1995
DOI: 10.1007/bf03226369
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Quantitation of levamisole in plasma using high performance liquid chromatography

Abstract: A rapid and sensitive procedure is described for the quantitation of levamisole in plasma using high-performance liquid chromatography (HPLC). The procedure involves sample preparation using a reverse-phase C18 cartridge prior to chromatography and quantitation using peak area ratios (UV absorbance detection, 225 nm) of levamisole to the internal standard, quinine. The limit of detection was 21 ng/ml and the limit of quantification was 72 ng/ml, both contained in 1 ml of plasma. The recoveries were sufficientl… Show more

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Cited by 31 publications
(18 citation statements)
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“…The presence of levamisole is difficult to confirm as a result of its short half‐life (5.6 h), the lack of widespread access to testing, and the low sensitivity of urine and blood assays 10 . Management is supportive.…”
Section: Discussionmentioning
confidence: 99%
“…The presence of levamisole is difficult to confirm as a result of its short half‐life (5.6 h), the lack of widespread access to testing, and the low sensitivity of urine and blood assays 10 . Management is supportive.…”
Section: Discussionmentioning
confidence: 99%
“…Levamisole concentrations were determined using a high-performance liquid chromatography method adapted from Vandamme et al [26]. …”
Section: Methodsmentioning
confidence: 99%
“…Various techniques have been used for the determination of levamisole in biological fluids. They include gas chromatography with nitrogenphosphorus detection (GC-NPD) 2 and flame ionization (GC-FID) [3] and liquid chromatography (LC) with ultraviolet (UV) detection [4][5][6][7] . Several methods have been developed for levamisole quantification such as polarography 8 , by a turbidimetric method and flow-injection analysis 9 .…”
Section: Levamisolementioning
confidence: 99%