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SPE前处理-UHPLC-MS/MS测定MBR中两种 N-酰基高丝氨酸内酯
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Quantitative Determination of two N-acylhomoserine Lactones in MBR by SPE Pre-processing-UHPLC-MS/MS
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    选用N-己基高丝氨酸内酯(C6-HSL)和N-辛基高丝氨酸内酯(C8-HSL)两种酰基高丝氨酸内酯类(AHLs)为代表物,建立了固相萃取(SPE)-超高效液相色谱串联三重四级杆质谱(UHPLC-MS/MS)分析膜生物反应器(MBR)活性污泥中AHLs的方法.研究结果表明C6-HSL和C8-HSL在1~200 μg/L内有良好的线性关系(R2 > 0.998),方法的检出限为0.100 μg/L,定量限为1.000 μg/L,在3个浓度水平下的平均加标回收率为80.69% ~ 83.75%,相对标准偏差(RSD)为4.71%~7.25%.方法精确度高、重复性好、基质效应弱,适用于MBR活性污泥中痕量AHLs的测定.

    Abstract:

    A method was developed for the determination of AHLs (N-Hexanoyl-DL-homoserine lactone(C6-HSL) and N-Octanoyl-DL-homoserine lactone(C8-HSL) were chosen as the representatives) in activated sludge in MBRs by solid phase extraction(SPE) combined with ultrahigh pressure liquid chromatography-tandem mass spectrometry(UHPLC-MS/MS). The results showed that C6-HSL and C8-HSL presented good linear relations(R2>0.998) in the range of 1~200 μg/L. The limit of detection and quantitation were 0.100 μg/L and 1.000 μg/L, respectively. The average recoveries of AHLs at three spiked concentrations were in the range of 80.69%~83.75%, and the relative standard deviations(RSD) were 4.71%~7.25%. The developed method is sensitive, stable and has weak matrix effects, which is applicable to determine the trace AHLs in activated sludge in MBRs.

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黄瑾辉?覮,胡熠,顾岩岭,史亚慧. SPE前处理-UHPLC-MS/MS测定MBR中两种 N-酰基高丝氨酸内酯[J].湖南大学学报:自然科学版,2018,45(12):144~148

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  • 在线发布日期: 2019-01-11
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