共查询到20条相似文献,搜索用时 609 毫秒
1.
Feng QZ Zhao LX Yan W Ji F Wei YL Lin JM 《Analytical and bioanalytical chemistry》2008,391(3):1073-1079
Highly sensitive flow-injection chemiluminescence (CL) combined with molecularly imprinted solid-phase extraction (MISPE)
has been used for determination of 2,4-dichlorophenol (2,4-DCP) in water samples. The molecularly imprinted polymer (MIP)
for 2,4-DCP was prepared by non-covalent molecular imprinting methods, using 4-vinylpyridine (4-VP) and ethylene glycol dimethacrylate
(EGDMA) as the monomer and cross-linker, respectively. 2,4-DCP could be selectively adsorbed by the MIP and the adsorbed 2,4-DCP
was determined by its enhancing effect on the weak chemiluminescence reaction between potassium permanganate and luminol.
The enhanced CL intensity was linear in the range from 1 × 10−7 to 2 × 10−5g mL−1. The LOD (S/N = 3) was 1.8 × 10−8g mL−1, and the relative standard deviation (RSD) was 3.0% (n = 11) for 1.4 × 10−6g mL−1. The proposed method had been successfully applied to the determination of 2,4-DCP in river water.
Figure Effect of 4-VP content on the ultraviolet spectrum of 2,4-DCP in chloroform 相似文献
2.
A rapid, specific, and sensitive method has been developed using molecularly imprinted polymers (MIPs) as solid-phase extraction
sorbents for extraction of trace tetracycline antibiotics (TCs) in foodstuffs. MIPs were prepared by precipitation polymerization
using tetracycline as the template. Under the optimal condition, the imprinting factors for MIPs were 4.1 (oxytetracycline),
7.0 (tetracycline), 7.4 (chlortetracycline), 7.7 (doxycycline), respectively. Furthermore, the performance of MIPs as solid-phase
extraction sorbents was evaluated and high extraction efficiency of molecularly imprinted solid-phase extraction (MISPE) procedure
was demonstrated. Compared with commercial sorbents, MISPE gave a better cleanup efficiency than C18 cartridge and a higher
recovery than Oasis HLB cartridge. Finally, the method of liquid chromatography–tandem mass spectrometry coupled with molecular-imprinted
solid-phase extraction was validated in real samples including lobster, duck, honey, and egg. The spiked recoveries of TCs
ranged from 94.51% to 103.0%. The limits of detection were in the range of 0.1–0.3 μg kg−1.
Chromatograms obtained by direct injection of the spiked egg extracts (5 × 10-3 mmol L−1) and purification with MISPE 相似文献
3.
Saman Azodi-Deilami Majid Abdouss Seyed Alireza Hasani 《Central European Journal of Chemistry》2010,8(4):861-869
In this paper, a highly selective molecularly imprinted polymer (MIP) for tramadol hydrochloride, a drug used to treat moderate
to severe pain, was prepared and its use as solid-phase extraction (SPE) sorbent was demonstrated. The molecularly imprinted
solid-phase extraction procedure followed by high performance liquid chromatography with ultraviolet detector (MISPE-HPLC)
was developed for selective extraction and determination of tramadol in human plasma and urine. The optimal conditions for
molecularly imprinted solid-phase extraction (MISPE) consisted of conditioning with 1 mL methanol and 1 mL of deionized water
at neutral pH, loading of tramadol sample (50 μg L−1) at pH 7.5, washing using 1 mL acetone and elution with 3 × 1 mL of 10% (v/v) acetic acid in methanol. The MIP selectivity
was evaluated by checking several substances with similar molecular structures to that of tramadol. Results from the HPLC
analyses showed that the calibration curve of tramadol (using MIP from human plasma and urine) is linear in the ranges of
6–100 and 3–120 μg L−1 with good precisions (1.9% and 2.9% for 5.0 μg L−1), respectively. The recoveries for plasma and urine samples were higher than 81%.
相似文献
4.
Molecularly imprinted solid-phase extraction for the determination of fenitrothion in tomatoes 总被引:1,自引:0,他引:1
Organophosphorus insecticides are widely employed in agriculture, and residues of them can remain after harvesting or storage.
Pesticide residue control is an important task for ensuring food safety. Common chromatographic methods used in the determination
of pesticide residues in food require clean-up and concentration steps prior to quantitation. While solid-phase extraction
has been widely employed for this purpose, there is a need to improve selectivity. Due to their inherent biomimetic recognition
systems, molecularly imprinted polymers (MIP) allow selectivity to be enhanced while keeping the costs of analysis low. In
this work, a MIP that was designed to enable the selective extraction of fenitrothion (FNT) from tomatoes was synthesized
using a noncovalent imprinting approach. The polymer was prepared using methacrylic acid as functional monomer and ethyleneglycol
dimethacrylate as crosslinking monomer in dichloromethane (a porogenic solvent). The polymer was characterized by Fourier
transform infrared spectroscopy, solid-state nuclear magnetic resonance (NMR), scanning electron microscopy (SEM), and nitrogen
sorption porosimetry. The pore structure and the surface area were evaluated using the BET adsorption method. To characterize
the batch rebinding behavior of the MIP, the adsorption isotherm was measured, allowing the total number of binding sites,
the average binding affinity and the heterogeneity index to be established. A voltammetric method of quantifying FNT during
the molecularly imprinted solid-phase extraction (MISPE) studies was developed. The polymer was placed in extraction cartridges
which were then used to clean up and concentrate FNT in tomato samples prior to high-performance liquid chromatographic quantitation.
The material presented a medium extraction efficiency of 59% (for analyses performed with three different cartridges on three
days and a fortification level of 5.0 μg g−1) and selectivity when used in the preparation of tomato samples, and presented the advantage that the polymer could be reused
several times after regeneration.
Figure 相似文献
5.
A new molecularly imprinted polymer for selective extraction of cotinine from urine samples by solid-phase extraction 总被引:1,自引:0,他引:1
Cotinine, the main metabolite of nicotine in human body, is widely used as a biomarker for assessment of direct or passive
exposure to tobacco smoke. A method for molecularly imprinted solid-phase extraction (MISPE) of cotinine from human urine
has been investigated. The molecularly imprinted polymer (MIP) with good selectivity and affinity for cotinine was synthesized
using cotinine as the template molecule, methacrylic acid as the functional monomer, and ethylene glycol dimethacrylate as
the cross-linker. The imprinted polymer was evaluated for use as a SPE sorbent, in tests with aqueous standards, by comparing
recovery data obtained using the imprinted form of the polymer and a non-imprinted form (NIP). Extraction from the aqueous
solutions resulted in more than 80% recovery. A range of linearity for cotinine between 0.05 and 5 μg mL−1 was obtained by loading 1 mL blank urine samples spiked with cotinine at different concentrations in acetate buffer of pH
9.0, and by using double basic washing and acidic elution. The intra-day coefficient of variation (CV) was below 7% and inter-day
CV was below 10%. This investigation has provided a reliable MISPE–HPLC method for determination of cotinine in human urine
from both active smokers and passive smokers.
Figure 相似文献
6.
A selective molecularly imprinted polymer-solid phase extraction for the determination of fenitrothion in tomatoes 总被引:1,自引:0,他引:1
Leonardo Augusto de Barros Isarita Martins Susanne Rath 《Analytical and bioanalytical chemistry》2010,397(3):1355-1361
A new and selective sorbent for molecularly imprinted solid-phase extraction (MISPE) was developed and applied for the determination
of residues of fenitrothion (FNT) in tomatoes, using HPLC coupled to photodiode array detection (HPLC-DAD). Using FNT as the
template molecule, methacrylic acid as the functional monomer, ethylene glycol dimethacrylate as the cross-linker, toluene
as the porogenic solvent, and bulk polymerization as the synthetic method, a molecularly imprinted polymer (MIP) was synthesized.
In order to choose the medium which promotes the best molecular recognition of FNT by the MIP, the adsorption of FNT by the
MIP was studied in different media containing acetonitrile and toluene. Besides FNT, three structurally related compounds
were used to evaluate the selectivity of the FNT-molecularly imprinted polymer. The MIP exhibited the highest selective rebinding
to FNT. The method developed was validated, using fortified blank tomato samples. The extraction efficiency was 96%. The limits
of detection and quantitation were 0.050 and 0.130 μg g−1, respectively. The intra-day precision was 5.9% and the inter-day precision 8.1%. The accuracy was higher than 89% for a
concentration level around the maximum residue limit of 0.5 μg g−1. 相似文献
7.
Zhixiang Xu Shuang Chen Wei Huang Guozhen Fang Hua Pingzhu Shuo Wang 《Analytical and bioanalytical chemistry》2009,393(4):1273-1279
Estrone is one of the important potential endocrine-disrupting compounds, and the sensitive and reliable analytical methods
for the determination of estrone are required for the assurance of human health. In this paper, using estrone as template
molecule, 3-aminopropyltriethoxysilane as function monomer, and tetraethoxysilicane as cross-linker, a highly selective molecularly
imprinted microsphere was synthesized by surface molecular imprinting technique combined with a sol–gel process. The imprinted
material was characterized by the Fourier transform infrared and static adsorption experiments, and the results showed that
it exhibited good recognition and selective ability for estrone. A novel method for separation and determination of trace
estrone in environmental sample was developed using on-line molecularly imprinted solid-phase extraction coupled to high-performance
liquid chromatography. With a sample loading flow rate of 2.6 mL min−1 for a 9.6-min extraction, the enrichment factor obtained by the slopes of the linear portion in comparison with the direct
injection of 10 μL standard sample solution was 1,045. The detection limit (S/N = 3) was 5.7 ng L−1, and the relative standard deviations for nine replicate extractions of 5.0 μg L−1 estrone was less than 10.0%. This method was evaluated for quantitative determination of estrone in well and lake water samples
spiked at two levels (0.5 and 1.0 μg L−1) with recoveries ranging from 86% to 95%.
相似文献
8.
以吲哚美辛(IDM)为模板分子,丙烯酰胺(AA)为功能单体,乙二醇二甲基丙烯酸酯(EGDMA)为交联剂,本体聚合法制备过程中加入纳米胶体金,合成了吲哚美辛胶体金分子印迹聚合物(MIPs/Au),利用MIPs/Au表面胶体金对蛋白吸附作用,将抗吲哚美辛的多克隆抗体固定在MIPs/Au上,得到表面固定有抗体的新型聚合物(MIPs/Au-Ab)并对其进行了表征。制备了填充材料为MIPs/Au-Ab的固相萃取柱并对其上样、淋洗和洗脱条件进行了优化,并将所制备的新型萃取柱用于水样中IDM的分离富集。抗吲哚美辛抗体交联在聚合物表面,不仅增加了萃取柱的特异性吸附容量,而且有效地降低了MIP的非特异性吸附。 相似文献
9.
Molecular imprinted solid-phase extraction (MISPE) is a well known technique for the selective extraction and pre-concentration
of analytes, are present at low levels in chemically complex materials. Herein, water-soluble, molecularly imprinted polymers
(MIP) were prepared for solid-phase extraction of pseudoephedrine hydrochloride (PSE), which was monitored at 256 nm by the
UV spectroscopy. MISPE conditions were optimized to allow the selective and determination of PSE in aqueous samples and composite
materials, such as biological fluids and human urine. MIP was prepared by precipitation polymerization method, using methacrylic
acid as a functional monomer and ethylene glycol dimethacrylate as a cross-linking agent in either acetonitrile or chloroform.
The results suggest that the obtained MISPE exhibits high affinity for PSE, and the imprinted polymer demonstrates much higher
efficiency than a non-imprinted polymer (NIP). The imprinting-induced extraction was confirmed by the determination of recovery
values for NIP (4%) and MIP (80%) polymers, respectively. The binding capacity of the MIP for PSE was found of 47.6 mg g−1. 相似文献
10.
The synthesis and evaluation of a molecularly imprinted polymer (MIP) used as a selective solid-phase extraction sorbent and
coupled to high-performance liquid chromatography (HPLC) for the efficient determination of sulfamerazine (SMR) in pond water
and three fishes are reported. The polymer was prepared using SMR as the template molecule, methacrylic acid as the functional
monomer and ethylene glycol dimethacrylate as the crosslinking monomer in the presence of tetrahydrofuran as the solvent.
The SMR-imprinted polymers and nonimprinted polymers were characterized by FT-IR and static adsorption experiments. The prepared
SMR-imprinted material showed a high adsorption capacity, significant selectivity and good site accessibility. The maximum
static adsorption capacities of the SMR-imprinted and nonimprinted materials for SMR were 108.8 and 79.6 mg g−1, respectively. The relative selectivity factor of this SMR-imprinted material was 1.6. Several parameters influencing the
solid-phase extraction process were optimized. Finally, the SMR-imprinted polymers were used as the sorbent in solid-phase
extraction to determine SMR in pond water and three fishes with satisfactory recovery. The average recoveries of the MIP-SPE
method were 94.0% in ultrapure water and 95.8% in pond water. Relative standard deviations ranging from 0.3% to 5.2% in MIP
were acquired. The results for the SMR concentrations in crucian, carp and wuchang fish were 66.0, 127.1 and 51.5 ng g−1, respectively. The RSDs (n = 5) were 3.51%, 0.53% and 5.08%, respectively. The limit of detection (LOD) for SMR was 1 ng g−1 and the limit of quantitation (LOQ) was 3.5 ng g−1. 相似文献
11.
de Jesus Rodrigues Santos W Lima PR Tarley CR Kubota LT 《Analytical and bioanalytical chemistry》2007,389(6):1919-1929
Despite the increasing number of applications of molecularly imprinted polymers (MIP) in analytical chemistry, the synthesis
of polymers with hemin introduced as the catalytic center to mimic the active site of peroxidase remains as a challenge. In
the current work, a new type of molecularly imprinted polymer (MIP) was synthesized with 4-aminophenol (4-APh) as the template
and two monomers: hemin, which acts as the catalytic center, and methacrylic acid (MAA), which is used to build the active
sites. This work shows that MIP successfully mimics peroxidase. For this purpose, a flow injection analysis system coupled
to an amperometric detector was investigated through multivariate analysis. The determination of 4-APh was not affected by
the equimolar presence of structurally similar phenol compounds, including catechol, 4-chloro-3-methylphenol, 2-aminophenol,
guaiachol, chloroguaiachol and 2-cresol, thus highlighting the good performance of the imprinted polymer. Under the optimized
experimental conditions, an analytical curve covering a wide linear response range from 0.8 up to 500 μmol L−1 (r > 0.999) was obtained, and the method gave satisfactory precisions (n = 8), as evaluated via the relative standard deviation (RSD), of 4.1 and 3.2% for solutions of 4-APh of 50 and 500 μmol L−1, respectively. Recoveries of 96–111% from water samples (tap water and river water) spiked with 4-APh were achieved, thus
illustrating the accuracy of the proposed system.
Figure Schematic presentation of the synthesis of the MIP 相似文献
12.
A novel molecularly imprinted polymer solid-phase extraction (MISPE) with flow-injection chemiluminescence (CL) was developed
for the determination of pazufloxacin mesilate (PZFX). The molecularly imprinted polymer (MIP) was synthesized by using PZFX
as the imprinting molecule. A glass tube packed the particles of the MIP was employed as MISPE micro-column, which was connected
into the sampling loop of the eight-way injection valve for on-line selective preconcentration and extraction of PZFX. The
eluent of acetonitrile:acetic acid (9:1, v:v) was used as carrier for eluting the adsorbed PZFX to react with the mixture
of cerium(IV) and sodium sulfite in the flow cell to produce strong CL. The relative intensity of CL was linear to PZFX concentration
in the range from 2.5 × 10−9 to 2.5 × 10−7 g mL−1. The limit of detection was 7 × 10−10 g mL−1 (3 σ) and the relative standard deviation for 5 × 10−8 g mL−1of PZFX solution was 3.7% (n = 7). This method has been applied to the determination of PZFX in human urine. 相似文献
13.
A new post-chemiluminescence (PCL) phenomenon was observed when phenothiazine medications were injected into the reaction
mixture after the chemiluminescence (CL) reaction of luminol and potassium ferricyanide had finished. A possible reaction
mechanism was proposed based on studies of the kinetic characteristics of the CL, CL spectra, fluorescence spectra, and on
other experiments. The feasibility of determining various phenothiazine medications by utilizing these PCL reactions was examined.
A molecular imprinting–post-chemiluminescence (MI-PCL) method was established for the determination of chlorpromazine hydrochloride
using a chlorpromazine hydrochloride-imprinted polymer (MIP) as the recognition material. The method displayed high selectivity
and high sensitivity. The linear range of the method was 1.0×10−8∼1.0×10−6, with a linear correlation coefficient of 0.9985. The detection limit was 3×10−9 g/ml chlorpromazine hydrochloride, and the relative standard deviation for a 1.0×10−7 g/ml chlorpromazine hydrochloride solution was 4.0% (n=11). The method has been applied to the determination of chlorpromazine hydrochloride in urine and animal drinking water
with satisfactory results.
相似文献
14.
Yan Sun Laixin Luo Fang Wang Jianqiang Li Yongsong Cao 《Analytical and bioanalytical chemistry》2009,395(2):465-471
A novel method based on solid-phase extraction was studied for the extraction of amitrole (3-amino-1,2,4-triazole), and its
residue determination in apples has been developed. The samples were derivatized with 4-chloro-3,5-dinitrobenzotrifluoride
(CNBF). The derivatization conditions and the influence of elution composition on the separation were investigated. In pH
9.5 H3BO3–Na2B4O7 media, the reaction of amitrole with CNBF was complete at 60°C after 30 min. The separation of derivatized amitrole was achieved
at room temperature within 13 min by gradient elution mode with cetyltrimethylammonium bromide in mobile phase as ion-pair
reagent. The method correlation coefficient was 0.9996, in concentrations ranging from 1.66 to 415 mg L−1. The calculated recoveries of the proposed method were from 94.17% to 105.67%, and relative standard deviations were 1.57%
to 6.44% in the application to the quantitative determination of amitrole in apples. The detection limit of amitrole was 0.10 mg L−1 with a signal-to-noise ratio of 3.
Figure Residue determination of amitrole in apple by ion-pairing high-performance liquid chromatography 相似文献
15.
Hu ML Jiang M Wang P Mei SR Lin YF Hu XZ Shi Y Lu B Dai K 《Analytical and bioanalytical chemistry》2007,387(3):1007-1016
Molecularly imprinted polymers (MIPs) were prepared by precipitation polymerization using tebuconazole (TBZ) as a template.
Frontal chromatography and selectivity experiments were used to determine the binding capabilities and binding specificities
of different MIPs. The polymer that had the highest binding selectivity and capability was used as the solid-phase extraction
(SPE) sorbent for the direct extraction of TBZ from different biological and environmental samples (cabbage, pannage, shrimp,
orange juice and tap water). The extraction protocol was optimized and the optimum conditions were: conditioning with 5 mL
methanol:acetic acid (9:1), 5 mL methanol and 5 mL water respectively, loading with 5 mL aqueous samples, washing with 1.2 mL
acetonitrile (ACN):phosphate buffer (5:5, pH3), and eluting with 3 mL methanol. The MIPs were able to selectively recognize,
effectively trap and preconcentrate TBZ over a concentration range of 0.5–15 μmol/L. The intraday and interday RSDs were less
than 9.7% and 8.6%, respectively. The limit of quantification was 0.1 μmol/L. Under optimum conditions, the MISPE recoveries
of spiked cabbage, pannage, shrimp, orange juice and tap water were 62.3%, 75.8%, 71.6%, 89% and 93.9%, respectively. MISPE
gave better HPLC separation efficiencies and higher recoveries than C18 SPE and strong cation exchange (SCX) SPE.
Figure HPLC analysis of spiked pannage after MISPE (A) and after C18 SPE (B). HQ (1), E3 (2), p-NP (3), FTF (4), TBZ (5), PNZ (6),
HXZ (7)
Electronic supplementary material Supplementary material is available in the online version of this article at and is accessible for authorized users. 相似文献
16.
Hugo M. Oliveira Marcela A. Segundo José L. F. C. Lima Manuel Miró Victor Cerdà 《Analytical and bioanalytical chemistry》2010,397(1):77-86
In the present work, it is proposed, for the first time, an on-line automatic renewable molecularly imprinted solid-phase
extraction (MISPE) protocol for sample preparation prior to liquid chromatographic analysis. The automatic microscale procedure
was based on the bead injection (BI) concept under the lab-on-valve (LOV) format, using a multisyringe burette as propulsion
unit for handling solutions and suspensions. A high precision on handling the suspensions containing irregularly shaped molecularly
imprinted polymer (MIP) particles was attained, enabling the use of commercial MIP as renewable sorbent. The features of the
proposed BI-LOV manifold also allowed a strict control of the different steps within the extraction protocol, which are essential
for promoting selective interactions in the cavities of the MIP. By using this on-line method, it was possible to extract
and quantify riboflavin from different foodstuff samples in the range between 0.450 and 5.00 mg L−1 after processing 1,000 μL of sample (infant milk, pig liver extract, and energy drink) without any prior treatment. For milk
samples, LOD and LOQ values were 0.05 and 0.17 mg L−1, respectively. The method was successfully applied to the analysis of two certified reference materials (NIST 1846 and BCR
487) with high precision (RSD < 5.5%). Considering the downscale and simplification of the sample preparation protocol and
the simultaneous performance of extraction and chromatographic assays, a cost-effective and enhanced throughput (six determinations
per hour) methodology for determination of riboflavin in foodstuff samples is deployed here. 相似文献
17.
Guanidinoacetate methyltransferase deficiency is a recently discovered inborn defect of creatine biosynthesis which reduces
serum creatinine concentrations to as low as 0.58 μg mL−1 (or 0.00058 μg mL−1 after 1,000-fold dilution). To measure ultra trace levels of creatinine in diluted samples, molecularly imprinted solid-phase
extraction (MISPE) and molecularly imprinted polymer (MIP) sensor techniques have been found to be inadequate. A combination
of these techniques (i.e. MISPE hyphenated with use of an MIP-sensor), reported in this paper, has been found to be highly
suitable for direct assay of creatinine in highly diluted human blood serum without complicated pretreatment of the sample.
The proposed technique has the potential to enhance the sensitivity of creatinine measurement from μg mL−1 to ng mL−1 in highly dilute aqueous samples in which the concentrations of interfering constituents are reduced to negligible levels.
In this work the sensitivity to creatinine was found to be improved compared with that of the MIP-sensor method alone (limit
of detection, LOD, 0.00149 μg mL−1). After preconcentration by MISPE and use of the sensor the detection limit for creatinine was as low as 0.00003 μg mL−1 (RSD = 0.94%, S/N = 3; 50-fold preconcentration factor) in aqueous samples. 相似文献
18.
《Analytical letters》2012,45(18):2896-2913
AbstractA highly selective and effective method for the purification and preconcentration of norfloxacin (NFX) in seawater samples was developed based on molecularly imprinted solid-phase extraction (MISPE). The molecularly imprinted polymer was synthesized by precipitation polymerization. Methacrylic acid (MAA) and ethylene glycol dimethacrylate (EGDMA) were used as the functional monomer and crosslinker, respectively. The resulting molecularly imprinted polymer (MIP) showed high adsorption for NFX and was selective for its solid-phase extraction. An offline MISPE method followed by high performance liquid chromatography with diode array detection was established for the determination of NFX in seawater. The recoveries of spiked seawater samples using the MISPE columns were satisfactorily higher than 77.6%. The relative standard deviation was less than 5.60%, and the limit of detection was 0.027?μg L?1. Four seawater samples obtained from the Bohai Sea were analyzed, and NFX was found only at one location at a concentration of 0.280?μg L?1. 相似文献
19.
Aguinaga N Campillo N Viñas P Hernández-Córdoba M 《Analytical and bioanalytical chemistry》2008,391(4):1419-1424
This paper describes a headspace solid-phase microextraction (HS-SPME) procedure coupled to gas chromatography with mass spectrometric
detection (GC–MS) for the determination of eight PAHs in aquatic species. The influence of various parameters on the PAH extraction
efficiency was carefully examined. At 75 °C and for an extraction time of 60 min, a polydimethylsiloxane–divinylbenzene (PDMS/DVB)
fiber coating was found to be most suitable. Under the optimized conditions, detection limits ranged from 8 to 450 pg g−1, depending on the compound and the sample matrix. The repeatability varied between 7 and 15% (RSD). Accuracy was tested using
the NIST SRM 1974b reference material. The method was successfully applied to different samples, and the studied PAHs were
detected in several of the samples.
Figure Headspace SPME sampling followed by GC–MS facilitates routine monitoring of PAHs in aquatic species 相似文献
20.
Xiaoling Qi Xiaoming Yang Bin Wang Hong Yang 《International journal of environmental analytical chemistry》2013,93(3):268-278
A broad selective molecularly imprinted polymers-based solid phase extraction (MISPE) for levonorgestrel (LNG) from water samples was developed. Using LNG as a template molecule, acrylamide (AA) as functional monomer, ethylene glycol dimethacrylate (EGDMA) as linking agent and bulk polymerisation as a synthetic method, the molecularly imprinted polymers (MIPs) were synthesised and characterised. The MIPs displayed a high specific rebinding for LNG with the imprinting factor of 3.71. The Scatchard analysis showed that there was at least one class of binding site for LNG formed in the MIPs with the dissociation constant of 8.046?µg?mL?1. The results of selectivity testing indicated that the MIPs also exhibited high cross-reactivity with structurally related compounds (estrone, methylprednisolone and ethinyl estradiol), but no recognition with non-structurally related compound (indomethacin), suggesting that the MIPs could be used as a broad recognition absorbent. MISPE column was prepared by packing MIPs particles into a common SPE cartridge. The MISPE extraction conditions including loading, washing and eluting solutions were carefully optimised. Water samples spiked with LNG were extracted by MISPE column and detected by high-performance liquid chromatography. The recoveries were found to be 79.97?~?132.79% with relative standard deviations (RSD) of 1.92?~?10.43%, indicating the feasibility of the prepared MIPs for LNG extraction. 相似文献