Abstract: Embodiments of negative pressure wound therapy systems, apparatuses, and methods for operating the systems and apparatuses are disclosed. In some embodiments, the apparatus includes a negative pressure source, a connector port, at least one switch, and a controller. The negative pressure source is connected through the connector port to either (i) a wound dressing having a canister configured to store fluid aspirated from the wound or (ii) a wound dressing without a canister between the connector port and the wound dressing. The controller determines, based on a signal received from the at least one switch, whether the canister is positioned in the fluid flow path and adjusts one or more operational parameters of negative pressure wound therapy based on the determination. The switch is activated by the connection of either the canister or canisterless wound dressing to the apparatus.

Abstract: A vacuum cleaner including a suction inlet, a conduit in fluid communication with the suction inlet, a filter having a valve releasably connected to a filter inlet, the filter configured to collect debris drawn through the suction inlet. The vacuum cleaner further comprising a release mechanism moveable from a first position to a second position. In the first position, the filter is in fluid communication with the conduit to collect debris with the valve being open, and in the second position, the filter is disconnected from the conduit with the valve being closed. Movement of the release mechanism between the first and second positions closes the valve.

Abstract: The present invention refers to a cryogenic cooling system utilizing rocket propellant as the working fluid in a phase change closed loop process. The purpose of the system is to enable long term zero boil off storage of cryogenic liquid rocket propellant in space. The system will also enable transfer of cryogenic liquid from one tank volume to another in a propellant depot mode of operation.

Abstract: In some embodiments, a hand controller apparatus for controlling a tool in a robotic surgery system can include a body with a proximal end and a distally located interface end configured to be coupled to an input apparatus configured to control a surgical tool. The hand controller apparatus can also include a control lever attached to a pivot joint proximate a side surface of the body and extending along the body and away from the proximal end, the control lever being laterally moveable relative to the side surface of the body about the pivot joint. The hand controller apparatus can additionally include a lateral movement detector configured to magnetically or inductively detect a lateral movement of the control lever.

Abstract: Disclosed herein are devices and systems for stimulating and manipulating tissue, such as skin, fascia and muscle tissue, to reduce pain or discomfort. In one aspect, a tissue stimulation and manipulation device includes a manipulating head having a casing with an application area configured to contact at least one site of a subject; and a propulsion source capable of producing mechanical motion or linear energy; the propulsion source and application area are operatively positioned relative to one another such that the propulsion source and contact portions on the application area cooperate to manipulate tissue at the site of the subject. Also disclosed herein are methods for using the disclosed devices and systems to treat skin, fascia and muscle tissue.

Abstract: Recombinant herpes simplex virus 2 (HSV-2) vaccine vectors, virions thereof, compositions and vaccines comprising such, and methods of use thereof are each provided.

Abstract: Disclosed herein is a dry, self-supporting fibrous material, the fibers of which have been treated with a binder composition. The fibrous material can be slit into tapes or tows that are suitable for use in an Automated Tape Laying (ATL) or Automated Fiber Placement (AFP) process. This fibrous material is suitable for forming preforms which are configured to receive a matrix resin by resin infusion in the manufacturing of structural composite parts.

Abstract: An equipment box assembly includes a housing including a back wall, a bottom wall, a top wall, and first and second sidewalls defining a cavity. At least one mounting feature is on each of the first and second sidewalls. The housing is sized to fit between first and second adjacent studs with the first sidewall mounted to the first stud using the at least one mounting feature on the first sidewall and with the second sidewall mounted to the second stud using the at least one mounting feature on the second sidewall.

Abstract: The invention provides for an immunogenic composition comprising a. a directed adjuvant comprising at least an anti-CD32 moiety linked to a TLR9 ligand and a first peptidic alpha-helix; and b. a gastrin-17 peptide immunogen linked to a second peptidic alpha-helix coiled to the first alpha-helix, which peptide immunogen is any of (i) human gastrin-17 comprising the amino acid sequence of SEQ ID 1, or a fragment thereof comprising the amino acid sequence of SEQ ID 2, or at least the 4 N-terminal amino acids of SEQ ID 2; (ii) an analog of (i), preferably of rhesus monkey or murine origin; and/or (iii) a functionally active variant of any of (i) or (ii), with one, two, three or four point mutations in the amino acid sequence of SEQ ID 2. The invention further provides a kit for producing such immunogenic composition, a vaccine comprising such immunogenic composition and its medical use, such as for treating gastrin dependent diseases.

Abstract: A method of and apparatus for accelerating the cooling of a beverage can and/or ice tray utilizing at least one body that presents a density and thermal conductivity, defines a standard beverage can and/or ice tray receiving receptacle configured to form a minimum contact surface area of engagement with at least one can and/or tray, and preferably further defines a series of thru-holes, so as to promote accelerated cooling through conduction, convection within a compartment.

Abstract: A display mount includes a vertical adjustment mechanism configured to be operatively coupled to a wall and a horizontal adjustment mechanism having a first end portion operatively coupled to the vertical adjustment mechanism and a second end portion that is configured to be operatively coupled to a display. With the vertical adjustment mechanism operatively coupled to the wall and with the display operatively coupled to the horizontal adjustment mechanism: the vertical adjustment mechanism is configured to lower and raise the display vertically parallel to the wall without the display moving substantially horizontally away from and toward the wall; and the horizontal adjustment mechanism is configured to extend and retract the display horizontally away from and toward the wall without the display moving substantially vertically parallel to the wall.

Abstract: Embodiments of negative pressure wound therapy systems and methods for operating the systems are disclosed. In some embodiments, a system includes a negative pressure source, a wound dressing configured to be positioned over a wound, and optionally a canister configured to store fluid aspirated from the wound. The negative pressure source, wound dressing, and canister (when present) can be fluidically connected to facilitate delivery of negative pressure to the wound. The system can be configured to automatically detect whether the canister is positioned in the fluid flow path between the negative pressure source and the dressing while negative pressure source provides negative pressure to the wound dressing. Operation of the system can be adjusted based on whether presence of the canister has been detected. For example, a value of an operational parameter can be set to indicate that the canister is present.

Abstract: The present invention is a three-dimensional printing system which is capable of printing with multiple different printing materials, including homogenous materials, such as cement paste, or heterogeneous materials, such as concrete. Functionality is accomplished by novel, critical structures including but not limited to a movable gate capable of controlling the flow of printing materials without clogging or becoming otherwise damaged. The system has a print head that discharges printing material through a discharge aperture. The movable gate is rotatably connected to the print head, allowing it to cover the discharge aperture and cut off the flow of printing material when actuated and rotated into position. Certain embodiments also include hose positioning systems to prevent hoses delivering printing material from disconnecting or damaging the printed structure.

Abstract: When a user sees a content item presented by a social networking system, the user may select an option to save the content item. The saved content item may be reinserted in a newsfeed presented to the user, integrated into collections, archived, used for notifications to the user, or otherwise subsequently presented to the user. A plug-in may be used to save content items accessed through websites external to the social networking system. As privacy settings associated with a saved content item are modified, the modified privacy settings are applied to the saved content item, which may prevent the user saving the content item from subsequently viewing the saved content item.

Abstract: A fiber-reinforced polymeric composite structure having chemically active thermoset particles positioned in an interlaminar region between adjacent layers of reinforcement fibers and method of making the same. Upon curing of the composite structure, the chemically active functional groups on the thermoset particles form covalent bonds with the matrix resin surrounding the particles. In one embodiment, the particles are formed of a partially cured thermoset polymer with a degree of cure of less than 100%. In another embodiment, the particles are derived from a thermosettable resin composition, wherein the stoichiometry is such that there is a deficiency or an excess in the amount of curing agent that is necessary for reacting with 100% of the thermoset resin component. In some embodiments, the composition of the chemically active thermoset particles is the same or substantially the same as that of the matrix resin of the composite structure.

Abstract: A dirt collector that includes a housing and an air-permeable filter media extending from the housing such that the filter media and housing at least partially define a collection volume.

Abstract: An equipment box assembly includes a housing including a back wall, a bottom wall, a top wall, and first and second sidewalls defining a cavity. At least one mounting feature is on each of the first and second sidewalls. The housing is sized to fit between first and second adjacent studs with the first sidewall mounted to the first stud using the at least one mounting feature on the first sidewall and with the second sidewall mounted to the second stud using the at least one mounting feature on the second sidewall.

Abstract: Recombinant herpes simplex virus 2 (HSV-2) vaccine vectors, virions thereof, compositions and vaccines comprising such, and methods of use thereof are each provided.

Abstract: A vacuum cleaner that includes a suction source configured to generate a suction airflow, a dirt collector in fluid communication with the suction source and configured to separate debris from the suction airflow and the dirt collector is configured to store the debris separated from the suction airflow. The vacuum further includes an infrared sensor operable to output a signal corresponding to a distance to an amount of debris stored in the dirt collector, a controller that receives the signal, and the controller is operable to determine a fill level stored in the dirt collector based on the signal. A visual display displays the fill level stored in the dirt collector.

Abstract: A method of using an electronic toolset for locating, reading, adjusting and confirming adjustment of an implantable bodily fluid drainage system without requiring recalibration following adjustment from a current valve setting to a new valve setting using an electronic toolset including an adjustment tool having a magnetic element and an indicator tool including a sensor array. The need to remove the electronic toolset from the patient to recalibrate or zero the sensor array prior to confirming the new valve setting is eliminated. This is realized by disposing a ferromagnetic system component of the indicator tool in a magnet shield cage made of a metallic alloy to prevent magnetic fields produced by a magnetic element in the adjustment tool during the adjusting step from influencing the sensor array.