An apparatus for use in a minimally invasive prostate cancer detection system, using a fluorophore peptide dye conjugate compound which has at least one absorption wavelength in a range of 380 to 1400 nm, wherein said compound attaches to a prostate-specific membrane antigen (PSMA) expressed by a prostate cancer cell. A photo-acoustic imaging probe to be inserted in at least one of a rectum, urethra, or placed proximal the prostate. The probe having an emitter to emit a first signal at the prostrate and a prostate cancer, excite the conjugate compound and a receiver to receive a second signal from said conjugate compound, thereby indicating a cancerous region of the prostrate. A processor unit connected to said probe, is configured and operable for receiving and processing said to produce a tomographic representation of the prostrate.

A magnetic field sensor system includes a one-axis magnetic field generator that generates a magnetic field, three or more three-axis magnetic field detectors that detect a magnetic field for each axis and are arranged on a substantially straight line, and a calculator that calculates, from a detection result of the magnetic field, a spatial position or a spatial direction of the one-axis magnetic field generator. The calculator selects two or more three-axis magnetic field detectors, which generate no symmetry of magnetic fields, based on a preset judgment standard of symmetry of magnetic fields, and calculates the spatial position or the spatial direction of the one-axis magnetic field generator, based on detection results of the magnetic field between the selected two or more three-axis magnetic field detectors and the one-axis magnetic field generator.

Disclosed is a monitoring device including a first measurement device disposed inside an organ of a target, the first measurement device being configured to measure a first biosignal of the target and to transmit the first biosignal, a second measurement device disposed inside a skin tissue of the target, and the second measurement device being configured to measure a second biosignal of the target, to receive the first biosignal, and to transmit bioinformation comprising the first biosignal and the second biosignal, a drone configured to move to an area in which the target is positioned, to receive the bioinformation from the second measurement device, and to transmit the bioinformation, and an analyzer configured to monitor and analyze a condition of the target based on the bioinformation received from the drone.

Methods for monitoring equivalent inner diameter of arterioles by measuring blood pressure wave transient time from small arteries to arterioles and calculating, from the transient time and concurrently measured heart rate values, an equivalent inner diameter of arterioles.

Self-righting articles, such as self-righting capsules for administration to a subject, are generally provided. In some embodiments, the self-righting article may be configured such that the article may orient itself relative to a surface (e.g., a surface of a tissue of a subject). The self-righting articles described herein may comprise one 5 or more tissue engaging surfaces configured to engage (e.g., interface with, inject into, anchor) with a surface (e.g., a surface of a tissue of a subject). In some embodiments, the self-righting article may have a particular shape and/or distribution of density (or mass) which, for example, enables the self-righting behavior of the article. In certain embodiments, the self-righting article a tissue 10 interfacing components. In some embodiments, each tissue-interfacing component may comprise an electrically-conductive portion configured for electrical communication with tissue and an insulative portion configured to not be in electrical communication with tissue.

There is provided a method for controlling a flow of intestinal contents in the intestinal passageway of a patient's intestines. The method comprises gently constricting (i.e., without substantially hampering the blood circulation in the intestinal tissue wall) at least one portion of the intestinal tissue wall to influence the flow in the intestinal passageway, and stimulating the constricted wall portion to cause contraction of the wall portion to further influence the flow in the intestinal passageway. The method can be used for restricting or stopping the flow in the intestinal passageway, or for actively moving the fluid in the intestinal passageway, with a low risk of injuring the intestines.

A catheter for use in magnetic resonance imaging includes a catheter shaft having a proximal end and a distal end. A flexible lumen is supported on the distal end of the shaft, and the flexible lumen is configured to be expanded and contracted using a fluid introduced via the proximal end of the catheter shaft. A magnetic resonance coil formed on the flexible lumen such that the magnetic resonance coil may expand and contract with the flexible lumen. The magnetic resonance coil is coupled to an external match and tune circuit via magnetic resonance imaging device. The balloon coil includes nested bazooka or sleeve baluns along the length of the cable to minimize common mode currents on the outer surface of the cable to prevent high current hot spots that cause heating of the cable.

An infection detection device includes a housing having a display configured to output a level of infection at a surgical site, and a probe having a proximal end portion attached to the housing and a distal end portion configured for insertion into a surgical site. A detection device is integrated along the distal end portion of the probe and is configured to measure a level of infection at a surgical site. The detection device is configured to alert a user when a predetermined level of infection is detected at a surgical site.

Systems and methods for monitoring nutritional uptake of an individual are disclosed. The method can include monitoring microflora intestinal gas concentration levels associated with a patient and adjusting the volume of nutrient provided by the patient with an artificial feeding device based at least in part on the microflora intestinal gas levels associated with the patient. A microflora intestinal gas sensor can be used to monitor the microflora intestinal gas associated with the patient. The microflora intestinal gas sensor can monitor the microflora intestinal gas in a patient's exhaled breath or in the patient's digestive tract. The microflora intestinal gas sensor be included as part of an enteral feeding system at the distal end or outside end of an enteral feeding tube. Systems and methods for monitoring nutritional uptake of an infant based on microflora intestinal gas levels associated with the infant are also disclosed.

A temperature probe for monitoring temperatures of a surface of a tissue or organ within the body of a subject includes a section with a substantially two-dimensional arrangement and a plurality of temperature sensors positioned across an area defined by the substantially two-dimensional arrangement. Such an apparatus may be used in conjunction with procedures in which thermal techniques are used to diagnose a disease state or treat diseased tissue. Specifically, a temperature probe may be used to monitor temperatures across an area of a surface of a tissue or organ located close to the treated tissue to prevent subjection of the monitored tissue or organ to potentially damaging temperatures.