Abstract: Software, and a master system with hardware and connections, for validated drug clinical studies includes: creating data collection documents with unique identifiers; having operators complete security identification verification before proceeding; having secured operators fill out and sign specified data collection documents; creating permanent records of the preceding; tracking by unique identifiers in a local system; uploading to a central system; independently reviewing filled out signed data collection documents to accept or require clarifications; keeping permanent read only records of all originally filled out and signed documents; making document clarification requests; reviewing each response; assigning new unique identifier links to each version of every revision; iteratively repeating the above until the documents are clean, and storing and tracking every version of every document in the central system; providing a monitor query and document entry history of all changes to all documents to create a

Abstract: A pneumatic tire has a crown-reinforcing insert which extends from under the tread substantially, such as at least one-third of the sidewall height, into the sidewall of the tire. Apexes extend from the beads substantially, such as at least one-third of the sidewall height, into the sidewall of the tire, thereby effecting a substantial, such as at least one-third of the sidewall height, “overlap” between end portions of the crown-reinforcing insert and the apexes. Additionally, at least one belt extends from under the tread substantially into the sidewall, and the turn-ups of at least some of the plies extend quite high, such as at least one-third of the sidewall height, into the sidewall. This combination of features yields superior runflat performance.

Abstract: For drug clinical studies validation methodology; creating data collection documents with unique identifiers; having operators complete security identification verification before proceeding; having secured operators fill out and sign specified data collection documents; creating permanent records of the preceding; tracking by unique identifiers in a local system; uploading to a central system; independently reviewing filled out signed data collection documents to accept or require clarifications; keeping permanent read only records of all originally filled out and signed documents; making document clarification requests; reviewing each response; assigning new unique identifier links to each version of every revision; iteratively repeating the above until the documents are clean, and storing and tracking every version of every document in the central system; providing a monitor query and document entry history of all changes to all documents to create a secured audit trail.

Abstract: A ventilation or CPAP interface system adapted to be inserted into a nares of a user to secure the interface. A cannula adapted to be connected to a source of ventilation gas forms a first portion of an input gas flow passage to supply the ventilation gas to the user. A nasal insert adapted to be inserted the nares of the user forms a second portion of the input gas flow passage from the cannula to a distal end of the nasal insert. A seal portion adapted to engage a portion of the first naris is provided adjacent the distal end of the nasal insert. Ventilation interface system may optionally include feed tubes, y-connector, tube holder, and headgear.

Abstract: A ventilation interface and system is described which can be adapted to be connected to a source of ventilation. The ventilation interface and system may include variable exhaust ports. The ventilation interface system may optionally include feed tubes, y-connector, tube holder, and headgear.

Abstract: The ventilation interface for sleep apnea therapy interfaces a ventilation device to the patient's airways. The ventilation interface includes a pair of nasal inserts made from flexible, resilient silicone which are oval shaped in cross-section and slightly tapered from a base proximal the ventilation supply to the distal tip end. A bead flange is disposed about the exterior of each insert at the distal end of the insert. A bleed port for release of exhaled air is defined through a conical vent projecting normally to the path of the incoming air flow, and continues through a nipple extending to the exterior of the air conduit. In one embodiment, a pair of nasal inserts are integral with a nasal cannula body, with bleed ports axially aligned with each insert. In another embodiment, each insert is independently connected to a separate, thin-walled, flexible supply line.

Abstract: A ventilation interface and system is described which can be adapted to be connected to a source of ventilation. The ventilation interface and system may include improved headgear and nasal inserts with a curve.

Abstract: Use of physical vapor deposition methodologies to deposit nanoscale gold on activating support media makes the use of catalytically active gold dramatically easier and opens the door to significant improvements associated with developing, making, and using gold-based, catalytic systems. The present invention, therefore, relates to novel features, ingredients, and formulations of gold-based, heterogeneous catalyst systems generally comprising nanoscale gold deposited onto a nanoporous support.

Abstract: A ventilation or CPAP interface system adapted to be inserted into a nares of a user to secure the interface. A cannula adapted to be connected to a source of ventilation gas forms a first portion of an input gas flow passage to supply the ventilation gas to the user. A nasal insert adapted to be inserted the nares of the user forms a second portion of the input gas flow passage from the cannula to a distal end of the nasal insert. A seal portion adapted to engage a portion of the first naris is provided adjacent the distal end of the nasal insert. Ventilation interface system may optionally include feed tubes, y-connector, tube holder, and headgear.

Abstract: A ventilation or CPAP interface system adapted to be inserted into a nares of a user to secure the interface. A cannula adapted to be connected to a source of ventilation gas forms a first portion of an input gas flow passage to supply the ventilation gas to the user. A nasal insert adapted to be inserted the nares of the user forms a second portion of the input gas flow passage from the cannula to a distal end of the nasal insert. A seal portion adapted to engage a portion of the first naris is provided adjacent the distal end of the nasal insert. Ventilation interface system may optionally include feed tubes, y-connector, tube holder, headgear and a headgear flange.

Abstract: The present invention pertains to the discovery that B. anthracis possesses a luxS gene that encodes a functional LuxS polypeptide, and that B. anthracis synthesizes a functional AI-2 quorum-sensing molecule. The invention provides mutant B. anthracis bacteria lacking the function of the luxS gene, which do not produce a functional AI-2 molecule and have growth defects compared to wild-type B. anthracis. The invention also concerns methods for inhibiting the growth of B. anthracis, or for preventing or treating B. anthracis infection, by inhibiting the activity of the B. anthracis LuxS polypeptide, or by exposure of the B. anthracis to furanone. In particular, the invention concerns the use of furanone, a compound that inhibits AI-2-mediated quorum-sensing, to inhibit the growth of B. anthracis, to inhibit B. anthracis toxin production, particularly that of protective antigen, and to prevent or treat B. anthracis infection. The invention also provides methods to prevent B.

Abstract: The ventilation interface for sleep apnea therapy interfaces a ventilation device to the patient's airways. The ventilation interface includes a pair of nasal inserts made from flexible, resilient silicone which are oval shaped in cross-section and slightly tapered from a base proximal the ventilation supply to the distal tip end. A bead flange is disposed about the exterior of each insert at the distal end of the insert. In one embodiment, a valve is disposed between the nasal inserts and a source of positive airway pressure, the valve having a rim with a one-way diaphragm pivotally attached to the valve body with an inflatable bladder depending from the rim which seals against an exit port during inspiration and deflates to uncover the exit port on expiration. Another embodiment has nasal inserts without positive airway pressure but with a removable filter in the inserts for filtering inspired air.

Abstract: The present invention pertains to a copolymer polyols based on tertiary amine based polyols and to polyurethane products made therefrom. The use oof such copolymer polyols reduces the amount of amine catalysts needed for the production of polyurethane foam.

Abstract: The ventilation interface for sleep apnea therapy interfaces a ventilation device to the patient's airways. The ventilation interface includes a pair of nasal inserts made from flexible, resilient silicone which are oval shaped in cross-section and slightly tapered from a base proximal the ventilation supply to the distal tip end. A bead flange is disposed about the exterior of each insert at the distal end of the insert. A bleed port for release of exhaled air is defined through a conical vent projecting normally to the path of the incoming air flow, and continues through a nipple extending to the exterior of the air conduit. In one embodiment, a pair of nasal inserts are integral with a nasal cannula body, with bleed ports axially aligned with each insert. In another embodiment, each insert is independently connected to a separate, thin-walled, flexible supply line.

Abstract: A nasal ventilation interface comprising a hollow body having at least one and preferably two nasal apertures, and at least one and preferably two inhale apertures, and at least one and preferably two nasal insert tubes each associated with one of the nasal apertures and having an annular sleeve that forms a seal with a nostril of the patient. The hollow body has at least one and preferably two exhale apertures and at least one valve assembly associated with the exhale apertures that are capable of preventing air from passing through the exhale aperture upon the patient inhaling and allowing air to pass through the exhale aperture upon exhaling. The hollow body may also have at least one and preferably two filters for retaining heat and moisture from the exhale air and transferring the retained heat and moisture into the inhale air.

Abstract: A ventilation or CPAP interface system adapted to be inserted into a nares of a user to secure the interface. A cannula adapted to be connected to a source of ventilation gas forms a first portion of an input gas flow passage to supply the ventilation gas to the user. A nasal insert adapted to be inserted the nares of the user forms a second portion of the input gas flow passage from the cannula to a distal end of the nasal insert. A seal portion adapted to engage a portion of the first naris is provided adjacent the distal end of the nasal insert. Ventilation interface system may optionally include feed tubes, y-connector, tube holder, and headgear.

Abstract: An apparatus and a method for molding a lofted material and preserving the inherent loft characteristics associated with such a material are provided. The apparatus has a first mold and a second mold that cooperate to provide a three-dimensional aspect to the lofted material. The first mold has a surface with a projecting element and a first level portion while the second mold has a surface with a recessed element and a second level portion. The projecting element is formed to fit in the recessed element when the first and second molds are brought into relatively close relation. A uniform preset gap is maintained between the projecting element and the recessed element when the first mold is closed relative to said second mold, or vice-versa, such that the inherent loft characteristics associated with the lofted material are substantially preserved during a molding operation.

Abstract: A system and method are disclosed for communicating multimedia information. Exemplary embodiments provide a Video-to-Optical apparatus (“V2O”) that can be used over either a private or a public optical network and transfers multimedia information in SONET/SDH frame format. The V2O uses SONET/SDH frames to transmit high-resolution stereoscopic images and other multimedia information through an optical network with high efficiency, high accuracy and low latency. The V2O interfaces with a visualization graphics-server on one side and the optical network on the other. The V2O apparatus can be placed in an optical network that offers an end-to-end OC 3 or higher rate circuit. A plurality of multimedia visualization centers can be coupled to the optical network.

Abstract: Compositions and methods for wrinkle reduction in fabrics, including washable clothes, dry cleanable clothes, linens, bed clothes, draperies, window curtains, shower curtains, table linens, and the like requiring little, if any, pressing, ironing, and/or steaming are disclosed.