4.8 Article

Optical-based microbubble for on-demand droplet release from static droplet array (SDA) for dispensing one droplet into one tube

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BIOSENSORS & BIOELECTRONICS
卷 240, 期 -, 页码 -

出版社

ELSEVIER ADVANCED TECHNOLOGY
DOI: 10.1016/j.bios.2023.115639

关键词

Static droplet array (SDA); Microfluidics; On-demand release; Laser-responsive

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Static droplet arrays are important for high-capacity screening assays, but extracting target droplets remains a challenge. This study presents an optical-based on-demand droplet release system using a 1064 nm laser to push out droplets. The system has a high success rate and low residual volume, making it suitable for high-throughput screening assays.
Static droplet array (SDA) is a pivotal tool for high-capacity screening assays, yet extraction and collection the target droplets that contain unique analytes or cells from the SDA remains one major technical bottleneck that limits its broader application. Here we present an optical-based on-demand droplet release (OODR) system by incorporating a 1064 nm laser-responsive indium tin oxide (ITO) layer into a chamber array-based droplet microfluidic chip. By focusing the 1064 nm laser onto the ITO layer, microbubbles can be created via local heating to selectively push-out the droplets from the chamber. Then the released droplet is readily exported in a one-droplet-one-tube (ODOT) manner by the inherent capillary force into pipette tip. Releasing of the droplets containing fluorescein sodium demonstrated -100% successful rate (9 out of 6400 droplets were successfully released) and low residual (only -5% of the droplet volume remains in the chamber). White or fluorescence image-based releasing of single-cell-droplets directly after cell loading or multi-cells-droplets derived from onchip single-cell cultivation for both E. coli and yeast cells further demonstrated the wide applicability of OODR. The present system is user-friendly and has the potential to be applied in various high-throughput screening assays, including single molecule/cell analysis, drug screening, and phenotype-based cell sorting.

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