Exploring the possibilities of capacitively coupled contactless conductivity detection in combination with liquid chromatography for the analysis of polar compounds using aminoglycosides as test case

被引:10
作者
Jankovics, Peter [1 ,2 ,3 ]
Chopra, Shruti [1 ]
El-Attug, Mohamed N. [1 ,4 ]
Cabooter, Deirdre [1 ]
Wolfs, Kris [1 ]
Noszal, Bela [2 ]
Van Schepdael, Ann [1 ]
Adams, Erwin [1 ]
机构
[1] Katholieke Univ Leuven, Fac Pharmaceut Sci, Lab Pharmaceut Anal, B-3000 Louvain, Belgium
[2] Semmelweis Univ, Dept Pharmaceut Chem, H-1092 Budapest, Hungary
[3] Natl Inst Pharm, H-1051 Budapest, Hungary
[4] Tripoli Univ, Fac Pharm, Dept Pharmaceut Chem, Tripoli, Libya
关键词
(CD)-D-4; LC; Aminoglycosides; Ion-pairing reagents; Explorative study; TANDEM-MASS-SPECTROMETRY; PULSED ELECTROCHEMICAL DETECTION; CAPILLARY-ELECTROPHORESIS; QUANTITATIVE-DETERMINATION; MICROCHIP ELECTROPHORESIS; DETECTION CE-(CD)-D-4; FUNDAMENTAL-ASPECTS; GENTAMICIN SULFATE; STRAY CAPACITANCE; PART I;
D O I
10.1016/j.jpba.2014.12.015
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The analysis of highly polar (often charged) compounds which lack a strong UV absorbing chromophore is really challenging. Despite the numerous analytical methods published, the demand for a simple, robust and cheap technique for their analysis still persists. Here, reversed phase (RP) liquid chromatography (LC) with capacitively coupled contactless conductivity detection (CID) was explored for the first time as a possible method for separation and detection of various aminoglycoside (AMG) antibiotics which were taken as typical test compounds: tobramycin (TOB), spectinomycin, streptomycin, amikacin, kanamycin A and kanamycin B. (CD)-D-4 was performed using a commercially available as well as a laboratory made cell. As ion-pairing reagents (IPR) four perfluorinated carboxylic acids were used: pentafluoropropionic acid, heptafluorobutyric acid, nonafluoropentanoic acid (NFPA) and pentadecafluorooctanoic acid (PDFOA). 0.125 mM NFPA-acetonitrile (ACN) (90:10) or 0.125 mM PDFOA-ACN (70:30) as mobile phases were suitable to detect TOB with reasonable retention times. However, NFPA was preferred for practical reasons. Its applicable concentration range in the mobile phase was strongly restricted by loss of chromatographic performance at lower levels and excessive background conductivity at higher levels. Overall repeatability and robustness of the method were rather poor which was explained by the relatively low IPR levels. Selectivity between the tested AMGs was mainly influenced by the number of protonated amino groups per molecule making it impossible to separate compounds of equal net charges. Problems encountered with gradient elution, hydrophilic interaction liquid chromatography (HILIC) and separation at high pH without IPRs are also discussed. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:155 / 168
页数:14
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