泉州师范学院学报
泉州師範學院學報
천주사범학원학보
Journal of Quanzhou Normal College
2013年
2期
61~64
,共null页
毛细管电泳 电化学发光 对乙酰氨基酚
毛細管電泳 電化學髮光 對乙酰氨基酚
모세관전영 전화학발광 대을선안기분
electrochemiluminescence; capillary electrophoresis; paracetamol
联吡啶钌是一种电化学发光试剂,对乙酰氨基酚对其电致发光信号有增敏作用.基于此原理,建立了毛细管电泳电化学发光分析方法用于测定对乙酰氨基酚.讨论了磷酸盐缓冲液pH值、浓度等实验参数对于对乙酰氨基酚检测的影响.在最佳实验条件下,检测电位1.15V;钌联吡啶浓度5mmol/L;检测池缓冲溶液50mmol/L(pH7.5);流动缓冲液50mmol/L(pH7.5);进样高压10kV;进样时间8s,运行高压12kV,在3min内可实现对乙酰氨基酚的分离检测,对乙酰氨基酚在0.05~10mg/L内呈良好线性,检出限为0.01rag/L.对1.0mg/L对乙酰氨基酚进行7次重复测定,所得电化学发光信号和迁移时间的RSD分别为3.5%和1.6%(n=7).在优化的实验条件下,应用此法测定了实际样品中对乙酰氨基酚的含量,回收率为92%~105%.
聯吡啶釕是一種電化學髮光試劑,對乙酰氨基酚對其電緻髮光信號有增敏作用.基于此原理,建立瞭毛細管電泳電化學髮光分析方法用于測定對乙酰氨基酚.討論瞭燐痠鹽緩遲液pH值、濃度等實驗參數對于對乙酰氨基酚檢測的影響.在最佳實驗條件下,檢測電位1.15V;釕聯吡啶濃度5mmol/L;檢測池緩遲溶液50mmol/L(pH7.5);流動緩遲液50mmol/L(pH7.5);進樣高壓10kV;進樣時間8s,運行高壓12kV,在3min內可實現對乙酰氨基酚的分離檢測,對乙酰氨基酚在0.05~10mg/L內呈良好線性,檢齣限為0.01rag/L.對1.0mg/L對乙酰氨基酚進行7次重複測定,所得電化學髮光信號和遷移時間的RSD分彆為3.5%和1.6%(n=7).在優化的實驗條件下,應用此法測定瞭實際樣品中對乙酰氨基酚的含量,迴收率為92%~105%.
련필정조시일충전화학발광시제,대을선안기분대기전치발광신호유증민작용.기우차원리,건립료모세관전영전화학발광분석방법용우측정대을선안기분.토론료린산염완충액pH치、농도등실험삼수대우대을선안기분검측적영향.재최가실험조건하,검측전위1.15V;조련필정농도5mmol/L;검측지완충용액50mmol/L(pH7.5);류동완충액50mmol/L(pH7.5);진양고압10kV;진양시간8s,운행고압12kV,재3min내가실현대을선안기분적분리검측,대을선안기분재0.05~10mg/L내정량호선성,검출한위0.01rag/L.대1.0mg/L대을선안기분진행7차중복측정,소득전화학발광신호화천이시간적RSD분별위3.5%화1.6%(n=7).재우화적실험조건하,응용차법측정료실제양품중대을선안기분적함량,회수솔위92%~105%.
A simple method is developed for the determination of paracetamol by electrochemi- lurninescence(ECL)detection with the aid of capillary electrophoresis, which is based on the fact that the ECL intensity of Ru(bpy)2 3 + can be enhanced in the presence of paracetamol in PBS medium. Sample solution is injected to separation capillary of 40 cm length (25 μm i.d.) by electrokinetic iniection for 8 s at 10 kV. Under the optimized condition, the linear range from 0.05-10 mg/L for paracetamol and detection limit (S/N=3) of 0.1mg/L is achieved. The RSD of migration time and ECL intensity for continuous injections of lmg/L paracetamol (n = 7) are 1.6% and 3.5%, respectively.This method has been applied to the analysis of paracetamol in real samples, and the recovery ranged from 92% to 105%.