Abstract:
The present invention pertains to compositions having improved delivery of pharmaceutical actives. These compositions comprise pharmaceutical actives in an anhydrous solvent. These compositions may take the form of liquid elixirs placed into the mouth and eventually swallowed, or can be delivered via liquid-filled drops, metered liquid dosing devices, atomizers and liquid-releasing, edible capsules.
Abstract:
The present invention relates to a novel process for the preparation of specific sterically hindered nitroxyl ethers from their corresponding sterically hindered nitroxyl radicals by reacting it with an aldehyde and a hydroperoxide. This nitroxyl ether formation may be carried out from different starting nitroxyl radicals, which are subsequently further reacted to the desired compounds. The compounds prepared by this process are effective as stabilizers for polymers against harmful effects of light, oxygen and/or heat and as flame-retardants for polymers.
Abstract:
A drive system for double toggle mechanisms used to move upper and lower platens with an electric servo motor-gear box drive shaft driving a crank arm arranged to drive a respective double toggle mechanism in turn connected to the platen. The drive shaft axis is located below the toggle mechanism link pivots and driven in a direction so that the motor acts to assist the double toggle mechanism in lifting the platen, reducing the servo motor peak load. The various components are arranged for symmetrical loading of the pivots concerning the toggle links to increase the evenness of the platen when being raised or lowered.
Abstract:
The present invention concerns tunable distributed Bragg reflector (DBR) semiconductor lasers, in particular a DBR laser with a branched optical waveguide 5 within which a plurality of differently shaped lasing cavities may be formed, and a method of operation of such a laser. The laser may comprise a phase control section (418), gain section (420, 422), a sampled grating DBR (412) giving a comb-line spectrum and two tunable, chirped DBRs (414, 416) for broadband frequency training and a coupling section (410).
Abstract:
The present invention relates to spirocyclic amide derivatives of the formula I, pharmaceutically acceptable salts thereof, a process for their preparation, pharmaceutical compositions containing them, and their use in therapy.
Abstract:
A system and method are provided to allow demand loading and discarding of Java executable image (JXE) files. The virtual machine allocates an address space for a requested JXE program. The read-only portion of the JXE file is memory mapped from its nonvolatile location to the allocated memory space using read-only mapping and the read/write section of the JXE file are loaded into memory. When a page of the JXE program is needed, a page fault occurs if the read-only portion has not been loaded into memory. The operating system's page fault handler retrieves the needed page(s) from the nonvolatile storage location based upon the mapping data that resulted from the previously performed memory mapping. Because the read-only section of the JXE file is memory mapped using read-only mapping, the operating system's paging process is free to discard previously loaded memory pages that contain read-only portions of the JXE file.
Abstract:
Method and apparatus for providing GPS pseudorange correction and carrier phase correction information for navigation or surveying activities over a selected geographic region S of arbitrary size. In a navigation mode, a virtual reference station (VRS), positioned near a selected location L, receives differential GPS (DGPS) correction signals, translates these signals into a selected format, and broadcasts this DGPS information in this format for use by a local user. In a survey mode, the VRS receives corrected GPS information, translates this information into a selected format and broadcasts this translated and corrected GPS information and the VRS location, for use by a mobile station in forming a baseline vector from the GPS mobile station to the VRS location.
Abstract:
The present invention is an orally administered liquid pharmaceutical composition that demonstrates excellent physical stability while delivering concentrated levels of the pharmaceutical active(s). Specifically, these compositions for extended periods do not allow the active to precipitate or settle out of solution. Among the advantages of this invention is that the compositions do not require agitation/shaking prior to use as a method to re-suspend or dissolve active drug material to insure even and consistent dosing.
Abstract:
The invention relates to liquid sulphur-containing antioxidants and to compositions comprising them. The novel lubricant compositions comprise the reaction product of a selected group of 5-tert-butyl-4-hydroxy-3-methyl(or tert-butyl)phenyl substituted carboxylic acid esters with thiodiethylene glycol and a mono-hydroxy alcohol with a carbon chain length higher than 4 C-atoms. The novel lubricant compositions are highly resistant to oxidative degradation and are capable of reducing the negative effects of deposits, such as black sludge, in motor combustion engines, particularly spark ignition internal combustion engines.