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We demonstrated a unique optofluidic lab-on-a-chip device that can measure optically encoded forward scattering signals. From the design of the spatial pattern, we can measure the position and velocity of each cell in the flow and generate a 2-D cell distribution plot over the cross section of the channel. Moreover, we have demonstrated that the cell distribution is highly sensitive to its size and stiffness. The latter is an important biomarker for cell classification and our method offers a simple and unequivocal method to classify cells by their size and stiffness. We have proved the concept using live and fixed HeLa cells. Due to the stiffness and size difference of neutrophils compared to other types of white blood cells, we have demonstrated detection of neutrophils from other blood cells. Finally, we have performed the test using 5 μL of human blood. In a greatly simplified blood preparation process, skipping the usual steps of anticoagulation, centrifuge, antibody labelling or staining, filtering, etc., we have demonstrated that our device and detection principle can count neutrophils in whole human blood. Our system is compact, inexpensive and simple to fabricate and operate, having a commodity laser diode and a Si PIN photoreceiver as the main pieces of hardware. Although the results are still preliminary, the studies indicate that this optofluidic device holds promise to be a point-of-care and home care device to measure neutrophil concentration, which is the key indicator of the immune functions for cancer patients undergoing chemotherapy.
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http://dx.doi.org/10.1039/c2lc40560a | DOI Listing |
Lab Chip
September 2025
Department of Electrical & Electronic Engineering, The University of Hong Kong, Pokfulam Road, Hong Kong.
Traditional biophysical cytometry has been limited by its low-dimensional phenotyping characteristics, often relying on only one or a few cellular biophysical phenotypes as readouts. This has perpetuated the perception that biophysical cytometry lacks the power to determine cellular heterogeneity. Here, we introduce a multimodal biophysical cytometry platform, termed quantitative phase morpho-rheological (QP-MORE) cytometry, which simultaneously captures a collection of high-resolution biophysical and mechanical phenotypes of single cells at ultrahigh throughput (>10 000 cells per s).
View Article and Find Full Text PDFNat Commun
August 2025
Department of Bio and Brain Engineering, Korea Advanced Institute of Science and Technology (KAIST), 291 Daehak-ro, Yuseong-gu, Daejeon, 34141, Republic of Korea.
Wearable sensors allow non-invasive monitoring of sweat metabolites, but their reliance on molecular recognition elements limits both physiological coverage and temporal resolution. Here we report an all-flexible chronoepifluidic surface-enhanced Raman spectroscopy (CEP-SERS) patch for label-free and chronometric profiling of sweat metabolites. The CEP-SERS patch integrates plasmonic nanostructures in epifluidic microchannels for chronological sweat sampling and molecular analysis.
View Article and Find Full Text PDFSmall
August 2025
BIOS Lab-on-a-Chip Group, EEMCS Faculty, MESA+ institute, University of Twente, Enschede, 7500 AE, The Netherlands.
Assemblies structured from colloids exhibit promise for advanced applications, including photonic devices, electrochemical energy storage systems, and catalytic supports. Despite observing diverse morphologies, a comprehensive understanding of the underlying formation mechanisms remains elusive. In this work, it is proposed that the coordination interactions between metal sulfide nanoparticles (MS NPs) and fluorosurfactants at the droplet interface influence the morphology of assemblies during the evaporation-induced self-assembly in droplet microfluidics.
View Article and Find Full Text PDFNat Commun
August 2025
New Cornerstone Science Laboratory, State Key Laboratory of Extreme Photonics and Instrumentation, College of Optical Science and Engineering, Zhejiang University, Hangzhou, China.
As a counterintuitive phenomenon, optical pulling of an object has been attracting increasing attention in recent years, owing to its intriguing underlying physics of light momentum transfer and potential for multi-directional manipulation. Due to the difficulty in engineering wave vectors for long-range optical pulling with a single beam, to date, the pulling range of an object is experimentally limited to hundreds of micrometres. Here, we demonstrate ultra-long-range optical pulling of a micro-droplet with an optical nanofibre based on the Minkowski-photon-momentum engineering.
View Article and Find Full Text PDFAdv Mater
August 2025
School of Microelectronics, College of Materials Science and Engineering, Nanjing University of Science and Technology, Nanjing, 210094, China.
Sustained amplified stimulated emission (ASE) under continuous-wave (cw) excitation is a prerequisite for any new gain material being developed for lasing applications. Despite the great success achieved in colloidal quantum dot (QD) lasers, the cw light amplification is hampered by the high pump threshold and thermal effects of QD solids. Herein, the first-ever cw ASE and lasing from QDs relevant for practical implementations are realized by adopting the microfluidic dot-in-matrix design.
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