CN1594373A - Use of methylacrylic acid_vinyl glycol dimethyl acrylate polymers - Google Patents
Use of methylacrylic acid_vinyl glycol dimethyl acrylate polymers Download PDFInfo
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- CN1594373A CN1594373A CN 200410013388 CN200410013388A CN1594373A CN 1594373 A CN1594373 A CN 1594373A CN 200410013388 CN200410013388 CN 200410013388 CN 200410013388 A CN200410013388 A CN 200410013388A CN 1594373 A CN1594373 A CN 1594373A
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Abstract
The invention discloses the use of methylacrylic acid_vinyl glycol dimethyl acrylate polymers, wherein methylacrylic acid_vinyl glycol dimethyl acrylate polymer is used as adsorbing medium for efficient enriching for basic substances in biological and environmental samples, thus can be applied to the fields of environmental monitoring, drug and excitant detecting and pesticide residue detecting.
Description
Technical field
The present invention relates to the purposes of methacrylic acid-vinyl ethylene glycol dimethacrylate polymkeric substance, relate in particular to the methacrylic acid-application of vinyl ethylene glycol dimethacrylate polymkeric substance in the basic sample solution pre-treatment.
Background technology
The analytic target of facing along with modern separate analytical technique becomes increasingly complex, and the content of analysans is more and more lower, and the pretreatment technology of sample shared status in the sample analysis technology is also more and more important.Various pretreatment technologies emerge in an endless stream with corresponding sorbing material, and its common purpose is and can carries out the interference that sample substrate is also removed in maximum enrichment simultaneously to the analysans in the sample.
In the analysis of and the biological sample of paying close attention to, environmental sample etc. interested people, basic sample solution accounts for significant proportion.As drugs and stimulant substance major part is alkaline matter, and sterilant and many medicines that uses clinically also are alkaline matter.For the analysis of this type of alkaline matter, because they are present in the complicated matrix (as urine sample, blood sample) mostly, and content is lower, directly analyzes comparatively difficulty, generally must be through carrying out qualitative and quantitative analysis after the enrichment of pre-treatment and the removal of impurities.Existing sample pre-treatments analytical procedure comprises traditional liquid-liquid extraction, the Solid-Phase Extraction that grows up from the beginning of the eighties at the end of the seventies, and the solid-phase microextraction that grows up the nineties or the like.For back two kinds of technology, used enrichment material then is mainly and can be used for neutrality, acidity and alkaline universal material, as the octadecyl silane material, and styrenic polymer, polydimethylsiloxane or the like lacks corresponding specific aim and selectivity.
Methacrylic acid-vinyl ethylene glycol dimethacrylate polymkeric substance, its structural formula is:
Methacrylic acid and vinyl ethylene glycol dimethacrylate have comparatively widely at polymeric material field to be used, and it can be used as the intelligent material of pH sensitivity, is applied to drug release, enzyme immobilization, chemical sensor etc.This polymkeric substance is applied to the synthetic field of molecularly imprinted polymer also morely, and they are respectively the most common monomer and linking agents.But this base polymer does not draw attention as the performance of non-imprinted polymer material.
Summary of the invention
The present invention is exactly a kind of new purposes that methacrylic acid-vinyl ethylene glycol dimethacrylate polymkeric substance is provided at the problems referred to above.
Technical scheme provided by the invention is: the methacrylic acid-application of vinyl ethylene glycol dimethacrylate polymkeric substance in sample pre-treatments.
Above-mentioned methacrylic acid-vinyl ethylene glycol dimethacrylate polymkeric substance can adopt the method or the preparation of following method of bibliographical information: with the methacrylic acid is monomer, the vinyl ethylene glycol dimethacrylate is a linking agent, with toluene and lauryl alcohol is pore-creating agent, Diisopropyl azodicarboxylate is an initiator, obtains methacrylic acid-vinyl ethylene glycol dimethacrylate polymer materials by the thermal-initiated polymerization reaction.Concrete operations condition of the present invention is:
Monomer: methacrylic acid (MAA) 1mmol
Linking agent: vinyl ethylene glycol dimethacrylate (EGDMA) 4mmol
Pore-creating agent: toluene 200mg, lauryl alcohol 1.6g
Initiator: Diisopropyl azodicarboxylate (AIBN) 8mg
Mixing and stirring under the room temperature, logical nitrogen deoxygenation 5min pours into sealed vessel or in vinyl modification quartz capillary (sealing two ends), 60 ℃ of initiation reaction 16h.
In the polymer materials that sealed vessel reaction obtains, be milled to Powderedly after the taking-up, remove toluene and lauryl alcohol with methanol wash, the particle (as 30～50 microns) of certain size is got in flotation, is packed in the solid phase extraction column to use.
The integral post material that obtains in kapillary uses after removing pore-creating agent with methyl alcohol.
The present invention is an adsorption medium with methacrylic acid-vinyl ethylene glycol dimethacrylate polymkeric substance, can carry out enrichment efficiently at the alkaline matter in biological and the environmental sample, can be used for a plurality of Application Areass such as environmental monitoring, drugs drug-testing, agricultural residual detection.Have good specific aim and selectivity.After particularly being applied to coupling technique (Solid-Phase Extraction/solid-phase microextraction and gas-chromatography/liquid chromatography coupling), can be used for the routine of sample, quick, high throughput analysis.
Methacrylic acid-vinyl ethylene glycol dimethacrylate polymkeric substance has hydrophobic skeleton structure and carboxylic acid group's acid functional group, and it has very big potentiality as a class at the adsorption medium of basic sample solution.In addition, this base polymer is with low cost in addition, synthetic method is simple, mild condition, for protein characteristics such as close friend comparatively, all make it satisfy the basic demand that becomes the universal adsorption medium of analyzing at basic sample solution, can be used for every field such as biology, medicine, drugs and stimulant analysis, environmental monitoring.
Description of drawings
Fig. 1 is 5 μ g/mL urine sample solid-phase microextraction color atlass in the embodiment of the invention 1;
Fig. 2 is 5 μ g/mL urine samples, 20 μ L direct injection color atlass among the embodiment 1:
Fig. 3 is a drug abuse suspect urine sample solid-phase microextraction color atlas among the embodiment 1;
Fig. 4 is 1 a μ g/mL serum sample solid-phase microextraction color atlas in the embodiment of the invention 2;
Fig. 5 is 1 μ g/mL sample direct injection (5 a μ L) color atlas in the embodiment of the invention 2.
Embodiment
Embodiment 1:
Methacrylic acid-vinyl ethylene glycol dimethacrylate polymer capillary integral post is used for managing the ketamine that interior solid-phase microextraction-liquid chromatography coupling technique is analyzed urine sample
Methacrylic acid-vinyl ethylene glycol dimethacrylate polymer capillary integral post preparation: get the quartz capillary 20cm of 250 microns internal diameters, behind 1mol/L sodium hydroxide and 1mol/L hydrochloric acid activation, logical 160 ℃ of oven dry of nitrogen.Pour into the methanol solution of (γ-methacryloyl) propyl trimethoxy silicane after the cooling, 40 ℃ of reaction 12h.Behind methyl alcohol flush away unreacted reactant, dry up kapillary with nitrogen.Get methacrylic acid 50mg, vinyl ethylene glycol dimethacrylate 430mg, toluene 110mg, lauryl alcohol 0.8g, AIBN 4mg stirs after the mixing, and logical nitrogen 5min pours in the kapillary with syringe, and seal with silicon rubber at two ends.60 ℃ of reaction 16h in baking oven.With methyl alcohol flush away pore-creating agent and unreacted reactant.
Capillary pipe solid phase micro-extraction-liquid chromatography coupling technique is analyzed the ketamine in the urine sample:
Extraction conditions: with methacrylic acid-vinyl ethylene glycol dimethacrylate polymer capillary integral post is the extraction kapillary, activate successively through methyl alcohol, phosphate buffered saline buffer, sample solution extract stream speed control is made as 0.04mL/min, the extraction time is 10min, the direct desorb 5min of flow velocity 0.02mL/min is controlled to analytical column with moving phase again with phosphate buffered saline buffer washing kapillary in the extraction back.
The liquid-phase chromatographic analysis condition: with 15mm * 4.6mm i.d.Kromasil ODS post is analytical column, and moving phase is that 0.05mol/L ammonium acetate buffer (pH4.5) mixes with 70: 30 (volume ratio) with methyl alcohol, and flow velocity 1mL/min, ultraviolet detection wavelength are 223nm.
Urine analysis: get healthy human urine's sample centrifuging and taking supernatant liquor and use, add volume ratio 1: 1 phosphate buffer soln (pH6.0) as sample substrate.Ketamine is marked liquid add in the above-mentioned sample, obtaining concentration is a series of activities curve test soln of 0.05 μ g/mL～10 μ g/mL.After extraction, mapping obtains working curve to concentration with peak area, and linearly dependent coefficient is 0.9999, detects and is limited to 6.4ng/mL, and the detectability 189.5ng/mL that obtains than the direct injection method has improved 19.74 times.Accompanying drawing 1 is 5 μ g/mL urine sample solid-phase microextraction color atlass, and accompanying drawing 2 is 5 μ g/mL urine samples, 20 μ L direct injection color atlass, and peak 1 is a ketamine among the figure.Method in a few days RSD is 0.9%, and RSD is 1.6% in the daytime.
Actual urine analysis: drug abuse suspect urine sample records and contains ketamine 1.88 μ g/mL in its urine sample after handling with quadrat method, sees accompanying drawing 3, and peak 1 is a ketamine.
Embodiment 2:
Methacrylic acid-vinyl ethylene glycol dimethacrylate polymer capillary integral post is used for managing Theobromine, theophylline and the caffeine of interior solid-phase microextraction-liquid chromatography coupling technique serum analysis
Methacrylic acid-vinyl ethylene glycol dimethacrylate polymer capillary integral post preparation: with embodiment 1
Theobromine, theophylline and caffeine in solid-phase microextraction in the pipe-liquid chromatography coupling technique serum analysis:
Extraction conditions: with methacrylic acid-vinyl ethylene glycol dimethacrylate polymer capillary integral post is the extraction kapillary, activate successively through methyl alcohol, phosphate buffered saline buffer, sample solution extract stream speed control is made as 0.04mL/min, the extraction time is 6min, the direct desorb 5min of flow velocity 0.02mL/min is controlled to analytical column with moving phase again with phosphate buffered saline buffer washing kapillary in the extraction back.
The liquid-phase chromatographic analysis condition: with 15mm * 4.6mm i.d.Kromasil ODS post is analytical column, and moving phase is that 0.05mol/L ammonium acetate buffer (pH4.5) mixes with 70: 30 (volume ratio) with methyl alcohol, and flow velocity 1mL/min, ultraviolet detection wavelength are 270nm.
Serum sample is analyzed: get healthy human serum centrifuging and taking supernatant liquor and use, added phosphate buffer soln and regulate pH to 3.0 in 1: 5 by volume.Theobromine, theophylline and caffeine mark liquid are added in the above-mentioned sample, and obtaining concentration is a series of activities curve test soln of 0.05 μ g/mL～2 μ g/mL.After extraction, mapping obtains working curve to concentration with peak area, and linearly dependent coefficient is followed successively by 0.9990,0.9998 and 0.9990.Detection is limited to 12.0,8.0 and 6.5ng/mL.Method in a few days deviation RSD is 1.9,1.2 and 2.9%, and deviation RSD is 2.8,2.4 and 1.4% in the daytime.Accompanying drawing 4 is the solid-phase microextraction figure of serum sample, and accompanying drawing 5 is the color atlas of direct injection, and peak 1 is a Theobromine among the figure, and peak 2 is a theophylline, and peak 3 is a caffeine.
The reusability of extraction capillary column: after serum sample had extracted, cleaning kapillary with phosphate buffer soln can reuse, and extraction efficiency does not have reduction.Use capillary pressure not find to raise repeatedly.These phenomenons show that this method can be used for the actual sample analysis, and the reusable analysis cost that makes of kapillary reduces.
Claims (1)
1. methacrylic acid-the application of vinyl ethylene glycol dimethacrylate polymkeric substance in the basic sample solution pre-treatment.
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| Application Number | Priority Date | Filing Date | Title |
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| CN 200410013388 CN1252099C (en) | 2004-06-29 | 2004-06-29 | Use of methylacrylic acid_vinyl glycol dimethyl acrylate polymers |
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| CN 200410013388 CN1252099C (en) | 2004-06-29 | 2004-06-29 | Use of methylacrylic acid_vinyl glycol dimethyl acrylate polymers |
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| CN1594373A true CN1594373A (en) | 2005-03-16 |
| CN1252099C CN1252099C (en) | 2006-04-19 |
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Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101516448A (en) * | 2006-09-19 | 2009-08-26 | 巴斯夫欧洲公司 | Cosmetic preparations based on molecularly imprinted polymers |
| CN101858898A (en) * | 2010-05-18 | 2010-10-13 | 华中师范大学 | Monolithic column solid phase extraction sample pretreatment method |
| CN111592121A (en) * | 2020-05-13 | 2020-08-28 | 欣格瑞（山东）环境科技有限公司 | Acrylic copolymer, novel environment-friendly corrosion and scale inhibitor composition and application |
-
2004
- 2004-06-29 CN CN 200410013388 patent/CN1252099C/en not_active Expired - Fee Related
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101516448A (en) * | 2006-09-19 | 2009-08-26 | 巴斯夫欧洲公司 | Cosmetic preparations based on molecularly imprinted polymers |
| CN101516448B (en) * | 2006-09-19 | 2014-07-16 | 巴斯夫欧洲公司 | Cosmetic preparations based on molecularly imprinted polymers |
| CN101858898A (en) * | 2010-05-18 | 2010-10-13 | 华中师范大学 | Monolithic column solid phase extraction sample pretreatment method |
| CN101858898B (en) * | 2010-05-18 | 2012-08-29 | 华中师范大学 | Monolithic column solid phase extraction sample pretreatment method |
| CN111592121A (en) * | 2020-05-13 | 2020-08-28 | 欣格瑞（山东）环境科技有限公司 | Acrylic copolymer, novel environment-friendly corrosion and scale inhibitor composition and application |
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| CN1252099C (en) | 2006-04-19 |
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