Abstract: The present disclosure relates to a microfluidic concentrating particlizers including a particle generator, a particle concentrator, and a fluid movement network. The particle generator includes a sample inlet microchannel and a reagent inlet microchannel. The sample inlet microchannel is operable to direct a source sample. The reagent inlet microchannel is operable to direct reagent. The source sample and reagent come in contact to form a sample fluid dispersion including sample-modified particulates and fluid. The particle concentrator includes a filtering chamber fluidly coupled to the particle generator to concentrate sample-modified particulates relative to the fluid. The fluid movement network includes multiple pumps to generate fluidic flow through both the particle generator and the particle concentrator.

Abstract: In one example in accordance with the present disclosure, a chemical lysis system is described. The chemical lysis system includes a microfluidic channel to serially feed individual cells from a volume of cells to at least one chemical lysing device. Each chemical lysing device includes at least one lysing chamber to receive, from the microfluidic channel, a single cell to be lysed. The chemical lysing device also includes an orifice disposed in each lysing chamber to receive a lysing agent and a sensor to detect a state within the lysing chamber. A controller of the chemical lysis system analyzes a ruptured cell.

Abstract: A particle monitoring system may include a flow passage, a particle imager to image a targeted particle within the flow passage, electrodes supported proximate the flow passage, a power source connected to the electrodes and a controller to cause the power source to charge to electrodes so as to (1) apply an electric field balanced with respect to gravity so as to hold, levitate and rotate a targeted particle within the flow passage during imaging and (2) release the targeted particle following the imaging

Abstract: In one example in accordance with the present disclosure, a method is described. The method includes receiving, in a microfluidic channel, serially fed cells to be encapsulated. Each cell is individually lysed and a lysate of each cell is transported to a downstream analysis device. The lysate of an individual cell is encapsulated with an encapsulating fluid.

Abstract: In one example in accordance with the present disclosure, a cell marking system is described. The cell marking system includes a microfluidic channel to serially feed individual cells from a volume of cells into at least one marking chamber. The at least one marking chambers hold an individual cell to be marked. The cell marking system also includes a marker application device per marking chamber to selectively apply a marker to the individual cell disposed within a respective marking chamber.

Abstract: The present disclosure relates to a microfluidic device including a microfluidic substrate and dry reagent-containing polymer particles. The microfluidic substrate includes a microfluidic-retaining region within the microfluidic substrate that is fluidly coupled to multiple microfluidic channels. The dry reagent-containing polymer particles include reagent and a degradable polymer. The reagent is releasable from the degradable polymer when exposed to release fluid. The dry reagent-containing particles are retained within the microfluidic substrate at the microfluidic-retaining region in position to release reagent into the egress microfluidic channel upon flow of release fluid from the ingress microfluidic channel through the microfluidic-retaining region.

Abstract: A particle monitoring system may include a volume for containing a fluid in which particles are suspended, a photosensitive layer, a light encoding layer sandwiched between the volume and the photosensitive layer and electrodes to apply an electric field to the fluid within the volume and proximate the photosensitive layer.

Abstract: In one example in accordance with the present disclosure, a cell analysis system is described. The cell analysis system includes at least one cell analysis device. Each cell analysis device includes a channel to serially feed individual cells from a volume of cells into a lysing chamber. The cell analysis device also includes at least one feedback-controlled lysing element in the lysing chamber to agitate a cell. The cell analysis system also includes a controller to analyze the cell. The controller includes a lysate analyzer to analyze properties of the lysate and a rupture analyzer to analyze parameters of an agitation when a cell membrane ruptures.

Abstract: A surface enhanced Raman spectroscopy (SERS) sensor may include a nano structured surface and a nonstoichiometric oxide layer. The nano structured surfers may include a first peak, a second peak and a valley between the first peak and the second peak. The non-stoichiometric oxide layer may include a first portion on the first peak and a second portion on the second peak.

Abstract: An example system includes an input channel to flow nucleic segments therethrough, a mixing portion coupled to the input channel, a separation chamber in fluid communication with the second end of the input channel, at least two output channels coupled to the chamber, and an integrated pump to facilitate flow through the separation chamber. The mixing portion is to include at least two different categories of beads having different sizes from each other and having a probe to attach to a corresponding nucleic acid segment. The separation chamber has a passive separation structure including an array of columns spaced apart to facilitate separation of the different categories of beads and attached corresponding nucleic acid segment into at least two flow paths based on a size of the category of the beads. Each output channel is to receive separated categories of beads and attached nucleic acid segments.

Abstract: In one example in accordance with the present disclosure, a cell analysis system is described. The cell analysis system includes a substrate. Formed in the substrate is a feedback-controlled lysis system to rupture a cell membrane. The feed-back-controlled lysis system includes at least one lysing chamber to receive a single cell to be lysed. A lysing element of the feedback-controlled lysis system agitates the single cell and a sensor detects a state within the lysing chamber. The cell analysis system also includes a microfluidic channel formed in the substrate to 1) serially feed individual cells from a volume of cells to the feedback-controlled lysis system and 2) deliver a lysate of a ruptured cell to at least one analysis chamber. The cell analysis system also includes at least one analysis chamber formed in the substrate to process the lysate and a controller to determine when a cell membrane has ruptured.

Abstract: In one example in accordance with the present disclosure, a cell sorting device is described. The cell sorting device includes a microfluidic channel to serially transport individual cells from a volume of cells along a flow path. A sensor disposed in the microfluidic channel distinguishes between a cell to be analyzed and waste fluid. The cell sorting device includes at least two fluid transport devices disposed within the microfluidic channel. The at least two fluid transport devices include a cell ejector to, responsive to detection of a cell to be analyzed, eject the cell to be analyzed from the cell sorting device and a waste transport device to direct the waste fluid to a waste reservoir.

Abstract: An apparatus includes a polymer base layer having a surface. A die that includes a fluid manipulation surface that is substantially coplanar with the surface of the polymer base layer. The die includes a control electrode to generate an electric field to perform microfluidic manipulation of fluid across the fluid manipulation surface of the die.

Abstract: An example system includes an input channel having a first end and a second end to receive particles through the first end, a separation chamber, at least two output channels, and an integrated pump to facilitate flow through the separation chamber. The separation chamber is in fluid communication with the second end of the input channel. The separation chamber has a passive separation structure, the passive separation structure including an array of columns spaced apart to facilitate separation of particles in a flow based on a size of the particles. Each output channel is in fluid communication with the separation chamber to receive separated particles. The integrated pump is positioned within at least one of the input channel or one of the at least two output channels.

Abstract: An example system includes an input channel to receive particles through a first end, a separation chamber, at least two output channels, an integrated pump to facilitate flow through the separation chamber and a cell analysis portion. The separation chamber is in fluid communication with a second end of the input channel. The separation chamber has a passive separation structure including an array of columns spaced apart to facilitate separation of particles into at least two flow paths based on a size of the particles. The size associated with a first flow path of the at least two flow paths corresponds to a cell. A first output channel is to receive the first flow path corresponding to a cell. The cell analysis portion is coupled to the first output channel and is to perform at least one analysis associated with cells in the first output channel.

Abstract: A particle classification system may include a volume to contain a fluid having a suspended particle, electrodes proximate the volume to apply an electric field to rotate the suspended particle, a focused light source, a scattered light sensor to sense light from the focused light source that has scattered upon impinging the rotating suspended particle and a controller to classify the particle based at least in part upon signals from the scattered light sensor.

Abstract: Examples relate to conducting Polymerase Chain Reactions (PCR). An example device for conducting PCR includes a primer applicator to add a first multi-primer set of a primer library to a first test chamber of a test chamber array. The example device also includes an amplification analyzer to determine if amplification has occurred in the first test chamber. The example device includes a device controller to instruct the primer applicator to apply a second multi-primer set of the primer library to the first test chamber in response to a detection by the amplification analyzer that amplification has not occurred in the first test chamber. Example devices instruct the primer applicator to apply a first primer subset of the first multi-primer set to a second test chamber of the test chamber array in response to a detection by the amplification analyzer that amplification occurred in the first test chamber.

Abstract: Examples include a fluid device. The fluid device includes a substrate, a sensor coupled on the substrate. A reservoir is formed in the substrate adjacent to the sensor. A deformable cover is disposed to seal the sensor and the reservoir on the substrate.

Abstract: A cellular object imaging system may include a growth platform. The growth platform may include a body having a cellular fluid suspension region, a media supply passage extending within the body to the cellular object fluid suspension region, at least one fluid pump on the body to selectively deliver media to the cellular object fluid suspension region, a waste discharge passage extending within the body from the cellular object fluid suspension region and a cellular object rotator on the body adjacent the cellular object fluid suspension region to rotate a cellular object within the cellular object fluid suspension region. The cellular object fluid suspension region permits optical imaging of the cellular object suspended in a fluid during rotation by the cellular object rotator.

Abstract: In one example, an analysis chip includes a substrate for surface-enhanced spectroscopy including an ordered nanostructure surface to receive a liquid including a number of analytes. The received liquid is to be guided by the ordered nanostructure surface over the substrate to separate the number of analytes.