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Concentrating Single Cells in Picoliter Droplets for Phospholipid Profiling on a Microfluidic System
Weifei Zhang1, Nan Li1,2, Ling Lin2
1Department of Chemistry, Beijing Key Laboratory of Microanalytical Methods and Instrumentation, MOE Key Laboratory of Bioorganic Phosphorus Chemistry & Chemical Biology, Tsinghua University, Beijing, 100084, China.
Small (Weinheim an Der Bergstrasse, Germany)
|November 27, 2019
Summary
Researchers developed an integrated microfluidic system for single-cell lipid analysis. This system reveals cellular lipid heterogeneity, aiding disease research and drug treatment studies.
Area of Science:
- Biochemistry
- Cell Biology
- Analytical Chemistry
Background:
- Cellular membrane lipids are crucial for cellular function.
- Alterations in lipid profiles are linked to various diseases.
- Understanding intercellular lipid heterogeneity is vital for disease research.
Purpose of the Study:
- To develop an integrated microfluidic system for on-line single-cell lipid analysis.
- To investigate intercellular heterogeneity in lipid composition.
- To assess changes in lipid homeostasis before and after drug treatment.
Main Methods:
- An integrated microfluidic system combining droplet-based inkjet printing, dielectrophoretic electrodes, and de-emulsification.
- On-line single-cell encapsulation, manipulation, and mass spectrometry (MS) detection.
- Comparison of lipid profiles between normal and cancer cells, and drug-treated cells.
Main Results:
- The integrated system achieved improved single-cell encapsulation rates.
- Reduced matrix and oil phase interference in MS detection.
- Observed significant differences in lipid heterogeneity between normal and cancer cells.
- Demonstrated clear changes in lipid profiles of cells post-drug treatment.
Conclusions:
- The developed microfluidic system is effective for analyzing single-cell lipid heterogeneity.
- This technology provides a promising tool for studying the link between lipid homeostasis and diseases.
- The system facilitates the understanding of cellular responses to drug treatments.

