以高效液相層析儀檢測農產品中亞速爛殘留量

依序以含0.1% 醋酸之乙(v/v)溶液、丙酮、水及乙醚萃取農產品中亞速爛,再以矽酸鎂固相萃取匣及中性氧化鋁固相萃取匣淨化之,所得檢液以高效液相層析儀配合紫外光檢出器檢測。亞速爛添加0.1 ∼ 0.3ppm濃度於柑橘中之平均回收率為83.5 ∼ 90.9% ,添加0.05 ∼ 0.2 ppm 濃度於甘蔗中之平均回收率為80.6 ∼86.7%,最低檢出量均為0.01 ppm...

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Bibliographic Details
Published in藥物食品分析 Vol. 9; no. 1; pp. 40 - 44
Main Authors 李宗璘(Li, Tsung-lin), 李婉媜(Lee, Wan-chen), 張碧秋(Chang, Pi-chiou), 周薰修(Chou, Shin-shou)
Format Journal Article
LanguageChinese
Published 台灣 衛生福利部食品藥物管理署 01.03.2001
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Summary:依序以含0.1% 醋酸之乙(v/v)溶液、丙酮、水及乙醚萃取農產品中亞速爛,再以矽酸鎂固相萃取匣及中性氧化鋁固相萃取匣淨化之,所得檢液以高效液相層析儀配合紫外光檢出器檢測。亞速爛添加0.1 ∼ 0.3ppm濃度於柑橘中之平均回收率為83.5 ∼ 90.9% ,添加0.05 ∼ 0.2 ppm 濃度於甘蔗中之平均回收率為80.6 ∼86.7%,最低檢出量均為0.01 ppm
Asulam was extracted with 0.1% acetic acid in acetonitrile, acetone, water and diethyl ether successively. Following after clean up withflorisil and neutral alumina solid phase extraction cartridge, the elute was determined by HPLC with UV detector. Recoveries were carriedout by spiking the standard asulam at the levels of 0.1~0.3 and 0.05~0.2 ppm to citrus and sugarcane, respectively. The average recoverieswere 83.5 to 90.9 % for citrus and 80.6 to 86.7 % for sugarcane, and both detection limits was 0.01 ppm.
ISSN:1021-9498