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Rapid Method for Measuring Rotenone in Water at Piscicidal Concentrations
Author(s) -
Dawson V. K.,
Harman P. D.,
Schultz D. P.,
Allen J. L.
Publication year - 1983
Publication title -
transactions of the american fisheries society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.696
H-Index - 86
eISSN - 1548-8659
pISSN - 0002-8487
DOI - 10.1577/1548-8659(1983)112<725:rmfmri>2.0.co;2
Subject(s) - rotenone , environmental science , environmental chemistry , chemistry , biological system , biology , biochemistry , mitochondrion
A high‐performance liquid chromatography (HPLC) procedure that is rapid, specific, and sensitive (limit of detection <0.005 mg/liter) was developed for monitoring application and degradation rates of rotenone. For analysis, a water sample is buffered to pH 5 and injected through a Sep Pak(R) C 18 disposable cartridge. The cartridge adsorbs and retains the rotenone which then can be eluted quantitatively from the cartridge with a small volume of methanol. This step effectively concentrates the sample and provides sample cleanup. The methanol extract is analyzed directly by HPLC on an MCH 10 reverse‐phase column; methanol: Water (75:25, volume : Volume) is the mobile phase and flow rate is 1.5 ml/minute. The rotenone is detected by ultraviolet spectrophotometry at a wavelength of 295 nm. Received November 29, 1982 Accepted May 24, 1983