CN1601272A - Ethylene equol molecular engram solid phase extracting small pole and its its prepn process - Google Patents

Ethylene equol molecular engram solid phase extracting small pole and its its prepn process Download PDF

Info

Publication number
CN1601272A
CN1601272A CN 200410046861 CN200410046861A CN1601272A CN 1601272 A CN1601272 A CN 1601272A CN 200410046861 CN200410046861 CN 200410046861 CN 200410046861 A CN200410046861 A CN 200410046861A CN 1601272 A CN1601272 A CN 1601272A
Authority
CN
China
Prior art keywords
diethylstilbestrol
des
phase extraction
solid phase
stiboestrol
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
CN 200410046861
Other languages
Chinese (zh)
Other versions
CN1265195C (en
Inventor
陈波
马金余
刘程
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
HUNAN NUEL TECHNOLOGIES Co Ltd
Original Assignee
HUNAN NUEL TECHNOLOGIES Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by HUNAN NUEL TECHNOLOGIES Co Ltd filed Critical HUNAN NUEL TECHNOLOGIES Co Ltd
Priority to CN 200410046861 priority Critical patent/CN1265195C/en
Publication of CN1601272A publication Critical patent/CN1601272A/en
Application granted granted Critical
Publication of CN1265195C publication Critical patent/CN1265195C/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Landscapes

  • Other Investigation Or Analysis Of Materials By Electrical Means (AREA)
  • Steroid Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

The invention discloses a molecular impriting solid-phase extraction small column capable of high-selectively purifying and enriching diethyl stiboestrol (DES) from sample solution for determining residual amount of artificially-synthetic estrin diethyl stiboestrol (DES) in animal food and its preparation method. Said invention uses diethyl stiboestrol as molecular template to prepare molecular imprinting polymer, it is a cross-linked polymer with fixed hole size and form and definite arranged function group, and has the 'memory' function for steresotructure of diethyl stiboestrol template molecule, so that said material can be fileld into polypropylene small column so as to can obtain the diethyl stiboestrol molecular imprinting solid-phase extraction small column. As compared with general solvent extraction method and C18 solid-phase extraction method said invented imprinting column is more simple, quick and higher in efficiency.

Description

Diethylstilbestrol molecular imprinted solid phase extraction cartridge and preparation method thereof
Technical field
The present invention relates to the analytical chemistry field, specifically be applied to measure the high selectivity purifying of the sample solution of synthetic estrogen diethylstilbestrol (DES) residual quantity in the animal food, diethylstilbestrol molecular imprinted solid phase extraction cartridge of enrichment and preparation method thereof.
Background technology
(Diethylstilbestrol DES) is a kind of synthetic estrogen with phenolic hydroxyl structure to diethylstilbestrol, and many countries such as America and Europe forbid using it in the animal feed.Because the abuse of diethylstilbestrol, the residue detection of diethylstilbestrol in the animal food has been caused great attention both domestic and external.If measure in accordance with regulations, the residual situation of diethylstilbestrol is in animal tissue and the body fluid: the concentration in muscle, fat is very low, usually<0.5 μ g/kg, the concentration in the liver<2 μ g/kg, though concentration is the highest in excreta and the bile, also has only 0.5~20 μ g/kg.In order to make low concentration sample influential on detecting device, be necessary sample is carried out the enrichment of DES with concentrated.Under the usual conditions, extract DES with organic solution and can obtain the good recovery, but also extracted a large amount of liposoluble substances simultaneously, be difficult for separating, want extraction with NaOH with DES, but NaOH again with fatty acid generation saponification.Directly extract again less than the good recovery with rare NaOH solution.The Solid-Phase Extraction method is a kind of simple, convenient, suitable pre-service.But C 18Solid phase extraction column can not well separate DES and fat.
Summary of the invention
The object of the present invention is to provide and a kind ofly can simply, fast, efficiently measure the high selectivity purifying of the sample solution of synthetic estrogen diethylstilbestrol (DES) residual quantity in the animal food and diethylstilbestrol molecular imprinted solid phase extraction cartridge of enrichment and preparation method thereof.
Technical scheme of the present invention is achieved in that
(1) diethylstilbestrol molecular imprinted solid phase extraction cartridge: be to be filled in the pillar of polypropylene shell with diethylstilbestrol (DES) the microsphere polymkeric substance 0.2~1.0g that is ground to 10~60 μ m.
(2) preparation method of diethylstilbestrol molecular imprinted solid phase extraction cartridge: may further comprise the steps
(1). the preparation of diethylstilbestrol (DES) microsphere polymkeric substance:
With polymer raw template molecule stilbestrol Diethylstilbestrol (DES), function monomer methacrylic acid (MAA), crosslinking chemical Ethylene glycol dimethacrylate (EDMA), press template molecule: function monomer: crosslinking chemical=1~5: 4~10: 20~100, join in the round-bottomed flask successively, add initiating agent azoisobutyronitrile (AIBN), pore-foaming agent ethanol, chloroform, ether etc. again, ultrasonic 5~30min, logical nitrogen 5~40min, vacuum is reacted 5~48h in 40~90 ℃ of water-baths;
(2) the microsphere polymkeric substance is ground to about 10~60 μ m, uses V (acetic acid)/ V (ethanol)=5~30: 95~70 flushings, tiny particle is removed in the acetone sedimentation;
(3) the quality 0.2~1.0g of weighing molecularly imprinted polymer;
(4) be filled in the pillar of polypropylene shell;
Because diethylstilbestrol (DES) microsphere polymkeric substance is a kind of cross-linked polymer that fixing hole size and shape is arranged and the functional group of determining arrangement is arranged, it has " memory " function to the spatial structure of DES template molecule, can be applicable to be used for measure high selectivity purifying, the enrichment of the sample solution of animal food synthetic estrogen diethylstilbestrol (DES) residual quantity.
This trace post is more simple, quick, efficient than usual vehicle extraction, C18 solid phase extraction.The pillar of selection polypropylene material shell helps the last DES solid phase extraction column that obtains can carry out online fast purification, elution in microwave cavity, and forms integrated on-line system with chromatographic fractionation system.
Embodiment
Below the invention will be further described by embodiment.
Embodiment 1:
(1). the preparation of diethylstilbestrol (DES) microsphere polymkeric substance:
The reaction raw materials tabulation
The molecular weight reaction consumption
Reaction reagent
(g/mol) molar weight (mmol) quality (g) actual amount
Diethylstilbestrol
268.4 0.50 0.134 270mg
DES
Methacrylic acid MAA 68.01 2.0 0.136 0.136ml
Ethylene glycol dimethacrylate
198.22 10.0 1.687 2.0ml
EDMA
Azoisobutyronitrile AIBN 164.21 0.12 19.7 19.7g
Acetonitrile 6ml
Cause
Chloroform 6ml
The hole
Ether 6ml
Agent
Above-mentioned three kinds of liquid 6ml
Successively join in round-bottomed flask by the consumption of above table reaction reagent Diethylstilbestrol (MES), methacrylic acid (MAA), Ethylene glycol dimethacrylate (EDMA), azoisobutyronitrile (AIBN), pore-foaming agent, ultrasonic 15min, logical nitrogen 5min, sealing, 60 ℃ of water-baths, 24h.
(2), the preparation of diethylstilbestrol molecular imprinted solid phase extraction cartridge
The microsphere polymkeric substance is ground to about 26 μ m, uses V (acetic acid)/ V (ethanol)=10: 90 flushings, tiny particle is removed in the acetone sedimentation, obtains particle diameter in a certain interval
3, the quality 0.2~1.0g of weighing microsphere polymkeric substance;
4, the microsphere polymkeric substance is filled in the solid phase pillar
(3) the diethylstilbestrol molecular imprinted solid phase extraction cartridge is used for measuring high selectivity purifying, the enrichment of the sample solution of animal food synthetic estrogen diethylstilbestrol (DES) residual quantity.
Concrete operations are as follows:
(1) earlier with the pillar washed with methanol,
(2) add sample solution 1.5ml;
(3) elute soln is the mixed solution of methyl alcohol, second alcohol and water, and the ratio of organic solvent and water is 0.5~4: 1.The effluent volume scope is at 2~10 pillar volumes.

Claims (2)

1. the diethylstilbestrol molecular imprinted solid phase extraction cartridge is characterized in that it being diethylstilbestrol (DES) the microsphere polymkeric substance 0.2~1.0g that will be ground to 10~60 μ m, is filled in the pillar of polypropylene shell.
2. the preparation method of diethylstilbestrol molecular imprinted solid phase extraction cartridge is characterized in that may further comprise the steps
(1). the preparation of diethylstilbestrol (DES) microsphere polymkeric substance:
With polymer raw template molecule stilbestrol Diethylstilbestrol (DES), function monomer methacrylic acid (MAA), crosslinking chemical Ethylene glycol dimethacrylate (EDMA), press template molecule: function monomer: crosslinking chemical=1~5: 4~10: 20~100, join in the round-bottomed flask successively, add initiating agent azoisobutyronitrile (AIBN), pore-foaming agent ethanol, chloroform, ether etc. again, ultrasonic 5~30min, logical nitrogen 5~40min, vacuum is reacted 5~48h in 40~90 ℃ of water-baths; '
(2) the microsphere polymkeric substance is ground to about 10~60 μ m, uses V (acetic acid)/ V (ethanol)=5~30: 95~70 flushings, tiny particle is removed in the acetone sedimentation;
(3) the quality 0.2~1.0g of weighing molecularly imprinted polymer;
(4) be filled in the pillar of polypropylene shell.
CN 200410046861 2004-10-26 2004-10-26 Ethylene equol molecular engram solid phase extracting small pole and its its prepn process Expired - Fee Related CN1265195C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN 200410046861 CN1265195C (en) 2004-10-26 2004-10-26 Ethylene equol molecular engram solid phase extracting small pole and its its prepn process

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN 200410046861 CN1265195C (en) 2004-10-26 2004-10-26 Ethylene equol molecular engram solid phase extracting small pole and its its prepn process

Publications (2)

Publication Number Publication Date
CN1601272A true CN1601272A (en) 2005-03-30
CN1265195C CN1265195C (en) 2006-07-19

Family

ID=34665719

Family Applications (1)

Application Number Title Priority Date Filing Date
CN 200410046861 Expired - Fee Related CN1265195C (en) 2004-10-26 2004-10-26 Ethylene equol molecular engram solid phase extracting small pole and its its prepn process

Country Status (1)

Country Link
CN (1) CN1265195C (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN100374860C (en) * 2006-02-16 2008-03-12 上海交通大学 Process for producing chloromycetin molecular engram solid phase extraction small column
CN100382869C (en) * 2006-03-13 2008-04-23 中山大学 Molecular blotting solid phase microextraction coating preparation method
CN101177501B (en) * 2007-10-30 2010-05-19 湖北出入境检验检疫局检验检疫技术中心 Method for preparing progesterone molecular engram polymer
CN102580353A (en) * 2012-02-23 2012-07-18 宁波市疾病预防控制中心 Preparation method of solid phase extraction column of molecular imprinted of phenolic environmental estrogens
CN104193875A (en) * 2014-06-25 2014-12-10 齐鲁工业大学 Preparation method and application of magnetic diethylstilbestrol molecularly-imprinted polymer
CN108519445A (en) * 2018-02-11 2018-09-11 桂林理工大学 A kind of method of trace estrogen in separation and concentration environmental water sample
CN114950394A (en) * 2022-06-01 2022-08-30 江苏大学 Preparation method of magnetic surface molecularly imprinted nano material for selective adsorption separation of diethylstilbestrol

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN100374860C (en) * 2006-02-16 2008-03-12 上海交通大学 Process for producing chloromycetin molecular engram solid phase extraction small column
CN100382869C (en) * 2006-03-13 2008-04-23 中山大学 Molecular blotting solid phase microextraction coating preparation method
CN101177501B (en) * 2007-10-30 2010-05-19 湖北出入境检验检疫局检验检疫技术中心 Method for preparing progesterone molecular engram polymer
CN102580353A (en) * 2012-02-23 2012-07-18 宁波市疾病预防控制中心 Preparation method of solid phase extraction column of molecular imprinted of phenolic environmental estrogens
CN102580353B (en) * 2012-02-23 2014-04-16 宁波市疾病预防控制中心 Preparation method of solid phase extraction column of molecular imprinted of phenolic environmental estrogens
CN104193875A (en) * 2014-06-25 2014-12-10 齐鲁工业大学 Preparation method and application of magnetic diethylstilbestrol molecularly-imprinted polymer
CN104193875B (en) * 2014-06-25 2016-03-23 齐鲁工业大学 The preparation method of stilboestrol magnetic molecularly imprinted polymer and application thereof
CN108519445A (en) * 2018-02-11 2018-09-11 桂林理工大学 A kind of method of trace estrogen in separation and concentration environmental water sample
CN114950394A (en) * 2022-06-01 2022-08-30 江苏大学 Preparation method of magnetic surface molecularly imprinted nano material for selective adsorption separation of diethylstilbestrol

Also Published As

Publication number Publication date
CN1265195C (en) 2006-07-19

Similar Documents

Publication Publication Date Title
CN100374860C (en) Process for producing chloromycetin molecular engram solid phase extraction small column
CN101130580A (en) Tsiklomitsin molecular engram polyalcohol and uses of the same
CN1632563A (en) Streptomycin molecular engram solid phase extraction column and preparing process and application thereof
CN107501045B (en) Method for separating and purifying butanetriol from fermentation liquor by using macroporous adsorption resin
CN102000549B (en) Preparation method and application of novel melamine molecule imprinting adsorbing material
CN1815224A (en) Capillary liquid-phase chromatographic collumn and making method
CN101246150B (en) Tsiklomitsin molecular engram integral column preparation method
CN102580353B (en) Preparation method of solid phase extraction column of molecular imprinted of phenolic environmental estrogens
CN1601272A (en) Ethylene equol molecular engram solid phase extracting small pole and its its prepn process
CN101733082A (en) Method for preparing rhodamine B molecular engram solid phase extraction stuffing and application thereof
CN100390211C (en) High polarity polystyrene adsorption resin preparation method and its uses in separating bocconine
CN104693336A (en) Sulfonyl modified strong cationic hypercrosslinked resin and preparation method thereof
CN102279232A (en) Method for efficiently separating and purifying multiresidue sulfonamide antibiotics in biological sample
CN101721516A (en) Preparation method of gardenia extract
CN103772595B (en) A kind of preparation method of multi-template molecular engram monolithic rod
CN103232572A (en) Molecular imprinting polymer for roxarsone detection, and preparation method thereof
CN102070753B (en) Brodifacoum (anticoagulation raticide) molecularly imprinted polymer and use thereof of as solid phase extraction agent
CN105601789A (en) Rutin-Cu2+ ligand molecularly imprinted polymer and preparation method and application thereof
CN102507820B (en) Method for detecting trichlorfon and monocrotophos
CN101921370A (en) Method for preparing molecularly imprinted polymer used for detecting valnemulin
CN105085827A (en) Preparation method of tanshinol surface molecularly-imprinted polymer
CN108484816B (en) Phenothiazine drug family specific molecularly imprinted polymer, chemiluminescence kit and detection method
CN105223258A (en) Amikacin and streptomysin double-template molecularly imprinted solid phase extraction column and using method
CN102565243B (en) Method for preparing organic arsines molecular imprinting monolithic column and application thereof
CN102250285A (en) Semi-covalent molecularly imprinted polymer used for selectivity separating phenols, preparation method thereof, and application thereof

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant
C19 Lapse of patent right due to non-payment of the annual fee
CF01 Termination of patent right due to non-payment of annual fee