A microfluidic system for introduction of nanolitre sample in inductively coupled plasma mass spectrometry using electrokinetic flow combined with hydrodynamic flow

被引:19
作者
Cheng, Heyong [1 ]
Xu, Zigang [2 ]
Liu, Jinhua [3 ]
Wang, Xiuzhong [1 ,4 ]
Yin, Xuefeng [1 ]
机构
[1] Zhejiang Univ, Dept Chem, Inst Microanalyt Syst, Hangzhou 310027, Zhejiang, Peoples R China
[2] Zhejiang Univ, Dept Chem, Inst Analyt & Appl Chem, Hangzhou 310027, Zhejiang, Peoples R China
[3] Hangzhou Normal Univ, Coll Mat Chem & Chem Engn, Hangzhou 310036, Zhejiang, Peoples R China
[4] Qingdao Agr Univ, Coll Chem & Pharmaceut Sci, Qingdao 266109, Peoples R China
基金
中国国家自然科学基金;
关键词
NANO-LIQUID CHROMATOGRAPHY; INJECTION-ANALYSIS; CHIP; SEPARATION; NEBULIZER;
D O I
10.1039/c1ja10273g
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A microfluidic system for introducing nanolitre sample in inductively coupled plasma mass spectrometry using electrokinetic flow combined with hydrodynamic flow was developed, which consisted of a microfluidic chip, a syringe pump, a high voltage power supply, a homemade microflow nebulizer and a heated single pass spray chamber. In the microfluidic chip, the sample in the reservoir S automatically flew across the intersection P-1 to the reservoir SR under hydrodynamic pressure. Two porous polymer plugs C-1 and C-2 were created on the microchip to isolate electrokinetic flow from the pressure-driven flow. Once a high voltage between S and buffer reservoir B was applied, the sample was driven through the porous polymer plug C-1 into the metering channel by electrokinetic force. Simply changing the sampling time can freely optimize the sampling volume down to 0.18 nL, which was injected into the nebulizer by the pressure-driven makeup solution. The nanolitre sample introducing system has the advantages of low sample consumption, satisfactory precision, low sampling dead volume (0.38 nL) and low sampling dead time (0.42 s). The proposed system was successfully applied to determine platinum content in a serum sample of a cancer patient on cisplatin chemotherapy. The sample consumption of 1.8 nL was about 10(5) times less than that with the conventional sampling system. The sample throughput up to 112 h(-1) could be achieved with the detection limit of 64 ng L-1 for Pt-195. The content of Pt in the sample was 8.4 +/- 0.3 mu g L-1, agreeing well with that (8.5 +/- 0.3 mu g L-1) determined by the conventional sampling system.
引用
收藏
页码:346 / 353
页数:8
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