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    Chinese Journal of Chromatography
    2020, Vol. 38, No. 5
    Online: 08 May 2020

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    Contents
    Volume 38, Number 5 Content
    2020, 38 (5):  0-0. 
    Abstract ( 17 )   PDF (5084KB) ( 19 )  
    Advances in dispersive liquid-liquid microextraction and its application to analysis of biological samples
    SHI Yiwei, ZHANG Ning, CAO Wen, HONG Zhanying
    2020, 38 (5):  491-501.  DOI: 10.3724/SP.J.1123.2019.10026
    Abstract ( 347 )   HTML ( 24 )   PDF (3328KB) ( 146 )  

    Dispersive liquid-liquid microextraction (DLLME) is a mini-extraction technology with merits of low cost, environment friendliness, and high extraction efficiency; moreover, this method is easy to operate and requires only a short operation time. In this paper, several extraction models, including normal dispersive liquid-liquid microextraction, ionic liquid dispersive liquid-liquid microextraction, and ultrasound-assisted dispersive liquid-liquid microextraction, are reviewed according to the type of extraction solvents and dispersive methods. This paper also summarizes the application of DLLME to the analysis of biological samples in the last five years.

    Application of capillary electrophoresis in enzyme inhibitors screening from natural products
    LI Feng, ZHANG Yanmei, KANG Jingwu
    2020, 38 (5):  502-515.  DOI: 10.3724/SP.J.1123.2019.12012
    Abstract ( 78 )   HTML ( 4 )   PDF (4537KB) ( 42 )  

    As aberrant enzyme functions are often closely associated with various diseases, enzymes represent one of the most important drug target groups. Historically, natural products have been the most productive sources for drug discovery. However, the complexity of the components leads to a bottleneck in separation and purification, thus restricting activity-based drug screening. Due to the unique advantages such as high separation efficiency and without sample matrix interference, the advantage of capillary electrophoresis (CE) directly applied to extracts without purification for activity-based drug screening is of great attractive. In this review, we have summarized the application of CE for screening enzyme inhibitors in natural products during the last decade. In particular, we discuss important examples for screening inhibitors of transferases (kinases), hydrolases, oxidoreductases, etc. We also present an overview of the technical details concerning the separation modes in CE and enzyme kinetics. Finally, we provide future prospects for the application of CE to the screening of active ingredients in natural products.

    Synthesis of a chiral metal-organic framework using zinc oxide as zinc source for enantioselective adsorption of 2, 2'-furoin racemate
    WANG Cuijie, GAO Yu, LI Xinglin, ZHAO Wuduo, YU Ajuan, ZHANG Shusheng
    2020, 38 (5):  516-521.  DOI: 10.3724/SP.J.1123.2019.10024
    Abstract ( 96 )   HTML ( 6 )   PDF (2995KB) ( 38 )  
    Supporting Information

    Chiral metal-organic frameworks (CMOFs), [Zn(L-mal)(H2O)2]n were prepared by using zinc oxide instead of the traditional metal inorganic salt as the zinc source, and their chiral separation performance was investigated. Equal amounts of ZnO and L-malic acid were dissolved in H2O, and[Zn(L-mal)(H2O)2]n were obtained by allowing the mixture to stand at room temperature for 24 h. Then, 100 mg[Zn(L-mal)(H2O)2]n as the adsorbent was added to 250 μL 1 g/L 2, 2'-furoin racemate, and 4.5 mL isopropanol and 1 mL methanol were selected as the extraction solvent and elution solvent, respectively, for selective adsorption experiments. The final filtrate was analyzed by high performance liquid chromatography (HPLC). The results showed that[Zn(L-mal)(H2O)2]n exhibited better selective adsorption ability for R-2, 2'-furoin with 20% enantiomeric excess (ee). This work provides a new method for the green preparation of CMOF and expands its application in the field of chiral separation.

    Synthesis of magnetic graphene oxide modified with dodecylamine and its application for the determination of seven endocrine-disrupting chemicals in environmental water samples
    GUO Jinghao, TONG Changlun
    2020, 38 (5):  522-528.  DOI: 10.3724/SP.J.1123.2019.10007
    Abstract ( 93 )   HTML ( 5 )   PDF (2084KB) ( 50 )  

    Magnetic graphene oxide (MGO) modified with dodecylamine (DDA) was synthesized in this work. The as-prepared MGO-DDA was characterized by Fourier transform infrared spectroscopy, X-ray diffraction, and vibrating sample magnetometer measurements. The material was used as the absorbent in magnetic solid-phase extraction (MSPE) for seven environmental endocrine-disrupting chemicals (EDCs):estrone (E1), β-estradiol (E2), estriol (E3), 17α-ethynylestradiol (EE2), hexoestrol (HEX), androstendione (AND), and bisphenol A (BPA). MSPE combined with HPLC-UV was developed for the determination of EDCs in environmental water samples. The effects of the amount of adsorbent, adsorbing time, and the type and volume of eluents on the recoveries of the EDCs were investigated. Under the optimal conditions, good linear relationships between the UV signals and the EDC concentrations were obtained, with R2 greater than 0.999. The limits of detection for all the EDCs were between 0.10 and 0.23 nmol/L. The MSPE-HPLC-UV method was successfully applied to the analysis of the seven EDCs in environmental water samples such as lake water and sewage water samples. The recoveries of all the EDCs in spiked lake water and sewage water samples were between 73.9% and 114.7%, and the RSDs ranged from 0.7% to 11.8%. Thus, the proposed MSPE-HPLC-UV method is simple, reliable, sensitive, and low-cost.

    Simultaneous determination of 16 flavonoids and ferulic acid in honey by solid phase extraction and high performance liquid chromatography-tandem mass spectrometry
    HOU Jianbo, XIE Wen, QIAN Yan, SHI Yingzhu, LU Shun, SHENG Tao, CHEN Wenbin
    2020, 38 (5):  529-537.  DOI: 10.3724/SP.J.1123.2019.06030
    Abstract ( 132 )   HTML ( 10 )   PDF (1898KB) ( 98 )  

    Flavonoids are polyphenol compounds that are widely distributed in honey; they play an important role in its antioxidant activity and aid in distinguishing various species of honey. An analytical method based on solid phase extraction and high performance liquid chromatography with tandem mass spectrometry (SPE-HPLC-MS/MS) for the simultaneous determination of rutin, myricetin, morin, quercetin, naringenin, hesperetin, luteolin, genistein, kaempferol, isorhamnetin, apigenin, pinocembrin, wogonin, chrysin, galangin, genkwanin, and ferulic acid in honey was developed and validated. The honey samples were diluted with HCl solution (pH 2) and cleaned up on a C18 column by solid phase extraction; the methanol eluent was filtered through a nylon membrane and analyzed by LC-MS/MS on an ODS-3 column (150 mm×4.6 mm, 3 μm). Quantitative detection was performed by LC-MS/MS in the multiple reaction monitoring (MRM) mode under negative electrospray ionization (ESI-) conditions. The external standard method was used for quantitation. The method validation data were obtained. The calibration standard curve solutions were prepared by honey matrix-matching; the linear range was 0-200 μg/kg, with correlation coefficients of the calibration standard curves greater than 0.997. The limits of quantification (LOQs) of this method were 20 μg/kg. The recoveries were in the range of 64.5%-113%, and the relative standard deviations were 1.4%-14.5% at three spiked levels (20, 40, and 100 μg/kg). The developed method is convenient, rapid, and effective, and it is suitable for the determination and confirmation of flavonoids in honey samples.

    Rapid determination of multiple prohibited and restricted veterinary drug residues in fish and shrimp by ultra high performance liquid chromatography-tandem mass spectrometry
    CHEN Xinglian, LIN Tao, LIU Xingyong, MEI Wenquan, WANG Li, GENG Huichun, CHENG Long, WANG Luxiang
    2020, 38 (5):  538-546.  DOI: 10.3724/SP.J.1123.2019.09017
    Abstract ( 118 )   HTML ( 17 )   PDF (1703KB) ( 118 )  
    Supporting Information

    A method was established for the rapid determination of 28 prohibited and restricted veterinary drugs of five classes (sulfonamides, quinolones, chloramphenicols, nitrofurans metabolites and triphenylmethane) in fish and shrimp by ultra high performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS) coupled with simultaneous extraction and purification. After optimizing the sample pretreatment methods and chromatographic conditions, the samples were hydrolyzed with hydrochloric acid. The five kinds of residual drugs were simultaneously extracted with acetonitrile after nitrofuran metabolites derivatized with 2-nitrobenzaldehyde. The extraction solutions were dehydrated with sodium chloride and salted out. The acetonitrile layer was purified with n-hexane and concentrated to near dryness. The residues were dissolved in 1.0 mL methanol. Then, the solutions were purified by dispersive solid phase extraction with C18, N-(n-propyl)ethylenediamine (PSA) and amino bonded silica gel (NH2) sorbents. The residues were separated on a ZORBAX C18 chromatographic column (50 mm×2.1 mm, 1.8 μm). The MS data were acquired in positive and negative multiple reaction monitoring (MRM) modes, and quantitated by the isotope internal standard method. With this approach, the linear relationships of the 28 veterinary drugs were good. The linear correlation coefficients were greater than 0.99. The limits of detection and limits of quantification were in the range of 0.1-0.8 μg/kg and 0.3-2.7 μg/kg, respectively. The average recoveries at three spiked levels (1, 5, and 20 fold of the LOQs) were 70.0%-120% with relative standard deviations of 0.9%-10.0%. The method is simple, rapid, accurate and sensitive, and it is suitable for the rapid determination of various prohibited and restricted drugs in fish and shrimp.

    Determination of five protopanaxadiol ginsenosides in ginseng by solid-phase extraction-ultra performance liquid chromatography
    SONG Chunying, ZHANG Huarong, GUO Zhimou, YAN Jingyu, JIN Gaowa, LIANG Xinmiao
    2020, 38 (5):  547-553.  DOI: 10.3724/SP.J.1123.2019.09003
    Abstract ( 96 )   HTML ( 13 )   PDF (894KB) ( 65 )  

    A new method based on solid-phase extraction-ultraperformance liquid chromatography (SPE-UPLC) was developed for the determination of five protopanaxadiol ginsenosides in ginseng. The ginsenosides were extracted from ground ginseng samples using water-saturated n-butanol and purified on a hydrophilic solid-phase extraction column. Chromatographic separation was achieved on an ACQUITY UPLC BEH Shield RP18 column (100 mm×2.1 mm, 1.7 μm) by linear gradient elution using an acetonitrile/water mobile phase. Five protopanaxadiol ginsenosides were detected by a photodiode array detector, and they showed a strong positive linear correlation (r2>0.999) in the range of 5-500 μg/mL. In addition, the instrument precision ranged between 0.95% and 2.62% (n=6), with the sample stability between 0.90% and 2.15% (n=8) within 22 h. Intra- and inter-day repeatabilities were 5.35%-6.47% (n=6) and 5.56%-6.34% (n=8), respectively. Sample recoveries and the corresponding relative standard deviations (RSDs) were 87.16%-101.92% and 1.54%-4.01% (n=6), respectively. Hydrophilic chromatography materials were used in SPE, and the extract was directly loaded and purified without pretreatment. Besides, with the use of UPLC, the analysis time was greatly shortened. The developed method is simple and rapid, with high throughput, thus being suitable for the quantitative analysis of the five protopanaxadiol ginsenosides in ginsengs.

    Direct chemome profiling of Boschniakia rossica using online pressurized extraction-ultrahigh-performance liquid chromatography-ion trap-time-of-flight mass spectrometry
    LI Ting, XU Xia, CHANG Anqi, LIU Wenjing, SONG Qingqing, SONG Yuelin, TU Pengfei
    2020, 38 (5):  554-563.  DOI: 10.3724/SP.J.1123.2019.10006
    Abstract ( 60 )   HTML ( 6 )   PDF (2558KB) ( 33 )  

    An online pressurized extraction-ultrahigh-performance liquid chromatography-ion trap-time-of-flight mass spectrometry (online PLE-UHPLC-IT-TOF-MS) platform was configured for the rapid and direct profiling of the chemical constituents of Boschniakia rossica (B. rossica). Notably, only a sub-microgram amount (0.5 mg) of B. rossica was placed in an empty guard column core, which was then filled up with normal-phase silica gel as an extraction vessel. The guard column core was placed inside a guard column holder in the column oven (70℃) and connected to the UHPLC-IT-TOF-MS system via metal tubing. The extraction phase was maintained for 3 min with 0.1% (v/v) formic acid as the extraction solvent. The extraction and elution phases for the entire measurement were segmented by a 6-port/2-channel electronic valve. In the elution phase, 0.1% (v/v) aqueous formic acid-acetonitrile containing 0.1% (v/v) formic acid was the mobile phase, and the components of interest that accumulated at the front of the column were eluted into the IT-TOF-MS system for detection. A total of 48 compounds were observed, and according to the literature, database, and mass fragmentation pathways, 45 compounds, including 10 phenylethanol glycosides, 14 iridoid glycosides, and 21 phenylalanine glycosides, were identified from B. rossica. This study provides reliable information regarding the chemical composition and quality evaluation of B. rossica. Moreover, it offers a promising analytical pipeline for the chemical composition characterization of traditional Chinese medicines.

    Simultaneous determination of cucurbitacin B, E and I in plasma, urine, and melon and fruit vegetables by ultra performance liquid chromatography-triple quadrupole mass spectrometry using atmospheric pressure chemical ionization
    ZHANG Xiaoyi, ZHANG Xiuyao, CAI Xinxin, LI Ruifen
    2020, 38 (5):  564-571.  DOI: 10.3724/SP.J.1123.2019.09018
    Abstract ( 90 )   HTML ( 10 )   PDF (1036KB) ( 52 )  

    A method for the determination of cucurbitacin B (CuB), cucurbitacin I (CuI) and cucurbitacin E (CuE) in plasma, urine and melon and fruit vegetables was developed by ultra performance liquid chromatography-triple quadrupole mass spectrometry (UPLC-MS/MS). The target analytes in plasma and urine were extracted and cleaned-up by solid supported liquid-liquid extraction, while those in melon and fruit vegetables were extracted with acetonitrile and then diluted with water. CuB, CuI and CuE were separated on an XBridge BEH C18 column (100 mm×3.0 mm, 2.5 μm) with gradient elution using mobile phases of methanol and 0.025% (v/v) ammonia aqueous solution. An atmospheric pressure chemical ionization interface was used as the ion source and the analysis was performed in negative ionization multiple reaction monitoring (MRM) mode. The cucurbitacins in plasma and urine were quantified by the matrix working standard curve internal standard method, while those in melon and fruit vegetables were quantified by the solvent standard curve external standard method. Oleandrin was used as the internal standard. The average recoveries were 89.0%-113% for the three cucurbitacins in plasma and urine, with RSDs of 1.7%-12.2% (n=6). The average recoveries were 87.6%-114% for the three cucurbitacins in melon and fruit vegetables, with RSDs of 4.1%-11.1% (n=6). The limit of detection (S/N=3) of the three cucurbitacins was 0.03 μg/L in plasma and urine, and 5-10 μg/kg in melon and fruit vegetables. The method is simple, sensitive and accurate. It has been used for the determination of cucurbitacins in bitter bottle gourd and in the plasma and urine of patients poisoned by bitter bottle gourd, CuB was successfully detected.

    Fast high-performance liquid chromatography quantification of ten phenolic acids in honey using chemometric second-order calibration method
    ZHANG Xiaohua, LÜ Minming, ZHENG Jingjing, MU Shuting, LIU Panhua, CHEN Zheng
    2020, 38 (5):  572-580.  DOI: 10.3724/SP.J.1123.2019.09013
    Abstract ( 82 )   HTML ( 6 )   PDF (4603KB) ( 36 )  

    This study aims at the determination of ten phenolic acids in honey using high-performance liquid chromatography-diode array detection (HPLC-DAD) combined with a chemometric second-order calibration method. First, the accuracy of the model was investigated by analysis of the calibration samples and validation samples. Satisfactory results were obtained; the ten phenolic acids exhibited good linearity, and the correlation coefficient (R) was in the range 0.9982-0.9999, with average recoveries of 97.6% to 101.1%, which proved that the model was stable and reliable. Second, the types and operating conditions of the SPE columns were determined by experiments using simulated honey; HLB column was selected, washed with 0.1%(v/v) formic acid aqueous solution, and eluted with methanol. Finally, the phenolic acid contents in jujube flower honey were determined under the optimum conditions for simulated honey. The recoveries of the analytes were 62.1%-93.8%, which met the requirements considering the variety of target analytes and the complexity of the honey substrate. In addition, the efficiency of the method was validated by figures of merit and statistical parameters, including sensitivity (SEN), selectivity (SEL), root-mean-square error of prediction (RMSEP), limit of detection (LOD), and limit of quantification (LOQ); the obtained results were satisfactory. This method is simple, fast, and accurate, and it can be used for the quantitative analysis of the target analytes in complex substrates.

    Unified form of liquid chromatography plate height equation
    DAI Chaozheng, XU Xiaoping
    2020, 38 (5):  581-586.  DOI: 10.3724/SP.J.1123.2019.08024
    Abstract ( 79 )   HTML ( 4 )   PDF (852KB) ( 41 )  

    The effects of radial diffusion and mobile phase heating on the column efficiency during chromatographic separation were investigated. Starting from the heat transfer equation, an equation of plate height for liquid chromatography was derived using the principle of chromatographic dynamics, with consideration of the mobile phase friction and electric heat generation:

    This equation summarized the relationship between plate heights for high performance liquid chromatography (HPLC), ultra performance liquid chromatography (UPLC), capillary electrochromatography (CEC), and eliminate stagnant fluid layer chromatography (ESFLC) and various factors. The last term in the equation represented the contribution of radial diffusion and column heating to the plate height. When the linear velocity of the mobile phase was low and the column diameter was fine, the contribution of the frictional heat generation of the mobile phase to the plate height approached zero, and the plate height equation reduced to the Horvath and Lin equation. When the linear velocity of the mobile phase was too high, friction heat was generated in the column system. The temperature difference between the axis and the edge of the column increased, resulting in a decrease in the column efficiency. The temperature difference between the axis and the edge of the column was proportional to the square of the velocity of the mobile phase. The authors clearly point out that the column efficiency in liquid chromatography is closely related to the inner diameter of the column. The use of a column with a small inner diameter is conducive to high analytical speed and high efficiency, a very high mobile phase line velocity would serious degrade the column efficiency.

    Application of serum amino acid profile in urolithiasis based on gas chromatography-mass spectrometry
    GAO Yao, GONG Sisi, ZHANG Tianwen, TANG Minjie, ZHANG Beiying, CHEN Min, OU Qishui, MAO Houping
    2020, 38 (5):  587-594.  DOI: 10.3724/SP.J.1123.2019.07030
    Abstract ( 133 )   HTML ( 5 )   PDF (1488KB) ( 39 )  

    An overall workflow based on gas chromatography-mass spectrometry (GC-MS) was established for the analysis of the serum amino acid profile between urolithiasis patients (n=80, age (46.82±13.39) years) and healthy controls (n=37, age (43.46±12.79) years). The raw data from GC-MS analysis were processed by multivariate statistical methods to build the model. Following this, student's t-test and logistic regression were performed and receiver operator characteristic (ROC) curve was plotted to identify the potential biomarkers. Good linearities were observed for the target amino acids, with correlation coefficients (R2) greater than 0.9985. The limits of detection (LODs) were 0.1-4.0 μmol/L. The results indicated a significant discrimination between the urolithiasis and control groups. Five significantly differentially expressed amino acids (variable importance in projection (VIP)>1 and p < 0.05) were found to provide the scientific evidence for the early diagnosis of urolithiasis, while the sensitivity of the integrated five differential amino acids was up to 97.3%. In particular, the area under the curve (AUC) of serine reached 0.819, which suggested a great clinical screening value.

    Determination of eight vitamin E in vegetable oils by gas chromatography-mass spectrometry and its application on authentication of sesame oil
    SHEN Weijian, WANG Hong, LU Huiyuan, YU Keyao, HU Guoshen, WEI Xueyuan, WU Bin
    2020, 38 (5):  595-599.  DOI: 10.3724/SP.J.1123.2019.09011
    Abstract ( 225 )   HTML ( 26 )   PDF (843KB) ( 153 )  

    A method was established for the determination of eight vitamins E (α-, β-, γ-, δ-tocopherol and α-, β-, γ-, δ-tocotrienol) in vegetable oils using gas chromatography-mass spectrometry (GC-MS). The targets were extracted with methanol, and analyzed by GC-MS in the selected ion monitoring (SIM) mode after concentration to a constant volume, and quantified using the external standard method. Baseline separation were achieved for all the target compounds. The linearities of all the compounds were between 0.01 and 1 mg/L. The limits of detection (LODs) and limits of quantification (LOQs) were in the range of 0.03-0.25 mg/kg and 0.10-0.83 mg/kg, respectively. The average recoveries of all the targets in sesame oil samples were between 87.5% and 107.4% at three spiked levels (10, 50, and 250 mg/kg), and the RSDs were all less than 7.5%. The tocopherols and tocotrienols contents in sesame oil samples and in six lower-price vegetable oils (soybean, rapeseed, sunflower, peanut, corn and palm oils) were determined by the above mentioned method. The results showed that the vitamin E profiles of sesame oil were significantly different from those of the other six vegetable oils. Therefore, vitamin E can be used as a discriminating parameter for detecting the adulteration of sesame.

    Three-dimensional quantitative structure-activity relationship study on gas chromatographic retention index of the fragrance compounds of Liliumspp
    JIAO Long, WANG Yuan, TAI Wenliang, LIU Huanhuan, XUE Zhiwei, WANG Yanzhao
    2020, 38 (5):  600-605.  DOI: 10.3724/SP.J.1123.2019.07033
    Abstract ( 101 )   HTML ( 6 )   PDF (1353KB) ( 34 )  

    Quantitative structure-activity relationship models on the gas chromatographic retention index of the 38 volatile fragrance compounds of Liliumspp were investigated and established by comparative molecular field analysis (CoMFA) and comparative molecular similarity index (CoMSIA) methods. The robustness and predictive performance of the developed models were assessed using external test set validation and leave-one-out cross validation. Further, the effects of the molecular structure on the gas chromatographic retention indices of these compounds were intuitively studied in light of the three-dimensional contour maps of molecular fields provided by the developed CoMSIA and CoMFA models. The validation results demonstrated that both the models could accurately predict the retention indices of the investigated components. The influence of the molecular structure on the retention indices could be reasonably explained by these models. Moreover, the prediction accuracy of the CoMSIA model was slightly higher than that of the CoMFA model. Obviously, the proposed CoMSIA model is more promising for the analysis of the volatile fragrance compounds of Lilium spp.

    Determination of impurity components in the perfluoroisobutyrile based on home-made gas-circulating system
    LIU Jing, HUANG Qingdan, WANG Yong, ZENG Lian, ZHANG Yaru
    2020, 38 (5):  606-610.  DOI: 10.3724/SP.J.1123.2019.10014
    Abstract ( 68 )   HTML ( 10 )   PDF (976KB) ( 33 )  

    A method for the determination of impurity components in perfluoroisobutyrile (C4F7N) gas was established by setting up a sealed pipe gas composition test system comprising an automatic six-way valve and gas chromatography-tandem mass spectrometry (GC-MS) apparatus. C4F7N commercial gases were purchased from an abroad company (AC company) and a domestic Chinese company (DC company). These gases were subjected to qualitative and quantitative analyses by our test system and separated on an Agilent GS-GASPRO column (30 m×0.32 mm×5 μm). The results showed that the C4F7N commercial gas contained N2, O2, C3HF7 and a trace amount of C3F6. In the C4F7N commercial gas from the AC company, the total amount of impurities was 0.13%, and the C4F7N content was 99.87%. In the C4F7N gas from DC Company, the total amount of impurities was 0.83%, and the C4F7N content was 99.17%. The C4F7N contents of the gases from both the companies were consistent with the claimed value (≥ 99%). The determination of the impurities C4F7N can be beneficial for the subsequent study of its insulation performance and thermal stability.

    Determination of carbendazim residues in Procambarus clarkii by high performance liquid chromatography-triple quadrupole mass spectrometry
    LI Yameng, GAN Jinhua, LI Jincheng, WU Lidong, LI Qin, XIAO Yushi, PENG Jie, CHEN Jianwu, LIU Huan
    2020, 38 (5):  611-616.  DOI: 10.3724/SP.J.1123.2019.10009
    Abstract ( 73 )   HTML ( 12 )   PDF (959KB) ( 51 )  

    A novel method based on high performance liquid chromatography-triple quadrupole mass spectrometry (HPLC-MS/MS) was established for the determination of carbendazim in Procambarus clarkii. The sample was extracted by ethyl acetate under alkaline conditions and centrifuged. The supernatant was concentrated by rotary evaporation, redissolved, and then enriched and purified on a mixed-mode cation exchange solid phase extraction column (MCX). A C18 column was used with acetonitrile and water as mobile phases in a gradient elution. Ionization was performed using an electrospray positive ion source (ESI+), and detection was achieved by MS/MS in multiple reaction monitoring (MRM) mode. The linearity for carbendazim was good in the range of 0.5-50.0 μg/L; the linear equation was y=0.19988x+0.01842; and the correlation coefficient (r2) was 0.9985. The limit of detection (LOD) and limit of quantification (LOQ) were 0.25 μg/kg and 0.50 μg/kg, respectively. At spiked levels of 0.5, 1.0, 5.0, and 50.0 μg/kg, the recoveries ranged from 83.9% to 105.5%, and the relative standard deviation ranged from 1.1% to 3.2%. This method is simple and effective for the determination of carbendazim residues in P. clarkii.