State Key Laboratory of Physical Chemistry of Solid Surfaces, College of Chemistry and Chemical Engineering, College of Energy, Department of Physics, Institute of Artificial Intelligence, Xiamen Heart Research Center Affiliated with Xiamen University, Xiamen University, Xiamen, 361005, China.
Key Laboratory for Modern Measurement Technology and Instruments of Zhejiang Province, China Jiliang University, Hangzhou, 310018, China.
Biosens Bioelectron. 2024 May 1;251:116101. doi: 10.1016/j.bios.2024.116101. Epub 2024 Feb 2.
Abnormal levels of uric acid (UA) in urine serve as warning signs for gout and metabolic cardiovascular diseases, necessitating the monitoring of UA levels for early prevention. However, the current analytical methods employed suffer from limitations in terms of inadequate suitability for home-based applications and the requirement of non-invasive procedures. In this approach, creatinine, a metabolite with a constant excretion rate, was incorporated as an endogenous internal standard (e-IS) for calibration, presenting a rapid, pretreatment-free, and accurate strategy for quantitative determination of UA concentrations. By utilizing urine creatinine as an internal reference value to calibrate the signal fluctuation of surface-enhanced Raman spectroscopy (SERS) of UA, the quantitative accuracy can be significantly improved without the need for an external internal standard. Due to the influence of the medium, UA, which carries a negative charge, is selectively adsorbed by Au@Ag nanoparticles functionalized with hexadecyltrimethylammonium chloride (CTAC) in this system. Furthermore, a highly convenient detection method was developed, which eliminates the need for pre-processing and minimizes matrix interference by simple dilution. The method was applied to the urine detection of different volunteers, and the results were highly consistent with those obtained using the UA colorimetric kit (UACK). The detection time of SERS was only 30 s, which is 50 times faster than UACK. This quantitative strategy of using urinary creatinine as an internal standard to correct the SERS intensity of uric acid is also expected to be extended to the quantitative detection needs of other biomarkers in urine.
尿液中尿酸 (UA) 水平异常是痛风和代谢性心血管疾病的警告信号,因此需要监测 UA 水平以进行早期预防。然而,目前使用的分析方法在适用于家庭应用方面存在局限性,并且需要非侵入性程序。在这种方法中,肌酐作为一种具有恒定排泄率的代谢物被用作内标 (e-IS) 进行校准,提供了一种快速、无需预处理且准确的定量测定 UA 浓度的策略。通过利用尿肌酐作为内部参考值来校准 UA 的表面增强拉曼光谱 (SERS) 的信号波动,可以显著提高定量准确性,而无需外部内标。由于介质的影响,带负电荷的 UA 在该体系中被十六烷基三甲基氯化铵 (CTAC) 功能化的 Au@Ag 纳米粒子选择性吸附。此外,还开发了一种非常方便的检测方法,通过简单稀释消除了预处理的需要,并最大限度地减少了基质干扰。该方法应用于不同志愿者的尿液检测,结果与 UA 比色试剂盒 (UACK) 的检测结果高度一致。SERS 的检测时间仅为 30 秒,比 UACK 快 50 倍。这种使用尿肌酐作为内标校正尿酸 SERS 强度的定量策略也有望扩展到尿液中其他生物标志物的定量检测需求。