4.8 Article

Simplified, Shear Induced Generation of Double Emulsions for Robust Compartmentalization during Single Genome Analysis

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 14, Issue 18, Pages 20528-20537

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.1c22692

Keywords

microfluidics; double emulsion; droplet; shell thickness; coalescence; compartmentalization; single-cell barcoding

Funding

  1. Gordon and Betty Moore Foundation [GBMF9195]
  2. University of Illinois at Urbana-Champaign through the UIUC Startup Grant

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This study demonstrates that double emulsion (DE) drops can address the instability issue of single emulsion (SE) drops and prevent content mixing. A simple DE drop maker is also developed, allowing for the production of single-core DEs at various flow rates and better control over shell thickness. DE drops show excellent stability during thermal cycling and maintain the monodispersity throughout the workflow. DE drops have advantages for multistep reactions due to their resistance to content mixing.
Drop microfluidics has driven innovations for high throughput, low input analysis techniques such as single-cell RNA-seq. However, the instability of single emulsion (SE) drops occasionally causes significant merging during drop processing, limiting most applications to single-step reactions in drops. Here, we show that double emulsion (DE) drops address this critical limitation and completely prevent drop contents from mixing. DEs show excellent stability during thermal cycling. More importantly, DEs undergo rupture into the continuous phase instead of merging, preventing content mixing and eliminating unstable drops from the downstream analysis. Due to the lack of drop merging, the monodispersity of drops is maintained throughout a workflow, enabling the deterministic manipulation of drops downstream. We also developed a simple, one-layer DE drop maker compatible with simple surface treatment using a plasma cleaner. The device allows for the robust production of single-core DEs at a wide range of flow rates and better control over the shell thickness, both of which have been significant limitations of conventional two-layer devices. This approach makes the fabrication of DE devices much more accessible, facilitating its broader adoption. Finally, we show that DE droplets eliminate content mixing and maintain compartmentalization of single virus genomes during PCR-based amplification and barcoding, while SEs mixed contents due to merging. With their resistance to content mixing, DE drops have key advantages for multistep reactions in drops, which is limited in SEs due to merging and content mixing.

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