Abstract: An electric double-layer ultracapacitor configured to maintain desired operation at an operating voltage of three volts, where the capacitor includes a housing component, a first and a second current collector, a positive and a negative electrode electrically coupled to one of the first and second current collectors, and a separator positioned between the positive and the negative electrode. The capacitor may also include a protective coating disposed on an inner surface of the housing for the ultracapacitor.

Abstract: An electric double-layer ultracapacitor configured to maintain desired operation at an operating voltage of three volts, where the capacitor includes a housing component, a first and a second current collector, a positive and a negative electrode electrically coupled to one of the first and second current collectors, and a separator positioned between the positive and the negative electrode. The capacitor may also include an electrolyte in ionic contact with the electrodes and the separator, the electrolyte having acetonitrile and a quaternary ammonium salt with a molarity of less than one.

Abstract: A surgical device comprising: (a) a stylet comprising: one or more support rods; (b) a hand piece comprising: one or more housing structures defining a cavity; and one or more actuating mechanisms comprising: one or more levers attached to one or more pivot axes in the hand piece and configured to form one or more slidable joints in communication with the one or more support rods; wherein the one or more levers are configured to be assembled by: being placed into the hand piece along the assembly direction before the stylet so the stylet may be placed into the hand piece over the one or more levers; or being placed into the hand piece along the assembly direction after the stylet so the one or more levers is placed into the hand piece over the stylet and in communication with the stylet.

Abstract: A forceps comprising: (a) a stylet having a hollow tube having a proximal end region and a longitudinal axis; one or more assemblies that are extendable through the hollow tube, the one or more assemblies comprising: one or more support rods and one or more functional attachments; (b) a hand piece comprising: one or more housing structures defining a cavity; one or more actuating mechanisms comprising: a bearing fitting; a shuttle in communication with the bearing fitting constrained by a plurality of guide ridges; a socket housed by the shuttle; and one or more levers in communication with stylet so that movement of the one or more levers causes movement of the hollow tube and movement of the one or more assemblies; and wherein the movement of the hollow tube and the movement of the one or more assemblies are relative to each other.

Abstract: A forceps comprising: (a) a stylet comprising; (i) a hollow tube having a longitudinal axis; (ii) assemblies, that are extendable through the hollow tube, comprising; (1) support rods; (2) functional attachments at the end of the support rods; (b) a hand piece comprising; (i) housing structures defining a cavity that houses the stylet; (ii) actuating mechanisms, in communication with the stylet, comprising; (1) a bearing fitting located on the stylet; (2) a shuttle in communication with the bearing fitting, and constrained by a plurality of guide ridges so that the shuttle is movable along a longitudinal axis and restricted from rotational movement around the longitudinal axis; (3) a socket housed by the shuttle, the socket receiving the bearing fitting and being rotatable relative to the shuttle; and (4) levers in communication with the stylet that causes movement of the hollow tube and the assemblies are relative to each other.

Abstract: An electric double-layer ultracapacitor configured to maintain desired operation at an operating voltage of three volts, where the capacitor includes a housing component, a first and a second current collector, a positive and a negative electrode electrically coupled to one of the first and second current collectors, and a separator positioned between the positive and the negative electrode. At least one of the positive electrode and the negative electrode can include a treated carbon material, where the treated carbon material includes a reduction in a number of hydrogen-containing functional groups, nitrogen-containing functional groups and/or oxygen-containing functional groups.

Abstract: Dosage forms containing pharmaceutical compositions for use in devices to produce a spray or mist delivery of the compositions include dosage blister compartments and a dispensing blister compartment, wherein crushing of the compartments delivers the compositions in a desired spray pattern. Certain dosage forms include a plurality of dosage chambers each containing a component or a portion of a pharmaceutical composition, the contents of which are mixed or combined just prior to or during administration.

Abstract: The present disclosure is directed to processes for manufacturing internally pierced shaped articles for unit-dose packaging with at least one formed recess (e.g., a blister), in particular for unit-dose packaging of pharmaceutical dosage forms. In certain embodiments, the first step of the process is directed to drawing the film material (e.g., metal-plastic foil) with one or more plungers to form a primary contour, the contour having a depth of at least 100% and up to 150% of the depth of the formed recess. The second stage involves shaping the primary contour with one or more plunger(s) to the desired formed recess, with a depth that is less than the depth of the primary contour, while substantially maintaining the surface area of the primary contour formed in the first stage. The formed recess may be formed using warm-forming or cold-forming techniques. The third stage involves the automatic placing of an internal piercing device stably into the shaped article.

Abstract: Intranasal delivery devices include dosage forms containing medical compositions for use in the intranasal devices, and methods of delivering medical compositions to the nasal mucosa of users. The devices dispense a predetermined quantity of fluid into the nasal passage of a user, in which the predetermined quantity of fluid is contained in, or produced in a dosage form or blister that is crushed by a plunger with sufficient force to drive the dosage form against a piercing mechanism, piercing the dosage form and forcing the liquid contents from the dosage form and through a delivery channel into a spray to be directed into the nasal passage of a user. The plunger is connected to a trigger device by a linkage that confers a mechanical advantage to the trigger mechanism.

Abstract: A method of care is described that includes administering an effective amount of ?-hydroxy-?-methylbutyrate (HMB) to an adult or elderly patient to improve the patient's quality of life during or after hospitalization of the patient. The improved quality of life may encompass the general health, physical health, or mental health of the patient.

Abstract: In one embodiment, an apparatus cascades groups of serialized data streams through devices, and performs operations based on information communicated therein. A received group of serialized data streams is aligned, but not framed, and forwarded to a next device (e.g., a next stage in a linear or tree cascaded formation of devices). Eliminating the framing and subsequent serialization operations performed on the received group of serialized data streams reduces the latency of communications through the cascaded devices, which can be significant when considered in relation to the high-speed communication rates. The received group of serialized data streams is also framed to create a sequence of data frames for processing (e.g., associative memory lookup operations, controlling multiplexing of received downstream serialized data streams, general or other processing) within the device.

Abstract: An embodiment includes a chordal replacement system comprising: a pledget coupled to a first suture length and at least one of a first needle and a first ferrule; a second suture length coupled to the pledget and at least a second needle; and a third suture length coupled to the pledget and at least a third needle; wherein the second and third suture lengths are not monolithic with each other and do not constitute a single suture. Other embodiments are described herein.

Abstract: A laparoscopic forceps comprising a handpiece including a distal end portion; a tubular member protruding from the distal end portion of the handpiece, the tubular member having a distal end, a pair of jaws having legs that are disposed within the tubular member and partially protruding from the distal end of the tubular member, the pair of jaws and the tubular member being movable relative to each other in a direction parallel to a longitudinal axis of the tubular member; wherein each of the pair of jaws has an arcuate section, and the pair of jaws are closable by advancing the tubular member over the arcuate section of the jaws; and an operable mechanism for creating relative motion between the pair of jaws and the tubular member along a direction parallel to the axis of the tubular member, wherein at the distal end portion of the tubular member there is a profile shape that is non-circular.

Abstract: A tool for depositing multilayer coatings onto a substrate. In one configuration, the tool includes a includes an in-line organic material deposition station operating under at least one of a pressure or temperature controlled environment. In another, it further is of a hybrid design that incorporates both in-line and cluster tool features. In this latter configuration, at least one of the deposition stations is configured to deposit an inorganic layer, while at least one other deposition station is configured to deposit an organic layer. The tool is particularly well-suited to depositing multilayer coatings onto discrete substrates, as well as to encapsulating environmentally-sensitive devices placed on the flexible substrate.

Abstract: An article comprising: a housing comprising: i. a barrel portion, wherein a shaft capable of unidirectional or bidirectional movement is disposed within the barrel portion; wherein the shaft comprises a proximal end and a distal end; and wherein a pair of jaws is located at the distal end of the shaft; and ii.

Abstract: A hybrid tissue scaffold is provided which comprises a porous primary scaffold having a plurality of pores and a porous secondary scaffold having a plurality of pores, wherein the secondary scaffold resides in the pores of the primary scaffold to provide a hybrid scaffold. The pores of the porous primary scaffold may have a pore size in a range of 0.50 mm to 5.0 mm, and the pores of the porous secondary scaffold may have a pore size in a range of 50 ?m to 600 ?m. The primary scaffold may provide 5% to 30% of a volume of the hybrid scaffold.

Abstract: A tool for depositing multilayer coatings onto a substrate. The tool includes a housing defining a vacuum chamber connected to a vacuum source, deposition stations each configured to deposit a layer of multilayer coating on the substrate, a curing station, and a contamination reduction device. At least one of the deposition stations is configured to deposit an inorganic layer, while at least one other deposition station is configured to deposit an organic layer. In one tool configuration, the substrate may travel back and forth through the tool as many times as needed to achieve the desired number of layers of multilayer coating. In another, the tool may include numerous housings adjacently spaced such that the substrate may make a single unidirectional pass. The contamination reduction device may be configured as one or more migration control chambers about at least one of the deposition stations, and further includes cooling devices, such as chillers, to reduce the presence of vaporous layer precursors.

Abstract: The subject matter of this specification can be embodied in, among other things, a method that includes receiving, from a web browser, a request for a token that authorizes a third party server to access a user's data stored by a content provider server. The token specifies a first scope of authorization that indicates a portion of the user's data that the third party server is permitted to access. The method also includes determining if the first scope is substantially the same as or a subset of a second scope of a previously issued token and transmitting the token in response to the received request if the first scope is determined to be substantially the same as or a subset of the second scope.

Abstract: The present invention relates to systems and methods for providing a user indicia in a display at a local client browser. The user indicia is selected prior to a web transaction and is recognizable by the user. The user indicia is displayed in a web page of a web transaction during authentication. A user can recognize the user indicia prior to providing authentication information in a web transaction. An authentication system includes a web server that provides a web page having a security box identifier, and a client browser that receives the web page from the web server. In response to the security box identifier, the client browser inserts a user indicia into the received web page and outputs a modified web page including the user indicia for display.

Abstract: A hybrid tissue scaffold is provided which comprises a porous primary scaffold having a plurality of pores and a porous secondary scaffold having a plurality of pores, wherein the secondary scaffold resides in the pores of the primary scaffold to provide a hybrid scaffold. The pores of the porous primary scaffold may have a pore size in a range of 0.50 mm to 5.0 mm, and the pores of the porous secondary scaffold may have a pore size in a range of 50 ?m to 600 ?m. The primary scaffold may provide 5% to 30% of a volume of the hybrid scaffold.