Techniques for detecting cannabinoid, opioid, and virus aerosols in an exhaled breath are provided. An example method for analyzing exhaled breath includes receiving an aerosol breath sample, concentrating the aerosol breath sample onto an infrared-transparent coupon with an electrostatic precipitator, disposing the infrared-transparent coupon in an optical path of a spectroscopy system, detecting one or more infrared spectral features of the concentrated aerosol breath sample with the spectroscopy system, and analyzing the aerosol breath sample based on the one or more infrared spectral features.

A mask-based diagnostic apparatus is provided for detecting a biomarker contained in exhaled breath of a test subject. An exhaled breath condensate (EBC) collector converts breath vapor received from the lungs and airways of the test subject into a fluid biosample. The EBC collector including a thermal mass, a condensate-forming surface and a fluid conductor disposed on the condensate-forming surface. A fluid transfer system receives the fluid biosample from the EBC collector. A biomarker testing unit receives the fluid biosample from the fluid transfer system and tests the fluid biosample for a target biomarker. A testing system support is provided for supporting the EBC collector, the fluid transfer system and the biomarker testing unit. The testing system support is configured and dimensioned to fit inside a face mask. A face mask is provided forming an exhaled breath vapor containment volume to hold the exhaled breath vapor in proximity to the EBC collector to enable the condensate-forming surface cooled by the thermal mass to coalesce the exhaled breath vapor into the fluid biosample.

Described herein are various embodiments of an oxygen concentrator system and method of delivering oxygen enriched gas to a user. In some embodiments, oxygen concentrator system includes one or more components that improve the efficiency of oxygen enriched gas delivery during operation of the oxygen concentrator system.

A system (100) for assessing fluid responsiveness includes an infusion pump (24) in communication with at least one processor (32), and a plurality of physiological monitors (40,42,44,46) operable to receive physiological signals from an associated patient. Physiological signals (48,50) acquired from the associated patient (10) during a fluid challenge are synchronized with a timing signal (54) of the infusion pump (24) administering the fluid challenge. One or more dynamic indices and/or features (58) is calculated from the synchronized physiological signals (50), and one or more dynamic indices and/or features (50) is calculated from baseline physiological signals (48) acquired from the associated patient (10) prior to the fluid challenge. A fluid responsiveness probability value (64) of the patient (10) is determined based on dynamic indices and/or features (58) from the synchronized physiological signals (50) and dynamic indices and/or features (50) from the baseline physiological signals (48).

A breath sensor includes a base body, a first electrode provided on a part of a surface of the base body, a second electrode provided on a part of the surface of the base body, and a covering layer made of a material that does not pass moisture therethrough, the covering layer covering the second electrode with the base body. The base body is preferably made of a material whose surface potential changes due to attachment of moisture to one of a surface of the first electrode and the surface of the base body. A surface potential on a side of the first electrode of the base body changes when a breath containing moisture touches the surface of the first electrode.

A gas analysis system includes a gas analyzer which analyzes a gas acquired from a living body and a liquid separator which is detachably attached to the gas analyzer, and which separates a liquid component from the gas. In the gas analysis system, the liquid separator includes a magnet, and the gas analyzer includes a magnetic sensor which detects magnetism generated by the magnet, and a determining section which, based on the magnetism detected by the magnetic sensor, determines that the liquid separator is attached to the gas analyzer.

A wireless sensor platform design and a single walled carbon nanotube/ionic liquid-based chemidosimeter system can incorporated into a highly sensitive and selective chemical hazard badge that can dosimetrically detect an analyte down to a sub parts-per-million concentration.

Devices and systems for monitoring weaning of a subject from a respiratory ventilator including a processing logic configured to characterize distinct patterns in a series of CO.sub.2 waveforms, the distinct patterns indicative of the effectiveness of a weaning process; and to provide an indication relating to the effectiveness of the weaning process.

According to the present invention, the temperature is set to 37° C. (310 K) with respect to an equation that gives a redox potential E according to the Nernst equation, and the resulting redox potential E of hydrogen/hydrogen ion is E=−0.061×pH+0.031×pH.sub.2 (V). At pH=7.4, E=−0.451+0.031×pH.sub.2 (V). A hydrogen gas index pH.sub.2 of a subject is measured, and E is calculated using the above equation. According to a potential verification method according to the present invention, the potential before and after blow-in is measured by blowing air and air containing hydrogen gas into a phosphate buffer solution, and correction is carried out as necessary to obtain a linear regression line, whereby a change in a potential associated with changes in the hydrogen gas index pH.sub.2 can be checked and the redox potential obtained by the calculation can be recognized as being close to an actual redox potential.

A user device and a breath analysis device (or other types of portable devices) use a pairing and communication protocol that address user convenience and connectivity issues. For example, a breath analysis device is associated with a unique identifier and the unique identifier is associated with an account corresponding to the user. Likewise, a user device is associated with a user device identifier and the user device identifier is associated with the account corresponding to the user. The breath analysis device and the user device can use at least one of the identifiers to determine whether the user device is authorized to pair with the breath analysis device, and vice-versa. If authorized, the breath analysis device and user device can pair with one another. Once paired, the user device may wirelessly communicate with the breath analysis device for various purposes, such as to retrieve and display breath analysis test results.