UV resonance Raman detection and quantitation of domoic acid in phytoplankton

被引:17
|
作者
Wu, Q
Nelson, WH [1 ]
Treubig, JM
Brown, PR
Hargraves, P
Kirs, M
Feld, M
Desari, R
Manoharan, R
Hanlon, EB
机构
[1] Univ Rhode Isl, Dept Chem, Kingston, RI 02881 USA
[2] Univ Rhode Isl, Sch Oceanog, Kingston, RI 02881 USA
[3] MIT, George Russell Harrison Spect Lab, Cambridge, MA 02138 USA
关键词
D O I
10.1021/ac991052d
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Cultures of the phytoplankton diatom, Pseudonitzischia multiseries, have been harvested under controlled growth conditions ranging from late logarithmic to late stationary phase (17-58 days). The amount of domoic acid (DA) present in the growth media and in the homogenized cells has been determined by HPLC. Defined samples of media, homogenized cells, whole cells, and whole cells in media have been laser excited at 251 nm for the purpose of selectively exciting intense UV resonance Raman spectra from DA in the samples. Neither media nor cell component spectra from algae seriously interfere with DA spectra. The spectral cross sections for the dominant 1652-cm(-1) mode of DA have been determined for 242-, 251-, and 257-nm excitation, Maximum sensitivities are achieved with 251-nm excitation because cross sections for DA are maximum, and interference from other algal components becomes very small. DA concentrations that have been determined with 251-nm excitation by resonance Raman methods correlate closely with values determined independently with HPLC, especially at higher DA concentrations. The UV resonance Raman analysis of DA in phytoplankton algae is shown to be very sensitive and quantitative as well as rapid and nonintrusive.
引用
收藏
页码:1666 / 1671
页数:6
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