An inserter apparatus (e.g., a continuous analyte monitoring inserter apparatus) includes an outer member; an inner member; a transmitter carrier configured to support a transmitter and biosensor assembly during insertion of a biosensor, the transmitter carrier including a bias member; and a pivot member configured to pivot at times relative to the transmitter carrier and support an insertion device during biosensor insertion. The outer member is configured to press the bias member against the pivot member during insertion of the biosensor. During a first stroke portion of the insertion apparatus, the pivot member is prevented from pivoting. In a second stroke portion, pivoting is allowed, and the bias member causes, pivoting of the pivot member and retraction of the insertion device. Other systems and methods embodiments are provided.

A vehicle trim assembly includes a first trim component having an interior facing surface and an exterior facing surface, the first trim component including an extended portion, a second trim component including an edge defining a groove configured to engage with the extended portion of the first trim component, and a single chip sensor overmolded with the second trim component such that the single chip sensor is integrated into the second trim component. The single chip sensor is formed with the second trim component in a multi-shot injection molding process.

This disclosure describes multi-fluid kits for three-dimensional printing, three-dimensional printing kits, and methods of sensing metal ions using three-dimensional printed ion sensors. In one example, a multi-fluid kit for three-dimensional printing can include a fusing agent and an ion-sensing agent. The fusing agent can include water and an electromagnetic radiation absorber. The electromagnetic radiation absorber can absorb radiation energy and convert the radiation energy to heat. The ion-sensing agent can include water and a redox-active inorganic salt.

A method for manufacturing a weighing system (10) includes, first, modeling a blank that includes a base (12) having at least one wall (26) and a lever (20) hinged to the base (12) via thin-section joints (14) and secured to the base (12) via material bridges. The lever (20) has a lever portion adjacent to the wall (26), wherein the wall (26) and the lever portion adjacent to the wall are each provided with an aperture (32, 34), and wherein the apertures (32, 34) are both aligned with each other. The manufacturing method further includes thereafter cutting open the material bridges. Before the material bridges are cut open, however, a fixing bolt (36) is pushed into the apertures (32, 34) in such a way that it engages positively in the apertures (32, 34) during the cutting open of the material bridges.

A sensor casing is disclosed that has an open receiving space which has a peripheral edge as a creep barrier at the open end. The receiving space is filled with a potting compound. The cured potting compound forms a concave surface with respect to the peripheral edge. A method for potting an open receiving space of a sensor casing of this kind is also disclosed. The peripheral edge has an outwardly declining slope which allows temporary overfilling of the receiving space during a potting process so as to form a stable convex potting compound surface.

Method of analysis. In the method, a first emulsion and a second emulsion substantially separated from one another by a spacer fluid may be formed. The first emulsion, the spacer fluid, and the second emulsion may be flowed in a channel from a fluid inlet to a fluid outlet of a heating and cooling station having two or more temperature-controlled zones, such that each emulsion is thermally cycled to promote amplification of a nucleic acid target in droplets of the emulsion. Amplification data may be collected from individual droplets of each emulsion downstream of the heating and cooling station. A level of the nucleic acid target present in each emulsion may be determined based on the amplification data collected from the individual droplets of the emulsion.

An electrode-modified heavy metal ion microfluidic detection chip, comprising a microfluidic module (1) and a three-electrode sensor (2), wherein the microfluidic module (1) is integrally molded by 3D printing, and the interior thereof has a microchannel (10) and a sensor slot (11); and the three-electrode sensor (2) comprises three electrodes (21, 22, 23) printed on a card-shaped bottom plate (20), among which the working electrode (21) is a porous nano-NiMn2O4 modified bare carbon electrode, and the three-electrode sensor (2) is inserted into the sensor slot (11) that matches same to form the microfluidic detection chip.

A soft-melted parison is disposed in molds forming a shape of a measurement pipeline portion 10, the parison is expanded by means of gas inflow, and blow molding is performed. The shapes of a pipe body 11, a fluid inlet portion 12, and a fluid outlet portion 13 are formed by an inner mold of the molds. Ultrasonic wave input-output portions 14a and 14b bulging outwards in a sealed manner are formed on both sides positioned in the oblique direction of the pipe body 11 with respect to a center line of the pipe body 11. Parts of the ultrasonic wave input-output portions 14a and 14b are wall surfaces 15a and 15b for attaching ultrasonic wave transmission-reception units. The measurement pipeline portion 10 is obtained by cutting end portions of the fluid inlet portion 12 and the fluid outlet portion 13 after the parison is solidified.

A microneedle biosensor includes a microneedle and a substrate. One end of the microneedle is connected to the substrate, an outer surface of the microneedle is provided with a working electrode and a first electrode, an outer surface of the working electrode is provided with an enzyme, and an outer surface of the microneedle biosensor is covered with a biocompatible film. A method for manufacturing a microneedle biosensor includes: manufacturing the substrate and the microneedle in an additive mode simultaneously; spray-printing and curing the working electrode and the first electrode on the outer surface of the microneedle; spray-printing and drying the enzyme on the outer surface of the working electrode; and using biocompatible liquid for spray-printing, and drying the biocompatible liquid to form the biocompatible film. The substrate, the microneedle, the working electrode, the first electrode, the enzyme and the biocompatible film are all manufactured through a full printing method.

Provided is a composite material capable of measuring bending deformation, the composite material including: a first conductive composite body that is bendable; a dielectric body that is bendable and compressible; and a second conductive composite body that is bendable, wherein the first conductive composite body and the second conductive composite body are respectively stacked on both surfaces of the dielectric body, and heights of the first conductive composite body and the second conductive composite body from the dielectric body are different from each other.