A method includes receiving first fluid property data from a sample flowline of a focused sampling system and receiving second fluid property data from a guard flowline of the focused sampling system. The sample flowline and the guard flowline are each configured to sample formation fluid from a hydrocarbon reservoir, the formation fluid includes native formation fluid and a contaminant, and the first fluid property data includes an optical density of the native formation fluid and the second fluid property data includes an optical density of the contaminant

Provided herein are an optical test platform and corresponding method of manufacturing the same. The test platform may include a shell defining a cavity for receiving a sample tube, a first aperture, and a second aperture. The first aperture and the second aperture of the shell may each be configured to optically couple the cavity with an exterior of the shell. The test platform may further include a first window and a second window embedded in the shell. The first window may seal a first aperture and the second window may seal a second aperture. The first window and second window may each permit the optical coupling of the cavity with the exterior of the shell. The first window and the second window may be optically coupled via the cavity, and the shell may prohibit optical coupling between the first window and the second window through the shell.

An improved system, method and interface for automated rapid antimicrobial susceptibility testing (AST) is disclosed which includes, in one aspect, a carrier population station comprising a workstation having a graphic user interface (GUI). The GUI accepts information from a lab technologist, including information related to a scope of testing to be performed on a microorganism containing sample. The GUI controls intelligent assignment of microorganism containing samples to test panels in a manner that maximize utilization of the test carrier by grouping together samples of similar tests scopes and advantageously testing those samples using one multiplexed test panel. Customizing workflow in accordance with test scope to facilitate parallel processing of multiple samples advantageously reduces laboratory waste, decreases test latencies, increases AST system throughput and efficiency, and thus lowers the costs to the AST lab.

Provided herein are an optical test platform and corresponding method of manufacturing the same. The test platform may include a shell defining a cavity for receiving a sample tube, a first aperture, and a second aperture. The first aperture and the second aperture of the shell may each be configured to optically couple the cavity with an exterior of the shell. The test platform may further include a first window and a second window embedded in the shell. The first window may seal a first aperture and the second window may seal a second aperture. The first window and second window may each permit the optical coupling of the cavity with the exterior of the shell. The first window and the second window may be optically coupled via the cavity, and the shell may prohibit optical coupling between the first window and the second window through the shell.

An optical measuring device for measuring light emitted from a sample includes a container cavity for receiving a container in which the sample is enclosed; a light detection unit for detecting light from the sample; a light guide path for guiding the light from the sample to the light detection unit; and a light absorbing unit for absorbing incident light. An end of the light guide path to receive the incident light faces the container cavity, a light exit end of the light guide path faces the light detection unit, and the light absorbing unit covers the perimeter of the light guide path other than the light-receiving-end and the light exit end thereof.

Method and devices for calibrating optical density reflective color fluids to be deposited on substrate are disclosed. Some methods comprise depositing a quantity of a keying color fluid on a first region of the substrate; applying a voltage level to a reflective color fluid application device; depositing, in response to the voltage level applied, a quantity of reflective color fluid on the first region of the substrate and on a second region of the substrate; performing reflectance measurements of the first region and of the second region; performing optical density calculations as a function of the reflectance measurements; varying the voltage level applied to the reflective color fluid application device in response to said optical density calculation until the optical density calculation is within a calibrated range of optical densities.

Instruments, systems, and methods for measuring optical density of microbiological samples are provided. In particular, optical density instruments providing improved safety, efficiency, comfort, and convenience are provided. Such optical density instruments include a handheld portion and a base station. The optical density instruments may be used in systems and methods for measuring optical density of biological samples.

Methods for detecting and treating polymicrobial infections, wherein a mixed population of microbes (e.g., bacteria) are present in a patient sample and the microbes are not first isolated from the sample. For example, the present invention describes specific polymicrobial infections and methods of treating said infections, wherein a particular antibiotic or a group of antibiotics are selected based on the composition of the polymicrobial infections.

An identification apparatus includes a plurality of irradiation units disposed at different positions in a conveyance width direction to irradiate a specimen with a converging ray in different irradiation conditions, the specimen being conveyed in a predetermined conveyance direction by a conveyance unit, a plurality of light-capturing units configured to capture scattered light from the specimen, each of the plurality of light-capturing units corresponding to a different one of the plurality of irradiation units, an acquisition unit configured to acquire identification information for identifying a property of the specimen, based on the light captured by the light-capturing units; and a placement unit configured to place the specimen on a position corresponding to any one of the plurality of irradiation units in accordance with a characteristic value of the specimen at an upstream side of the plurality of irradiation units in the conveyance direction.

A prism for measuring liquid concentration includes: an accommodating space for accommodating a liquid; an interface formed on a bottom surface of the accommodating space; a first light transmission surface and a second light transmission surface respectively formed on two side surfaces of the accommodating space; a third light transmission surface and a light emitting surface respectively formed relative to the interface. When a first incident light beam enters the prism, the first incident light beam is reflected to the light emitting surface by the interface, and exits the prism from the light emitting surface. When a second incident light beam enters the prism to the first light transmission surface, the second incident light beam exits the prism to the accommodating space from the second incident light beam, passes through the liquid and the second light to the prism, and exits the prism from the third light transmission surface.