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    Chinese Journal of Chromatography
    2015, Vol. 33, No. 12
    Online: 08 December 2015

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    Reviews
    Recent advances in preparative electromigration techniques for proteins
    HAO Feiran, FU Bin, ZHANG Yangjun, QIAN Xiaohong
    2015, 33 (12):  1226-1233.  DOI: 10.3724/SP.J.1123.2015.09010
    Abstract ( 378 )   [Full Text(HTML)] () PDF (1939KB) ( 95 )  

    Preparative electromigration techniques are a category of separation and preparation techniques based on differential electromigration principle. These techniques are widely applied in biomacromolecule and proteome researches. Related techniques mainly include preparative electrophoresis, preparative electrochromatography, preparative isoelectric focusing and free flow electrophoresis and so on. We review each kind of the preparative electromigration techniques on its apparatus designs, applications, advantages and disadvantages in detail. Microscale preparative electrophoresis is a hot spot in recent years. Its high resolution, high recovery and high efficiency make it a more prominent role in the biological sample analysis. In this review, we focus on some advances in microscale preparative electrophoresis and also give an outlook on preparative electromigration techniques in the future.

    Articles
    Preparation and applications of 4-methyl imidazole magnetic surface molecularly imprinted polymers
    QI Yuxia, ZHAO Lijuan, MA Meihua, WEI Chanling, LI Ya, LI Wenjing, GONG Bolin
    2015, 33 (12):  1234-1241.  DOI: 10.3724/SP.J.1123.2015.08035
    Abstract ( 576 )   [Full Text(HTML)] () PDF (1724KB) ( 74 )  

    The magnetic surface molecularly imprinted polymers (MIPs) with specific recognition of 4-methyl imidazole (4-MI) were prepared by using 4-MI as template molecule, methacrylic acid (MAA) as functional monomer and Fe3O4 as magnetic fluid. The polymers were characterized by of Fourier transform infrared spectrometer (FT-IR) analysis, X-ray diffraction (XRD) analysis, transmission electron microscopy (TEM) and vibrating sample magnetometer (VSM). The results demonstrated that an imprinted polymer layer was successfully coated onto the surface of modified Fe3O4 nanomaterials, resulting in a narrow diameter distribution and good magnetic responsibility. The ultraviolet (UV) spectrophotometry was used to demonstrate the interaction between 4-MI and MAA. It was found that one 4-MI molecule was entrapped by one MAA molecule, which was the main existing form of subject and object. By UV spectrophotometric method to study the adsorption performance of magnetic molecularly imprinted polymers, the specific adsorption equilibrium and selectivity were evaluated by batch rebinding studies. The Scatchard analysis showed that there were two kinds of binding sites in the Fe3O4@(4-MI-MIP). The corresponding maximum adsorption capacities of 4-MI onto Fe3O4@(4-MI-MIP) were 40.31 mg/g and 23.07 mg/g, and the dissociation constants were 64.85 mg/L and 30.41 mg/L, respectively. The kinetic experimental data were correlated with second-order kinetic model. The magnetic molecularly imprinted polymers were used for the adsorption of 4-methyl imidazole in environmental water samples, and good results were obtained.

    Simultaneous determination of 121 veterinary drugs in pork by QuEChERS and ultra performance liquid chromatography-tandem mass spectrometry
    GUO Haixia, XIAO Guiying, ZHANG Xiqing, WANG Minglin, LI Li, LENG Lei, GAO Hongliang
    2015, 33 (12):  1242-1250.  DOI: 10.3724/SP.J.1123.2015.09016
    Abstract ( 572 )   [Full Text(HTML)] () PDF (920KB) ( 282 )  

    A method has been developed for the simultaneous determination of the 10 kinds of 121 veterinary drugs (including chloramphenicols, β -agonists, sulfonamides, 4-quinolones, nitroimidazoles, macrolides, avermections, polyether antibiotics, tetracycline antibiotics, cephalosporins, etc.) in pork using QuEChERS method coupled with ultra performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS). The drugs were extracted with Na2EDTA-McIlvaine buffer solution (pH=4) and acetonitrile. Anhydrous sodium sulfate was used for the salting-out process. The solutions divided into two groups were cleaned-up by different mixed sorbents. The drugs were analyzed by UPLC-MS/MS in multiple reaction monitoring (MRM) mode via electrospray ionization. Among the 121 drugs, 5 drugs were quantified by internal standard method, and the other 116 drugs were quantified by external standard method. The calibration curves of the 121 drugs were linear in the range of 0.02-40 μg/L with the correlation coefficients more than 0.99. The limits of quantification (LOQs, S/N=10) were 0.05-10 μg/kg. The average recoveries of 8 drugs at LOQ level in pork ranged from 41.7% to 59.6% with the relative standard deviations (RSDs) of 1.7%-13.5%. The average recoveries of 10 drugs at LOQ level in pork ranged from 122.6% to 163.2% with the RSDs of 0.6%-14.8%. The average recoveries of 103 drugs at LOQ level in pork ranged from 60.3% to 118.3% with the RSDs of 0.4%-16.7%. The proposed method is rapid, simple, sensitive, reliable and cost-effective.

    Rapid screening and confirmation of non-target pigment in Chinese softshell turtle by liquid chromatography coupled to time of flight mass spectrometry
    LI Shiyan, WANG Yang, ZHOU Fan, ZHENG Chongying, ZHANG Haiqi, HE Zhongyang, HE Xin
    2015, 33 (12):  1251-1256.  DOI: 10.3724/SP.J.1123.2015.08008
    Abstract ( 301 )   [Full Text(HTML)] () PDF (1397KB) ( 106 )  

    A method of non-target pigment screening in Chinese softshell turtle has been established by using liquid chromatography coupled to time of flight mass spectrometry (LC-Q-TOF MS). After being purified by a simple acetonitrile extraction work, the non-target pigment in 20 Chinese softshell turtle samples was detected by liquid chromatography-photodiode array detection (LC-DAD). The S7 sample, which has a strong spectral response, was chosen to extract the mass spectrometry information of the non-target pigment on different gradient elution conditions. In order to get the characteristic molecular mass ion (564.39773 Da and 564.39561 Da) of the non-target pigment, qualitative spectral full scan with negative sample was used. The molecular formula generation data and the literature information prompted speculation that the non-target pigment was canthaxanthin with the formula of C40H52O2. By comparing the canthaxanthin standard material MS/MS information, the result was confirmed accurate. A strategy of LC-Q-TOF MS method for the qualitative analysis of unknown compounds is discussed, and the results indicated that the described method can be effectively applied to qualitative analysis for non-target pigment in Chinese softshell turtle.

    Determination of 135 pesticides and their metabolites in Angelica sinensis by ultra-fast liquid chromatography-tandem mass spectrometry coupled with solid-phase extraction
    LIU Jie, TONG Ling, MENG Wenting, ZHAO Yunli, YU Zhiguo
    2015, 33 (12):  1257-1268.  DOI: 10.3724/SP.J.1123.2015.09014
    Abstract ( 464 )   [Full Text(HTML)] () PDF (1899KB) ( 199 )  

    A method using solid-phase extraction (SPE) followed by ultra-fast liquid chromatography-tandem mass spectrometry (UFLC-MS/MS) has been established for simultaneously quantitative determination of 135 pesticides and their metabolites (organophosphorus pesticides, pyrethroid pesticides and carbamate pesticides, etc.) in Angelica sinensis. The pesticide residues were extracted from the samples by acetonitrile, cleaned-up with a primary secondary amine (PSA) column and then analyzed using UFLC-MS/MS in multiple reaction monitoring (MRM) mode with positive electrospray ionization. The pesticide residues were quantified by matrix matched standard solution-internal standard method. All of the pesticides had good linear responses with r>0.99. The average recoveries of the pesticides at the spiked levels of 10, 50, 100 μg/kg ranged from 71.3%-119.7% with the RSDs of 1.0%-19.9%, except for clethodim (62.0%-68.2%). The limits of quantification of the 135 pesticides and their metabolites were 1.0-10.0 μg/kg. The results demonstrated that the method is simple, fast, sensitive and can be used for the analysis of the multiclass of pesticide residues in Angelica sinensis.

    Determination of rutin, quercetin and kaempferol in althaea rosea (L) Gavan for Uyghur medicine by high performance liquid chromatography
    MUHETAER·Tu'erhong, RESALAT·Yimin, CHU Ganghui, YIN Xuebo, MUNIRA·Abudukeremu
    2015, 33 (12):  1269-1273.  DOI: 10.3724/SP.J.1123.2015.05008
    Abstract ( 630 )   [Full Text(HTML)] () PDF (850KB) ( 87 )  

    Uyghur medicine is one important part of the national medicine system. Uyghur medicine modernization, namely the study of effective components with modern technologies, is the only way for the scientification, standardization, and industrialization of Uyghur medicine. Here we developed a selective extraction method for rutin, quercetin and kaempferol in Althaea rosea (L) Gavan. The three active species were determined by high performance liquid chromatography (HPLC) with HC-C18 column (250 mm×4.6 mm, 5 μm) and the mobile phase of CH3OH-0.4% H3PO4(50:50, v/v). Rutin, quercetin and kaempferol were baseline separated with each other and the interference species with flow rate of 1.0 mL/min and column temperature of 30 ℃. Under the optimal conditions, linear correlation were obtained in the mass concentration range of 12.5-150 μg/mL (r=0.9998) for rutin, 12.5-125 μg/mL (r=0.9999) for quercetin, and 12.5-125 μg/mL (r=0.9988) for kaempferol. The recoveries (n=5) of rutin, quercetin and kaempferol were 100.25% (RSD=1.1%), 97.60% (RSD=0.47%) and 97.75% (RSD=0.71%), respectively. The method can be used to determine the contents of rutin, quercetin and kaempferol in Althaea rosea (L) Gavan and provide the guidance for the analysis of the flavonoids in other Uyghur medicines.

    Chemometric study of the retention mechanism on butyl column: effect and relation of pH and pKa
    KOUSKOURA Maria G, MITANI Constantina V, MARKOPOULOU Catherine K
    2015, 33 (12):  1274-1286.  DOI: 10.3724/SP.J.1123.2015.06037
    Abstract ( 372 )   [Full Text(HTML)] () PDF (2257KB) ( 46 )  

    Reversed phase chromatographic separations are optimized for analytes containing ionizable groups by adjustment of pH of mobile phases. As it seems the pKa values of compounds affect their retention because of the variety in their solvation. However, it is of stressful need to predict their behavior taking into account also a series of other parameters. This work focuses on the development of ten different models, using partial least squares regression, which will identify and quantify the impact of several factors in the chromatographic behavior of 104 analytes. The combined effect of their numerous characteristics is obvious since along with pH (at 2.3 and 6.2), factors such as lipophilicity, molecular volume, polar surface area and the presence of specific moieties in their structures are not diminished. On the contrary, they work increasing or counterbalancing several effects on the retention time. The models compiled can be applied to predict with reliability (R2>0.865 and Q2>0.777) the behavior of unknown drugs.

    Determination of 2-methylisoborneol and geosmin in drinking water using headspace solid phase micro-extraction coupled with gas chromatography-mass spectrometry
    CHENG Jianguo, LIU Kaiying, BAI Mindong, CHENG Chao, YU Yixuan, ZHOU Xinying
    2015, 33 (12):  1287-1293.  DOI: 10.3724/SP.J.1123.2015.08031
    Abstract ( 674 )   [Full Text(HTML)] () PDF (897KB) ( 183 )  

    The odorous compounds of 2-methylisoborneol (2-MIB) and geosmin (GSM) heavily produced and released in water source are one of the most important factors leading to off-flavor emergencies and resident water consumption panic in drinking water. A headspace solid phase micro-extraction (HS-SPME) combined with gas chromatography-mass spectrometry (GC-MS) method was established for the simultaneous determination of these two trace earthy and musty compounds in reservoir water, reservoir soil and tap water. The conditions of HS-SPME, such as salt amount, extraction time and extraction temperature, were optimized based on orthogonal analysis. The qualitative and quantitative analyses of 2-MIB and GSM were carried out in the electron impact (EI)-selective ion scanning mode. The results showed that the linear relationship between peak area and concentration of 2-MIB and GSM was good enough (r2≥0.998) from 5 to 1000 ng/L, the limits of detection were 0.72 ng/L for 2-MIB, 0.34 ng/L for GSM and the limits of quantification were 2.40 ng/L for 2-MIB, 1.13 ng/L for GSM. When the target samples spiked in the range of 10-600 ng/L, the average recoveries of the target compounds were 93.6%-107.7% (RSD≤6.1%, n=6). Based on the above method, the target compounds in reservoir water, reservoir soil and tap water in a certain region of Liaoning Province were analyzed. The results showed that the two target odors in reservoir water were 3.0-3.6 ng/L. As for the extract of the soil around the reservoir, 2-MIB was 8.1 ng/L and GSM was 17.8 ng/L. The odorous substances were not detected in the tap water. This method is simple, accurate, reliable, highly sensitive and no need of organic solvents. And it is suitable for the detection of 2-MIB and GSM in drinking water.

    Non-target screening of organic pollutants in sediments and sludges using gas chromatography-mass spectrometry and automated mass spectral deconvolution
    WANG Gang, MA Huilian, WANG Longxing, CHEN Jiping, HOU Xiaohong
    2015, 33 (12):  1294-1300.  DOI: 10.3724/SP.J.1123.2015.08022
    Abstract ( 491 )   [Full Text(HTML)] () PDF (1424KB) ( 189 )  

    A screening method in the combination of ultrasonic extraction, gas chromatography-mass spectrometry detection and automated mass spectrometry deconvolution technique was developed for non-target screening of non-polar and weak polar pollutants in sediments and sludges. The samples were extracted by ultrasonication for 20 min using dichloromethane for three times. The extraction solutions were cleaned-up by gel permeation chromatography and a silica gel column, and then 3 g of copper powder was used to remove the sulfur by ultrasonication for 10 min. Parallel experiments were carried out for 5 times and the RSDs were ranged from 5.8% to 14.9%. Automated mass spectral deconvolution & identification system (AMDIS) would improve the resolution of overlapping peaks, and identify the pure mass spectrum of the analytes in the cases of stronger background interference and co-extracted substances covering. Standard spectrum databases, such as NISTDRUG, NISTEPA, NISTFDA, Mass Spectral Library, etc, would qualitatively identify the organic pollutants in the samples. As a result, a total of 290 organic pollutants were identified, of which 190 and 153 pollutants were found in sediments and sludges, respectively. The identified pollutants included the Environmental Protection Agency (EPA) priority pollutants, pharmaceuticals, herbicides, antioxidants, intermediates, organic solvents and chemical raw materials. The proposed method is proved to be a promising one for non-target screening of complex matrix samples with the advantages of higher sensitivity and better repeatability.

    Determination of solubility parameters for asymmetrical dicationic ionic liquids by inverse gas chromatography
    WANG Jun, YANG Xuzhao, WU Jinchao, SONG hao, ZOU Wenyuan
    2015, 33 (12):  1301-1306.  DOI: 10.3724/SP.J.1123.2015.07030
    Abstract ( 554 )   [Full Text(HTML)] () PDF (894KB) ( 101 )  

    Inverse gas chromatographic (IGC) technology was used to determine the solubility parameters of three asymmetrical dicationic ionic liquids ([PyC5Pi]NTf2]2, [MpC5Pi]NTf2]2 and [PyC6Pi]NTf2]2) at 343.15-363.15 K. Five alkanes were applied as test probes including octane (n-C8), decane (n-C10), dodecane (n-C12), tetradecane (n-C14), hexadecane (n-C16). Some thermodynamic parameters were obtained by IGC data analysis, such as the specific retention volumes of the solvents (Vg0), the molar enthalpies of sorption (ΔH1s), the partial molar enthalpies of mixing at infinite dilution (ΔHl), the molar enthalpies of vaporization (ΔHv), the activity coefficients at infinite dilution (Ω1), and Flory-Huggins interaction parameters (χ12) between ionic liquids and probes. The solubility parameters (δ2) of the three dicationic ionic liquids at room temperature (298.15 K) were 28.52-32.66 (J·cm-3)1/2. The solubility parameters (δ2) of cationic structure with 4-methyl morpholine are bigger than those of the cationic structure with pyridine. The bigger the solubility parameter (δ2) is, the more the carbon numbers of linking group of the ionic liquids are. The results are of great importance to the study of the solution behavior and the applications of ionic liquid.

    Preparation of octadecyl methacrylate-based polymer stationary phase by in-situ polymerization for open tubular capillary electrochromatography
    ZHOU Sunying, CHEN Jinyun, TAN Jingjing, LIN Xucong, XIE Zenghong
    2015, 33 (12):  1307-1313.  DOI: 10.3724/SP.J.1123.2015.07010
    Abstract ( 456 )   [Full Text(HTML)] () PDF (5242KB) ( 71 )  

    The preparation of porous polymethacrylate-based open tubular capilary columns by in-situ copolymerization of octadecyl methacrylate (OMA), and ethylene dimethacrylate (EDMA) in N,N-dimethylformamide (DMF) solvent are proposed. The parameters of the preparation procedure of the stationary phase are discussed in detail. The surface of the cross-section of an open tubular (OT) column by scanning electron microscope (SEM) showed wrinkle configuration, which is expedient to enhance proportion of stationary phase and column capacity. Efficient separation of six alkyl benzene homologous series (namely, toluene, ethylbenzene, propylbenzene, butylbenzene, amylbenzene and hexylbenzene) were performed by CEC using the prepared column, and their elution order was in agreement with their hydrophobicity. So, the OT columns bonded with octadecyl ligands yielded reversed-phase retention behavior toward nonpolar solutes. In addition, the separation of four antiepileptics was also investigated with satisfactory effectiveness. The column efficiency range was 35300-49800 plates/m. The results showed that the C18-OT column of organic matrix for reversed-phase chromatography was successfully prepared via in-situ polymerization in this work. Hereby, this new column thus offers a promising new alternative in OT-CEC and will be useful in separation science.

    Technical Notes
    Impurity profile study of cefalotin sodium by two-dimensional liquid chromatography-quadrupole time-of-flight mass spectrometry
    QIU Ya, QIN Feng, WEN Hongliang, ZHAO Jingdan, LIU Hao, YANG Meicheng
    2015, 33 (12):  1314-1319.  DOI: 10.3724/SP.J.1123.2015.07027
    Abstract ( 522 )   [Full Text(HTML)] () PDF (883KB) ( 131 )  

    A two-dimensional liquid chromatography-quadrupole time-of-flight mass spectrometry (2D-LC-QTOF MS) method to profile the impurities of cefalotin sodium was developed. A Symmetry C18 column (250 mm×4.6 mm, 5 μm) was used in the first dimensional chromatography, with gradient elution using pH 2.5 phosphate buffer and acetonitrile as the mobile phases. The column temperature was maintained at 40 ℃ with an ultraviolet detection of 220 nm for analysis. An ACQUITY UPLC BEH C18 column (50 mm×2.1 mm, 1.7 μm) was used in the second dimensional chromatography, with gradient elution using water containing 0.1% (v/v) formic acid and acetonitrile containing 0.1% (v/v) formic acid as the mobile phases. The column temperature was maintained at 40 ℃. An HLB C18 column (30 mm×2.1 mm, 20 μm) was used as the trap column. The data were collected in positive ion mode. The ion source temperature was set at 100 ℃ and the electrospray ionization (ESI) needle voltage was set at 1000 V. The nebulizer gas temperature was set at 500 ℃. The molecular formulas of the impurities were determined by their exact masses and isotope distributions. And the structures were determined by the protonated molecular ions and the manufacturing process of cefalotin sodium. Six impurities of cefalotin sodium were characterized and the origination of the impurities was deduced. Three of them were unknown impurities to the best of our knowledge. It was confirmed that the Chinese Pharmacopoeia 2010 has mistaken impurity A of cefalotin sodium. The results indicated that the 2D-LC-QTOF MS method could be used to investigate the impurity profile of cefalotin sodium, and it is simple and sensitive.

    Simultaneous determination of four aflatoxins in Citrus reticulatablanco by ultra performance liquid chromatography coupled with immunomagnetic beads for enrichment and purification
    XING Yanyan, TONG Ling, CHEN Nan, YU Zhiguo, ZHAO Yunli
    2015, 33 (12):  1320-1326.  DOI: 10.3724/SP.J.1123.2015.06001
    Abstract ( 532 )   [Full Text(HTML)] () PDF (2521KB) ( 111 )  

    Immunomagnetic beads (IMBs) were formed by coupling the ProtElut NHS (N-hydroxysuccinimide) magnetic beads and anti-aflatoxins monoclonal antibody. The synthesized IMBs presented uniform size, good magnetic property and specific selectivity. In this work, a novel and facile pretreatment method of sample enrichment and purification based on the IMBs for the determination of aflatoxins (AFs) (AFB1, AFB2, AFG1, AFG2) in Citrus reticulatablanco samples by ultra performance liquid chromatography (UPLC) were developed. The sample was extracted with 20%(v/v) methanol-PBS buffer solution (pH 7.4), followed by a cleanup procedure with the IMBs. The target compounds were eluted using 1 mL methanol. The four afatoxins were separated on an ACQUITY UPLC HSS T3 C18 column (100 mm×2.1 mm, 1.8 μm) adopting a gradient program within 12 min. The UPLC equipped with a fluorescence detector with a special mercury/xenon lamp was used to detect the aflatoxins. The satisfactory correlation coefficients (r2>0.999) of the four aflatoxins were obtained within their respective linear ranges. The limits of detection (S/N=3) were between 0.013 μg/kg and 0.038 μg/kg, and the limits of quantification (S/N=10) were between 0.044 μg/kg and 1.2 μg/kg. The recoveries were in the range of 63.9%-115.0% with the relative standard deviations (RSDs) of 0.4%-14.2%. The validation results meet the requirements of trace assay. It's indicated that the IMBs were good pretreatment alternatives and the developed method is simple, fast, accurate, and can be applied for the simultaneous determination of the four aflatoxins in Citrus reticulatablanco.

    Measurement of 11 benzophenone ultraviolet-filters in cosmetics by high performance liquid chromatography
    QU Baocheng, BIAN Haitao, MAO Xiqin, LI Jin
    2015, 33 (12):  1327-1332.  DOI: 10.3724/SP.J.1123.2015.06042
    Abstract ( 367 )   [Full Text(HTML)] () PDF (766KB) ( 94 )  

    A sample preparation and analytical method with liquid-liquid extraction (LLE) and high performance liquid chromatography (HPLC) was developed to detect 11 benzophenone ultraviolet-filters in cosmetics. The target compounds were extracted by the mixed solutions of tetrahydrofuran (THF)/methanol/water or dichloromethane/water at proper ratios. The extracts were centrifuged and filtered to remove matrix compounds, and then analyzed by HPLC. The separation of analytes was carried out on a Diamonsil-C18 column (150 mm×4.6 mm, 5 μm) with 0.1%(v/v) formic acid aqueous solution (containing 10 mmol/L ammonium acetate) as mobile phase A and methanol containing 0.1%(v/v) formic acid as mobile phase B. The spiked recoveries of the method (n=7) were 93.4%-103.8% with the relative standard deviations of 0.1%-4.2%. The limits of detection (LODs) were in the range of 4.0-30 μg/g and the limits of quantitation (LOQs) ranged from 15 to 100 μg/g. The method was applied to the determination of 42 cosmetic samples randomly purchased from the supermarket in Dalian. Five benzophenone series were always detected, in which the content of benzophenone-3 in sunscreen cream and the content of benzophenone-2 in perfume were very high and reached 2785 μg/g and 2106 μg/g, respectively. The results showed that the developed method is efficient, reliable and sensitive, which can be applied to the determination of benzophenones in cosmetics.

    Determination of inorganic anions and gluconate by two-dimensional ion chromatography
    CHEN Ailian, DING Hui, FANG Linmei, SHI Chaoou
    2015, 33 (12):  1333-1337.  DOI: 10.3724/SP.J.1123.2015.08036
    Abstract ( 658 )   [Full Text(HTML)] () PDF (1048KB) ( 123 )  

    A new two-dimensional ion chromatography method was developed to parallelly analyze two different types of samples with the application of valve switching technology-suppressed conductivity and pulsed amperometric analysis system, for concurrent determination of chloride, nitrite, sulfate, nitrate four inorganic anions and gluconate. The first dimensional chromatography was using Ionpac AG18+Ionpac AS18 anion analysis columns with a suppressed conductivity detector for the separation and detection of Cl-, NO2-, SO42- and NO3-. Respectively, the elution was 5 and 20 mmol/L NaOH at an isocratic flow rate of 1.0 mL/min and sample injection volume of 25 μL. The second dimensional chromatography was utilizing two guard columns, CarboPac PA1 and CarboPac PA20, with 90 mmol/L NaOH solution for the isocratic eluent of 0.8 mL/min. Gluconate was enriched by an AG15 column and switched into the pulsed amperometric detector. The results showed that: each inorganic anion in 0.1-5.0 mg/L and gluconate in 0.0856-4.2825 mg/L had a good linear relationship (R2≥0.9945). The RSDs of the peak areas were between 1.05%-1.94%. The limits of detection were 0.61-2.17 μg/L for the anions and 24.24 μg/L for the gluconate. The recoveries were between 90.3%-102.8%. The two detection modes parallelly have good separation efficiency, detection accuracy and the precision of the separation and are suitable for the analysis of complex samples.