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首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Rapid, sensitive and simultaneous determination of fluorescence-labeled polyamines in human hair by high-pressure liquid chromatography coupled with electrospray-ionization time-of-flight mass spectrometry
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Rapid, sensitive and simultaneous determination of fluorescence-labeled polyamines in human hair by high-pressure liquid chromatography coupled with electrospray-ionization time-of-flight mass spectrometry

机译:高压液相色谱-电喷雾电离飞行时间质谱快速,灵敏,同时测定人发中的荧光标记多胺

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The rapid, sensitive and simultaneous determination of six polyamines, i.e., ornithine (ORN), 1,3-diaminopropane (DAP), putrescine (PUT), cadaverine (CAD), spermidine (SPD) and spermine (SPM), in human hairs was performed by ultra-performance liquid chromatography (UPLC) with fluorescence (FL) detection and electrospray-ionization time-of-flight mass spectrometry (ESI-TOF-MS). The primary (-NH2) and secondary (-NH) amines in the polyamine structures were first labeled with 4-(N,N-dimethylaminosulfonyl)-7-fluoro-2,1,3-benzoxadiazole (DBD-F) at 60 degrees C for 30 min in the mixture of 0.1 M borax (pH 9.3) and acetonitrile (CH3CN). The resulting derivatives were perfectly separated using an ACQUITY UPLC (TM) BEH C-18 column (1.7 mu m, 100 mm x 2.1 mm i.d.) by a gradient elution with a mixture of water-acetonitrile containing 0.1% formic acid (HCOOH). The separated polyamine derivatives were sensitively detected with both FL and TOF-MS. The detection limits in FL and TOF-MS were 11-86 and 2-5 fmol, respectively. However, the determination of several polyamines by FL detection was interfered with by endogenous substances in the hair. Therefore, the simultaneous determination in hair was carried out by the combination of UPLC separation and the ESI-TOF-MS detection. The Structures of the polyamines were identified from the protonated-molecular ions [M+H](+) obtained from the TOF-MS measurement. A good linearity was achieved from the calibration curves, that was obtained by plotting the peak area ratios of the analytes relative to the internal standard (IS), i.e., 1,6-diaminohexane (DAH), against the injected amounts of each polyamine (0.05-50 pmol, r(2) > 0.999). The proposed method was applied to the determination in the hairs of healthy volunteers. The mean concentrations of ORN, DAP, PUT, CAD, SPD and SPM in 1 mg of human hairs (n = 20) were 1.46, 0.18,1.18, 0.11, 1.97 and 0.98 pmol, respectively. Because the proposed method provides a good mass accuracy and the trace detection of the polyamines in hair, this analytical technique seems to be applicable for the determination of various biological compounds in hair.
机译:快速,灵敏,同时测定人发中的六种多胺,即鸟氨酸(ORN),1,3-二氨基丙烷(DAP),腐胺(PUT),尸胺(CAD),亚精胺(SPD)和精胺(SPM)通过具有荧光(FL)检测和电喷雾电离飞行时间质谱(ESI-TOF-MS)的超高效液相色谱(UPLC)进行。首先在60度下用4-(N,N-二甲基氨基磺酰基)-7-氟-2,1,3-苯并恶二唑(DBD-F)标记多胺结构中的伯(-NH2)和仲(-NH)胺在0.1 M硼砂(pH 9.3)和乙腈(CH3CN)的混合物中加热30分钟。使用ACQUITY UPLC TM BEH C-18柱(1.7μm,100mm×2.1mm i.d.),通过用含有0.1%甲酸(HCOOH)的水-乙腈的混合物进行梯度洗脱,将得到的衍生物完全分离。分离的多胺衍生物可以通过FL和TOF-MS灵敏地检测到。 FL和TOF-MS的检出限分别为11-86和2-5 fmol。但是,通过FL检测确定几种多胺会受到头发中内源性物质的干扰。因此,通过UPLC分离和ESI-TOF-MS检测相结合,可同时测定头发。从通过TOF-MS测量获得的质子化分子离子[M + H](+)鉴定多胺的结构。从标定曲线获得了良好的线性,该标定曲线是通过将分析物相对于内标(IS)(即1,6-二氨基己烷(DAH))的峰面积比相对于每种多胺的进样量( 0.05-50 pmol,r(2)> 0.999)。该方法用于健康志愿者头发的测定。 1 mg人发(n = 20)中ORN,DAP,PUT,CAD,SPD和SPM的平均浓度分别为1.46、0.18、1.18、0.11、1.97和0.98 pmol。因为所提出的方法提供了良好的质量准确度和头发中多胺的痕量检测,所以这种分析技术似乎可用于测定头发中的各种生物化合物。

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