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建立了同时检测猪组织中9种β-受体阻断剂( BBs)残留的超快速液相色谱-四极杆/线性离子阱质谱方法。均质试样经β-葡糖醛苷酶/芳基硫酸酯酶水解,乙腈提取,硅藻土与 BondElut 分散固相萃取填料双重快速净化,以0.1%(v / v)甲酸水溶液-甲醇为流动相使用 Kinetex TM C18-XB 色谱柱(150 mm×2.1 mm,2.6μm)超快速液相色谱分离,优化多反应监测(MRM)离子对后,采用预设定多反应监测( sMRM)-信息依赖性采集( IDA)-增强子离子扫描(EPI)模式检测,在线 EPI 谱库定性分析,内标法定量。结果表明,9种 BBs 在线性范围内的线性关系良好( r≥0.995);定量限(LOQ,S / N≥10)均达到0.5μg / kg;3个添加水平(0.5、1.0和5.0μg / kg)下的回收率为87.5%~111.8%;RSD 为4.0%~12.5%。该方法快速、准确、灵敏,可有效用于猪组织样品中多种 BBs 残留的同时测定。

A highly sensitive method using ultra-fast liquid chromatography coupled with qua-drupole/linear ion trap mass spectrometry(UFLC-Q/Trap MS)was developed to simultaneous-ly screen and confirm nine β-blockers(BBs)in porcine tissues(porcine muscle,liver and kid-ney). The method was used for trace determination of atenolol,pindolol,acebutolol,metopro-lol,carazolol,labetalol,bisoprolol,propranolol and penbutolol. The homogenized tissues were hydrolyzed by β-glucuronidase/aryl sulfatase and extracted with acetonitrile,followed by con-tinuous purification procedures of disperse solid phase extraction( d-SPE)with diatomaceous earth and BondElut cartridge. The ultra-fast chromatographic separation was conducted on a Kinetex TM C18-XB column(150 mm×2. 1 mm,2. 6 μm)using 0. 1%(v/v)formic acid aqueous solution and methanol as mobile phases in gradient elution. The optimized ion transitions were employed in the mixed-mode of scheduled multiple reaction monitoring( sMRM)-information dependent acquisition(IDA)-enhanced product ion(EPI)scan. Qualification analysis was per-formed through spectra-matching with on-line lab-built MS/MS library. For quantification stable isotope-labelled analogues of the analytes were used as internal standards. As a result,in por-cine liver,kidney and muscle,the nine BBs showed good linearity with all the correlation coef-
ficients(r)more than 0. 995 in the range of 0. 1-20 μg/L. The limits of quantification(LOQ,S/N≥10)were 0. 5 μg/kg for all the analytes. The developed method gave average recoveries of 87. 5% -111. 8% spiked at 0. 5,1.0 and 5. 0 μg/kg with the relative standard deviations of 4. 0% -12. 5%. The proposed method can be used to screen and confirm the nine BBs in a single run, which makes it effective in surveillance and detection of the BBs residues in porcine tissues.

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