Lou Yingying, Xiao Huiquan, Zou Xiaocong, Xu Zenghui, Sun Zhiwei, Li Zan, Ji Zhongyin, You Jinmao
College of Chemistry and Chemical Engineering, Shaoxing University, Shaoxing, 312000, P. R. China.
Shandong Technician Institute, Liaocheng, 252027, P. R. China.
J Fluoresc. 2025 Jan 13. doi: 10.1007/s10895-024-04098-6.
The fluorescence detection of amino compounds and the evaluation of their content in environmental samples are vital, not only for assessing food quality but also for studying soil organic matter. Here, we present the synthesis and application of a novel fluorescent probe, 4-(9-acridone)benzylmethyl carbonochloride (APE-Cl), for detecting amino compounds via a chloroformate reaction with fluorescence detection. The complete derivatization reaction of APE-Cl with amino compounds can be accomplished in aqueous acetonitrile within 5 min at room temperature, using 0.2 M borate buffer (pH = 9.0). APE-amine derivatives exhibited intense fluorescence with an excitation maximum at λex 254 nm and an emission maximum at λem 418 nm. All derivatives demonstrated high stability, strong fluorescence, and elevated ionization potential under atmospheric pressure chemical ionization (APCI-MS) in positive ion detection mode. The method, combined with gradient elution, provides baseline resolution of common amine derivatives on a reversed-phase C18 column. The LC separation for the derivatized amines shows good reproducibility with aqueous acetonitrile as the mobile phase. The relative standard deviations (n = 6) for each amine derivative are < 3.99%. The detection limits (at a signal-to-noise ratio of 3) per injection ranged from 1.68 to 11.2 femtomole. The established pre-column derivatization method for determining amino compounds in practical samples proved to be satisfactory.
氨基化合物的荧光检测及其在环境样品中的含量评估至关重要,这不仅对于评估食品质量,而且对于研究土壤有机质都具有重要意义。在此,我们介绍一种新型荧光探针4-(9-吖啶酮)苄基甲基氯甲酸酯(APE-Cl)的合成及应用,该探针通过氯甲酸酯反应与荧光检测来检测氨基化合物。在室温下,使用0.2 M硼酸盐缓冲液(pH = 9.0),APE-Cl与氨基化合物的完全衍生化反应可在乙腈水溶液中5分钟内完成。APE-胺衍生物表现出强烈的荧光,最大激发波长为λex 254 nm,最大发射波长为λem 418 nm。在大气压化学电离(APCI-MS)正离子检测模式下,所有衍生物均表现出高稳定性、强荧光和较高的电离电位。该方法与梯度洗脱相结合,可在反相C18柱上实现常见胺衍生物的基线分离。以乙腈水溶液为流动相,衍生化胺的液相色谱分离具有良好的重现性。每种胺衍生物的相对标准偏差(n = 6)< 3.99%。每次进样的检测限(信噪比为3时)范围为1.68至11.2飞摩尔。所建立的用于测定实际样品中氨基化合物的柱前衍生化方法被证明是令人满意的。