High-performance liquid chromatography (HPLC) and different high-performanc
e capillary electrophoresis (HPCE) methods have been developed for the dete
ction and quantitation of cyanobacterial toxins in environmental samples.
Cyanobacteria, also known as blue-green algae, are responsible for toxic co
ntamination of fresh water. Several serious episodes involving microcystins
have been reported in recent years; the most common and toxic of these hep
atotoxins is microcystin-LR (MC-LR). Sensitive analytical methodologies are
required for determination of these compounds because of the implications
for human health when the toxins are present in drinking water.
Different modes of operation of HPCE were used and the results obtained wer
e compared with those obtained by HPLC. Citrate buffer resulted in good sep
aration of the microcystins when capillary electrophoresis was used in capi
llary zone electrophoresis (CZE) and capillary isotachophoresis (CITP) mode
s; borate buffer containing sodium dodecyl sulphonate (SDS) was used in mic
ellar electrokinetic chromatography (MEKC). Conditions were optimized and t
he methods were applied to water samples and cyanobacterial cells containin
g microcystins. Results obtained by use of HPLC-UV and different modes of o
peration of CE-UV were compared in terms of sensitivity, selectivity, and e
fficiency.