1995
DOI: 10.1111/j.1365-2621.1995.tb06300.x
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Highly Sensitive Method for Urea Detection in Wine

Abstract: Trace amounts of urea (less than 50 @L) in wine were accurately determined using a modified high performance liquid chromatography (HPLC-fluorometric) technique. Appropriate selection of eluent, HPLC columns, and chiral derivatives for the o-phthalaldehyde solution provided a 20-fold enhancement of sensitivity over established methods. A linear relationship was observed at concentrations from 0.5-500 &g/L of aqueous urea solution. The threshold level for detectability of urea in wine was 5 pg/L. The method is … Show more

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Cited by 14 publications
(12 citation statements)
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“…As the temperature rose by 5ЊC, K increased by 50%, and the required treatment period decreased by about 33%. Similar results were reported in table wines (Kodama, 1995). At 35ЊC, the urea content showed the sharpest decline.…”
Section: Temperature and Treatment Time Effectssupporting
confidence: 89%
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“…As the temperature rose by 5ЊC, K increased by 50%, and the required treatment period decreased by about 33%. Similar results were reported in table wines (Kodama, 1995). At 35ЊC, the urea content showed the sharpest decline.…”
Section: Temperature and Treatment Time Effectssupporting
confidence: 89%
“…It could, therefore, be separated from wine by filtration through nitrocellulose filters with a pore size Ͻ1.0 µm (Kodama, 1995). One unit of urease was defined as the amount of enzyme activity that released 1 µmol ammonia from urea (5000 mg/L)/min at 37ЊC and a pH of 4.0 (0.1 mol/L citrate) (Kodama, 1995).…”
Section: Acid Ureasementioning
confidence: 99%
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“…Recent methods in the literature for determination of urea in wines are based on enzymic analysis and monitoring of the pH change using two capillary glass electrodes capable of quantifying changes of pH of 0.001 units produced in the hydrolysis by urease [6]; on HPLC with a previous derivatisation reaction for facilitating separation [7,8] or on derivatisation with 1-phenyl-propan-1,2-dione 2-oxime in ethanol and photometric monitoring at 540 nm [9].…”
Section: Introductionmentioning
confidence: 99%
“…Adsorption is not considered as an alternative removal method since urea does not show high affinity to common adsorbents [3]. Urea rejection by reverse osmosis membranes is also not efficient [4,5]. An attractive, alternative removal method is based on the hydrolysis of urea by urease immobilized on a suitable support material.…”
Section: Introductionmentioning
confidence: 99%