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Published on: March 8, 2024
Pipetting-driven microfluidic immunohistochemistry to facilitate enhanced immunoreaction and effective use of
Segi Kim1, Seyong Kwon1, Chang Hyun Cho1
1Department of Bio and Brain Engineering, Korea Advanced Institute of Science and Technology (KAIST), 291 Daehak-ro, Yuseong-gu, Daejeon 34141, Republic of Korea. jekyun@kaist.ac.kr.
Insights
This study introduces a novel microfluidic immunohistochemistry (IHC) platform operated by a manual pipette. This easy-to-use system significantly reduces processing time and antibody waste for disease diagnosis.
Area of Science:
- Biotechnology
- Medical Diagnostics
- Analytical Chemistry
Background:
- Immunohistochemistry (IHC) is crucial for cancer diagnosis and research but is time-consuming and costly.
- Existing microfluidic IHC platforms require specialized equipment, limiting real-world application.
- Continuous flow in microfluidic systems leads to inefficient antibody use.
Purpose of the Study:
- To develop a novel, user-friendly microfluidic IHC platform.
- To eliminate the need for external pumps or controllers in microfluidic IHC.
- To enhance antigen-antibody reactions and reduce antibody waste.
Main Methods:
- A microfluidic IHC device operated solely by manual pipetting was developed.
- Bidirectional fluid flow was induced via repetitive manual pipetting.
- Breast cancer cell and tissue sections were stained using the developed platform.
Main Results:
- The platform achieved effective immunostaining in under 2 minutes of pipetting.
- Staining intensity was comparable to conventional IHC methods requiring 1 hour.
- The system demonstrated efficient antibody utilization and sample preservation.
Conclusions:
- The manual pipetting-based microfluidic IHC platform offers a convenient and accessible solution.
- This approach simplifies microfluidic IHC for practical use in clinical and research settings.
- The system enhances efficiency and reduces costs associated with IHC.
Abstract:
Immunohistochemistry (IHC), which has been used to detect antigens in cells of a tissue section using an immunoreaction between an antibody and an antigen, is a practical tool for identifying the type and stage of diseases in cancer diagnosis and scientific research. However, conventional IHC requires long, laborious process times and high costs. Although microfluidic IHC platforms have been developed to overcome these limitations, the application of microfluidic IHC in real-world environments is still limited due to the additional equipment needed to operate the microfluidic systems. In addition, continuous flow in a microfluidic channel leads to a waste of unbound antibodies. In this study, we demonstrate a novel and easy-to-use microfluidic IHC platform operated only using a manual pipette that is commonly available in research laboratories or hospitals. No other device such as a pump or a controller is required to operate our system. Bidirectional flows of the antibody solution in a microfluidic device are induced by repetitive manual pipetting which facilitates the enhanced antigen-antibody reaction and enables the effective use of a limited amount of antibody. When breast cancer cell and tissue sections are reacted with antibodies using our platform, pipetting for less than 2 min is sufficient to obtain immunostaining results without damaging the sample. The staining intensity by our method is similar to that of the sample stained for 1 h by a conventional batch process. We believe that this pipetting-based approach to the operation of a microfluidic system allows end users to use microfluidic IHC more conveniently and easily in real-world environments.
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