TY - JOUR
T1 - Development of a capillary zone electrophoretic method for the rapid separation and detection of hepatotoxic microcystins
AU - Li, Paul C. H.
AU - Hu, Shen
AU - Lam, Paul K. S.
PY - 1999/1
Y1 - 1999/1
N2 - Analysis of trace amounts of various hepatotoxic microcystins in marine and freshwater samples is very important since these toxins, especially microcystin-LR, have been demonstrated to have tumour-promoting activity. In this study, instead of measuring the total amount of microcystins, we developed a capillary zone electrophoretic method for the separation and detection of individual toxin standards. No additives were used for enhancement of resolution. This technique is characterized by a high separation efficiency, short analysis time and small sample volume. In order to improve the detection sensitivity, a laser-induced fluorescence detector was used, and the labelling of microcystins was accomplished through a two-step procedure. First, the microcystin standards were converted into cysteine conjugates, followed by derivatization with Fluorescein 5-Isothiocyanate (FITC). After derivatization, the FITC-labelled microcystins were directly injected, separated and detected in 8 min. This method was shown to be a promising technique for sensitive and rapid analysis of individual microcystin toxins. Copyright (C) 1999 Elsevier Science Ltd.
AB - Analysis of trace amounts of various hepatotoxic microcystins in marine and freshwater samples is very important since these toxins, especially microcystin-LR, have been demonstrated to have tumour-promoting activity. In this study, instead of measuring the total amount of microcystins, we developed a capillary zone electrophoretic method for the separation and detection of individual toxin standards. No additives were used for enhancement of resolution. This technique is characterized by a high separation efficiency, short analysis time and small sample volume. In order to improve the detection sensitivity, a laser-induced fluorescence detector was used, and the labelling of microcystins was accomplished through a two-step procedure. First, the microcystin standards were converted into cysteine conjugates, followed by derivatization with Fluorescein 5-Isothiocyanate (FITC). After derivatization, the FITC-labelled microcystins were directly injected, separated and detected in 8 min. This method was shown to be a promising technique for sensitive and rapid analysis of individual microcystin toxins. Copyright (C) 1999 Elsevier Science Ltd.
UR - http://www.scopus.com/inward/record.url?scp=0032845313&partnerID=8YFLogxK
UR - https://www.scopus.com/record/pubmetrics.uri?eid=2-s2.0-0032845313&origin=recordpage
U2 - 10.1016/S0025-326X(99)00012-0
DO - 10.1016/S0025-326X(99)00012-0
M3 - RGC 21 - Publication in refereed journal
SN - 0025-326X
VL - 39
SP - 250
EP - 254
JO - Marine Pollution Bulletin
JF - Marine Pollution Bulletin
IS - 1-12
ER -