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List of Issues

    Chinese Journal of Chromatography
    2018, Vol. 36, No. 2
    Online: 08 February 2018

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    Preparation of hydrophilic polymer brushes magnetic microspheres by surface-initiated for magnetic dispersive solid phase extraction of tetracycline antibiotic residues from honey
    ZHOU Shaodan, TANG Jiaqi, JIA Bo, LÜ Yunkai
    2018, 36 (2):  85-93.  DOI: 10.3724/SP.J.1123.2017.10026
    Abstract ( 745 )   [Full Text(HTML)] () PDF (3969KB) ( 151 )  

    Activators regenerated by electron transfer-atom transfer radical polymerization (ARGET-ATRP) was applied to the continuous grafting of polybasic polymers and poly(ethylene glycol) (PEG) brushes on the surface of the magnetic microspheres (MMs). At first, the MMs were coated with silica gel, modified by amino group, and then 2-bromoisobutyryl bromide was grafted on the surface of MMs. After that, the hydrophilic polymer brushes magnetic microspheres (HMMs) were prepared by polymerization on the surface of the MMs. HMMs were characterized by transmission electron microscope (TEM) and Fourier transform-infrared (FT-IR) spectrometer. The adsorption performance to protein was studied. The results demonstrated that HMMs have the relatively uniform particle size, good dispersity and excellent protein resistance properties. Tetracycline antibiotics (TCs, tetracycline hydrochloride, chlortetracycline hydrochloride and doxycycline hydrochloride) in honey samples were determined by magnetic dispersion solid phase extraction (MDSPE) using the prepared HMMs and high performance liquid chromatography (HPLC). The average recoveries were obtained in the range of 85.8%-94.5%. The limits of detection (LODs) and limits of quantification (LOQs) of the proposed method were in the ranges of 1.92-2.56 μg/kg and 6.40-8.53 μg/kg, respectively. The proposed method was successfully applied to fast clean-up and enrichment of the TCs residues in honey.

    Preparation and evaluation of a new type of amino-bonded silica chromatographic stationary phase for the determination of lactose
    XUE Kunpeng, HU Shuai, TU Bingfang, YAO Lixin, LI Liangxiang, WANG Shaoqing, GUO Deyong
    2018, 36 (2):  94-99.  DOI: 10.3724/SP.J.1123.2017.09022
    Abstract ( 642 )   [Full Text(HTML)] () PDF (820KB) ( 141 )  

    A method for the separation and determination of lactose and sucrose using high performance liquid chromatography-refractive index (HPLC-RI) detection base on the prepared amino-bonded silica gel chromatographic stationary phase was established. The method was accorded to the content determination method in Pharmacopoeia of the People's Republic of China (2015). Then, a series of chromatographic behaviors of lactose and sucrose such as the retention times, resolutions and peak area stabilities were investigated on three different types of amino-bonded silica columns (300 mm×4.6 mm, 5 μm). The mobile phase was acetonitrile-water (70:30, v/v) with isocratic elution, the flow rate was 1.0 mL/min and the injection volume was 10 μL. The resolution of lactose and sucrose was 3.03 by isopropyl side chain protected amino column, and the peak shape of each target compound was good. The relative standard deviation (RSD) of peak area of lactose was 1.14%, less than 2.0% prescribed in the Pharmacopoeia of the People's Republic of China (2015). Therefore, this method meets the requirements of lactose content determination, and is suitable as the quality control method in the above mentioned Pharmacopoeia.

    Preparation of phenyl-modified silica nanoflake fibers and the solid-phase microextraction of polycyclic aromatic hydrocarbons
    ZHOU Shanshan, JIN Panxia, WANG Ziyi, WANG Xuemei, DU Xinzhen
    2018, 36 (2):  100-106.  DOI: 10.3724/SP.J.1123.2017.10009
    Abstract ( 474 )   [Full Text(HTML)] () PDF (4066KB) ( 203 )  

    A novel silica-based solid-phase microextraction (SPME) fiber was successfully fabricated by the immobilization of silica nanoflakes (SiO2NFs) onto the hydrothermally treated nickel-titanium alloy (NiTi) wire using sol-gel method, followed by self-assembled surface modification of phenyltrichlorosilane. The extraction performance of the fabricated fiber was evaluated using typical aromatic compounds in direct-immersion mode of SPME. The fiber exhibited the high extraction capability and good extraction selectivity for polycyclic aromatic hydrocarbons (PAHs) in water samples. The influences of stirring rate, extraction temperature, extraction time and ionic strength on the extraction efficiencies were optimized coupled to HPLC with UV detection. Under the optimized conditions, the five PAHs presented good linearity in the certain mass concentration ranges with correlation coefficients (r) greater than 0.999, and LODs ranged from 0.013 to 0.108 μg/L. The intra-day and inter-day RSDs were from 4.1% to 5.9% and 4.8% to 6.8% for the PAHs at the spiked level of 50 μg/L with the single fiber, respectively. The recoveries of the five PAHs in real water samples spiked at 10 μg/L and 30 μg/L ranged from 90.8% to 105.7% and 93.6% to 103.1%, respectively. Moreover, the phenyl-modified SiO2NFs coated NiTi fiber has high stability and good preparation reproducibility. The developed method is suitable for the concentration and determination of the target PAHs in environmental water samples.

    Two-dimensional liquid chromatography separation and high resolution mass spectrometry analysis for proteome of rice leaves based on different extraction methods
    CHAI Shuangshuang, MA Youning, GAO Huanhuan, QIN Meiling, YANG Huan, ZHANG Hantong, HE Qiao, LIN Xiaoyan
    2018, 36 (2):  107-113.  DOI: 10.3724/SP.J.1123.2017.09051
    Abstract ( 581 )   [Full Text(HTML)] () PDF (1609KB) ( 157 )  

    A two-dimensional liquid chromatography (2D LC) system was developed to separate proteins from rice leaves, which was extracted by phenol method, followed by the analysis with linear trap quadrupole orbitrap mass spectrometry (LTQ/Orbitrap MS). After proteins were extracted with phenol method, the enzymolytic peptides were separated by offline two-dimensional RP-RP system and detected by LTQ/Orbitrap MS, yielding 2712 proteins. Liquid chromatography separation system (1D LC and 2D LC) and protein extraction methods (phenol method, sodium dodecyl sulfate method (SDS method) and trichloroacetic acid/acetone method (TCA/acetone method)) were compared. Proteins identified by 2D LC were 2712, 2415 and 1914 with the above three extraction methods, respectively. The proteins were 2.7-fold, 2.5-fold and 1.9-fold the number of proteins identified by 1D LC respectively. And in terms of 2D LC, the proteins identified by phenol method were 297 and 798 more than SDS method and TCA/acetone method, respectively. Some proteins with extreme properties, such as very acidic or basic protein and high relative molecular mass proteins, were only identified in phenol method. Furthermore, proteins, which were extracted by different extraction methods and separated by 2D LC, were classified according to biological functions. It was found that protein functions by the three extraction methods were complementary. However, phenol method had the most variety of functions. The method provides technological support for rice proteomics and reference for research techniques of other crop proteomics.

    Rapid determination of 25 drug residues in aquatic products by ultra performance liquid chromatography-quadrupole/electrostatic field orbitrap high resolution mass spectrometry
    ZHANG Xianchen, LI Rong, ZHANG Pengjie, WU Xia, HUA Hongbo, YANG Luqi, LU Junwen, RONG Yutang
    2018, 36 (2):  114-124.  DOI: 10.3724/SP.J.1123.2017.10010
    Abstract ( 762 )   [Full Text(HTML)] () PDF (3086KB) ( 156 )  

    An ultra performance liquid chromatography-quadrupole/electrostatic field orbitrap high resolution mass spectrometry (UPLC-Q Orbitrap HRMS) method was developed for the rapid screening of 25 drug residues in aquatic products by the application of a novel enhanced matrix removal of lipids (EMR-Lipid). The samples were extracted with acetonitrile, cleaned-up with EMR-Lipid, and salted out with 3.0 g sodium chloride and 3.0 g sodium sulfate. The separation of the 25 drug residues was performed on an ACQUITY UPLC BEH C18 column (100 mm×2.1 mm, 1.7 μm) with gradient elution. Acetonitrile containing 0.1% (v/v) formic acid and 0.1% (v/v) formic acid aqueous solution were used as mobile phases. The compounds were detected by Full scan/date dependent MS/MS (Full MS/dd-MS2) via heated electrospray ionization (HESI) source. The calibration curves were linear with correlation coefficients (r) greater than 0.997. The limits of detection (LODs) ranged from 0.1 μg/kg to 1.0 μg/kg. The average spiked recoveries of the 25 target compounds were between 70.1% and 108.9% with relative standard derivations (RSDs) from 2.1% to 13.8%. Compared with the previous methods, this method has characteristics of simpler sample preparation and higher sensitivity.

    Rapid screening of 24 tranquillizer drugs in fish and fishery products by ultra-high performance liquid chromatography-quadrupole/electrostatic field orbitrap high resolution mass spectroscopy
    LI Rong, YANG Luqi, ZHANG Pengyun, LUO Yangdan, ZHANG Pengjie, GAO Yongqing
    2018, 36 (2):  125-135.  DOI: 10.3724/SP.J.1123.2017.10002
    Abstract ( 677 )   [Full Text(HTML)] () PDF (3005KB) ( 161 )  

    A method was developed for the simultaneous determination of 24 tranquillizer drugs in fish and fishery products using ultra-high performance liquid chromatography-quadrupole/electrostatic field orbitrap high resolution mass spectrometry (UPLC-Q-Orbitrap HRMS). The samples were extracted with acetonitrile. Then, the extracts were concentrated, dissolved by 50% (v/v) methanol aqueous solution, cleaned up with hexane saturated by acetonitrile. The separation was performed on an ACQUITY UPLC® BEH C18 column (100 mm×2.1 mm, 1.7 μm) with the gradient elution using acetonitrile and water both containing 0.1% (v/v) formic acid as mobile phases. The drugs were analyzed by full MS scan/data dependent MS2 (Full MS/dd-MS2)(Top 1) mode by heating electrospray ion (HESI) source. The results were quantified by external standard method. The calibration curves of the 24 tranquillizer drugs were linear in their respective linear range, the decision coefficients (r2) were no less than 0.9968. The average spiked recoveries of the 24 tranquillizer drugs were 58.9%-122.9%, and the relative standard deviations (RSDs) were 0.1%-16.4% in the six kinds of fish and fishery products at three spiked levels. The limits of quantification (LOQs) of the 24 tranquillizer drugs were 0.1-5.0 μg/kg. The method is simple, rapid, sensitive, reliable and suitable for the screening of the 24 tranquillizer drugs in fish and fishery products.

    Simultaneous determination of seven high risk pesticide residues in royal jelly by high performance liquid chromatography-tandem mass spectrometry
    LI Yinghong, ZHOU Ping, XU Quanhua, ZHAO Huan, SHAO Qiaoyun
    2018, 36 (2):  136-142.  DOI: 10.3724/SP.J.1123.2017.10012
    Abstract ( 775 )   [Full Text(HTML)] () PDF (820KB) ( 249 )  

    A method was developed for the simultaneous determination of seven high risk pesticides in the royal jelly, eg. tau-fluvalinate, triadimenol, coumaphos, haloxyfop, carbendazim, thiophanate-ethyl and thiophanate-methyl by high performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS). First, the royal jelly samples were extracted with acetonitrile under alkaline conditions. After dehydration by anhydrous sodium sulfate, the extracts were enriched and purified through solid-phase extraction (SPE) with Oasis HLB cartridges. Finally, the pesticides were detected by HPLC-MS/MS method. The separation was carried out on a Venusil MP C18 column with gradient elution. Methanol (containing 0.1% (v/v) formic acid) and 0.5 mmol/L ammonium acetate aqueous solution (containing 0.1% (v/v) formic acid) were used as the mobile phases. The detection was achieved using electrospray ionization in positive ion (ESI+) mode and multiple reaction monitoring (MRM) mode for data collection. Quantification was carried out using internal standard method. The results showed that the seven high risk pesticides were linear in the range of 5-100 μg/kg. The linear correlation coefficients (r2) were 0.9921-0.9996. The limits of detection (LODs) and limits of quantification (LOQs) of the seven high risk pesticides were 0.5-2.0 μg/kg and 1.0-5.0 μg/kg, respectively. The average recoveries at the three spiked levels were 80.5%-101.3%, and the relative standard deviations were 3.6%-9.4% (n=3). This method is simple, effective and sensitive, and is suitable for the determination of the pesticide residues in royal jelly.

    Determination of carbendazim and thiabendazole in wine and beer by ultra high performance liquid chromatography-high resolution mass spectrometry coupled with dispersive micro solid-phase extraction
    GAO Jie, CHEN Dawei, ZHAO Yunfeng
    2018, 36 (2):  143-149.  DOI: 10.3724/SP.J.1123.2017.10018
    Abstract ( 647 )   [Full Text(HTML)] () PDF (823KB) ( 124 )  

    A rapid method was established for the determination of carbendazim and thiabendazole in wine and beer by ultra high performance liquid chromatography-Q Orbitrap high resolution mass spectrometry and dispersive micro solid-phase extraction (DMSPE) based on a strong cation exchange adsorbent (PCX). For the pretreatment method, the amount of PCX, the volume percentage of acetonitrile, the volume percentage of ammonium hydroxide and the volume of eluent were optimized. The analytes were separated on a BEH C18 column (50 mm×2.1 mm, 1.7 μm) and detected using targeted single ion monitoring-data dependent tandem mass spectrometry (tSIM-ddMS2) scan mode. The method showed a good linearity within a certain concentration ranges with correlation coefficients R2 ≥ 0.9999. The detection limits of carbendazim and thiabendazole in wine and beer were 0.02 and 0.01 μg/L, and the quantification limits were 0.06 and 0.03 μg/L. The average recoveries of carbendazim and thiabendazole at the spiked levels of 0.1, 1.0 and 100 μg/L were in the ranges of 95.6%-110.2% and 87.5%-102.8%, with intra-day precision (RSDr) ranges from 1.8%-5.2% and 1.3%-4.8%, and inter-day precision (RSDR) ranges from 4.3%-8.7% and 4.8%-9.4%. The method is rapid, simple and sensitive for the simultaneous determination of carbendazim and thiabendazole in wine and beer.

    Determination of sedative and β-receptor hormone residues in feed by ultra high performance liquid chromatography-tandem mass spectrometry
    SUN Shanshan, ZHU Lijun, HU Yanxi, LIU Yufeng, XU Liang
    2018, 36 (2):  150-158.  DOI: 10.3724/SP.J.1123.2017.10025
    Abstract ( 530 )   [Full Text(HTML)] () PDF (931KB) ( 102 )  

    An analysis and detection method for eight sedatives and fifteen β-receptor hormones in feed was established by ultra high performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS). The sample was extracted with acetonitrile-1% (v/v) trichloroacetic acid aqueous solution (7:3, v/v), and purified by cationic solid phase extraction column. The extracts were separated on an Agilent Zorbax Eclipse Plus C18 chromatographic column (100 mm×3.0 mm, 1.8 μm) and then quantified via internal standard method. The results showed that the linear relationships of the 23 targets were good in the range of 2.0-200.0 μg/L (r2> 0.99). The average recoveries of the targets spiked in the matrix of feed samples were within 75.1%-102.4% in three spiked levels of 5.0, 10, 50 μg/kg, and the relative standard deviations (RSDs) were within 4.3%-14.3% (n=6). This method with high purification efficiency and extensive scope of application can be applied to screening and detecting sedatives and β -receptor hormones in feed.

    Determination of metformin hydrochloride, melamine and dicyandiamide in metformin hydrochloride preparations by tandem dual solid phase extraction cartridges-high performance liquid chromatography-electrospray ionization multi-stage mass spectrometry
    ZHOU Yanfen, WANG Fanghuan, WANG Zelan, ZHAN Haijuan, LIU Wanyi, MENG Zhe
    2018, 36 (2):  159-166.  DOI: 10.3724/SP.J.1123.2017.10014
    Abstract ( 684 )   [Full Text(HTML)] () PDF (1394KB) ( 176 )  

    A method for the confirmation and quantification of metformin hydrochloride and its relative substances melamine and dicyandiamide using tandem dual solid phase extraction (SPE) cartridges and high performance liquid chromatography-electrospray ionization multi-stage mass spectrometry (HPLC-ESI-MSn) was developed. The samples were extracted with anhydrous ethanol containing 0.1% (v/v) acetic acid under ultrasound-assisted conditions. The extracts were concentrated and purified using Cleanert PCX and C18 tandem dual solid phase extraction cartridges, and eluted with 5% (v/v) ammonia methanol solution. The separation was performed on a Kromasil-C18 column (100 mm×4.6 mm, 3.5 μm) with gradient elution. The detection was performed in selected ion monitoring (SIM) mode using electrospray ionization multi-stage mass spectrometry. The external standard method was used for quantification. The extraction solvents, types of SPE cartridges and eluents were optimized by comparing the recoveries under different conditions. The results showed that the detector response of each target compound was linear in corresponding mass concentration ranges with the correlation coefficients (r2) ≥ 0.9992. The limits of detection (LODs) and the limits of quantification (LOQs) of the three analytes were 1.48-13.61 μg/kg and 5.96-45.67 μg/kg, respectively. The recoveries of the three analytes were 65.02%-118.33% spiked at low, medium and high levels. The relative standard deviations (RSDs) were no more than 13.41%. The method is reliable, easy, and has a better purification effect. The method can be applied to the routine analysis of metformin hydrochloride and its relative substances melamine and dicyandiamide in different preparations of metformin hydrochloride.

    Determination of organic acids in the root exudates of Cr-hyperaccumulator Leersia hexandra Swartz using high performance liquid chromatography
    WU Chancui, LIU Jie, ZHANG Xuehong
    2018, 36 (2):  167-172.  DOI: 10.3724/SP.J.1123.2017.09009
    Abstract ( 946 )   [Full Text(HTML)] () PDF (799KB) ( 306 )  

    High performance liquid chromatography (HPLC) was used for the separation and quantification of the low molecular-mass organic acids in the root exudates of Cr-hyperaccumulator Leersia hexandra Swartz. Eight organic acids, oxalic, tartaric, formic, malic, lactic, acetic, maleic and citric acids, were separated on an XSelect HSS T3 column (250 mm×4.6 mm, 5 μm) within 13 min with the mobile phase of 40 mmol/L potassium dihydrogen phosphate-phosphorous acid at pH 2.40, a flow-rate of 1.0 mL/min, a detection wavelength of 205 nm and a column temperature of 25℃. This is a simple and highly sensitive method for the separation of the eight organic acids with well-shaped peaks. The limits of detection (LODs) for the eight acids ranged from 0.12 mg/L to 12.32 mg/L. Under the optimized conditions, tartaric, malic, lactic, maleic and citric acids in the root exudates were detected with high linearities, acceptable recoveries and excellent precisions. The contents of these acids calculated in the root exudates were (130.90±1.44) μg/g (root dry weight (DW)) for tartaric acid, (1031.34±4.38) μg/g (root DW) for malic acid, (65.54±1.01) μg/g (root DW) for lactic acid, (0.96000±0.00367) μg/g (root DW) for maleic acid and (201.50±1.13) μg/g (root DW) for citric acid. The proposed HPLC method is quite suitable for the simultaneous determination of organic acids in the root exudates of Leersia hexandra Swartz, and can be used in other plant root exudates as well.

    One-step extraction method of phthalate esters in vegetable oils
    JIN Xiangzi, KAW Han Yeong, WANG Zhao, ZOU Yilin, LI Wanying, GUO Ziyu, SUN Huaze, ZHAO Jinhua, LI Donghao
    2018, 36 (2):  173-178.  DOI: 10.3724/SP.J.1123.2017.09029
    Abstract ( 706 )   [Full Text(HTML)] () PDF (840KB) ( 146 )  

    In order to develop a fast investigation method for phthalate esters (PAEs) from vegetable oils, a gas-liquid micro-extraction (GLME) technique that combined with GC-MS was established. A vegetable oil sample (0.1 g) was directly added into the GLME device. The integrated process of extraction, clean-up, and concentration of PAEs was completed within 5 min. Internal standard method was applied to ensure the accuracy of the results. Soybean oil, blend oil, olive oil, and sesame oil were spiked with 200 μg/kg of a mixed 15 PAEs standard, and the ranges of the recoveries and RSDs were between 60.0% to 112.3% and 0.9% to 28.4%, respectively. Compared with some traditional sample pretreatment methods such as liquid-liquid extraction, liquid-liquid micro-extraction, gel permeation chromatography, this method is simple and fast, with high accuracy, good repeatability and low matrix effect. This study verified the suitability of the GLME method for field detection of food products in food safety sector and exhibits great significance for the completion of food safety system in China.