液相色谱-串联质谱法测定柑橘中虫酰肼残留量
LC-MS/MS Determination of Residual Amount of Tebufenozide in Orange
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摘要: 提出了液相色谱-串联质谱法测定柑橘中虫酰肼残留量的方法。样品用1%(体积分数,下同)乙酸-乙腈溶液先后提取2次,提取液定容为25 mL。分取8.0 mL经N-丙基乙二胺(PSA)和十八烷基硅烷(ODS)键合相净化,取所得净化液5.00 mL,在60 ℃氮气吹至近干后供液相色谱-串联质谱分析。0.1%乙酸-乙腈溶液定容至1 mL。以ACQUITY UPLC BEH C18色谱柱为分离柱,以不同体积比混合的0.1%乙酸溶液和乙腈为流动相梯度洗脱,采用电喷雾正离子源模式多反应监测检测。方法的测定下限(10S/N)为0.005 mg·kg-1。以空白柑橘样品为基体进行加标回收试验,所得回收率在77.1%~90.1%之间,相对标准偏差(n=5)均小于13%。Abstract: A method of LC-MS/MS for the determination of residual amount of tebufenozide in orange was proposed. The sample was extracted twice with a mixture solution of 0.1% (φ) acetic acid-acetonitrile, and the extracts were made up to 25 mL. An aliquot of 8.0 mL was taken and purified with PSA and ODS. A portion (5.00 mL) of the purified solution was evaporated to near-dryness at 60 ℃ by N2-blowing, and the residue was dissolved, made up to 1.0 with 0.1% (φ) acetic acid-acetonitrile, and used for LC-MS/MS analysis. ACQUITY UPLC BEH C18 column was used as stationary phase, and the mixture of acetonitrile and 0.1% (φ) acetic acid solution mixed in different ratio was used as mobile phase in gradient elution. ESI+ as well as multi-reactions monitor was adopted in MS/MS. Value of detection limit (10S/N) of the method found was 0.005 mg·kg-1. On the base of blank orange sample, test for recovery was made by standard addition method; values of average recovery found were in the range of 77.1%-90.1% with RSD′s (n=5) less than 13%.