Abstract: Disclosed is a fastener that includes a nut with a threaded bore that includes a head on one end, a cylindrical outer surface and a tapered ramp on the other end, a bolt that includes a head, a threaded portion engaged with the threaded bore, a recess next to the bolt head and an enlarged shank between the threads and the recess, where the outer diameter of the recess is smaller than a major diameter of the threaded bore of the nut and where an outer diameter of the shank is larger than a major diameter of the bolt threads, and a sleeve with a unthreaded bore positioned between the tapered ramp and the bolt head with one end crimped into the recess such that the internal diameter of the crimped sleeve bore is smaller than the major diameter of the threads on the bolt.

Abstract: A magnetic filter carriage (16) for use in filtering contaminants from fluid in a high pressure fluid flow comprises a frame (18, 20, 22) arranged to support a plurality of magnet filter rods (42), such that the rods (42) are each supported at both ends thereof in a fixed orientation, for example parallel to one another. The frame (18, 20, 22) is adapted to be inserted within a pressure vessel (4) across the direction of fluid flow between a fluid inlet (7) and a fluid outlet (9) of the pressure vessel (4), and may be arranged such that more than about 90% of the flow across the vessel (4) passes through the frame (18, 20, 22). The rods (42) are mounted in a plurality of cassettes (36) which are easily removable for cleaning or replacement.

Abstract: Methods and apparatus are disclosed for filling a therapeutic substance or drug within a hollow wire that forms a stent. The stent is placed within a chamber housing a fluid drug formulation. During filling, the chamber is maintained at or near the vapor-liquid equilibrium of the solvent of the fluid drug formulation. To fill the stent, at least a portion of the stent is placed into contact with the fluid drug formulation until a lumenal space defined by the hollow wire is at least partially filled with the fluid drug formulation via capillary action. After filling is complete, the stent is retracted such that the stent is no longer in contact with the fluid drug formulation. The solvent vapor pressure within the chamber is reduced to evaporate a solvent of the fluid drug formulation. A wicking means may control transfer of the fluid drug formulation into the stent.

Abstract: Broadly speaking, embodiments of the present invention provide a wearable audio device including one or a plurality of microphones, a sound recognition systems and a controller to control the device based on one or more recognized sounds or classes of sound. Embodiments use stored sound models.

Abstract: A computer implemented method for automatically generating lyric videos comprising receiving an audio selection, determining timing information of the audio selection, and determining lyric information of the audio selection. The method includes receiving tone information of the audio selection and generating video content based on at least one of the timing information, the lyric information, and the tone information of the audio selection. The method also includes rendering a lyric video based on the video content and the audio selection.

Abstract: A system for monitoring and detecting the gait and other health related parameters of a user. One such parameter is monitoring of medication compliance and treatment session attendance done by a medication and liquid dispensing apparatus, which combines mechanical dispensing of medication. These parameters are provided in standard of care summaries to care providers, and are continually reported by the Optimum Recognition Blueprint as Standard of Care Summaries to care providers, as well as communicated to the end-user by the Virtual Caregiver Interface.

Abstract: A conveyor or drive chain wear monitor includes two sensors spaced apart from one another a predetermined distance which is less than the distance between the two selected measuring points on a chain. Two timers are provided, one of which is a chain speed timer and the other of which is the chain wear timer. The two timers are both controlled by the spaced sensors. The problem of sensor beams being broken by irrelevant beam breaking obstacles located between the successive spaced measuring points is solved by providing an ignore obstacle software routine in the wear monitor computer. The ignore obstacle software routine allows a user to program the monitor to ignore any number of irrelevant obstacles which might occur between two spaced measuring points on a chain.

Abstract: Sampling wands are provided that have features added to improve the collection of trace residues from surfaces, and also features to improve the release of the sampled residue into a detection system. The improved features include, but are not limited to a system to deliver solution or other reagents onto the sampling ticket before sampling to improve the collection of residues through enhanced release of particles from the surface, dissolution of the residue, and/or increased adherence of the residue to the ticket, and a system to deliver solution or other reagents after sampling but before analysis to improve release of the residue into the detection system.

Abstract: A stent is formed from a wire having an outer member, a radiopaque core member disposed within a portion of the outer member, and an annular lumen between the radiopaque core member and the outer member. A substance is disposed in the annular lumen to be eluted through at least one opening disposed through the outer member. A plurality of radiopaque core members are disposed within portions of the outer member and are separated by lumens defined by the inner surface of the outer member. The lumens and annular lumens are in fluid communication with each other. In a method for making the stent, a composite wire including an outer member, an intermediate member, and a core member is shaped into a stent pattern and processed to remove the intermediate member and portions of the radiopaque core member, without damaging the outer member.

Abstract: A medical device having a first portion, a second portion, and at least one connector connecting the first and second portion is formed using additive manufacturing. The method includes forming a plurality of layers of a first portion of the medical device, placing a first removable masking plate over the first portion with an opening of the masking plate aligned with a point of the first portion, forming at least one layer of a first connector on the first portion, wherein the first connector is formed in the opening of the removable masking plate, forming a plurality of layers of a second portion of the medical device, wherein a first layer of the plurality of layers of the second portion is formed partially on the first connector and partially on the removable masking plate, and removing the first removable masking plate.

Abstract: A method of making a medical device includes forming a precursor medical device using additive manufacturing. The precursor medical device includes a first portion, a second portion, a first connector, and a second connector. The first connector connects the first portion to the second portion and is configured to remain. The second connector connects the first portion to the second portion and are configured to be removed. The second connector is formed such that the second connector is less ductile than the first portion, the second portion, and the first connector. The precursor medical device is processed to remove the second connector without adversely affecting the first portion, the second portion, and the first connector.

Abstract: A computer implemented method for automatically generating musical works including receiving a lyrical input and receiving a musical input. The method includes analyzing the lyrical input to determine at least one lyrical characteristic and analyzing the musical input to determine at least one musical characteristic. Based on the at least one lyrical characteristic, the method includes correlating the lyrical input with the musical input to generate a synthesizer input. The method includes sending the synthesizer input and the at least one voice characteristic to a voice synthesizer. The method may also include receiving, from the voice synthesizer, a vocal rendering of the lyrical input. The method includes receiving a singer selection corresponding to at least one voice characteristic, and generating a musical work from the vocal rendering based on the lyrical input, the musical input, and the at least one voice characteristic.

Abstract: Broadly speaking, embodiments of the present invention provide a wearable audio device including one or a plurality of microphones, a sound recognition systems and a controller to control the device based on one or more recognised sounds or classes of sound. Embodiments use stored sound models.

Abstract: One embodiment of the present invention includes an approach for efficient start-up for secured connections and related services. A client machine receives, via an application program, a request to send a secure message to a server machine. The client machine transmits a plurality of messages to the server machine that includes a first message comprising at least two of user authentication data, entity authentication data, key exchange data, and encrypted message data. The client machine receives, from the server machine, a second message that includes a first master token comprising a first set of session keys for encrypting and authenticating messages exchanged with the server machine.

Abstract: An apparatus configured to couple to an electrical penetration assembly is disclosed in which the apparatus comprises a connector comprising an inorganic seal to seal an inorganic flange and/or housing to an electrical penetration assembly.

Abstract: A method for forming a membrane includes a step of dissolving a lithium salt in a solution including an ionomer that includes protogenic groups to form a modified solution. A membrane is formed from the solution containing the lithium salt and the ionomer that includes protogenic groups. The membrane is dried and then contacted with water to form a plurality of pores therein.

Abstract: A firearm support system (FSS) includes a buffer tube mount (BTM) having a first complementary component and a receiver comprising a second complementary component configured to selectively receive the first complementary component. The BTM comprises a shelf that extends from a ring of the BTM.

Abstract: Analytical instruments are provided that can include a sample inlet component with the sample inlet component including a first sampling port; a plurality of sample capturing assemblies; and a first valve assembly in fluid communication with both the sampling port and the sample capturing assemblies. The instrument can further include a sample analysis component in fluid communication with the first valve assembly of the sample inlet component; and an instrument control component in controlling communication with both the sample inlet component and the analysis component. Instrumental analysis methods are provided that can include continuously providing sample to at least one of a plurality of sample capturing assemblies; and selectively analyzing the contents of at least one of the plurality of sample capturing assemblies.

Abstract: Methods and apparatus are disclosed for filling a therapeutic substance or drug within a hollow wire that forms a stent. The stent is placed within a chamber housing a fluid drug formulation. During filling, the chamber is maintained at or near the vapor-liquid equilibrium of the solvent of the fluid drug formulation. To fill the stent, at least a portion of the stent is placed into contact with the fluid drug formulation until a lumenal space defined by the hollow wire is at least partially filled with the fluid drug formulation via capillary action. After filling is complete, the stent is retracted such that the stent is no longer in contact with the fluid drug formulation. The solvent vapor pressure within the chamber is reduced to evaporate a solvent of the fluid drug formulation. A wicking means may control transfer of the fluid drug formulation into the stent.