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, a portion of the stent is placed into contact with the fluid drug formulation until a lumenal space defined by the hollow wire is 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: A system and method for determining access and use of sensor and communication peripheral subsystems on a wireless device using resource consumption for the purpose of notifying and securing user privacy.

Abstract: In various embodiments, a method comprises scanning a directory structure to generate a scan result comprising a plurality of discovered systems, identifying one or more accounts associated with at least one of the plurality of discovered systems, configuring a security appliance to change one or more old passwords to one or more new passwords for the one or more accounts, and changing, with the configured security appliance, the one or more old passwords to the one or more new passwords.

Abstract: Methods, systems, and computer program products for initializing one or more components of a system, the system comprising an integrated circuit that comprises at least one processor, are disclosed. A method includes initializing at least one component of the system, determining a temperature of the integrated circuit using a temperature sensing device embedded on the integrated circuit, comparing the determined temperature to a predetermined suitable temperature operating range of at least one additional component to yield a comparison result, and initializing the at least one additional component based on the comparison result. The at least one additional component may be initialized on the condition that the determined temperature of the integrated circuit is within the predetermined suitable temperature operating range of the at least one additional component.

Abstract: In some aspects, techniques and systems for improving a well survey are described. An error analysis is performed to identify errors associated with operating a well survey instrument in a magnetic environment at a wellbore location. Based on the error analysis, an instrument performance model (IPM) is selected for a well survey by the well survey instrument. In some cases, the IPM is selected such that the errors satisfy specifications of the IPM.

Abstract: A mobile device comprising a software application configured to detect the sound of a product use event; provide a user reward using said software application in response to said detection; capture data relating to said product use event; and provide said captured data to a remote computer system for analysis.

Abstract: A firearm support system, has a stock unit configured to be carried by a firearm, the first unit having a first complementary component and a belt unit configured to be carried by a belt, the second unit having a second complementary component configured for selective engagement with the first complementary component.

Abstract: Various embodiments of methods and systems for continuous transdermal monitoring (“CTM”) are disclosed. One exemplary method for CTM begins by monitoring an output signal from an accelerometer. The accelerometer output signal may indicate acceleration and deceleration of a body part of a user, such as the user's wrist. Based on the accelerometer output signal, it may be determined that the body part of the user has decelerated to a minimum, e.g., substantially zero. With a determination that the body part has decelerated to the minimum, e.g., substantially zero, or has not accelerated beyond the minimum, e.g., substantially zero, the method may determine a reading from a pulse oximeter associated with the accelerometer. Advantageously, the pulse oximetry reading, or a reading from other sensors associated with the accelerometer, may be optimally accurate as motion artifact may be minimized. The pulse oximetry reading may be recorded for later query and/or rendered for the benefit of the user.

Abstract: Various embodiments of methods and systems for continuous transdermal monitoring (“CTM”) are disclosed. One exemplary embodiment of a continuous transdermal monitoring system comprises a sensor package. The sensor package may include a pulse oximetry sensor having a plurality of light detectors arranged as an array. One exemplary method for continuous transdermal monitoring begins by positioning a pulse oximetry sensor system, similar to the system described immediately above, adjacent to a target tissue segment. Then, the method continues by detecting a light reflected by the target tissue segment. Then, the method continues by transmitting a pulse oximetry reading(s), based at least in part on the light reflected by the target tissue segment, of the target tissue segment. Then, the method continues by analyzing the pulse oximetry reading(s).

Abstract: In various embodiments, a method comprises scanning a directory structure to generate a scan result comprising a plurality of discovered systems, identifying one or more accounts associated with at least one of the plurality of discovered systems, configuring a security appliance to change one or more old passwords to one or more new passwords for the one or more accounts, and changing, with the configured security appliance, the one or more old passwords to the one or more new passwords.

Abstract: Various embodiments of methods and systems for continuous transdermal monitoring (“CTM”) are disclosed. One exemplary method for CTM begins by monitoring an output signal from an accelerometer. The accelerometer output signal may indicate acceleration and deceleration of a body part of a user, such as the user's wrist. Based on the accelerometer output signal, it may be determined that the body part of the user has decelerated to a minimum, e.g., substantially zero. With a determination that the body part has decelerated to the minimum, e.g., substantially zero, or has not accelerated beyond the minimum, e.g., substantially zero, the method may determine a reading from a pulse oximeter associated with the accelerometer. Advantageously, the pulse oximetry reading, or a reading from other sensors associated with the accelerometer, may be optimally accurate as motion artifact may be minimized. The pulse oximetry reading may be recorded for later query and/or rendered for the benefit of the user.

Abstract: A system for treating a vascular condition includes a catheter having an inner member and an outer member, the outer member concentrically arranged about the inner member and a retractable drug delivery device disposed at a distal end of the inner member. A coating disposed on at least a portion of an outer surface of the retractable drug delivery device includes at least one therapeutic agent.

Abstract: Various embodiments of methods and systems for continuous transdermal monitoring (“CTM”) are disclosed. One exemplary embodiment of a continuous transdermal monitoring system comprises a sensor package. The sensor package may include a pulse oximetry sensor having a plurality of light detectors arranged as an array. One exemplary method for continuous transdermal monitoring begins by positioning a pulse oximetry sensor system, similar to the system described immediately above, adjacent to a target tissue segment. Then, the method continues by detecting a light reflected by the target tissue segment. Then, the method continues by transmitting a pulse oximetry reading(s), based at least in part on the light reflected by the target tissue segment, of the target tissue segment. Then, the method continues by analyzing the pulse oximetry reading(s).

Abstract: Biodegradable magnesium alloy implantable medical devices are protected to delay onset of corrosion, and thus biodegradability, or to corrode more uniformly. The protection allows for extended effective use of the devices while maintaining biodegradability. Examples of protective coatings include conversion coatings that at least partially remove exposed second phases from a surface of the magnesium alloy and coatings that provide a barrier between water and the surface of the magnesium alloy.

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, a portion of the stent is placed into contact with the fluid drug formulation until a lumenal space defined by the hollow wire is 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: A storage and display case comprising an at least partially transparent housing dimensioned to receive at least one article to be displayed; a door attached to the housing, the door configured to open and close; a channel configured to receive an air filter; one or more feet on a bottom of the housing; and one or more receiving members on a top of the housing, the one or more receiving members configured to accept one or more feet of another storage and display case allowing multiple storage and display cases to be stacked stably.

Abstract: A document printing system configured to print documents received from a user device. The system comprises a remote server and a first local print server. The remote server is configured to communicate with one or more local print servers located on respective local networks, including the first local print server. The remote server receives print jobs from remote user devices and to maintain a global queue of print jobs. The first local print server is coupled to a first local network and to an input device for receiving user instructions. The first local print server receives print jobs from user devices, maintains a first local queue of print jobs, processes print jobs from the global queue of documents, and instructs a printing device to print a document in accordance with a print job, based upon user instructions received at the input device.

Abstract: A digital sound identification system for storing a Markov model is disclosed. A processor is coupled to a sound data input, working memory, and a stored program memory for executing processor control code to input sound data for a sound to be identified. The sample sound data defines a sample frequency domain data energy in a range of frequency. Mean and variance values for a Markov model of the sample sound are generated. The Markov model is stored in the non-volatile memory. Interference sound data defining interference frequency domain data is inputted. The mean and variance values of the Markov model using the interference frequency domain data are adjusted. Sound data defining other sound frequency domain data are inputted. A probability of the other sound frequency domain data fitting the Markov model is determined. Finally, sound identification data dependent on the probability is outputted.

Abstract: Embodiments of the invention provide a method of processing natural rubber latex using an extruder including a plurality of process zones by processing coagulant with latex to produce a coagulum and serum. In some embodiments, the coagulant can include an acid, a metal salt, or a mixture of both. Some embodiments can include a coagulum wash stage, and a deresination step. In some embodiments, the extruder can be operated to move coagulum through the extruder to remove at least some fraction of water to form a substantially dewatered coagulum, and a drying step to form a dried coagulum. In some embodiments, a stabilizer such as an antioxidant can be introduced into the extruder, and processed to remain in some fraction in the dried coagulum. Some alternative embodiments include a latex processing method of providing a flow of coagulant, and combining latex with the flowing using an emulsion dispensing bar.