中国粮油学报
中國糧油學報
중국량유학보
JOURNAL OF THE CHINESE CEREALS AND OILS ASSOCIATION
2009年
7期
138-141
,共4页
尹青岗%王锋%周洪杰%张海伟%谢芳%哈益明
尹青崗%王鋒%週洪傑%張海偉%謝芳%哈益明
윤청강%왕봉%주홍걸%장해위%사방%합익명
玉米赤霉烯酮%高效液相色谱%荧光检测器%玉米
玉米赤黴烯酮%高效液相色譜%熒光檢測器%玉米
옥미적매희동%고효액상색보%형광검측기%옥미
zearalenone%HPLC%FLD%maize
研究了高效液相色谱法测定玉米中玉米赤霉烯酮的方法.样品借鉴了GB/T 19540-2004中提取玉米赤霉烯酮的方法,通过Oasis HLB净化柱对提取液净化,以agilent extent C18色谱柱为分离柱,乙腈-水(V水:V乙腈=55:45)为流动相进行荧光检测(λex=235 nm,λem=460 nm).玉米赤霉烯酮的质量浓度在12~2 400μ/kg范围内呈良好线性,相关系数为0.9994,对添加高、中、低3个浓度玉米赤霉烯酮的玉米样品进行加标回收试验,平均回收率分别为96.736%、93.839%、86.240%,变异系数在1%~10%之间,最低检测限为10μ/kg.此方法对玉米中玉米赤霉烯酮的检测是可行的,且可给谷物中玉米赤霉烯酮检测方法优化提供参考.
研究瞭高效液相色譜法測定玉米中玉米赤黴烯酮的方法.樣品藉鑒瞭GB/T 19540-2004中提取玉米赤黴烯酮的方法,通過Oasis HLB淨化柱對提取液淨化,以agilent extent C18色譜柱為分離柱,乙腈-水(V水:V乙腈=55:45)為流動相進行熒光檢測(λex=235 nm,λem=460 nm).玉米赤黴烯酮的質量濃度在12~2 400μ/kg範圍內呈良好線性,相關繫數為0.9994,對添加高、中、低3箇濃度玉米赤黴烯酮的玉米樣品進行加標迴收試驗,平均迴收率分彆為96.736%、93.839%、86.240%,變異繫數在1%~10%之間,最低檢測限為10μ/kg.此方法對玉米中玉米赤黴烯酮的檢測是可行的,且可給穀物中玉米赤黴烯酮檢測方法優化提供參攷.
연구료고효액상색보법측정옥미중옥미적매희동적방법.양품차감료GB/T 19540-2004중제취옥미적매희동적방법,통과Oasis HLB정화주대제취액정화,이agilent extent C18색보주위분리주,을정-수(V수:V을정=55:45)위류동상진행형광검측(λex=235 nm,λem=460 nm).옥미적매희동적질량농도재12~2 400μ/kg범위내정량호선성,상관계수위0.9994,대첨가고、중、저3개농도옥미적매희동적옥미양품진행가표회수시험,평균회수솔분별위96.736%、93.839%、86.240%,변이계수재1%~10%지간,최저검측한위10μ/kg.차방법대옥미중옥미적매희동적검측시가행적,차가급곡물중옥미적매희동검측방법우화제공삼고.
A method was established for determination of mycotoxin zearalenone(ZEN) in maize by high performance liquid chromatography(HPLC). Using the method of GB/T 19540:2004 as reference, samples were cleaned up through Oasis HLB column. Extracted samples were analyzed by HPLC on an agilent extent C18 column with acetonitrile/water (45 :55) as mobile phase (1.0 mL min 1 ), and fluorescence detection (λex = 235 urn, λem = 460 nm) was conducted. Re-salts: The calibration graphs are linear up from 12~2 400 μg/kg for ZEN in maize and correlation coefficient is 0.9994.For maize samples added with high, middle or low level of ZEN reference material, the recovery is 86.240%, 93. 839%,96.736%, respectively. The relative standard deviations are 1% ~ 10%, and the minimum detection limit is 10 μg/kg.This determination method for ZEN is feasible and may also provide reference to improve ZEN determination in other cereal grains.