Droplet microfluidics has emerged as a versatile and powerful tool for various analytical applications, including single-cell studies, synthetic biology, directed evolution, and diagnostics. Initially, access to droplet microfluidics was predominantly limited to specialized technology labs. However, the landscape is shifting with the increasing availability of commercialized droplet manipulation technologies, thereby expanding its use to non-specialized labs. Although these commercial solutions offer robust platforms, their adaptability is often constrained compared to in-house developed devices. Consequently, both within the industry and academia, significant efforts are being made to further enhance the robustness and automation of droplet-based platforms, not only to facilitate technology transfer to non-expert laboratories but also to reduce experimental failures. This Perspective article provides an overview of recent advancements aimed at increasing the robustness and accessibility of systems enabling complex droplet manipulations. The discussion encompasses diverse aspects such as droplet generation, reagent addition, splitting, washing, incubation, sorting, and dispensing. Moreover, alternative techniques like double emulsions and hydrogel capsules, minimizing or eliminating the need for microfluidic operations by the end user, are explored. These developments are foreseen to facilitate the integration of intricate droplet manipulations by non-expert users in their workflows, thereby fostering broader and faster adoption across scientific domains.
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http://dx.doi.org/10.1063/5.0242599 | DOI Listing |
Cell Rep Med
March 2025
Nuffield Department of Clinical Neurosciences & Kavli Institute for Nanoscience Discovery, University of Oxford, Oxford, UK. Electronic address:
Accurate diagnosis of early Parkinson's disease requires platforms suitable for detecting minute amounts of neuronally derived biomarkers in the massive protein excess of easily accessible biofluids such as blood. Here, we describe an on-chip droplet-confined fluorescence reporting assay that identified α-synuclein on the membrane of L1CAM+ extracellular vesicles (EVs) immunocaptured from human serum and corroborate this finding by super-resolution direct stochastic optical reconstruction microscopy (dSTORM) microscopy. Using conditioned media from neuroblastoma cells expressing α-synuclein mutants or patient-derived induced pluripotent stem cell (iPSC) neurons with α-synuclein gene triplication, we found that association of α-synuclein with the L1CAM+ EV surface is increased under pathological conditions.
View Article and Find Full Text PDFCyborg Bionic Syst
March 2025
Key Laboratory of Biomimetic Robots and Systems (Beijing Institute of Technology), Ministry of Education, Beijing 100081, China.
Digital microfluidic chips (DMCs) have shown huge potential for biochemical analysis applications due to their excellent droplet manipulation capabilities. The driving force is a critical factor for characterizing and optimizing the performance of droplet manipulation. Conducting numerical analysis of the driving force is essential for DMC design, as it helps optimize the structural parameters.
View Article and Find Full Text PDFAnal Chem
March 2025
Queensland Micro and Nanotechnology Centre, Griffith University, Nathan, QLD 4111, Australia.
Double emulsions are highly structured dispersion systems that generate double-layered droplets. Double emulsions offer an effective platform for encapsulating liquid samples. Multilayer protection, controlled release of encapsulated materials, and stability make double emulsions superior to single emulsions in handling sensitive liquid samples.
View Article and Find Full Text PDFMicromachines (Basel)
January 2025
Biomedical and Chemical Engineering, The Catholic University of Korea, 43 Jibong-ro Wonmi-gu, Bucheon-si 14662, Gyeonggi-do, Republic of Korea.
Microfluidic devices are greatly affected by the materials used. The materials used in previous studies had problems in various aspects, such as processing, adsorption, and price. This study will investigate the materials needed to overcome such problems.
View Article and Find Full Text PDFMicromachines (Basel)
January 2025
Laboratory for Future Interdisciplinary Research of Science and Technology (FIRST), Institute of Integrated Research, Institute of Science Tokyo, R2-9, 4259 Nagatsuta-cho, Midori-ku, Yokohama 226-8501, Japan.
Step emulsification (SE) is renowned for its robustness in generating monodisperse emulsion droplets at arrayed nozzles. However, few studies have explored poly(dimethylsiloxane) (PDMS)-based SE devices for producing monodisperse oil-in-water (O/W) droplets and polymeric microspheres with diameters below 20 µm-materials with broad applicability. In this study, we present a PDMS-based microfluidic SE device designed to achieve this goal.
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