主办:上海医药工业研究院
   中国药学会
   中国化学制药工业协会
ISSN 1001-8255   CN 31-1243/R   ZYGZEA

Archive

  • 2014 Volume 45 Issue 9
    Published: 10 September 2014
      

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  • MA Yuzhen1, WANG Weijian2
    2014, 45(9): 871-873.
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    An HPLC method was established for the determination of related substances in edrophonium chloride injection. A C18 column was used, with the mobile phase of 7.0 mg/ml tetramethylammonium bromide solution (adjusted to pH 3.0 with phosphoric acid)∶acetonitrile (80∶20) at the detection wavelength of 273 nm. The related substances could be effectively detected and separated with edrophonium chloride completely. It was linear for the related substance dimethylaminophenol in the concentration range of 0.09 - 1.5 μg/ml. Its recovery was 98.2%, with RSD of 1.76%.
  • ZHAO Qi, ZHANG Changqing, HU Haifeng*
    2014, 45(9): 873-875.
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    A pressurized capillary electrochromatography(pCEC) method was established for the determination of WF16616, an antifungal lipopeptide compound. The method was conducted with the mobile phase of acetonitrile∶6.5 mmol/L phosphate buffer (pH 5.2) (48∶52) at the flow rate of 0.08 ml/min, the detection wavelength of 212 nm,and the separation voltage of 11 kV. The calibration curve for WF16616 was linear in the concentration range of 0.06 -1.60 mg/ml. The average recovery was 101.17%, with RSD of 3.28%.
  • JIN Shumin1, WANG Hongxia2, TIAN Yulu2, WANG Huaxin1, BAI Li1*
    2014, 45(9): 876-879.
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    An LC-MS/MS method was established for the determination of nine components in San-Huang-Tang-Min decoction. A C18 column was used with the mobile phase of acetonitrile∶water (containing 2 mmol/L ammonium acetate and 0.08% formic acid) by gradient elution. Multiple reaction monitoring scanning mode was performed combined with the ion switching technology. Coptisine, berberine and astragaloside Ⅳ were detected by the positive ion
    scanning mode while protocatechuic acid, rutin, timosaponin B-Ⅱ, timosaponin A-Ⅲ, methylophiopogonanone A and methylophiopogonanone B were detected by the negative ion scanning mode. The calibration curves for the above nine compounds were linear in their corresponding injection amounts. Their average recoveries were 90.9% - 108.7%, with RSDs of 1.2% - 4.7%.
  • CHENG Zhihong, SONG Dingzhong, HOU Huimin*, YUAN Jie, HAO Wusi
    2014, 45(9): 880-882.
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    A head-space capillary GC method was established for the determination of ethyl acetate, n-hexane and six kinds of resin residues in alisol extract. A Rtx-5 column was used for the determination of ethyl acetate and n-hexane, while a Stabilwax-DB column was used for the determination of benzene, toluene, p-xylene, o-xylene, styrene,and divinylbenzene. FID detector was used with temperature programmed control using nitrogen as the carrier gas. Eight residual solvents were separated completely. The calibration curves for the above eight compounds were linear in the ranges of 2.05 - 20.5 μg, 24.88 - 734.7 μg, 0.04 - 0.80 μg, 0.05 - 0.84 μg, 0.03 - 0.85 μg, 0.04 - 0.87 μg, 0.03 - 0.91 μg and 0.09 - 0.91 μg, respectively. The recoveries of ethyl acetate and n-hexane were 112.02% and 91.65%, with RSDs less than 3.45%, while the recoveries of the others were 85.05% - 96.32%, with RSDs less than 5.20%.
  • ZHANG Qiong1,2, SHAO Lei2, ZHANG Runsheng3, LIANG Chen3, ZHANG Yurong3*
    2014, 45(9): 883-890.
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    Drugs can form a variety of metabolites in metabolic processes in vivo. These drugs themselves and/or their metabolites can be used as markers to detect drug abuse population in biological samples. Some analytical techniques such as HPLC, GC, LC-MS and GC-MS methods are used to detect different drug metabolic markers, which can identify the type and time of drug-related personnel's abuse of drugs. In this paper, the metabolic markers of morphine, cannabis,cocaine, amphetamines and ketamine in vivo were summarized. This paper also introduced the detection methods and research progress of these metabolic markers in a variety of biological samples.
  • AN Chenhong, SHANG Zhenhua*
    2014, 45(9): 891-895.
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  • ZHANG Hui, LI Minghua, QIAO Yufeng
    2014, 45(9): 896-898.
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  • LIU Guiming1, HUANG Chaofeng2, LIU Qing2
    2014, 45(9): 899-45104.
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  • WANG Xiaowen, CHEN Lei
    2014, 45(9): 45104-45107.
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  • ZHOU Bin1,2, WU Xiaoming1*
    2014, 45(9): 45113-45116.
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  • WU Linping
    2014, 45(9): 45117-45120.
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