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A Microfluidic Chip for Detecting Cholangiocarcinoma Cells in Human Bile
Lien-Yu Hung1, Nai-Jung Chiang2,3, Wei-Chun Tsai1
1Department of Power Mechanical Engineering, National Tsing Hua University, Hsinchu, Taiwan.
Scientific Reports
|June 28, 2017
Summary
A new microfluidic system offers a sensitive method for detecting cholangiocarcinoma (CCA) cells in bile. This innovative approach aids in early diagnosis of biliary tract cancer, overcoming limitations of current methods.
Area of Science:
- Oncology
- Biotechnology
- Medical Diagnostics
Background:
- Cholangiocarcinoma (CCA) is a significant cause of liver cancer, often diagnosed late due to limitations in current detection methods.
- Existing diagnostic techniques for CCA are expensive, labor-intensive, and have low sensitivity, particularly in early stages.
Purpose of the Study:
- To develop and validate a novel microfluidic system for the sensitive detection of bile duct cancer cells in human bile.
- To provide a more efficient and accurate diagnostic tool for cholangiocarcinoma.
Main Methods:
- Partially purified human bile was processed through a microfluidic chip.
- The system incorporated cell capture, immunofluorescence (IF) staining with CCA-specific biomarkers, and optical detection modules.
- The system was tested on cell cultures, spiked blood samples, and clinical bile specimens.
Main Results:
- Successful capture and identification of CCA cells from various sample types were demonstrated.
- The system detected >2, 0, and 1 positive cells in 7.5 ml of bile from advanced stage, healthy, and chemotherapy-treated patients, respectively.
- Proof-of-concept validation confirmed the system's ability to identify cancer cells.
Conclusions:
- The developed microfluidic system shows promise as a tool for detecting cancer cells in bile.
- This technology has the potential for early-stage CCA detection, even when cancer cells are present at low densities.
- The system offers a sensitive and potentially cost-effective alternative for cholangiocarcinoma diagnosis.

