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首页> 外文期刊>RSC Advances >Development of a HPLC-FL method to determine benzaldehyde after derivatization with N-acetylhydrazine acridone and its application for determination of semicarbazide-sensitive amine oxidase activity in human serum
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Development of a HPLC-FL method to determine benzaldehyde after derivatization with N-acetylhydrazine acridone and its application for determination of semicarbazide-sensitive amine oxidase activity in human serum

机译:N-乙酰肼a啶酮衍生化后测定苯甲醛的HPLC-FL方法的建立及其在人血清中氨基脲敏感的胺氧化酶活性测定中的应用

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摘要

A novel fluorescence labeling reagent N -acetylhydrazine acridone (AHAD) was designed and synthesized. A highly sensitive high performance liquid chromatography (HPLC) method coupled with fluorescence detection to determine benzaldehyde after derivatization with AHAD was developed. Optimum derivatization was obtained at 40 °C for 30 min with trichloroacetic acid as catalyst. Benzaldehyde derivative was separated on a reversed-phase SB-C18 column in conjunction with a gradient elution and detected by fluorescence detection at excitation and emission wavelengths of 371 nm and 421 nm. The established method exhibited excellent linearity over the injected amount of benzaldehyde of 0.003 to 5 nmol mL ~(?1) . The method was successfully applied to the determination of serum semicarbazide-sensitive amine oxidase (SSAO) activity in humans. SSAO is a significant biomarker because serum SSAO activity is elevated in patients with Alzheimer's disease, vascular disorders, heart disease and diabetes mellitus. It was demonstrated that the SSAO activity of the hyperglycemic group (60 ± 4 nmol mL ~(?1) h ~(?1) ) was significantly higher than that of normal blood sugar group (44 ± 4 nmol mL ~(?1) h ~(?1) ) with P < 0.05.
机译:设计并合成了一种新型的荧光标记试剂N-乙酰肼a啶酮(AHAD)。开发了一种高灵敏的高效液相色谱(HPLC)方法,结合荧光检测,用AHAD衍生化后即可测定苯甲醛。以三氯乙酸为催化剂,在40°C下进行30分钟的最佳衍生。苯甲醛衍生物在反相SB-C18色谱柱上与梯度洗脱一起分离,并通过荧光检测在371 nm和421 nm的激发和发射波长下进行检测。建立的方法在苯甲醛的注入量为0.003至5 nmol mL〜(?1)时表现出极好的线性。该方法已成功地用于测定人类血清对氨基脲敏感的胺氧化酶(SSAO)活性。 SSAO是重要的生物标志物,因为阿尔茨海默氏病,血管疾病,心脏病和糖尿病患者的血清SSAO活性升高。结果表明,高血糖组的SSAO活性(60±4 nmol mL〜(?1)h〜(?1))明显高于正常血糖组(44±4 nmol mL〜(?1))。 h〜(?1)),P <0.05。

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