Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Bridging the Gap - Advancing Microfluidics From Laboratory to Point-of-Care.

IEEE reviews in biomedical engineering·2026
Same author

Monitoring algal blooms in eutrophic inland lakes using OLCI: Overcoming cloud and sun-glint effects on low-quality imagery.

Journal of hazardous materials·2026
Same author

Ultrasensitive Nucleic Acid Testing: From Foundational Research to Clinical Translation.

ACS nano·2025
Same author

Standalone self-compartmentalizing microfluidic chip for digital single-cell antimicrobial susceptibility testing.

Journal of pharmaceutical and biomedical analysis·2025
Same author

Design, Synthesis and Anti-Inflammation Evaluation of <i>N</i>-Acyl Tryptophan Derivatives as Promising P2Y<sub>14</sub>R Antagonists Against Lipopolysaccharide-Induced Acute Lung Injury.

Drug design, development and therapy·2025
Same author

A Finger-Actuated Microfluidic System for Point-Of-Care Detection of SARS-CoV-2 and Influenza A.

Analytical chemistry·2025

Related Experiment Video

Updated: Dec 14, 2025

A Microfluidic Platform for Precision Small-volume Sample Processing and Its Use to Size Separate Biological Particles with an Acoustic Microdevice
11:32

A Microfluidic Platform for Precision Small-volume Sample Processing and Its Use to Size Separate Biological Particles with an Acoustic Microdevice

Published on: November 23, 2015

14.2K

A scalable microfluidic chamber array for sample-loss-free and bubble-proof sample compartmentalization by simple

Baobao Lin1, Zijian Guo, Zhi Geng

  • 1Department of Biomedical Engineering, School of Medicine, Tsinghua University, Beijing, 100084, China. pliu@tsinghua.edu.cn.

Lab on a Chip
|July 23, 2020
PubMed
Summary

A new self-compartmentalization device with capillary burst valves enables efficient sample partitioning for bioassays. This microfluidic platform achieves 100% sample utilization, enhancing applications like digital PCR (dPCR).

More Related Videos

A Microfluidic Chip for ICPMS Sample Introduction
11:16

A Microfluidic Chip for ICPMS Sample Introduction

Published on: March 5, 2015

11.6K
Microfluidic Chips Controlled with Elastomeric Microvalve Arrays
18:11

Microfluidic Chips Controlled with Elastomeric Microvalve Arrays

Published on: October 1, 2007

21.6K

Related Experiment Videos

Last Updated: Dec 14, 2025

A Microfluidic Platform for Precision Small-volume Sample Processing and Its Use to Size Separate Biological Particles with an Acoustic Microdevice
11:32

A Microfluidic Platform for Precision Small-volume Sample Processing and Its Use to Size Separate Biological Particles with an Acoustic Microdevice

Published on: November 23, 2015

14.2K
A Microfluidic Chip for ICPMS Sample Introduction
11:16

A Microfluidic Chip for ICPMS Sample Introduction

Published on: March 5, 2015

11.6K
Microfluidic Chips Controlled with Elastomeric Microvalve Arrays
18:11

Microfluidic Chips Controlled with Elastomeric Microvalve Arrays

Published on: October 1, 2007

21.6K

Area of Science:

  • Biotechnology
  • Microfluidics
  • Analytical Chemistry

Background:

  • Sample compartmentalization is crucial for bioanalytical techniques like multiplex polymerase chain reaction (PCR) and digital PCR (dPCR).
  • Existing methods often face challenges with sample utilization and interference from air bubbles.

Purpose of the Study:

  • To develop a novel self-compartmentalization device for efficient and scalable sample partitioning.
  • To demonstrate the device's capability in bioassays with high sample utilization.

Main Methods:

  • Designed a microfluidic device with an array of microchambers connected by a main microchannel.
  • Incorporated three capillary burst valves (CBVs) for sequential fluid switching and partitioning.
  • Optimized CBV burst pressures for controlled sample loading and isolation with air or oil.

Main Results:

  • Achieved a 100% sample utilization rate, unaffected by manual pipetting or air bubbles.
  • Demonstrated scalability from a few to tens of thousands of microchambers.
  • Successfully performed mock multiplex loop-mediated isothermal amplifications (LAMP) in a 144-microchamber array.

Conclusions:

  • The developed self-compartmentalization device offers a robust and versatile platform for sample discretization.
  • This technology has significant potential for advancing various bioanalytical applications requiring precise sample partitioning.