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首页> 外文期刊>Chromatographia >Development of a sensitive reagent, 1,2-benzo-3,4-dihydrocarbazole-9-ethyl-p-toluenesulfonate, for determination of bile acids in serum by HPLC with fluorescence detection, and identification by mass spectrometry with an APCI source
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Development of a sensitive reagent, 1,2-benzo-3,4-dihydrocarbazole-9-ethyl-p-toluenesulfonate, for determination of bile acids in serum by HPLC with fluorescence detection, and identification by mass spectrometry with an APCI source

机译:开发一种敏感试剂1,2-苯并3,4-二氢咔唑-9-乙基对甲苯磺酸盐,用于通过HPLC和荧光检测来测定血清中的胆汁酸,并通过APCI质谱进行鉴定

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摘要

A pre-column derivatization method with 1,2-benzo-3,4-dihydrocarbazole-9-ethyl-p-toluene-sulfonate (BDETS) as labeling reagent followed by high-performance liquid chromatography with fluorescence detection has been developed for sensitive determination of bile acids (BA). Derivatives were sufficiently stable to be efficiently analyzed by high-performance liquid chromatography. The derivatives also formed an intense protonated molecular ion corresponding to m/z (M + H)(+), and fragment ions at (MH+ - H2O)(+), (MH+ - 2H(2)O)(+), and (MH+ 3H(2)O)+, in positive-ion mass spectrometry with an APCl source. Collision- induced dissociation of the protonated molecular ion produced fragment products at m/z 319.1 and 246.1 corresponding to cleavage of the C-O and N-CO bonds of derivative molecules. Maximum yields close to 100% were observed when a 10 to 15-fold molar excess of the reagent was used in the presence of potassium citrate as catalyst. The derivatives fluoresced strongly, which enabled the direct injection with no significant disturbance from the main by-products from reagent degradation, for example 1,2-benzo-3, 4-dihydrocarbazole-9-ethanol (BDCE-OH). The limit of detection, at a signal-to-noise ratio of 3, was 12.94-21.94 fmol. Results from validation showed the method to be highly accurate and precise (<6.4%). Excellent linear responses were observed with correlation coefficients >0.9996.
机译:建立了一种以1,2-苯并-3,4-二氢咔唑-9-乙基对甲苯磺酸酯(BDETS)为标记试剂,然后进行高效液相色谱和荧光检测的柱前衍生化方法,用于灵敏测定胆汁酸(BA)。衍生物足够稳定,可以通过高效液相色谱法进行有效分析。衍生物还形成了对应于m / z(M + H)(+)的强质子化分子离子,并在(MH +-H2O)(+),(MH +-2H(2)O)(+)和(MH + 3H(2)O)+,在带有APCl源的正离子质谱分析中。碰撞诱导的质子化分子离子的解离在m / z 319.1和246.1处产生碎片产物,对应于衍生分子C-O和N-CO键的断裂。当在柠檬酸钾的存在下使用10-15倍摩尔过量的试剂时,观察到最大收率接近100%。衍生物发出强烈的荧光,可以直接注射而不会受到试剂降解的主要副产物(例如1,2-苯并-3、4-二氢咔唑-9-乙醇(BDCE-OH))的干扰。信噪比为3时,检测限为12.94-21.94 fmol。验证结果表明该方法具有很高的准确性和精确性(<6.4%)。观察到优异的线性响应,相关系数> 0.9996。

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