Substrates for the at-line coupling of capillary electrophoresis and surface-enhanced Raman spectroscopy

被引:24
作者
Dijkstra, RJ [1 ]
Gerssen, A [1 ]
Efremov, EV [1 ]
Ariese, F [1 ]
Brinkman, UAT [1 ]
Gooijer, C [1 ]
机构
[1] Free Univ Amsterdam, Dept Analyt Chem & Appl Spectroscopy, NL-1081 HV Amsterdam, Netherlands
关键词
surface-enhanced (resonance) Raman spectroscopy; capillary electrophoresis; at-line coupling; substrates;
D O I
10.1016/j.aca.2003.11.066
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
In this preliminary study, we evaluated four different types of substrate for the at-line coupling of capillary electrophoresis and surface-enhanced (resonance) Raman spectroscopy, CE-SER(R)S, with emphasis on spectral repeatability. We tested Sub I: etched silver foil, Sub2: a vapour-deposited silver film, Sub3: a silver oxalate-precoated silica TLC plate and Sub4: a silica TLC plate on which colloid and poly(Llysine) were manually added to the analyte spots, used earlier in at-line CE-SE(R)RS. All substrates were first tested by manual spotting using trans- 1,2-bis(4-pyridyl)ethylene (BPE) as a model compound for SERS and crystal violet (CV) as a model compound for SE(R)RS. The spectral features of the SE(R)RS spectra of BPE and CV showed a most satisfactory repeatability on all substrates. As expected, the signal intensities varied considerably between runs; this implies that quantification in at-line CE-SE(R)RS should rather be done by means of an on-line absorbance detector. In addition, the suitability of Sub1, Sub2 and Sub4 as deposition substrates after CE was explored using two cationic dyes: CV and basic fuchsin (1317). Good-quality SERRS spectra could be recorded on all three substrates. Although Sub1 and Sub2 have a poor water-sorptivity, they were found to be good substrates for at-line CE-SERRS. They do not require any post-deposition addition of silver colloid and could therefore become attractive alternatives for Sub4. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:127 / 134
页数:8
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