Abstract: The present disclosure involves mitigating biofilms through the use of a solution containing delmopinol and/or delmopinol salt. The solution is introduced to the biofilm through various techniques, such as a catheter or flushing a medical device lumen. The biofilm can be located in body cavities, wounds, or on medical devices. The solution is removed by suction or other means and may contain an antibiotic to increase its effectiveness. Agitation of the solution during contact with the biofilm may also be used to increase its efficacy. In some embodiments, the concentration of the solution ranges from 1 ?g/l up to a saturated solution, and the contact time can range from 1 second to 5 minutes. The concentrations may be higher or lower, and the contact time may be more or less than these ranges. This method provides an effective and efficient way to mitigate biofilms in various medical fields, including urology, gastroenterology, and wound care.

Abstract: The present disclosure provides nanoparticles comprising delmopinol and/or the sodium salt of delmopinol. Also provided are methods of using the nanoparticles and methods of making the nanoparticles.

Abstract: A method for testing a cell site during or after construction of the cell site is provided. In various embodiments, the method is implemented by a processor on a computing platform that includes a DU emulator. In those embodiments, the method includes establishing a first connection between a distributed unit (DU) emulator and a cell site router (CSR) of the cell site, wherein the DU emulator emulates functions of a DU; establishing a second connection between a radio unit (RU) and the CSR, wherein the RU is coupled to the DU emulator through the CSR; and causing, via the DU emulator, one or more tests to be performed at the cell site, wherein the one or more tests include at least one of a voltage standing wave ratio (VSWR) test, a passive intermodulation (PIM) test, a physical cell identifier (PCI) test, or a cable test.

Abstract: Systems and methods are provided for preventing a loss of throughput data connectivity from one or more active autonomous vehicles of the fleet communicating with a back office network by: collecting an average aggregate of the throughput data from the one or more active AVs communicating with the back office network; updating a set of records in a throughput data table corresponding to a plurality of mapped AV routes for the one or more active AVs, by processing a throughput data table record in the temporary buffer of updated throughput data to eliminate identified duplicate or out-of-date throughput data recorded in the throughput data table; and determining, by the back office network, whether one or more of the AV route segments or the final drop-off location exhibits the effect of an instance of the loss of throughput data connectivity between the AV and the back office network.

Abstract: Systems and methods are provided for preventing a loss of throughput data connectivity from one or more active autonomous vehicles of the fleet communicating with a back office network by: collecting an average aggregate of the throughput data from the one or more active AVs communicating with the back office network; updating a set of records in a throughput data table corresponding to a plurality of mapped AV routes for the one or more active AVs, by processing a throughput data table record in the temporary buffer of updated throughput data to eliminate identified duplicate or out-of-date throughput data recorded in the throughput data table; and determining, by the back office network, whether one or more of the AV route segments or the final drop-off location exhibits the effect of an instance of the loss of throughput data connectivity between the AV and the back office network.

Abstract: Embodiments of the invention include a medical device with one or more of a variety of features. More particularly, embodiments of the invention relate to endoscopic devices that include one or more features that improve the use of the device. Examples of such features include chamfered edges and corners on, for example, the end effectors, a surface with a controlled finish also on, for example, the end effectors, a jaw with teeth and/or a tang having various configurations, a handle having soft-grip features, and/or an elongate member with varied rigidity. Other examples of such features include a folded portion on, for example, the end effectors and/or a snap-fit clevis assembly.

Abstract: Embodiments of the invention include a medical instrument with a sealing device. In embodiments, the medical instrument is endoscopic device having a seal between an elongate shaft member and/or on a portion of a handle to, for example, prevent flow communication between a lumen of the elongate member and the external environment.

Abstract: Embodiments of the invention include a medical device with one or more of a variety of features. More particularly, embodiments of the invention relate to endoscopic devices that include one or more features that improve the use of the device. Examples of such features include chamfered edges and corners on, for example, the end effectors, a surface with a controlled finish also on, for example, the end effectors, a jaw with teeth and/or a tang having various configurations, a handle having soft-grip features, and/or an elongate member with varied rigidity. Other examples of such features include a folded portion on, for example, the end effectors and/or a snap-fit clevis assembly.

Abstract: Embodiments of the invention include a medical device with one or more of a variety of features. More particularly, embodiments of the invention relate to endoscopic devices that include one or more features that improve the use of the device. Examples of such features include chamfered edges and corners on, for example, the end effectors, a surface with a controlled finish also on, for example, the end effectors, a jaw with teeth and/or a tang having various configurations, a handle having soft-grip features, and/or an elongate member with varied rigidity.

Abstract: Embodiments of the invention include a medical instrument with a sealing device. In embodiments, the medical instrument is endoscopic device having a seal between an elongate shaft member and/or on a portion of a handle to, for example, prevent flow communication between a lumen of the elongate member and the external environment.

Abstract: Embodiments of the invention include a medical instrument with a sealing device. In embodiments, the medical instrument is an endoscopic device having a seal between an elongate shaft member and/or on a portion of a handle to, for example, prevent flow communication between a lumen of the elongate member and the external environment.

Abstract: Embodiments of the invention relate to a medical device having a proximal portion that can selectively receive other portions of the device. More specifically, embodiments of the invention relate to an endoscopic instrument with a handle portion configured to accommodate an elongate, flexible member and an end effector assembly of the endoscopic instrument for protection, coiling, looping, containment, packaging and for disposal. The device may have a variety of configurations.

Abstract: A feedhorn driving method and apparatus allows the establishment of multiple phase centers using only a single multimode feedhorn. At least two higher-order modes are extracted from the feedhorn and weighted in amplitude and phase. The phase center separation is established in accordance with an assigned weights. The feedhorn has application in i.a. moving target indication systems.

Abstract: The present invention provides a process for the preparation of p-toluic acid by liquid phase oxidation of p-xylene using oxygen or air as oxidant in the presence of p-toluic acid, water as solvent and cobalt salt or its combinations with salts of Ce, Mn as catalyst. Oxidation is carried out at 130-190° C. and pressure sufficient to keep water in liquid state. Oxidation step is followed by filteration to obtain p-toluic acid as major product. Unreacted p-xylene is recovered and recycled and the catalyst is recovered from aqueous phase and is recycled.

Abstract: A full thickness resection device comprises a control handle including an actuator wherein, when the device is in an operative position within a body lumen of a patient, the control handle remains outside the patient's body and a working head assembly coupled to a control handle by a flexible sheath, wherein, when the device is in the operative position; the working head assembly is located within a body lumen of the patient adjacent to a portion of tissue to be treated, the working head assembly including a tissue stapling mechanism including first and second tissue stapling members moveable relative to one another in combination with a first cable extending from the actuator through the flexible sheath to the first tissue stapling member so that, when the actuator is operated to draw the first cable proximally from the sheath, the first tissue stapling member is moved in a first direction relative to the second tissue stapling member.

Abstract: Embodiments of the invention include a medical instrument with a sealing device. In embodiments, the medical instrument is an endoscopic device having a seal between an elongate shaft member and/or on a portion of a handle to, for example, prevent flow communication between a lumen of the elongate member and the external environment.

Abstract: Embodiments of the invention relate to a medical device having a proximal portion that can selectively receive other portions of the device. More specifically, embodiments of the invention relate to an endoscopic instrument with a handle portion configured to accommodate an elongate, flexible member and an end effector assembly of the endoscopic instrument for protection, coiling, looping, containment, packaging and for disposal. The device may have a variety of configurations.

Abstract: Aspects of the invention are found in a heating component having a composite material coated on a support. The composite material includes a fluorinated or silicone polymer and inductively-heatable particles. Additional aspects of the invention are found in a heating belt having a flexible support coated with a composite material. The composite material includes a polymer material and inductively-heatable particles. Further aspects of the invention are found in a system for heating an article. The system includes a heating belt and a field generator. The heating belt includes a flexible support coated in a composite material. The composite material includes a polymeric matrix and inductively-heatable particles. The field generator induces a field about the heating belt. The inductively-heatable particles heat in the presence of the field.

Abstract: A feedhorn driving method and apparatus allows the establishment of multiple phase centers using only a single multimode feedhorn. At least two higher-order modes are extracted from the feedhorn and weighted in amplitude and phase. The phase center separation is established in accordance with an assigned weights. The feedhorn has application in i.a. moving target indication systems.

Abstract: Embodiments of the invention include a medical device with one or more of a variety of features. More particularly, embodiments of the invention relate to endoscopic devices that include one or more features that improve the use of the device. Examples of such features include chamfered edges and corners on, for example, the end effectors, a surface with a controlled finish also on, for example, the end effectors, a jaw with teeth and/or a tang having various configurations, a handle having soft-grip features, and/or an elongate member with varied rigidity.