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The integration of optical filtration functionality into a lens and a microfluidic chip represents a promising approach for reducing the size of a microfluidic device. Greenly fabricating a composite polydimethylsiloxane (PDMS) filter (C-filter) with optical amplification function for chlorophyll fluorescence detection was proposed in this work. The core idea is to make the PDMS microfluidic chip as one sub-filter (S-filter) and enable another sub-filter amplification function (F-lens). The S-filter was prepared by soaking a PDMS microfluidic chip into Sudan II dye solved with ethanol. The F-lens is manufactured by sequentially mixing ethanol-solved crystal violet and the dimethyl-methylhydrogenosiloxane and dimethyl-methylvinylsiloxane for lens molding. Experimental results show that ethanol can serve as an effective and green substitute for phenol and toluene for dye dissolving. The dimethyl-methylhydrogenosiloxane can well dissolve crystal violet. The S-filter can filter light within the wavelength range of 400-500 nm, while the F-lens can filter light in the wavelength range of 500-650 nm. The C-filter shows a transmittance of 99.33 % in the wave length range of 650-710 nm, which is superior to the 96.72 % transmittance of commercial filters and is well-suited for living algae detection.
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http://dx.doi.org/10.1016/j.saa.2025.126533 | DOI Listing |
Langmuir
September 2025
School of Biomedical Engineering, Anhui Medical University, Hefei 230032, China.
Optical manipulation techniques have been widely applied in the biomedical field. However, the key issues limiting the efficiency of optical manipulation techniques are the weak driving force of optical scattering and the small working range of optical gradient forces. The optothermal Marangoni convection enables effective control of flow fields through optical means, and particle manipulation based on this mechanism offers advantages such as a wide working range, strong driving force, and high flexibility.
View Article and Find Full Text PDFAdv Healthc Mater
September 2025
Department of Biomedical Engineering, University of Delaware, Newark, DE, 19716, USA.
Organ-on-chip (OOC) technologies, also called microphysiological systems (MPS), offer dynamic microenvironments that improve upon static culture systems, yet widespread adoption has been hindered by fabrication complexity, reliance on polydimethylsiloxane (PDMS), and limited modularity. Here, a modular MPS platform is presented, designed for ease of use, reproducibility, and broad applicability. The system comprises layered elastomeric inserts for dual monolayer cell culture, which is clamped within a reusable acrylic cassette for perfusion studies.
View Article and Find Full Text PDFJ Control Release
September 2025
Institute of Biomedical Engineering, University of Toronto, Toronto, Ontario M5S 3G9, Canada; The Keenan Research Centre for Biomedical Science of St. Michael's Hospital, Unity Health Toronto, Toronto, Ontario M5B 1T8, Canada; Leslie Dan Faculty of Pharmacy, University of Toronto, Toronto, Ontario M
Microfluidic hydrodynamic focusing (HF) has emerged as a powerful platform for the controlled synthesis of lipid nanoparticles (LNPs) and liposomes, offering superior precision, reproducibility, and scalability compared to traditional batch methods. However, the impact of HF inlet configuration and channel geometry on nanoparticle formation remains poorly understood. In this study, we present a comprehensive experimental and computational analysis comparing 2-inlet (2-way) and 4-inlet (4-way) HF designs across various sheath inlet angles (45°, 90°, 135°) and cross-sectional geometries (square vs.
View Article and Find Full Text PDFAnalyst
September 2025
School of Biomedical Engineering (Suzhou), Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei 230026, China.
Microfluidics-assisted spatially barcoded microarray technology offers a high-throughput, low-cost approach towards spatial transcriptomic profiling. A uniform barcoded microarray is crucial for spatially unbiased mRNA analysis. However, non-specific adsorption of barcoding reagents in microchannels occurs during liquid transport, causing non-uniform barcoding in the chip's functional regions.
View Article and Find Full Text PDFAnalyst
September 2025
Research Centre for Analytical Instrumentation, State Key Laboratory of Industrial Control Technology, Zhejiang University, Hangzhou 310027, P. R. China.
Rapid and efficient screening of foodborne pathogens is crucial for preventing bacterial spread and food poisoning. However, developing a multi-detection method that is easy to operate, offers good stability, and achieves high efficiency remains an enormous challenge. Existing multiplexed nucleic acid detection methods suffer from complex designs, leading to complicated operations, and non-robust sample introduction, causing primer/probe crosstalk and false-positive results.
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