# Extraction of electrokinetically separated analytes with on-demand   encapsulation

**Authors:** Xander F. van Kooten, Moran Bercovici, Govind V. Kaigala

arXiv: 1812.11497 · 2019-01-01

## TL;DR

This paper introduces a novel two-phase encapsulation technique that preserves electrokinetically separated analytes without continuous electric fields, enabling long-term storage and manipulation for molecular assays.

## Contribution

The authors develop a passive oil-phase encapsulation method that maintains analyte concentration post-electrophoretic separation, overcoming a key limitation of existing microchip electrokinetic techniques.

## Key findings

- Encapsulated DNA oligonucleotides remain concentrated for tens of minutes.
- The method achieves a 22-fold concentration increase over free diffusion.
- Single droplet manipulation enables off-chip detection and analysis.

## Abstract

Microchip electrokinetic methods are capable of increasing the sensitivity of molecular assays by enriching and purifying target analytes. However, their use is currently limited to assays that can be performed under a high external electric field, as spatial separation and focusing is lost when the electric field is removed. We present a novel method that uses two-phase encapsulation to overcome this limitation. The method uses passive filling and pinning of an oil phase in hydrophobic channels to encapsulate electrokinetically separated and focused analytes with a brief pressure pulse. The resulting encapsulated sample droplet maintains its concentration over long periods of time without requiring an electric field and can be manipulated for further analysis, either on- or off- chip. We demonstrate the method by encapsulating DNA oligonucleotides in a 240 pL aqueous segment after isotachophoresis (ITP) focusing, and show that the concentration remains at 60% of the initial value for tens of minutes, a 22-fold increase over free diffusion after 20 minutes. Furthermore, we demonstrate manipulation of a single droplet by selectively encapsulating amplicon after ITP purification from a polymerase chain reaction (PCR) mix, and performing parallel off-chip detection reactions using the droplet. We provide geometrical design guidelines for devices implementing the encapsulation method, and show how the method can be scaled to multiple analyte zones.

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Source: https://tomesphere.com/paper/1812.11497