Related Experiment Video
Updated: Jul 13, 2026

11:16
A Microfluidic Chip for ICPMS Sample Introduction
Published on: March 5, 2015
Fabrication of a monolithic sampling probe system for automated and continuous sample introduction in microchip-based
Qiao-Hong He1, Qun Fang, Wen-Bin Du
1Institute of Microanalytical Systems, Zhejiang University, Hangzhou, PR China.
Electrophoresis
|July 21, 2007
Summary
A new fabrication method creates integrated sampling probes on microfluidic chips for continuous capillary electrophoresis (CE) analysis. This system achieves high throughput and low sample consumption for analyzing amino acids.
Area of Science:
- Analytical Chemistry
- Microfluidics
- Separation Science
Background:
- Developing efficient sample introduction systems is crucial for chip-based capillary electrophoresis (CE).
- Traditional methods often face limitations in throughput and sample consumption.
Purpose of the Study:
- To develop a simple fabrication process for monolithic sampling probes on glass microfluidic chips.
- To integrate these chips with a continuous sample presentation system for chip-based CE.
- To evaluate the system's performance for high-throughput analysis of FITC-labeled amino acids.
Main Methods:
- Fabrication of monolithic sampling probes on glass chips using basic tools.
- Integration of microfluidic chips with a slotted-vial array for continuous sample introduction.
- Utilizing on-chip reservoirs for stable hydrostatic pressure during prolonged operation.
- Demonstration using FITC-labeled amino acids with Laser-Induced Fluorescence (LIF) detection.
- Application of gradient CE for enhanced separation efficiency.
Main Results:
- Achieved high throughput of 30-60 samples per hour with low carry-over (<1.0%).
- Demonstrated excellent reproducibility in peak height (3.3-3.6% RSD) and long-term analysis (6.8-7.5% RSD).
- Obtained extremely low sample consumption (30 nL per analysis).
- Reported separation efficiencies in the range of 0.8-2x10^5 plates/m.
- Gradient CE showed improved separation efficiency compared to isocratic methods.
Conclusions:
- The developed fabrication process and integrated system enable efficient, high-throughput, and low-consumption continuous analysis in chip-based CE.
- The system is versatile, applicable for both sample introduction and generating gradients for improved separations.
- This approach offers a significant advancement for automated and rapid analysis in microfluidic systems.

