高精度定量毛细管电泳法同时测定复合维生素B片中B_1、B_2、B_6、烟酰胺及泛酸钙
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  • 英文篇名:Simultaneous determination of vitamins B_1, B_2, B_6, niacinamide and calcium pantothenate in compound vitamin B tablets by high performance quantitative capillary electrophoresis
  • 作者:胡雯雯 ; 陶建伟 ; 王庆伟 ; 李静 ; 阎超 ; 许旭
  • 英文作者:HU Wenwen;TAO Jianwei;WANG Qingwei;LI Jing;YAN Chao;XU Xu;School of Chemical and Environmental Engineering, Shanghai Institute of Technology;Unimicro Technologies,Inc.;Pharmacy School, Shanghai Jiaotong University;
  • 关键词:毛细管电泳 ; 复合维生素B片 ; 含量测定
  • 英文关键词:capillary electrophoresis(CE);;compound vitamin B tablets;;content determination
  • 中文刊名:SPZZ
  • 英文刊名:Chinese Journal of Chromatography
  • 机构:上海应用技术大学化学与环境工程学院;上海通微分析技术有限公司;上海交通大学药学院;
  • 出版日期:2019-06-08
  • 出版单位:色谱
  • 年:2019
  • 期:v.37
  • 语种:中文;
  • 页:SPZZ201906013
  • 页数:5
  • CN:06
  • ISSN:21-1185/O6
  • 分类号:103-107
摘要
建立了高精度定量毛细管电泳法同时测定复合维生素B片中维生素B_1、B_2、B_6、烟酰胺和泛酸钙的方法。样品经乙腈-水(20∶80, v/v)超声提取后,采用全自动高精度定量毛细管电泳仪,以高精度进样阀定量进样,以40 mmol/L硼砂-硼酸缓冲液(pH 9.0)为背景电解质溶液,以工作电压为-10 kV电泳分离。维生素B_1、B_2、B_6、烟酰胺的检测波长为280 nm,然后切换至检测波长210 nm检测泛酸钙。结果表明,各组分之间均得到良好分离,峰面积日内重复性(RSD)为1.3%~1.9%,显著优于普通毛细管电泳。维生素B_1、B_2、B_6、烟酰胺及泛酸钙的浓度在各自线性范围内的相关系数(r)为0.996 8~0.999 8,检出限2.5~36.0 mg/L,平均回收率为94.1%~98.9%。该法准确可靠,可用于实际复合维生素B片中维生素B_1、B_2、B_6、烟酰胺和泛酸钙含量的同时测定。
        A high performance quantitative capillary electrophoresis method was developed for the simultaneous determination of vitamins B_1, B_2, B_6, nicotinamide, and calcium pantothenate in vitamin B tablets using a quantitative capillary electrophoresis instrument. The samples were extracted ultrasonically with acetonitrile-water(20∶80, v/v). The automatic high precision quantitative capillary electrophoresis instrument was used to realize quantitative injection through a 10 nL injection valve. The background electrolyte was selected as 40 mmol/L sodium borate buffer(pH 9.0), which was continuously supplied by a microfluidic injection pump. The working voltage was-10 kV. The detection wavelength of vitamins B_1, B_2, B_6, and nicotinamide was selected as 280 nm, which was then changed to 210 nm to detect calcium pantothenate. The result showed good linearities between the peak area and the concentration of vitamins B_1, B_2, B_6, nicotinamide, and calcium pantothenate in the correlation coefficients(r) range of 0.996 8-0.999 8. The limits of detection(LODs) were in the range of 2.5-36.0 mg/L. The average recoveries were 94.1%-98.9% with relative standard deviations(RSDs) as 1.3%-1.9%. The method is precise, reliable, and suitable for the simultaneous determination of vitamins B_1, B_2, B_6, nicotinamide, and calcium pantothenate in a real compound vitamin B tablet.
引文
[1] Chinese Pharmacopeia Commission.Drug Standard of Ministry of Public Health,Chemical Medicines and Preparations,Vol.1.Beijing:Chinese Pharmacopeia Commission,1989 中华人民共和国卫生部药典委员会.中华人民共和国卫生部药品标准,化学药品及制剂第一册.北京:中华人民共和国卫生部药典委员会,1989
    [2] Chen J Q,Wang J,He L H.Chinese Journal of Pharmaceutical Analysis,2012,32(6):1090 陈金泉,王军,何立环.药物分析杂志,2012,32(6):1090
    [3] Lu G R,Wang G Z.Journal of China Pharmaceutical University,1995,26(3):177 陆帼蓉,王桂珍.中国药科大学学报,1995,26(3):177
    [4] Wu F,Xu H Y.China Medical Herald,2007,4(31):95 吴芳,徐红艳.中国医药导报,2007,4(31):95
    [5] Zhang Y Y,Ding D Z.Journal of Pharmaceutical Research,2017,36(6):327 张媛媛,丁大中.药学研究,2017,36(6):327
    [6] Chen G L,Li Y L,Liu M,et al.Chinese Journal of Hospital Pharmacy,2006,26(10):1256 陈光龙,李玉兰,刘敏,等.中国医院药学杂志,2006,26(10):1256
    [7] Liu X L,Wu G,Zhong H B.Chinese Pharmaceutical Affairs,2003,17(4):241 刘晓琳,武谷,钟淮滨.中国药事,2003,17(4):241
    [8] Wu H X.Zheng A N,Su C Y,et al.Chinese Journal of chromatography,2017,35(4):439 吴宏星,郑艾妮,苏草茵,等.色谱,2017,35(4):439
    [9] Xu S,Xu W F,Jin P F,et al.China Pharmacist,2018,21(1):177 徐硕,徐文峰,金鹏飞,等.中国药师,2018,21(1):177
    [10] Guo Q S,Liu M K,Yu S,et al.Chinese Journal of Magnetic Resonance,2016,33(3):442 郭强胜,刘明珂,禹珊,等.波谱学杂志,2016,33(3):442
    [11] Eiff J,Monakhova Y B,Diehl B W K.J Agric Food Chem 2015,63(12):3135
    [12] Sim H,Kim B,Lee J.J AOAC Int,2016,99(5):1223
    [13] Chen P,Atkinson R,Wolf W R.J AOAC Int,2009,92(2):680
    [14] Huopalahti R,Sunell J.J Chromatogr A,1993,636:133
    [15] Boonkerd S,Detaevernier M R,Michotte Y.J Chromatogr A,1994,670:209
    [16] Pan Z W,Li Y Q,Chen Y L,et al.Chinese Journal of Chromatography,2007,25(4):594 潘仲巍,李玉琴,陈永雷,等.色谱,2007,25(4):594
    [17] Si X Y,Tan H R,Shi T T,et al.Chinese Agricultural Science Bulletin,2008,124(6):112 司雄元,檀华蓉,施婷婷,等.中国农学通报,2008,124(6):112
    [18] Ling B Z,Xu Y,Yao D,et al.Chromatographia,2015,78(7/8):543
    [19] Xu Y,Ling B Z,Zhu W J,et al.Biomed Chromatogr,2016,30(3):390
    [20] Han X M,Zu S C.Chinese Pharmaceutical Affairs,2012,26(8):891 韩秀梅,祖述春.中国药事,2012,26(8):891
    [21] Xiao H,Yan K,Zheng Y T,et al.Chinese Journal of chromatography,2018,36(4):381 肖汉,Yan Kevin,郑怡婷,等.色谱,2018,36(4):381