Modulation of mobile phase composition in flow-injection/sequential-injection chromatography exploiting multisyringe flow analysis

被引:0
|
作者
Mailen Fernández
Manuel Miró
Hilda M. González
Víctor Cerdà
机构
[1] University of the Balearic Islands,Department of Chemistry, Faculty of Sciences
[2] Cuban Sugar Research Institute,Department of Quality Assurance and Pharmaceutical Technology, Food and Pharmaceutical Sciences Institute
[3] University of Havana,undefined
来源
关键词
Monolithic column; Multisyringe liquid chromatography; Pyridoxine; Thiamine; Cyanocobalamin; Pharmaceutical preparations;
D O I
暂无
中图分类号
学科分类号
摘要
In this paper, a time-based multicommutated flow system is proposed for appropriate selection and modulation of mobile phase composition in flow-injection (FI)/sequential-injection (SI) chromatography. The novel flow assembly involves the on-line coupling of a short monolithic reversed-phase chromatographic column with a multisyringe flow injection set-up furnished with a set of solenoid valves. The proposed hyphenated technique was applied to the simultaneous spectrophotometric determination of thiamine (B1), pyridoxine (B6) and cyanocobalamin (B12) which were taken as model analytes. The separation method capitalizes on a dual isocratic elution protocol involving the use of a single forward stroke of the multisyringe pump for initial delivery of 50 mmol L−1 ammonium acetate (pH 7.0) for 2.4 min followed by 50 mmol L−1 ammonium acetate–methanol (80:20, v/v) for 6.4 min at 0.5 mL min−1 and room temperature. Detection was performed at the maximum wavelength for each target vitamin—280 nm for B1, 325 nm for B6, and 360 nm for B12. A first-order, two-level full-factorial design was utilized to ascertain the significant variables influencing the chromatographic separation and the magnitude of the interaction effects. The experimental design method revealed that resolution of the target vitamins is highly dependent on the pH, percentage of organic modifier, and their second-order interaction. The multisyringe flow-injection-based monolithic column separation method, which should be viewed as an expeditious and cost-effective alternative to the high-performance liquid chromatography counterpart, was applied to the separation and determination of B1, B6, and B12 in different pharmaceutical dosage forms in less than 9 min. Statistical comparison of the results from the proposed procedure with those from the HPLC method endorsed by the US Pharmacopeia revealed there were no significant differences at the 95 % confidence level.
引用
收藏
页码:817 / 825
页数:8
相关论文
共 50 条
  • [21] A SIMPLE INJECTION VALVE FOR FLOW-INJECTION ANALYSIS
    CHIPPERFIELD, JR
    WORSFOLD, PJ
    ANALYTICA CHIMICA ACTA, 1986, 181 : 283 - 285
  • [22] A VERSATILE INJECTION SYSTEM FOR FLOW-INJECTION ANALYSIS
    SOLLACARO, M
    DITTMAR, A
    LATER, R
    JOURNAL OF AUTOMATIC CHEMISTRY, 1992, 14 (03): : 101 - 105
  • [23] Application of phthalocyanines in flow- and sequential-injection analysis and microfluidics systems: A review
    van Staden, Jacobus Frederick
    TALANTA, 2015, 139 : 75 - 88
  • [24] SELECTIVITY IN FLOW-INJECTION ANALYSIS
    HANSEN, EH
    RUZICKA, J
    KRUG, FJ
    ZAGATTO, EAG
    ANALYTICA CHIMICA ACTA, 1983, 148 (APR) : 111 - 125
  • [25] OSCILLOGRAPHIC FLOW-INJECTION ANALYSIS
    ZHENG, JB
    LIU, P
    SHI, SH
    CHEMICAL JOURNAL OF CHINESE UNIVERSITIES-CHINESE, 1995, 16 (07): : 1016 - 1019
  • [26] FLOW-INJECTION ANALYSIS REVISITED
    RANGER, CB
    ANALYTICAL CHEMISTRY, 1982, 54 (11) : 1106 - 1106
  • [27] FLOW-INJECTION STRIPPING ANALYSIS
    DECASTRO, MDL
    IZQUIERDO, A
    ELECTROANALYSIS, 1991, 3 (06) : 457 - 467
  • [28] FLOW-INJECTION ANALYSIS OF PHARMACEUTICALS
    DECASTRO, MDL
    VALCARCEL, M
    JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 1989, 7 (12) : 1291 - 1300
  • [29] Reverse flow-injection analysis
    Mansour, Fotouh R.
    Danielson, Neil D.
    TRAC-TRENDS IN ANALYTICAL CHEMISTRY, 2012, 40 : 1 - 14
  • [30] Radiometric flow-injection analysis
    Myint, U.
    Tolgyessy, J.
    Journal of Radioanalytical and Nuclear Chemistry, 1995, 191 (02) : 413 - 426