic
18During F-FDG, the mixture after the fluoridation under the He effect behind decompression heating evaporate to dryness, find no remaining acetonitrile.Measure through radioactivity HPLC method in addition,
18Considerable change does not take place in F-FDG radiochemical purity in 8 hours, all greater than 95%.Measure through the TLC method, do not find
18F-FDG enantiomorph 2-18F-2-deoxidation-D-seminose (
18F-FDM) existence.Undue toxicity is checked: the tail vein gives
18Behind the F-FDG injection liquid 0.5mL, observed 48 hours, the mouse growth is normal, and no death and untoward reaction phenomenon take place, and dissects the back and observes, and does not see any organ damage.Sterility test and bacterial endotoxin inspection are all negative.
Reference:
[1] Li Jun, Li Guangyi, high tongued bell. novel
18The preparation and the quality control of F-deoxyglucose injection liquid. West China pharmaceutical journal, 2004,19 (1): 8～10.
[2]Lemaire?C，Damhaut?PH，Lauricella?B，et?al.Fast[
18F]FDG?synthesis?by?alkalinehydrolysis?on?a?low?polarity?solid?phase?support.J?Label?Compd?Radiopharm，2002，45(4)：435～447.
[3] Zhang Jinming, Tian Jiahe, Zhou Dan, etc. rapid automatized Synthetic 2-
18F-β-D-deoxyglucose. Chinese Journal of Nuclear Medicine, 2003,23 (1) :～54.
[4]Fuchtner?F，Steinbach?J，Mading?P，et?al.Basic?hydrolysis?of2-[
18F]fluoro-1，3，4，6-tetra-O-acetyl-D-glucose?in?the?preparation?of?2-[
18F]-fluoro-2-deoxy-D-glucose.Appl?Radiat?Isot，1996，47(1)：61～66.
[5]Hamacher?K，Coenen?HH，Stocklin?G.Efficient?stereospecific?synthesis?of?no-carrier-added2-[
18F]-fluoro-2-deoxy-D-glucose?using?aminopolyether?supported?nucleophilicsubstitution.J?Nucl?Med，1986，27(1)：235～238.
[6]Chaly?T，Dahl.JR.Thin?layer?chromatographic?detection?of?kryptofix?2.2.2in?the?routinesynthesis?of[
18F]2-fluoro-2-deoxy-D-glucose.Nucl?Med?Biol，1989，16(4)：385～387.
[7]Fowler?JS，Ido?T.Initial?and?subsequent?approach?for?the?synthesis?of?
18FDG.Sem?NuclMed，2002，32(1)：6～12.
[8] Tang Ganghua, Tang Xiaolan, Zhang Lan waits .2-
18Pharmacokinetic in the synthetic improvement of F-2-deoxidation-D-grape sugar and the mouse body. Chinese Pharmaceutical Journal, 2002,37 (4): 287～290.
[9]Taylor?MD，Roberts?AD，Nickles?RJ.Improved?the?yield?of?2-[
18F]fluoro-2-deoxyglucoseusing?a?microwave?cavity.Nucl?Med?Biol，1996，23：605-609.
[10]Toorongian?SA，Mulholland?GK，Jewett?DM，et?al.Routine?production?of2-deoxy-2-[
18F]fluoro-D-glucose?by?direct?nucleophilic?exchange?on?a?quaternary4-aminopyidinium?resin.Nucl?Med?Biol，1990，17(3)：273-279.
[11]Kim?DW，Choe?YS，Chi?DY，A?new?nucleophilic?fluorine-18?labeling?method?for?aliphaticmesylates：Reaction?in?ionic?liquids?shows?tolerance?for?water.Nucl?Med?Biol，2003，30：345-350
[12]Kim?DW，Jeong?JM，Lee?YS，et?al.Rapid?synthesis?of[
18F]FDG?without?an?evaporationstep?using?an?ionic?liquid.2004，61：1241-1246.
[13]Lemaire?C，Damhaut?Ph，Lauricella?B，et?al.Fast[
18F]FDG?synthesis?by?alkalinehydrolysis?on?a?low?polarity?solid?phase?support.J?Label?Compd?Radiopharm，2002，45：435-447.
[14]Meyer?GJ，Matzke?KH，Hamacher?K，et?al.The?stability?of?2-[
18F]-fluoro-2-deoxy-D-glucose?towards?epimerization?under?alkaline?conditions.Appl?Radiat?Isot，1999，51：37-41.
[15]Mosdzianowski?C，Lemaire?C，Simoens?E.et?al.Epimerization?study?on?[
18F]FDGproduced?by?an?alkaline?hydrolysis?on?solid?support?under?stringent?conditions.ApplRadiat?Isot，2002，56：871-875.
[16] Zhang Jinming, Tian Jiahe should be decided just to wait. and hydrolysis method is synthetic on the solid-phase extraction column
18F-FDG. isotropic substance, 2003,16 (3-4): 222-225.
[17]Van?Rijn?CJS，HerscheidJDM，Visser?GWM，et?al.On?the?stereoselectivity?of?the?reactionof?[
18F]acetylhypofluorite?with?glucals.Appl?Radiat?Isot，1985，36(2)：111-115
[18] TRACERlab FX
F-NSystem operation handbook (revised edition) chapter 3
Claims (9)
1.2-
18The synthesis technique of F-2-DDG is characterized in that, may further comprise the steps:
(a) nucleophilic fluorination reagent
18F
-Capture at post: pass through by medical cyclotron
18O (p, n)
18The F nuclear reaction is produced
18F
-Target water, under the rare gas element transmission, process places the QMA negatively charged ion pillar of radioactivity seeker,
18F
-Be trapped on the post, reclaim
18O
-Water;
(b) preparation of nucleophilic substitution reaction: under vacuum condition, the aprotic solvent that contains phase-transfer catalyst will
18F
-Wash-out is gone in the sealed reaction bottle, heating mixing solutions to 60～95 ℃, reduction vaporization, obtain the exsiccant phase-transfer catalyst-
18F
-Mixture; Described phase-transfer catalyst is selected from amino-polyether phase-transfer catalyst Kryptofix 2.2.2. or tetra-n-butyl ammonium salt;
(c) nucleophilic fluoridation: under the rare gas element effect, the precursor mannose triflate solution that is dissolved in aprotic solvent is pressed into described in the step b in the reaction flask, 80～90 ℃ of reacting by heating 5～10 minutes, decompression, cooling;
(d) capturing at post of fluorinated intermediates: under the rare gas element effect, water is pressed in the reaction flask, mixes with the fluorinated intermediates that obtains among the step c, and mixture is by the C18 pillar, and fluorinated intermediates is trapped on the post, dries up pillar with rare gas element;
(e) in the basic hydrolysis of post solid phase: alkaline solution is loaded onto in the C18 pillar, room temperature hydrolysis 2-3 minute;
(f) in post neutralization and separation and purification: with water wash C18 pillar, eluant is successively by C18 pillar, AG50w-X8 pillar, Al
2O
3Neutral pillar and the aseptic filter membrane of separating collected eluant, gets neutral
18F-FDG injection liquid, i.e. 2-
18F-2-DDG injection liquid.
2. synthesis technique according to claim 1 is characterized in that: described rare gas element is a He gas.
3. synthesis technique according to claim 1 is characterized in that: described aprotic solvent is selected from acetonitrile, DMSO or DMF.
4. synthesis technique according to claim 1 is characterized in that: in the steps d, described C18 pillar is 1 to 2 C18 pillar of banded successively.
5. synthesis technique according to claim 1 is characterized in that: in the steps d, transfer to AG50w-X8 pillar and Al through the effusive liquid of C18 pillar
2O
3The neutral pillar that separates captures phase-transfer catalyst, free F respectively
-, reclaim waste liquid.
6. synthesis technique according to claim 1 is characterized in that: among the step e, described alkaline solution is NaOH solution or KOH solution.
7. synthesis technique according to claim 1 is characterized in that: among the step f, described C18 pillar is 1 to 2 C18 pillar of banded successively.
8. synthesis technique according to claim 1 is characterized in that: among the step f, described AG50w-X8 pillar prepares as follows: smash sky C18 pillar or Al
2O
3The neutral pillar that separates discards weighting agent in the post, and pillar discards thimerosal after being immersed in earlier and sterilizing in 75% ethanol for disinfection, is immersed in the sterilized water again, discards sterilized water, dries, and after alcohol disinfecting and sterilized water processing, loads H
+Type AG50w-X8 resin gets the AG50w-X8 pillar.
9. according to claim 1,4,5,7, one of 8 described synthesis techniques, it is characterized in that: described QMA negatively charged ion pillar is a Sep Pak QMA negatively charged ion pillar, described C18 pillar is Sep Pak C18 pillar or Sep Pak plusC18 pillar, described Al
2O
3Neutral separation pillar is Sep Pak Al
2O
3The neutral pillar that separates.
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| CN100560548C (en) * | 2006-06-01 | 2009-11-18 | 郭启勇 | Adopt ionic liquid synthetic as phase-transfer catalyst 18The method of F mark positron radioactivity tracer agent |
| CN100560549C (en) * | 2006-06-23 | 2009-11-18 | 郭启勇 | Utilize ionic liquid synthetic as phase-transfer catalyst 18The method of F mark positron radioactivity tracer agent |
| EP1933330A1 (en) * | 2006-12-11 | 2008-06-18 | Trasis S.A. | Electrochemical 18F extraction, concentration and reformulation method for radiolabeling |
| CN101597228B (en) * | 2009-07-02 | 2013-12-25 | 中山大学附属第一医院 | <11>C-acetate preparation method |
| ITRM20110223A1 (en) * | 2011-04-28 | 2012-10-29 | Seventeen Srl | AUTOMATIC APPARATUS FOR THE SYNTHESIS OF PEPTIDIC-BASED RADIOPHARMACEUTICALS FOR DIAGNOSTIC AND / OR THERAPEUTIC USE. |
| WO2015071288A1 (en) * | 2013-11-13 | 2015-05-21 | Ge Healthcare Limited | Dual run cassette for the synthesis of 18f-labelled compounds |
| CN104086470A (en) * | 2014-07-04 | 2014-10-08 | 广州市原子高科同位素医药有限公司 | Positron nuclide labeled selenocysteine compound and application thereof |
| CN104262073B (en) * | 2014-09-30 | 2016-08-17 | 北京善为正子医药技术有限公司 | Small modules formula multifunction automatic18f labelling PET pharmaceutical synthesis instrument |
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| CN105152960B (en) * | 2015-10-11 | 2017-04-19 | 北京脑重大疾病研究院 | Automatic preparation method and device for ＜18＞F-(2S,4R)-4-fluoro-L-glutamine |
| CN105646601A (en) * | 2016-01-21 | 2016-06-08 | 甘肃圣普诺生物技术有限公司 | Hydrolyzation purification method for preparing 18F-FDG |
| CN106178594B (en) * | 2016-08-10 | 2019-06-04 | 周彤 | Repeatedly, rapid synthesis18The technique of F-FDG and used valve system |
| CN106631863B (en) * | 2016-09-06 | 2018-08-17 | 中山大学附属第一医院 | The radiation synthetic method of sub- glutamic acid-type PET developers |
| CN106902363B (en) * | 2017-02-27 | 2019-11-12 | 中山大学附属第一医院 | Radioactive composition, its single fraction preparation method and use |
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| CN113372399A (en) * | 2021-06-04 | 2021-09-10 | 江苏华益科技有限公司 | A kind of fluorine [ 2 ]18F]Synthesis method of deoxyglucose injection |
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