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Matrix Solid-phase Dispersion Extraction of Alkaloids from the Roots of Aconitum kusnezoffii Reichb 被引量:2
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作者 WEI Wei LI Xu-wen SHI Xiao-lei ZHOU Hong-yu YANG Rui-jie ZHANG Han-qi JIN Yong-ri 《Chemical Research in Chinese Universities》 SCIE CAS CSCD 2011年第1期23-27,共5页
Matrix solid-phase dispersion(MSPD) was developed for the extraction of four alkaloids, including aconitine, mesaconitine, hypaconitine and deoxyaconitine, from the roots ofAconitum kusnezoffii Reichb. The determina... Matrix solid-phase dispersion(MSPD) was developed for the extraction of four alkaloids, including aconitine, mesaconitine, hypaconitine and deoxyaconitine, from the roots ofAconitum kusnezoffii Reichb. The determination of the analyte was carried out by high performance liquid chromatography with UV detection. The alkaline alumina was used as sorbent. The mixture of acetonitrile and water was used as elution solvent. Several extraction parameters, such as type of sorbent, the ratio of sample to solid support material, type of the elution solvent and the volume of the elution solvent were tested. Mean recoveries ranged from 93.16% to 102.73%, with relative standard deviations from 0.27% to 4.17%. With the extraction efficiency and time expenditure taken into account, MSPD extraction should be a comparatively good method. 展开更多
关键词 Matrix solid-phase dispersion Aconitine-type alkaloid Aconitum kusnezoffii Reichb. extraction High-performance liquid chromatography 1005-9040(2011 )-01-023-05
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Solid-phase microextraction of endogenous metabolites from intact tissue validated using a Biocrates standard reference method kit 被引量:1
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作者 Runshan Will Jiang Karol Jaroch Janusz Pawliszyn 《Journal of Pharmaceutical Analysis》 SCIE CAS CSCD 2023年第1期55-62,共8页
Improved analytical methods for the metabolomic profiling of tissue samples are constantly needed.Currently,conventional sample preparation methods often involve tissue biopsy and/or homogenization,which disrupts the ... Improved analytical methods for the metabolomic profiling of tissue samples are constantly needed.Currently,conventional sample preparation methods often involve tissue biopsy and/or homogenization,which disrupts the endogenous metabolome.In this study,solid-phase microextraction(SPME)fibers were used to monitor changes in endogenous compounds in homogenized and intact ovine lung tissue.Following SPME,a Biocrates AbsoluteIDQ assay was applied to make a downstream targeted metabolomics analysis and confirm the advantages of in vivo SPME metabolomics.The AbsoluteIDQ kit enabled the targeted analysis of over 100 metabolites via solid-liquid extraction and SPME.Statistical analysis revealed significant differences between conventional liquid extractions from homogenized tissue and SPME results for both homogenized and intact tissue samples.In addition,principal component analysis revealed separated clustering among all the three sample groups,indicating changes in the metabolome due to tissue homogenization and the chosen sample preparation method.Furthermore,clear differences in free metabolites were observed when extractions were performed on the intact and homogenized tissue using identical SPME procedures.Specifically,a direct comparison showed that 47 statistically distinct metabolites were detected between the homogenized and intact lung tissue samples(P<0.05)using mixed-mode SPME fibers.These changes were probably due to the disruptive homogenization of the tissue.This study's findings highlight both the importance of sample preparation in tissue-based metabolomics studies and SPME's unique ability to perform minimally invasive extractions without tissue biopsy or homogenization while providing broad metabolite coverage. 展开更多
关键词 solid-phase microextraction Solvent extraction Metabolomics Sample preparation In vivo sampling
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Fast determination of multi-mycotoxins in corn by dispersive solid-phase extraction coupled with ultra-performance liquid chromatography with tandem quadrupole time-of-flight mass spectrometry 被引量:3
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作者 WANG Yan DONG Yan-jie +5 位作者 LI Zeng-mei DENG Li-gang GUO Chang-ying ZHANG Shu-qiu LI Da-peng ZHAO Shan-cang 《Journal of Integrative Agriculture》 SCIE CAS CSCD 2016年第7期1656-1666,共11页
A fast analytical method for the simultaneous determination of 9 mycotoxins, including alfatoxins (B1, B2, G1, and G2), fumonisins (B1, B2 and B3), zearalenone, and deoxynivalenol in corn using dispersive solid-ph... A fast analytical method for the simultaneous determination of 9 mycotoxins, including alfatoxins (B1, B2, G1, and G2), fumonisins (B1, B2 and B3), zearalenone, and deoxynivalenol in corn using dispersive solid-phase extraction method and ultra-performance liquid chromatography coupled to tandem quadrupole time-of-lfight mass spectrometry (UPLC-Q-TOF-MS) was developed and validated. Samples were extracted with acetonitrile-water (84:16, v:v, containing 1% acetic acid) using ultrasonic extraction. The extracts were puriifed with a dispersive SPE method using C18 as a cleaning agent. The ifnal clear extracts were dried by nitrogen blowing and subsequently redissolved in methanol-water (5:5, v:v). The samples were then analyzed by UPLC-Q-TOF-MS with 0.1% formic acid in ammonium acetate-methanol as mobile phase. The mean recoveries were ranged from 68.0 to 120.0%, and the relative standard deviation (RSD) ranged from 0.18 to 6.29%. Limits of detections ranged from 0.05 to 50 μg kg?1, and limits of quantiifcation ranged from 0.1 to 200 μg kg?1, which were below the legal limits set by the European Union for the legislated mycotoxins. The developed method was applied to 130 corn samples. Among the mycotoxins studied, alfatoxins B1 and fumonisins B1, B2 and B3 were the most predominant mycotoxins, and their concentrations were 0–593.12, 0–2.01×104, 0–6.94×103 and 0–3.05×103 μg kg–1, respectively. 展开更多
关键词 C18 CORN mycotoxins dispersive solid-phase extraction
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Trace determination and characterization of ginsenosides in rat plasma through magnetic dispersive solid-phase extraction based on core-shell polydopamine-coated magnetic nanoparticles 被引量:2
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作者 Ningning Zhao Shu Liu +3 位作者 Junpeng Xing Zifeng Pi Fengrui Song Zhiqiang Liu 《Journal of Pharmaceutical Analysis》 SCIE CAS CSCD 2020年第1期86-95,共10页
Enrichment of trace bioactive constituents and metabolites from complex biological samples is challenging.This study presented a one-pot synthesis of magnetic polydopamine nanoparticles(Fe3O4@-SiO2@PDA NPs)with multip... Enrichment of trace bioactive constituents and metabolites from complex biological samples is challenging.This study presented a one-pot synthesis of magnetic polydopamine nanoparticles(Fe3O4@-SiO2@PDA NPs)with multiple recognition sites for the magnetic dispersive solid-phase extraction(MDSPE)of ginsenosides from rat plasma treated with white ginseng.The extracted ginsenosides were characterized by combining an ultra-high-performance liquid chromatography coupled to a highresolution mass spectrometry with supplemental UNIFI libraries.Response surface methodology was statistically used to optimize the extraction procedure of the ginsenosides.The reusability of Fe3O4@-SiO2@PDA NPs was also examined and the results showed that the recovery rate exceeded 80%after recycling 6 times.Furthermore,the proposed method showed greater enrichment efficiency and could rapidly determine and characterize 23 ginsenoside prototypes and metabolites from plasma.In comparison,conventional methanol method can only detect 8 ginsenosides from the same plasma samples.The proposed approach can provide methodological reference for the trace determination and characterization of different bioactive ingredients and metabolites of traditional Chinese medicines and food. 展开更多
关键词 Fe3O4@SiO2@PDA NPs Multiple recognition sites Magnetic dispersive solid-phase extraction ENRICHMENT GINSENOSIDES
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Determination of phthalate esters in fat-containing foods by packed nanofiber solid-phase extraction column and gas chromatography 被引量:1
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作者 邱金丽 王羽 +1 位作者 周小玲 康学军 《Journal of Southeast University(English Edition)》 EI CAS 2016年第3期322-326,共5页
A new method for simultaneous determination of four phthalate esters ( PAEs) in commercial fat-containing foods was developed by the combination of a packed nanofibers column based on solid-phase extraction with gas... A new method for simultaneous determination of four phthalate esters ( PAEs) in commercial fat-containing foods was developed by the combination of a packed nanofibers column based on solid-phase extraction with gas chromatography-flame ionization detector ( GC-FID ). Conditions for obtaining optimum extraction efficiency such as extraction solvents, morphologies of adsorbent, ion strength and pH were investigated and optimized in detail. Under the optimized conditions, the limits of detection (LODs) found for dibutyl phthalate (DBP) , butyl benzyl phthalate (BBP), diethyl hexyl phthalate (DEHP) and di-n-octyl phthalate (DNOP) were 50, 25, 50 and 25 ng/g, respectively. Good linearity of four PAEs was achieved in the range of 50 to 4 000 ng/g. The proposed method was applied for analyzing different kinds of fat-containing samples. PAEs in commercial fat-containing samples can be highly extracted by a packed solid-phase extraction column of 5 mg polystyrene ( PS) nanofibers. The satisfactory average recoveries were obtained in the range of 96. 7% to 102. 3% , and the relative standard deviations (RSDs) below 5% were achieved. The proposed method reduces the organic solvent consumption, the complex and tedious procedures for sample pretreatment, and achieves high sensitivity and reproducibility for the investigated PAEs. 展开更多
关键词 phthalate esters (PAEs nanofibers solid-phase extraction gas chromatography fat-containing foods
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HPLC Determination of Captopril in Human Plasma with Pre-column Derivation and Solid-phase Extraction and Studies on Its Pharmacokinetic and Relative Bioavailability
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作者 丁劲松 张毕奎 +2 位作者 李焕德 刘义钊 邓航 《Journal of Chinese Pharmaceutical Sciences》 CAS 2001年第3期152-156,共5页
A new pre-column derivation HPLC method with solid-phase extraction to determine captopril in human plasma was established. Derivation products were extracted by a solid-phase extraction method after the reagent, p-a-... A new pre-column derivation HPLC method with solid-phase extraction to determine captopril in human plasma was established. Derivation products were extracted by a solid-phase extraction method after the reagent, p-a-dibromoacetophenone(p-BPB), was added in the plasma samples. The samples were analyzed in a VP-ODS column with UV-detector. The calibration curve of captopril was linear within the range of 5~1000 ngmL-1 with r=0.9987, the recovery of this method was 98.652.04%, within day and between day RSD were no more than 3.4% and 8.4% respectively. To study the pharmacokinetics and the relative bioavailability of captopril tablets, two formulations of captopril tablets were given to 18 healthy male volunteers according to a randomized 2-way cross-over design with a 1-week washout period. The respective AUC0~6 , Cmax and Tmax values of the two formulations were 424.5125.7 and 439.4113.3 mghL-1; 505.9244.6 and 504.8172.2 mgL-1; 0.6620.181 and 0.5280.176 h. Results from statistics analysis showed that there were no significant difference between the AUC0~6 , Cmax and Tmax values of the two formulations, The relative bioavailability of tablets I with respect to II was 96.114.6% from AUC0~6 measurement. Bioequivalance was observed between the two tablets. 展开更多
关键词 CAPTOPRIL solid-phase extraction HPLC PHARMACOKINETICS BIOAVAILABILITY
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Use of packed-fiber solid-phase extraction for sample clean-up and preconcentration of vitamin B_(12) before determination 被引量:5
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作者 Fang Fang Xue Jun Kang Zhi Yong Liu Yu Qin Ma Zhong Ze GU 《Chinese Chemical Letters》 SCIE CAS CSCD 2009年第12期1491-1494,共4页
A rapid and simple preconcentration step applying packed-fiber solid-phase extraction columns has been investigated to vitamin B12. The extraction performance of the new method was investigated preliminarily on vitami... A rapid and simple preconcentration step applying packed-fiber solid-phase extraction columns has been investigated to vitamin B12. The extraction performance of the new method was investigated preliminarily on vitamin functional drink. The analysis used a reversed-phase C18 column, with a photo-diode array detector at 220 nm. The samples were preconcentrated with packed-fiber solid-phase extraction columns. Good linearity was observed in vitamin functional drink. The repeatability of extraction performance, expressed as relative standard deviations, was from 3.5% to 4.3%. The limit of detection (LOD) is 5 ng mL^-1 (S/N = 3). Finally, the method had been applied for the determination of vitamin B12 in vitamin functional drink. 展开更多
关键词 Vitamin B12 NANOFIBERS Packed-fiber solid-phase extraction PRECONCENTRATION
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Comparison of simultaneous distillation extraction and solid-phase micro-extraction for determination of volatile constituents in tobacco flavor 被引量:8
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作者 钟科军 魏万之 +1 位作者 郭方遒 黄兰芳 《Journal of Central South University of Technology》 EI 2005年第5期546-551,共6页
The volatile and semi-volatile components in tobacco flavor additives were extracted by both simultaneous distillation extraction and solid-phase micro-extraction. Extraction conditions for solid-phase micro-extractio... The volatile and semi-volatile components in tobacco flavor additives were extracted by both simultaneous distillation extraction and solid-phase micro-extraction. Extraction conditions for solid-phase micro-extraction were optimized with information theory. Then, detection were accomplished by gas chromatography-mass spectrometry. Characteristic of each method was compared. Qualitative analysis and quantitative analysis of 6# tobacco flavor sample were accomplished through both simultaneous distillation extraction and solid-phase micro-extraction. The experimental results show that solid-phase micro-extraction method is the first choice for qualitative analysis and simultaneous distillation extraction is another good selection for quantitative analysis. By means of simultaneous distillation extraction, 20 components are identified, accounting for 92.77% of the total peak areas. Through solid-phase micro-extraction, there are 17 components identified accounting for 91.49% of the total peak areas. The main aromatic components in 6# tobacco flavor sample are propanoic acid, 2-hydroxy-, ethyl ester, menthol and menthyl acetate. The presented method has been successfully used for quality control of tobacco flavor. 展开更多
关键词 simultaneous distillation extraction solid-phase micro-extraction gas chromatography-mass spectrometry tobacco flavor
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Organic acids and inorganic anions in Bayer liquors by ion chromatography after solid-phase extraction 被引量:3
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作者 钟付金 陈晓青 +1 位作者 张树朝 李跃平 《Journal of Central South University of Technology》 EI 2007年第2期191-195,共5页
A method for the simultaneous separation and determination of organic acids and inorganic anions in Bayer liquors was developed by gradient ion chromatography with suppressed conductivity detection. Formate, acetate, ... A method for the simultaneous separation and determination of organic acids and inorganic anions in Bayer liquors was developed by gradient ion chromatography with suppressed conductivity detection. Formate, acetate, propionate, oxalate, succinate, glutarate, fluoride, chloride and sulfate were separated and determined in 33 min. The samples were pretreated with solid-phase extraction, which has high selectivity for removing a large number of metallic ions in the Bayer liquors, and filtered with a 0.45 μm filter membrane before being injected into the ion chromatographic system. The separation of six organic acids and three inorganic anions was achieved on an IonPac AS11-HC column with KOH as the eluent, and the detection was performed by a conductivity detection mode. No interference is found in the presence of fluorate, chlorate and sulphate when organic acids are determined. The calibration graphs of peak area for all the analytes are linear over a wide range. The relative standard derivation of the peak area of analytes is less than 2.14%. Under optimum conditions the detection ranges from 0.2 to 100.0 mg/L. The average recoveries of the added standards are between 94.3% and 102.8%. 展开更多
关键词 Bayer liquors organic acid inorganic anion ion chromatography solid-phase extraction
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Solid-phase extraction of trace Au(Ⅲ) with SDG and determination by the catalytic spectrophotometric method 被引量:2
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作者 LI Huizhi ZHAI Yubo 《Rare Metals》 SCIE EI CAS CSCD 2008年第6期560-565,共6页
The new catalytic kinetic spectrophotometric method for Au(III) determination was developed and validated. It was based on the catalytic effect of gold on the oxidation of sudan red III by ammonium peroxodisulfate ... The new catalytic kinetic spectrophotometric method for Au(III) determination was developed and validated. It was based on the catalytic effect of gold on the oxidation of sudan red III by ammonium peroxodisulfate ((NH4)2S2O8) with nitrilo triacetic acid as an activator in microemulsion and H2SO4 medium. Under optimum conditions, there was the linearity of the calibration curve in the concentration range from 0 to 20 μg/L Au(Ⅲ) at 520 nm. The relative standard deviation was 3.0% with a correlation coefficient of 0.9986. The detection limit achieved was 9.75 × 10^-5 μg/mL. A new method using a column packed with sulfhydryl dextrose gel (SDG) as a solid-phase extractant has been developed for the preconcentration and separation of Au(Ⅲ) ions. The method has been applied to the determination of trace gold with satisfactory results. 展开更多
关键词 analytical chemistry catalytic kinetic spectrophotometric method solid-phase extraction gold(Ⅲ)
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A novel signal feature extraction technology based on empirical wavelet transform and reverse dispersion entropy 被引量:3
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作者 Yu-xing Li Shang-bin Jiao Xiang Gao 《Defence Technology(防务技术)》 SCIE EI CAS CSCD 2021年第5期1625-1635,共11页
Feature extraction is an important part of signal processing,which is significant for signal detection,classification,and recognition.The nonlinear dynamic analysis method can extract the nonlinear characteristics of ... Feature extraction is an important part of signal processing,which is significant for signal detection,classification,and recognition.The nonlinear dynamic analysis method can extract the nonlinear characteristics of signals and is widely used in different fields.Reverse dispersion entropy(RDE)proposed by us recently,as a nonlinear dynamic analysis method,has the advantages of fast computing speed and strong anti-noise ability,which is more suitable for measuring the complexity of signal than traditional permutation entropy(PE)and dispersion entropy(DE).Empirical wavelet transform(EWT),based on the theory of wavelet analysis,can decompose a complex non-stationary signal into a number of empirical wavelet functions(EWFs)with compact support set spectrum,which has better decomposition performance than empirical mode decomposition(EMD)and its improved algorithms.Considering the advantages of RDE and EWT,on the one hand,we introduce EWT into the field of underwater acoustic signal processing and fault diagnosis to improve the signal decomposition accuracy;on the other hand,we use RDE as the features of EWFs to improve the signal separability and stability.Finally,we propose a novel signal feature extraction technology based on EWT and RDE in this paper.Experimental results show that the proposed feature extraction technology can effectively extract the complexity features of actual signals.Moreover,it also has higher distinguishing ability for different types of signals than five latest feature extraction technologies. 展开更多
关键词 Feature extraction Empirical mode decomposition Empirical wavelet transform Permutation entropy Reverse dispersion entropy
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Microwave Extraction Followed by Solid-phase Extraction for the Determination of Phthalate Esters in Fish Samples by Gas Chromatography 被引量:5
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作者 X. Zhang J. Wang R.H. Zhu 《Journal of Environmental Science and Engineering》 2010年第3期81-84,共4页
A new analytical procedure based on solid-phase extraction method coupled to GC-FID has been developed and validated for the determination of five phthalate esters (PAEs) (dimethyl-(DMP), diethyl-(DEP), di-n-bu... A new analytical procedure based on solid-phase extraction method coupled to GC-FID has been developed and validated for the determination of five phthalate esters (PAEs) (dimethyl-(DMP), diethyl-(DEP), di-n-butyl-(DBP), di-2-ethylhexyl- (DEHP), di-n-octyl-(DOP)) in fish samples. There was a good linear relationship in the range of 0.05-10μg with the detection limits of 0.09-0.16ng .The recoveries obtained for PAEs ranged from 88.6% to 96.4%with RSD of 4.2%-10.2%.The applicability of the developed method was demonstrated for real fish samples. 展开更多
关键词 Phthalate esters solid-phase extraction Capillary Gas Chromatography.
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Multiresidue Method for Determination of 67 Pesticides in Water Samples Using Solid-Phase Extraction with Centrifugation and Gas Chromatography-Mass Spectrometry 被引量:3
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作者 Abir Kouzayha Abdul Rahman Rabaa +3 位作者 Mohamad Al Iskandarani Daniel Beh Hélène Budzinski Farouk Jaber 《American Journal of Analytical Chemistry》 2012年第3期257-265,共9页
A new multi-residue method based on solid-phase extraction (SPE) with centrifugation was developed for determination and quantitation of 67 pesticides in water samples. Two SPE cartridges were tested: Chromabond C18 a... A new multi-residue method based on solid-phase extraction (SPE) with centrifugation was developed for determination and quantitation of 67 pesticides in water samples. Two SPE cartridges were tested: Chromabond C18 and Oasis HLB. Parameters that influence the extraction efficiency such as the eluent volume, the sample loading volume, the addition of organic solvent to water sample, sorbent drying and elute concentration were optimized. The innovation of this work was the examination of the use of a centrifugation technique in both the drying and elution steps. When combined with centrifugation, the volume of the elution solvent was reduced to 2 mL and the time for sorbent drying decreased also to 10 min under vacuum. Under the optimized conditions, this method showed good recoveries higher than 65% - 68% for the 67 analyzed pesticides using the C18 and HLB cartridges with relative standard deviations lower than 9.7% - 12.3%. Limits of quantification were between 2 and 20 ng.L–1. The simplicity of the described method, use of less of organic solvent, short procedure time, and good recoveries demonstrate the advantages of this environmentally friendly approach for routine analysis of numerous samples. 展开更多
关键词 MULTI-RESIDUE PESTICIDES solid-phase extraction CENTRIFUGATION Gas Chromatography-Mass SPECTROMETRY
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Comparison of liquid-liquid extraction-thin layer chromatography with solid-phase extraction-high-performance thin layer chromatography in detection of urinary morphine 被引量:1
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作者 Ali Ahadi Alireza Partoazar +1 位作者 Mohammad Hassan Abedi Khorasgani Seyed Vahid Shetab Boushehri 《The Journal of Biomedical Research》 CAS 2011年第5期362-367,共6页
Liquid-liquid extraction-thin layer chromatography (LLE-TLC) has been a common and routine combined method for detection of drugs in biological materials. Solid-phase extraction (SPE) is gradually replacing the tr... Liquid-liquid extraction-thin layer chromatography (LLE-TLC) has been a common and routine combined method for detection of drugs in biological materials. Solid-phase extraction (SPE) is gradually replacing the tra- ditional LLE method. High performance thin layer chromatography (HPTLC) has several advantages over TLC. The present work studied the higher efficiency of a new SPE-HPTLC method over that of a routine LLE-TLC method, in extraction and detection of urinary morphine. Fifty-eight urine samples, primarily identified as mor- phine-positive samples by a strip test, 'were re-screened by LLE-TLC and SPE-HPTLC. The results of LLE-TLC and SPE-HPTLC were then compared with each other. The results showed that the SPE-HPTLC detected 74% of total samples as morphine-positive samples whereas the LLE-TLC detected 48% of the same samples. We further discussed the effect of codeine abuse on TLC analysis of urinary morphine. Regarding the importance of morphine detection in urine, the present combined SPE-HPTLC method is suggested as a replacement method for detection of urinary morphine by many reference laboratories. 展开更多
关键词 morphine detection liquid-liquid extraction thin-layer chromatography solid-phase extraction highperformance thin layer chromatography
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Boiling Point Distribution of Hydrocarbon Types in Diesel Using Solid-Phase Extraction Followed by GC/FID-EIMS 被引量:1
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作者 Li Chengwei Tian Songbai Liu Zelong Zhu Xinyi 《China Petroleum Processing & Petrochemical Technology》 SCIE CAS 2008年第3期13-21,共9页
In this paper, a method was established to determine the boiling point distribution of hydrocarbon types in diesel. The diesel sample was separated into the saturate and aromatic fractions by means of solid-phase extr... In this paper, a method was established to determine the boiling point distribution of hydrocarbon types in diesel. The diesel sample was separated into the saturate and aromatic fractions by means of solid-phase extraction (SPE), and each fraction was analyzed by GC/FID-EIMS. According to the relationship between boiling point and retention time of n-paraffins in the chromatogram, the percentages of saturates and aromatics at each temperature interval were calculated. According to the average mass spectra of the saturate and aromatic fractions at each temperature interval, the hydrocarbon types of the sample were identified through summation of characteristic mass fragments. Using this method, the changes in composition of diesel during hydrotreating process were studied. The results showed that hydrogenation of aromatics is the main reaction during the hydrotreating process. The more rings the aromatics have, the easier the hydrogenation reactions would take place. The aromatics were converted into cycloparaffins via the hydrogenation and saturation process, leading to an increase in low boiling point fractions in the hydrotreated oil. 展开更多
关键词 boiling point distribution hydrocarbon type DIESEL GC/FID-EIMS solid-phase extraction
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Separation and Enrichment of Melamine in Feed by a New Molecularly Imprinted Solid-phase Extraction Column 被引量:1
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作者 Huang Huabin Zhuang Zhixia +2 位作者 Zhou Yanli Zhao Li Wang Xiaoru 《Animal Husbandry and Feed Science》 CAS 2014年第1期10-13,共4页
[ Objective] The research aimed to develop a new molecular imprinting solid-phase extraction column for the separation and enrichment of melamine in feed. [ Method] The molecular imprinting polymer of melamine was pre... [ Objective] The research aimed to develop a new molecular imprinting solid-phase extraction column for the separation and enrichment of melamine in feed. [ Method] The molecular imprinting polymer of melamine was prepared by mass polymerization method. This polymer was used as filler to prepare molecular imprinting polymer solid-phase extraction(MIP-SPE) column of melamine. The solid-phase extraction conditions were optimized and melamine content in concentrated solution was determined by using HPLC. [ Result] Melamine eould be separated selectively from feed and enriehed by self-made MIP-SPE column. It could wipe off complex matrix from feed and the addition recovery rate was 95%. The contrast experiment between MIP-SPE column and NMIP-SPE ( non-imprinted polymer- solid phase extraction) column showed that the extraction efficiency of the former was obviously higher than the latter. [ Conclusion] The home-made MIP- SPE column could be used to separate and enrich melamine in feed efficiently, with a broad application prospect. 展开更多
关键词 Molecular imprinting solid-phase extraction FEED MELAMINE
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Isolation and Purification of Unstable Iridoid Glucosides from Traditional Chinese Medicine by Preparative High Performance Liquid Chromatography Coupled with Solid-phase Extraction 被引量:1
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作者 LI Cun-man XIAO Yuan-sheng +3 位作者 XUE Xing-ya FENG Jia-tao ZHANG Xiu-li LIANG Xin-miao 《Chemical Research in Chinese Universities》 SCIE CAS CSCD 2011年第3期392-396,共5页
An efficient preparative method was successfully developed for isolation and purification of unstable components from medicinal plant extracts, using a combined method of preparative high performance liquid chro-matog... An efficient preparative method was successfully developed for isolation and purification of unstable components from medicinal plant extracts, using a combined method of preparative high performance liquid chro-matography(HPLC) and solid-phase extraction(SPE). The aim of this study was to obtain an effective method with high preparative efficiency and importantly to avoid the transformation of unstable compounds. The preparative HPLC system was based on an LC/MS controlled four-channel autopurification system. The SPE method was performed with a C18 packing material to trap the target compounds and to remove the acidic additive derived from the mobile phase. Using this method, the unstable iridoid glucosides(IGs) as model compounds were successfully isolated and purified from the extract of Hedyotis diffusa Willd. Six IGs(including one new minor IG) and one nucleotide compound were simultaneously obtained, each with a purity of 91% as determined by HPLC. The structures of the isolated compounds were identified by UPLC/Q-TOF MS, UV, 1D and/or 2D NMR. It was demonstrated that the combination of preparative HPLC with SPE is a versatile tool for preparative purification of unstable compounds from complex natural products. 展开更多
关键词 Unstable compound Isolation and purification Preparative high performance liquid chromatography solid-phase extraction Iridoid glucoside
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Determination of Trace Amount of Polycyclic Aromatic Hydrocarbons in Urban Sewage by Solid-phase Extraction Coupled with High Performance Liquid Chromatograph 被引量:2
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作者 WANG Jing-fei1,KANG Quan-ying1,RONG Nan1,2,WU Yi-hong1,LI Hong-bo1 1.Hebei Provincial Academy of Environmental Science,Hebei Provincial Laboratory of Water Environmental Science,Shijiazhuang 050037,China 2.College of Chemistry and Environmental Science,Hebei University,Baoding 071002,China 《Meteorological and Environmental Research》 CAS 2011年第10期91-94,共4页
[Method] This study aimed to determine trace amount of polycyclic aromatic hydrocarbons(PAHs) in urban sewage by using solid-phase extraction(SPE) coupled with high performance liquid chromatograph(HPLC).[Method] From... [Method] This study aimed to determine trace amount of polycyclic aromatic hydrocarbons(PAHs) in urban sewage by using solid-phase extraction(SPE) coupled with high performance liquid chromatograph(HPLC).[Method] From the aspects of solid-phase extraction column,elution solvent,elution volume,elution speed and so forth,the test conditions of SPE-HPLC method were optimized,and trace amount of PAHs in urban sewage was determined.[Result] The optimized solid-phase extraction conditions were SUPELCLEAN LC-18 solid-phase extraction column,methylene dichloride as elution solvent,15 ml elution volume,2 ml/min elution speed,5 ml/min loading speed,1 000 ml water with 200 ml methanol loading volume.Under the optimized extraction conditions,the recovery was high,namely 76.3%-105.2%;relative standard deviation was 3.8%-6.0%,showing good precision;detection limit was low,only 0.000 8-0.048 0 μg/L.[Conclusion] This method is user-friendly,with high sensitivity and good precision,and suitable for continuous determination of a large volume of water samples. 展开更多
关键词 solid-phase extraction(SPE) High performance liquid chromatograph(HPLC) Polycyclic aromatic hydrocarbons(PAHs) Urban sewage China
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Determination of Triclocarban, Triclosan and Methyl-Triclosan in Environmental Water by Silicon Dioxide/Polystyrene Composite Microspheres Solid-Phase Extraction Combined with HPLC-ESI-MS 被引量:1
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作者 Yinan Wang Pengfei Li +3 位作者 Yan Liu Bing Chen Jinyu Li Xikui Wang 《Journal of Geoscience and Environment Protection》 2013年第2期13-17,共5页
This paper developed a sensitive and efficient analytical method for triclocarban (TCC), triclosan (TCS) and Methyl-triclosan (MTCS) determination in environmental water, which involves enrichment by using silicon dio... This paper developed a sensitive and efficient analytical method for triclocarban (TCC), triclosan (TCS) and Methyl-triclosan (MTCS) determination in environmental water, which involves enrichment by using silicon dioxide/polystyrene composite microspheres solid-phase extraction and detection with HPLC-ESI-MS. The influence of several operational parameters, including the eluant and its volume, the flow rate and acidity of water sample were investigated and optimized. Under the optimum conditions, the limits of detection were 1.0 ng/L, 2.5 and 4.5 ng/L for TCC, TCS, and MTCS, respectively. The linearity of the method was observed in the range of 5-2000 ng/L, with correlation coefficients (r2) >.99. The spiked recoveries of TCC, TCS and MTCS in water sampleswereachieved in the range of 89.5% -96.8% with RSD below 5.7%. The proposed method has been successfully applied to analyze real water samples and satisfactory results were achieved. 展开更多
关键词 TRICLOCARBAN TRICLOSAN solid-phase extraction Silicon Dioxide/Polystyrene Composite MICROSPHERES HPLC-ESI-MS/MS
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Simultaneous Determination of Four Estrogens in Compost Based on Ultrasonic Solvent Extraction, Solid-Phase Extraction Clean-Up and Analysis by UHPLC-MS/MS 被引量:1
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作者 Miguel Ángel López Zavala Blanca Nelly Flores Arriaga Naoyuki Funamizu 《American Journal of Analytical Chemistry》 2016年第5期434-445,共12页
A rapid, cost effective and reliable analytical method was developed and validated for the simultaneous determination of four estrogens (17 β-estradiol, 17 α-ethinylestradiol, estrone, and estriol) in compost sample... A rapid, cost effective and reliable analytical method was developed and validated for the simultaneous determination of four estrogens (17 β-estradiol, 17 α-ethinylestradiol, estrone, and estriol) in compost samples from the biodegradation of biological infectious hazardous wastes. Ultrasonic solvent extraction, using methanol as extraction solvent, coupled with SPE clean-up, using cartridges HLB 60 mg - 6 ml Supelco&reg;<sup></sup> and acetonitrile for reconstitution of eluents, was used for the simultaneous extraction of the four estrogens. Mean recoveries in the range of 98% - 107% were obtained. All compounds were separated in a single gradient run by UHPLC Kinetex<sup>TM</sup> 2.6 μm XB-C18 100 &Aring;LC (50 × 4.6 mm) column. Analytes were detected via multiple reaction monitoring (MRM) using an AB SCIEX API-5000TM triple quadrupole (Applied Biosystems/MDS SCIEX) with electrospray ionization in negative mode. Isocratic mobile phase of Water:ACN (50:50) resulted to be the optimum. Limits of detection and quantification were on the order of 0.66 ng·g<sup>-1</sup> and 2 ng·g<sup>-1</sup> for all the estrogens. These limits were lower than most of the values reported in the literature for similar matrices. Suitable level of linearity, good repeatability and reproducibility with coefficients of variation is lower than 11.7%, 6.8% and 8.3%, respectively. 展开更多
关键词 COMPOST ESTROGENS solid-phase extraction Clean-Up UHPLC-MS/MS Ultrasonic Solvent extraction
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