毛细管电泳-电容耦合非接触式电导检测方法在低频率激励下的性能优化OA
Performance Investigation and Optimization of Capillary Electrophoresis with Capacitively Coupled Contactless Conductivity Detection at Low Excitation Frequencies
毛细管电泳-电容耦合非接触式电导检测(CE-C4D)方法具有进样量小、高通量、可检测阴阳离子、分析速度快和仪器易于小型化等优点,随着CE-C4D方法自身灵敏度不断提升,开发高灵敏度、小型化的CE-C4D仪器对该方法的推广应用至关重要.电容数字转换(CDC)检测技术仅依托单一芯片即可实现激励波形输出、电容值采集、24 bit模数转换和数字信号传输功能,有利于推动C4D仪器小型化的发展.然而,该技术固定工作于低频率激励条件(30 kHz,激励电压 3.3 V,参数不可调)下,这与传统 C4D 仪器采用的0.1~1 MHz级激励频率的特征存在显著差异.为深入探究低频率激励对C4D信号、分离效率和方法检出限的影响规律,本研究基于C4D等效电路模型,采用基于差分检测的电导测量模式,系统考察了电极长度、激励频率和电子电路等对CE-C4D信号强度和分离度的影响.结果表明,在1 MHz~30 kHz范围内,随着激励频率降低,Li+电泳谱图半峰宽明显展宽,由约1.24 s增至3.36 s,推测此现象是由低频率下检测有效区间增大所导致,但谱峰展宽不利于提高电泳分离效率.基于低频率激励下有效带宽较低的特性,本研究首次采用提升激励电压和电路增益的方式,优化并提升了CE-C4D技术在低频率激励下的方法灵敏度,对Li+的检出限可低至100 nmol/L.本研究结合模型分析和实验验证,进一步深化了对CE-C4D技术在低激励频率下信号响应特性的认识.
The capillary Electrophoresis-capacitively coupled contactless conductivity detection(CE-C4D)method offers many advantages such as small sample volume,high throughput,simultaneous detection of cations and anions,fast analysis speed,and easy miniaturization of instruments.With the continuous improvement of its own sensitivity,the development of CE-C4D instruments featuring both high sensitivity and miniaturization is crucial for the further promotion of this method.Capacitance-to-digital converter(CDC)detection technology is highly conducive to the miniaturization of C4D instruments,as it can realize functions including output of excitation waveform,capacitance acquisition,24-bit analog-to-digital conversion,and digital signal transmission through a single chip.However,this technique operates under low-frequency excitation(30 kHz,excitation voltage of 3.3 V with fixed parameters),which is significantly different from the traditional 100-kHz or MHz-level excitation frequencies.To conduct an in-depth study on the influencing factors of C4D signals,separation efficiency and method detection limit under low-frequency excitation,this work started from the equivalent circuit model of C4D and adopted a conductivity measurement model based on differential detection to systematically investigate the effects of electrode length,excitation frequency,and electronic circuits on CE-C4D signals and resolution.It was found that as the excitation frequency decreased from 1 MHz to 30 kHz,the half-peak width of the Li+electrophoretic chromatogram significantly broadened,approximately from 1.24 s to 3.36 s.This phenomenon was speculated to be caused by the increased effective detection interval under low frequencies,but peak broadening was unfavorable for improving electrophoretic separation efficiency.Based on this low-frequency characteristic(i.e.,low effective bandwidth),the method detection limit of CE-C4D technology under low-frequency excitation was optimized and improved for the first time by increasing the excitation voltage and circuit gain,achieving a detection limit of 100 nmol/L for Li+samples.Through model analysis and experimental research,this work further broadened the understanding of the signal response characteristics of CE-C4D technology under low excitation frequencies.
赵睿;景瑞斌;王永奇;樊新鸿;张正渊;陈宏刚;马玲
国网甘肃省电力公司电力科学研究院,兰州 730000国网甘肃省电力公司电力科学研究院,兰州 730000国网甘肃省电力公司电力科学研究院,兰州 730000国网甘肃省电力公司电力科学研究院,兰州 730000国网甘肃省电力公司电力科学研究院,兰州 730000国网甘肃省电力公司电力科学研究院,兰州 730000国网甘肃省电力公司电力科学研究院,兰州 730000
毛细管电泳电容耦合非接触式电导检测低频率激励检出限
Capillary electrophoresisCapacitively coupled contactless conductivity detectionLow frequency excitationLimit of detection
《分析化学》 2026 (6)
1084-1092,9
国网甘肃省电力公司科技项目(No.52272225000G)资助. Supported by State Grid Gansu Electric Power Company Science and Technology Project(No.52272225000G).
评论