We report an integrated microfluidic device for fine-scale manipulation and confinement of micro- and nanoscale particles in free-solution. Using this device, single particles are trapped in a stagnation point flow at the junction of two intersecting microchannels. The hydrodynamic trap is based on active flow control at a fluid stagnation point using an integrated on-chip valve in a monolithic PDMS-based microfluidic device. In this work, we characterize device design parameters enabling precise control of stagnation point position for efficient trap performance. The microfluidic-based hydrodynamic trap facilitates particle trapping using the sole action of fluid flow and provides a viable alternative to existing confinement and manipulation techniques based on electric, optical, magnetic or acoustic force fields. Overall, the hydrodynamic trap enables non-contact confinement of fluorescent and non-fluorescent particles for extended times and provides a new platform for fundamental studies in biology, biotechnology and materials science.

Traditional cultivation approaches in microbiology are labor-intensive, low-throughput, and yield biased sampling of environmental microbes due to ecological and evolutionary factors. New strategies are needed for ample representation of rare taxa and slow-growers that are often outcompeted by fast-growers in cultivation experiments. Here we describe a microfluidic platform that anaerobically isolates and cultivates microbial cells in millions of picoliter droplets and automatically sorts them based on colony density to enhance slow-growing organisms. We applied our strategy to a fecal microbiota transplant (FMT) donor stool using multiple growth media, and found significant increase in taxonomic richness and larger representation of rare and clinically relevant taxa among droplet-grown cells compared to conventional plates. Furthermore, screening the FMT donor stool for antibiotic resistance revealed 21 populations that evaded detection in plate-based assessment of antibiotic resistance. Our method improves cultivation-based surveys of diverse microbiomes to gain deeper insights into microbial functioning and lifestyles.

Trapping and manipulation of microscale and nanoscale particles is demonstrated using the sole action of hydrodynamic forces. We developed an automated particle trap based on a stagnation point flow generated in a microfluidic device. The hydrodynamic trap enables confinement and manipulation of single particles in low viscosity (1–10 cP) aqueous solution. Using this method, we trapped microscale and nanoscale particles $(100\text{nm}–15\mu \text{m})$ for long time scales (minutes to hours). We demonstrate particle confinement to within $1\mu \text{m}$ of the trap center, corresponding to a trap stiffness of $\sim {10}^{-5}–{10}^{-4}\text{pN}/\text{nm}$ .

Lasing from spherical microdroplets ejected into a liquid medium with a lower refractive index is observed in a microchannel. A microfabricated device that combines droplet production and excitation/detection has been utilized. Droplets of $50\mathrm{\mu }\mathrm{m}$ diameter containing a fluorescent dye were first detected and then excited through multimode fibers after their production at a T-junction. Images show intense lasing emission around the droplet rim. Spectra from the droplets exhibit morphology-dependent resonances that are redshifted relative to the bulk fluorescence emission from the dyes. The dependence of resonant peak intensities on the pump beam power is nonlinear.