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List of Issues

    Chinese Journal of Chromatography
    2017, Vol. 35, No. 1
    Online: 08 January 2017

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    Articles
    Tetrabromobisphenol A bis(2-hydroxyethyl ether) induced dysfunction of the respiratory chain oxidative phosphorylation and energy metabolism in rat pheochromocytoma cells by high performance liquid chromatography-electrospray ionization-tandem mass spectrometry
    LIU Qian, HU Ligang, ZHOU Qunfang, JIANG Guibin
    2017, 35 (1):  1-7.  DOI: 10.3724/SP.J.1123.2016.09001
    Abstract ( 701 )   [Full Text(HTML)] () PDF (2056KB) ( 139 )  

    Toxicological effects of tetrabromobisphenol A (TBBPA) derivatives are highly concerned due to their increasing usages in diverse fields. It has been reported that tetrabromobisphenol A bis(2-hydroxyethyl ether) (TBBPA-BHEE), a representative of TBBPA derivatives, can induce cellular toxicity on rat pheochromocytoma cells (PC12) through reactive oxygen species mediated caspase activation. Nevertheless, underlying molecular mechanisms of intracellular reactive oxygen species (ROS) formation and effects of TBBPA-BHEE on PC12 energy metabolism remain unclear. This study developed the method for quantification of ATP, ADP, AMP and cAMP (cyclic AMP) simultaneously in PC12 with HPLC-ESI-MS/MS. The disturbance of TBBPA-BHEE on the respiratory chain oxidative phosphorylation and energy metabolism in PC12 cells was investigated via evaluation of the four compounds. It was shown that the ratio of ADP to ATP (ADP/ATP) decreased in PC12 cells after TBBPA-BHEE stimulation, implying that TBBPA-BHEE accelerated the process of respiratory chain oxidative phosphorylation in PC12 mitochondria. In addition, the concentrations of cAMP and the ratio of AMP to ATP (AMP/ATP) decreased in PC12 cells upon TBBPA-BHEE treatment, which suggested that TBBPA-BHEE potentially induced the mitochondrial dysfunction and led to the consequent energy metabolism imbalance in PC12. The results not only provided insight in the toxicological effects of TBBPA-BHEE, but also confirmed that HPLC-ESI-MS/MS was a powerful tool for studies on the cellular respiratory chain oxidative phosphorylation and energy metabolism.

    Rapid analysis of complex samples using overlapping gas chromatography-mass spectrometry signals based on high-throughput approach
    LI Pao, CAI Wensheng, SHAO Xueguang
    2017, 35 (1):  8-13.  DOI: 10.3724/SP.J.1123.2016.06046
    Abstract ( 551 )   [Full Text(HTML)] () PDF (853KB) ( 95 )  

    Chemometric methods have been proved to be a powerful tool for the resolution of overlapping signals. However, a short elution region containing the signals of the target components must be determined prior to the calculation. It is difficult to achieve the high-throughput analysis for the gas chromatography-mass spectrometry (GC-MS) signals with long elution time. An approach based on moving window target transformation factor analysis (MWTTFA) and non-negative immune algorithm (NNIA) was developed for the resolution of multicomponent overlapping GC-MS signals. In the method, a rapid temperature program was used to make the analytes within a short retention time period, and then the chromatographic and mass spectral information of the components in the overlapping signals was calculated with the developed algorithm. In the calculation, MWTTFA was employed for testing the existence of a specific analyte in the signals, and the chromatographic information was extracted by NNIA. A mixture of 17 and 42 pesticide standard solutions were tested in full-scan mode within 10 min. The results showed that both the chromatographic and the mass spectra information of the components was extracted from the overlapping signals.

    Determination of four alkaloids in cell culture fluids by pipette tip solid phase microextraction-high performance liquid chromatography
    WANG Nani, SHOU Dan, WANG Xuping, ZHU Yan
    2017, 35 (1):  14-19.  DOI: 10.3724/SP.J.1123.2016.08001
    Abstract ( 512 )   [Full Text(HTML)] () PDF (3477KB) ( 109 )  

    A method for the determination of four alkaloids (phellodendrine, jatrorrhizine, palmatine, berberine) in cell culture fluids was developed by pipette tip solid phase microextraction (SPME) and high performance liquid chromatography (HPLC). A weak cation exchange monolithic stationary phase was prepared by in-situ polymerization in a pipette tip. Methacrylate acid, ethylene dimethacrylate and azodiisobutyronitrile were the functional monomer, the cross-linker and the initiator, respectively. The samples were cleaned-up using the microextraction tips. Phellodendrine, jatrorrhizine, palmatine and berberine were extracted from cell culture fluids. The analytes were separated on a reversed-phase Diamonsil C18 column (150 mm×4.6 mm, 5 μm) and eluted gradiently with acetonitrile and 0.05 mol/L potassium dihydrogen phosphate solution. The detection wavelength was 270 nm. The extraction performance was investigated by varying the elution solution types, the extraction and elution time and the molar ratios among monomers, cross-linkers and porogens. The analytes were quantified using external standard method. The established method was successfully applied for the pretreatment and determination of four alkaloids from Cortex Phellodendri in cell culture fluids. Under the optimal conditions, the limits of detection (S/N=3) for the analytes were 0.16-0.39 μg/L. The recoveries were in the range of 92.73%-97.91% and the relative standard deviations (RSDs) were ranged from 0.14% to 3.31% (n=6). The method is simple, sensitive and accurate. It can be used in the determination of alkaloids in cell culture fluids.

    Analysis of trace estrogens in toners by monolithic column online solid phase microextraction coupled with high performance liquid chromatography
    SONG Wenwen, LUO Xialin, LI Gongke, HU Yufei
    2017, 35 (1):  20-26.  DOI: 10.3724/SP.J.1123.2016.08012
    Abstract ( 493 )   [Full Text(HTML)] () PDF (5319KB) ( 120 )  

    A Poly(glycidyl methacrylate-co-ethyleneglycol dimethacrylate) (Poly(GMA-co-EDMA)) monolithic column was prepared in a capillary by in-situ polymerization. Glycidyl methacrylate (GMA) was chosen to be the monomer and ethyleneglycol dimethacrylate (EDMA) was utilized as crosslinking agent. The binary porogenic agents of methanol and n-hexane can develop the permeability of monolithic column and they were suitable to construct the online analysis apparatus. A series of experiments were carried out, and they demonstrated the monolithic column had good permeability with low column pressure (1.5×106 Pa at the washing flow rate of 0.5 mL/min). The enrichment factors of the prepared monolithic column for estradiol, ethynyl estradiol, estrone and diethylstilbestrol were 86, 116, 77 and 86, respectively. It was proved that the monolithic column was suitable for the online microextraction system by using the interface unit. A method was established for the analysis of trace estradiol, ethynyl estradiol, estrone and diethylstilbestrol in toners by monolithic column online solid phase microextraction coupled with high performance liquid chromatography. The limits of detection (S/N=3) were 0.05-0.20 μg/L. The recoveries in toner samples varied from 69.3% to 111.3%, and relative standard deviations were less than 5.0%. The method is efficient, sensitive, accurate, reliable and applicable to analyze trace estrogens in toners.

    Determination of oleanolic acid and ursolic acid in loquat leaf extract by chemical derivatization coupled with liquid chromatography-tandem mass spectrometry
    LUO Dan, FENG Yuqi, YAO Jinting, SUN Youbao, HUANG Taohong, HASHI Yuki
    2017, 35 (1):  27-31.  DOI: 10.3724/SP.J.1123.2016.08015
    Abstract ( 889 )   [Full Text(HTML)] () PDF (828KB) ( 148 )  

    A method for the determination of oleanolic acid (OA) and ursolic acid (UA) by liquid chromatography-tandem mass spectrometry (LC-MS/MS) was developed. By using derivatization reagents, N,N-dimethylethylenediamine (DMED) and d4-N,N-dimethylethylenediamine (d4-DMED), OA and UA in real samples and standard samples were derivatized separately. The derivative products of the standard samples were used as stable isotope internal standards, and accurately added to the samples and standard working solutions. Good linearities were obtained in the concentration range of 0.01-10 μ g/L with correlation coefficients (r2) greater than 0.99. The limits of detection of OA and UA were 0.92 ng/L and 1.06 ng/L, and the recoveries were between 98.7%-102.7% and 97.2%-105.0%, respectively. The method can be used for the detection of OA and UA in loquat leaf extract with high sensitivity.

    Holistic analysis of Liuwei Dihuang pills using ultrasonic cell grinder extraction and ultra-performance liquid chromatography
    ZHAO Tangjuan, CHEN Juan, SHI Yanping
    2017, 35 (1):  32-46.  DOI: 10.3724/SP.J.1123.2016.08025
    Abstract ( 440 )   [Full Text(HTML)] () PDF (9846KB) ( 71 )  

    An efficient holistic analysis strategy was developed and validated for quality control of the traditional Chinese medicine (TCM) preparation, Liuwei Dihuang pills (LWDHPs). In this strategy, eight bioactive components, i. e. allantoin, morroniside, loganin, peoniflorin, acteoside, paeonol, alisol B 23-acetate and pachymic acid from the six medicinal herbs composing LWDHPs were selected as the evaluation markers, and then they were simultaneously extracted by an ultrasonic cell grinder extraction (UCGE) method and separated in a single run by an ultra-performance liquid chromatographic method coupled with photodiode array detection (UPLC-PDA). Response surface methodology (RSM), a multivariate experimental design technique, was used to optimize the UCGE parameters based on Box-Behnken design (BBD) model. The optimum extraction conditions were obtained at a ratio of solvent to solid 45 mL/g, extraction time of 40 min and extraction temperature of 20℃. Under such conditions, the higher yields of the eight analytes were acquired compared with the traditional extraction methods, indicating that UCGE was a fast, easy and efficient method for extracting bioactive constituents from LWDHPs. Chromatographic separation was achieved on an HSS T3 column (50 mm×2.1 mm, 1.8 μm) using a linear gradient elution of acetonitrile and water. Because of the different UV characteristics of these components, five detection wavelengths were used for quantitative analysis. The proposed method was validated through linearity, limits of detection, limits of quantification, precision, stability, repeatability, and accuracy. The validated method was applied to analyze LWDHPs, which provided a reference for the quality evaluation of LWDHPs.

    Investigation of aromatic impurities in liquefied petroleum gas by solid-phase extraction sampling coupled with gas chromatography-mass spectrometry
    LI Hai-Fang, GAO Cuihua, LIN Jin-Ming
    2017, 35 (1):  47-53.  DOI: 10.3724/SP.J.1123.2016.08026
    Abstract ( 516 )   [Full Text(HTML)] () PDF (1203KB) ( 83 )  

    A dynamic solid-phase extraction system for sampling and synchronous preconcentration of aromatic impurities from liquefied petroleum gas (LPG) with graphitized carbon black (GCB) sorbents was constructed. The target aromatics (benzene, toluene, xylenes, styrene and naphthalene) were rapidly collected from LPG flow and analyzed with gas chromatography-mass spectrometry. Compared with C18 and poly (styrene-divinylbenzene) copolymer sorbents, the tandem packed GCB cartridges presented the highest extraction efficiency for capturing aromatics from LPG. The sampling efficiency, reproducibility and storage stability of aromatics on the adsorption GCB cartridge were evaluated. The quantification curves of eight aromatics in nitrogen simulative gas flow were linear in the range of 15-1000 μ g/m3. The developed sampling method presented good advantages of high recoveries (92.9%-109.0%), low method detection limits (1.0-6.2 μg/m3), together with excellent precision (relative standard deviations:0.6%-5.8%) and accuracy (relative errors:0.8%-8.2%), respectively.

    Quantification of intracellular adenosine 5'-triphosphate and its metabolites by high performance liquid chromatography analysis
    ZHU Huiyu, WU Danni, WANG Hailin
    2017, 35 (1):  54-58.  DOI: 10.3724/SP.J.1123.2016.08031
    Abstract ( 928 )   [Full Text(HTML)] () PDF (800KB) ( 253 )  

    This study was aimed to provide insight regarding the intracellular metabolites of adenosine 5'-triphosphate (ATP) and whether 2-tert-butyl-1,4-benzoquinone (TBBQ) affects cell metabolites. A rapid high performance liquid chromatography (HPLC) protocol was developed for the separation and quantitation of ATP and its metabolites (adenosine diphosphate (ADP) and adenosine monophosphate (AMP)) in cells. Chromatographic separation was performed using a Shimadzu HPLC system equipped with an Agela Venusil MP C18 column; isocratic elution was adopted. The mobile phase comprised solvent A (50 mmol/L disodium hydrogen phosphate and 15 mmol/L trimethylamine (TEA); pH adjusted to 7.88 using acetic acid (HAc)) and solvent B (methanol). The correlation coefficients of the three analytes were very high (R2≥0.9996), and the contents of the three metabolites in the MRC-5 cells were within the linear ranges (0.1-100 μ mol/L). The limits of detection for the detected three compounds were low. Samples were extracted from cells (after exposure and non-exposure to quinones) using 80% (v/v) methanol aqueous solution. The method developed in this study was successfully applied to detect ATP, ADP and AMP in MRC-5 cells, and the results demonstrated that ATP, ADP, AMP levels in cells were affected by TBBQ, but the relations between the concentration of TBBQ and the level of ATP, ADP and AMP were complex.

    Determination of anions in low molecular weight heparin by capillary electrophoresis with phthalate as the background electrolyte
    ZHANG Mingyu, KANG Jingwu
    2017, 35 (1):  59-64.  DOI: 10.3724/SP.J.1123.2016.08034
    Abstract ( 438 )   [Full Text(HTML)] () PDF (860KB) ( 58 )  

    The sulfate ester groups of low molecular weight heparins (LMWHs) are labile and easily hydrolyzed to produce free sulfate ions during the process of manufacture and storage. In addition, other anions such as chloride and acetylate are often introduced in the products. For monitoring the stability of the products, ion chromatography is the commonly used technique for determining the free anions in LMWHs. However, the column and the suppressor of ion chromatography are easily contaminated by LMWHs due to their relatively large molecules. Therefore, we developed a capillary electrophoresis (CE) method with indirect ultraviolet (UV) detection for determining the free anions in LMWHs, including sulfate, chloride, fluoride, phosphate and acetate. Unlike the commonly used anion separation CE method which uses chromate as the background absorption electrolyte, phthalate was used as the probe anion because its electrophoretic mobility matches better to all of the anions than chromate so that more narrow peaks could be obtained. Moreover, the molar absorptivity of phthalate at 230 nm (4754 L/(mol·cm)) was higher than that of chromate at 254 nm (2400 L/(mol·cm)). The combination of the narrow peak shape with the high molar absorptivity of the probe ion improves the detection sensitivity nearly to the lever of ion chromatography. Effects of various CE parameters on the separation of the anions were investigated and optimized. The method displayed excellent linearity in the concentration range from 0.002 to 1 mmol/L. The relative standard deviations (RSDs) for intraday (n=6) and interday (n=3) repeatabilities in terms of migration times and peak areas were all less than 3%. The limits of detection (S/N=3) and limits of quantitation (S/N=10) were determined as 0.4-0.8 μmol/L and 2-4 μmol/L for the above anions, respectively. The method was successfully applied for the stability monitoring of LMWHs.

    Rapid determination of micro gibberellins by non-aqueous capillary electrophoresis with reversed electroosmotic flow
    GUO Zhenpeng, WANG Xiaoyu, CHEN Yi
    2017, 35 (1):  65-69.  DOI: 10.3724/SP.J.1123.2016.08042
    Abstract ( 400 )   [Full Text(HTML)] () PDF (822KB) ( 60 )  

    A non-aqueous capillary electrophoresis (NACE) method for the rapid determination of micro gibberellins (GAs) was established. Dynamically poly(ethylene oxide) coated capillary was used, and electroosmotic flow (EOF) was reversed by using positive ions and adjusted by regulation the types and concentrations of the positive ions, running buffer, and pH of the buffer. With a buffer of 95% (v/v) methanol containing 10 mmol/L ammonium acetate at an acidity of 0.08% (v/v) acetic acid, the EOF was successfully reversed to separate the eight GAs in less than 10 min. Its applicability was validated by the determination of GAs in germinating wheat seeds, with relative standard deviations (RSDs)≤2.1% (intra-day) or ≤4.3% (inter-day) for migration times, and RSDs≤4.5% (intra-day) or≤6.9% (inter-day) for peak areas. The limits of detection (S/N=3) were in the range of 1.10-2.20 mg/L, with correlation coefficients (r2) of 0.9982-0.9993. The recoveries of the spiked samples were between 87.2% and 93.5%. The established method is simple, rapid, stable, and compatible with mass spectrometry, so it is valuable to be further studied.

    Purification and preparation of silybin and isosilybin by solid phase extraction
    ZHAO Xiaoshu, ZHANG Nazhen, LIU Min, DENG Fumei, WU Minghuo
    2017, 35 (1):  70-74.  DOI: 10.3724/SP.J.1123.2016.08046
    Abstract ( 557 )   [Full Text(HTML)] () PDF (830KB) ( 90 )  

    Silybin and isosilybin are mainly effective elements of silymarin. To improve the performance of treatment and decrease the side effects from the unknown components, purified silybin and isosilybin are in request. The main purpose of this research was to develop a solid phase extraction (SPE) method for the purification of silybin and isosilybin from silymarin extract. For the analysis of the samples, a liquid chromatography method with ultraviolet detector (LC-UV) was developed to separate the silybin and isosilybin from their impurities. The separation was achieved in 8 min and a total analytical time of 11 min with column washing and equilibration. In the SPE, three different SPE packings were tested, including hydrophilic-lipophilic balance (HLB), hydrophilic interaction chromatography (HILIC) and reverse phase C18 silica microspheres. Based on the selectivity against silybin and isosilybin, the C18 packings were chosen. After the optimization of the elution of SPE, the purity over 94% could be achieved for the silybin and isosilybin mixture with the recoveries of 70.5%-81.7% and 66.7%-81.8%, and the relative standard deviations (RSDs) of 2.7%-9.4% and 1.5%-6.1%, respectively. Though silybin and isosilybin could not be separated from each other by using SPE, this is a useful method for the purification of silybin and isosilybin mixture from the crude extract of their plant seeds due to its simplicity and efficiency.

    High-throughput method for cell phenotype analysis by gas chromatography coupled with mass spectrometry
    WANG Xiyue, GAO Peng, LIAN Lili, LOU Dawei, XU Guowang
    2017, 35 (1):  75-79.  DOI: 10.3724/SP.J.1123.2016.10004
    Abstract ( 457 )   [Full Text(HTML)] () PDF (1900KB) ( 83 )  

    A high-throughput method for cell phenotype analysis was developed based on 96-well plate culture and gas chromatography coupled with mass spectrometry (GC-MS). Forty-eight metabolites were selected as the sole energy for wild-type and its yfcC mutation E. coli (yfcC over-expression and yfcC deletion mutants) culture. The high-throughput phenotype analysis was achieved by investigating the catabolism difference of these metabolites among the three strains by GC-MS. The results showed that there were 14 metabolites changed significantly between wild-type and yfcC over-expression mutant E. coli. The metabolism ability of yfcC over-expression mutant E. coli for glycine and citric acid was much stronger than wild-type E. coli. For other metabolites, the wild-type strain showed stronger capabilities in metabolism. Among the 16 metabolites metabolized differentially between wild-type E. coli and its yfcC deletion mutant, metabolism ability of alanine, lactose, myo-inositol and citric acid in yfcC deletion mutant was much stronger. Other metabolites displayed the opposite results. Among the results acquired, we speculated that the faster metabolism of glycine in yfcC over-expression mutant E. coli might be caused by its promoted glyoxylate shunt. This high-throughput method for cell phenotype analysis was simple and efficient. It could provide more useful information about metabolism for gene study with unknown function.

    Communications
    Untargeted screening of acylcarnitines in urine by ultra-high performance liquid chromatography coupled with triple quadrupole mass spectrometry
    LI Shangfu, XIANG Li, CAI Zongwei
    2017, 35 (1):  80-85.  DOI: 10.3724/SP.J.1123.2016.09008
    Abstract ( 599 )   [Full Text(HTML)] () PDF (876KB) ( 132 )  

    A parent ion scan driven untargeted method was developed for the determination of acylcarnitines in the urine samples by ultra-high performance liquid chromatography coupled with triple quadrupole mass spectrometry (UHPLC-QqQ MS). The acylcarnitines were extracted with methanol and 1% (v/v) formic acid aqueous solution. After pretreatment, the samples were analyzed without derivatization. The data were acquired by scanning parent ions of three common fragment ions of acylcarnitines, which were m/z 60, 85 and 144. The three obtained chromatograms and their corresponding mass spectra were compared with the recognized acylcarnitine signals. Each parent ion that presented in all the three mass spectra was selected. The chromatograms of these ions were extracted. The generated peaks that had the same retention times in the three chromatograms were considered as candidate acylcarnitines. The structures of these candidates were identified by high resolution MS and MS/MS combined with searching against databases. Authentic standards were employed to confirm the results if they were available. A total of 37 acylcarnitines were identified in the urine samples by the method, including nine short-, 26 medium- and two long-chain acylcarnitines. A number of 14 acylcarnitines of them were unknown compounds which had not been included in the databases. This method could be extended to detect other biological samples, such as blood and tissues, for qualitative or quantitative analysis of acylcarnitines.

    Reviews
    Lipidomics and its analytical methods
    LIU Huwei, BAI Yu
    2017, 35 (1):  86-90.  DOI: 10.3724/SP.J.1123.2016.08006
    Abstract ( 693 )   [Full Text(HTML)] () PDF (1020KB) ( 373 )  

    Lipidomics is a very important research area in life science, which has showed close relationship with diseases and health. Since its introduction in 2003, lipidomics has become one of the hot topics in metabolomics, attracting great attention from scientific community. In this article, after brief introduction of lipidomics, different analytical methods are reviewed, including sample preparation, profiling analysis, targeted analysis, imaging analysis and data processing. The perspective in this area was also discussed.

    Recent developments in comprehensive two-dimensional gas chromatography for the analysis of persistent organic pollutants
    XIA Dan, GAO Lirong, ZHENG Minghui
    2017, 35 (1):  91-98.  DOI: 10.3724/SP.J.1123.2016.08029
    Abstract ( 729 )   [Full Text(HTML)] () PDF (1123KB) ( 192 )  

    The analysis of persistent organic pollutants (POPs) is relatively difficult because they are typical complex contaminants and present at trace levels. Many POP congeners cannot be effectively separated and analyzed by conventional one-dimensional gas chromatography (1D GC). Comprehensive two-dimensional gas chromatography (GC×GC) becomes a powerful separation technique for analyzing complex mixtures, with its higher peak capacity, higher resolution and sensitivity compared with 1D GC. This review summarizes the GC×GC applications in the analysis of POPs in the past decade, including the advance of GC×GC in solving the separation problems of some POPs such as polychlorinated dibenzo-p-dioxins, dibenzofurans, toxaphene, chlorinated parrafins, etc. The simultaneous analysis of multi-class organic pollutants and untargeted analysis of organic pollutants using GC×GC is also reviewed. The future trends of GC×GC in this field are also discussed.

    Research progress of aptamer application in solid phase extraction technique
    WANG Weiwei, LIU Suqin, XUE Yun, WANG Yan, YAN Chao
    2017, 35 (1):  99-104.  DOI: 10.3724/SP.J.1123.2016.08033
    Abstract ( 568 )   [Full Text(HTML)] () PDF (828KB) ( 192 )  

    Aptamers are short single-stranded oligonucleotides within randomly synthesized nucleic acid libraries by a systematic evolution of ligands by exponential enrichment. Because of specific identification for target molecule, solid phase extraction technique based on aptamers exhibits great potential for extraction, separation, purification and enrichment of trace-target analytes from complex samples, and it attracts more and more attention. This article brings a comprehensive survey of recent developments of solid phase extraction techniques based on aptamers, including the preparation of aptamer-based sorbents, the solid phase extraction procedure and the applications of aptamer-based solid phase extraction. Limits and prospects for aptamer-based solid phase extraction are also discussed.

    Latest developments of single cell analysis
    SHI Meng, SONG Zhihua, GENG Xuhui, WU Dapeng, GUAN Yafeng
    2017, 35 (1):  105-109.  DOI: 10.3724/SP.J.1123.2016.08039
    Abstract ( 454 )   [Full Text(HTML)] () PDF (792KB) ( 181 )  

    Single cell analysis can reveal the cellular components and physiological behavior diversity. It is on the cutting-edge of bio-analytical chemistry. Challenges on detection limit, resolution, and precise manipulation of cells are really tougher than ever before. This review includes the developments of several main techniques about separation, detection and imaging. At last, the future developments in separation and detection are discussed.

    Recent advances in capillary electrophoresis coupled with chemiluminescence detection
    YI Fang, HUANG Xiangyi, REN Jicun
    2017, 35 (1):  110-120.  DOI: 10.3724/SP.J.1123.2016.08043
    Abstract ( 595 )   [Full Text(HTML)] () PDF (2215KB) ( 81 )  

    Capillary electrophoresis (CE) is considered as a powerful method in many fields, such as biopharmaceuticals, environmental, food and public security analysis, owing to its high separation efficiency. However, the injection of small sample volumes and the short optical length lead to limited sensitivity. So it is necessary to couple with high sensitivity detector to realize the low concentration sample analysis. Chemiluminescence (CL) detection is characterized by providing low background with excellent sensitivity. By coupling with CL, both the high separation efficiency of CE and the high sensitivity of CL can be achieved at the same time. So far, this method has been widely applied to chemical analysis, drug screening, and environment monitoring. In this review, we briefly introduce some developments for CE-CL systems, and then put the emphasis on the applications in the past decades. Moreover, we discuss the perspectives of CE-CL system.

    Application progress of on-line two-dimensional liquid-chromatography in the analysis of traditional Chinese medicines
    GAO Wen, SONG Huipeng, YANG Hua, LI Ping
    2017, 35 (1):  121-128.  DOI: 10.3724/SP.J.1123.2016.08045
    Abstract ( 624 )   [Full Text(HTML)] () PDF (2613KB) ( 230 )  

    Traditional Chinese medicine (TCM) is a complex system, containing hundreds of components. The chemical profiling of TCMs is an important task and still facing great challenges. In recent years, the on-line two-dimensional liquid-chromatography (2D-LC) methods, emerging and powerful separation techniques, offer new possibilities for the global analysis of complex TCM samples. Recent advances of 2D-LC, including heart-cutting two-dimensional liquid-chromatography (heart-cutting LC-LC) and comprehensive two-dimensional liquid-chromatography (comprehensive LC×LC), applied to TCMs analysis are reviewed. Design and application of 2D-LC combined with turbulent flow chromatography (TFC) or cell membrane chromatography (CMC) applied for TCM bioactive components screening are described.

    Application advances of microfluidic chips for sorting circulating tumor cells in clinical samples
    BAO James Jianmin, WANG Dandan, LI Youxin
    2017, 35 (1):  129-137.  DOI: 10.3724/SP.J.1123.2016.09005
    Abstract ( 597 )   [Full Text(HTML)] () PDF (2651KB) ( 145 )  

    Cancer is becoming a common disease threatening seriously to the human health. Circulating tumor cells (CTCs) is a kind of cancer cells released from tumors and circulates with bloodstream. It is gradually discovered of the potential value of CTCs in diagnosis of cancer in initial stage, individual treatment and research of metastasis mechanism. However, it is a very challenge task for sorting the extremely few CTCs in blood. Microfluidic chip, a miniaturized, high-throughput and integrated platform, shows the unique advantages in the study of CTCs. With the progress of the research, the technology is no longer limited to the development of sorting method based on model samples, but scientists pay more attention to the analysis of clinical samples. To the best of our knowledge, there has been no paper summing up the progress of microfluidic chip techniques applied to the analysis of clinical samples recently. This review focuses on those microfluidic techniques that have been applied to sorting CTCs from the blood of cancer patients. Meanwhile, we predict the trends of sorting CTCs in clinical samples using microfluidic chip technology.