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[采用液相色谱-串联质谱联用同位素内标稀释技术测定鱼/贝类组织中环丙沙星残留量]

[Determination of ciprofloxacin residue in fish/shellfish tissues using liquid chromatography-tandem mass spectrometry with isotope internal standard dilution technique].

作者信息

Chen Xiaohong, Wang Yufei, Yao Xunping, Jin Micong

机构信息

Ningbo Key Laboratory of Poison Research and Control, Ningbo Municipal Center for Disease Control and Prevention, Ningbo 315010, China.

出版信息

Se Pu. 2009 Jan;27(1):39-43.

PMID:19449538
Abstract

Using isotope internal standard dilution technique, a high performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS) method has been developed for the identification and quantitative determination of ciprofloxacin residue in the tissues of various fishes/shellfishes. The homogenized tissue sample added with ciprofloxacin-D8 and phosphate buffer solution (pH 7.0) was extracted with acetonitrile under ultrasonication, and degreased with hexane. After solid-phase extraction (SPE) was performed on an Oasis MAX cartridge, the sample was separated on a Cloversil-C18 column (150 mm x 4.6 mm, 5 microm) by using the mobile phase consisting of CH3CN-0.05% CF3 COOH (25:75, v/v). The detection was carried out by LC-MS/MS using an electrospray ionization interface in multiple reaction monitoring (MRM) mode. The quantification using isotope-labelled internal standard was based on the peak area ratio of ciprofloxacin and deuterated internal standard in the MRM mode. The calibration curve was linear within the range of 0.1 - 50.0 microg/kg and the limit of quantification was 0.1 microg/kg (S/N > or = 10). The recovery was between 92.5% and 98.1%, and the relative standard deviation was less than 4.3%. The application of this method was further demonstrated by analyzing ten various real samples from local markets. The results show that this method is sensitive, accurate and suitable for the confirmative determination of ciprofloxacin residues.

摘要

采用同位素内标稀释技术,建立了一种高效液相色谱 - 串联质谱(HPLC-MS/MS)法,用于鉴定和定量测定各种鱼类/贝类组织中的环丙沙星残留。将添加了环丙沙星 - D8和磷酸盐缓冲溶液(pH 7.0)的匀浆组织样品用乙腈超声提取,并用正己烷脱脂。在Oasis MAX柱上进行固相萃取(SPE)后,样品在Cloversil-C18柱(150 mm×4.6 mm,5μm)上分离,流动相为CH3CN - 0.05% CF3COOH(25:75,v/v)。采用电喷雾电离接口在多反应监测(MRM)模式下通过LC-MS/MS进行检测。使用同位素标记内标进行定量基于MRM模式下环丙沙星和氘代内标的峰面积比。校准曲线在0.1 - 50.0μg/kg范围内呈线性,定量限为0.1μg/kg(S/N≥10)。回收率在92.5%至98.1%之间,相对标准偏差小于4.3%。通过分析来自当地市场的10个不同实际样品进一步证明了该方法的应用。结果表明,该方法灵敏、准确,适用于环丙沙星残留的确证测定。

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