1985
DOI: 10.1093/jaoac/68.5.950
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Rapid Liquid Chromatographic Determination of Patulin in Apple Juice

Abstract: A rapid method is described for the quantitative determination of patulin in apple juice. The mycotoxin is extracted from the sample with ethyl acetate and the extract is cleaned up by extraction with a sodium carbonate solution. Patulin is determined by reverse phase liquid chromatography using a μ.Bondapak C18covery is >75%.

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Cited by 7 publications
(8 citation statements)
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“…Patulin dissolved in a pH 4.0 acetic acid solution was more stable (9% loss of a 0.5 µg/mL solution after 130 min). Although the acetic acid solution did not completely prevent patulin from degradation, acidified water has been used in many methods to stabilize patulin before being injected into the HPLC system (Forbito and Babsky, 1985;Brause et al, 1996). The only advantage of dissolving samples in run buffer was that it resulted in a smoother chromatogram (Figure 2).…”
Section: Resultsmentioning
confidence: 99%
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“…Patulin dissolved in a pH 4.0 acetic acid solution was more stable (9% loss of a 0.5 µg/mL solution after 130 min). Although the acetic acid solution did not completely prevent patulin from degradation, acidified water has been used in many methods to stabilize patulin before being injected into the HPLC system (Forbito and Babsky, 1985;Brause et al, 1996). The only advantage of dissolving samples in run buffer was that it resulted in a smoother chromatogram (Figure 2).…”
Section: Resultsmentioning
confidence: 99%
“…Because of health-related concerns, it has been suggested that patulin be used as a quality indicator for apples used in food and drink (Rovira et al, 1993;Prieta et al, 1994). The World Health Organization (WHO), and many European countries, such as Switzerland, Sweden, Belgium, Russia, and Norway, have set the maxi-mum acceptable level of patulin in apple juice at 50 µg/L (Moller and Josefsson, 1980;Forbito and Babsky, 1985;Van Egmond, 1989;Stoloff et al, 1991, Rovira et al, 1993.…”
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confidence: 99%
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“…Not long after, various studies suggested patulin to be not only toxic to fungi and bacteria but also to animals (see below, Health Effects) and higher plants, including cucumber, wheat, peas, corn, and flax (Iyengar and Starky 1953;McCalla 1963, 1968;Berestets'kyi and Synyts'kyi 1973) As continued evidence for the negative health effects of patulin surfaced, many regulatory agencies began placing caps on patulin content within foods. European countries were among the 1st to address the concern, and today many countries across the world, particularly those within the EU, limit allowable patulin content within foods at 50 g/L (Moller and Josefsson 1980;van Egmond 1989;AIJN 1990;Stoloff and others 1991;Rovira and others 1993;Forbito and Babsky 1996;Gokmen and Akar 1998).…”
Section: History and Regulationmentioning
confidence: 99%
“…Furthermore, our method showed a better detection limit than those claimed by these authors. Relative to other methods which use one or more columns for purification, our method is faster, has similar or better recovery levels, and has the same or better sensitivity (Leuenberger et al, 1978;Stray, 1978, Forbito andBabsky, 1985;Kubacki and Goszcz, 1988; Lehmann and Wald, 1990;Tarter and Scott, 1991).…”
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confidence: 99%