摘要:
According to the present invention, in cases where a CHA function and a DKA function are mounted within a single package, a battery power supply that is used during the occurrence of power supply trouble is effectively utilized so that the supply of power can be separately controlled for each function. A CHA part and DKA part are disposed in a single control package. When trouble such as a power outage is detected, the CHA part blocks access requests from the host, and initiates end processing. When the end processing of the CHA part is completed, the package internal power supply control part stops the clock supply to the CHA part. Then, when the DKA part completes destage processing, the package internal power supply control part stops the supply of power to the DKA part. The power consumption of the package is lowered in stages in accordance with the progress of the end processing.
摘要:
Electroporation electrodes are laminated to a permeable membrane to form an electrode membrane. Such an electrode membrane is useful for a continuous controlled delivery of a therapeutic agent through the skin or mucosa, when placed in direct contact with the skin or mucosa and by application of electric field pulses at specified intervals. An electrode membrane can be assembled such that it incorporates an iontophoretic electrode in the same device. This device can be jointly utilized for electroporation and iontophoretic drug delivery through the skin and mucosal membrane.
摘要:
The present invention provides an adhesive gel composition for iontophoretic formulations which is useful for the application through the skin or the mucosa, which excels in all of drug absorption, drug stability, gel shape retention and gel adhesion, which is easy to prepare and fill at the time of production, and which can be produced at low costs and a method for producing the same. The adhesive gel composition for iontophoretic formulations is produced by mixing an ionic synthetic polymer(s), a nonionic synthetic polymer(s), a naturally-occurring polymer(s), a polyhydric alcohol(s), a crosslinking agent(s) and a drug(s). In the production of the adhesive gel composition for iontophoretic formulations, oxygen dissolved in the gel is positively removed by carrying out replacement with nitrogen and/or vacuum kneading at the time of the ingredients are mixed and kneaded.
摘要:
To enable processing both the image data of RGB and the image data of CMYK and enhance printing speed, the following measures are taken. An image processor for printing according to the present invention is provided with an expander for expanding both the image data in the first color space of RGB and others and the image data in the second color space of CMYK and others and image data supply means for converting expanded image data to the image data in the second color space and supplying it to a print engine if the expanded image data is the image data in the first color space or supplying expanded image data to the print engine without converting it if the expanded image data is the image data in the second color space. If image data in the first color space is supplied from a host computer and if image data in the second color space is supplied, the image data is also once compressed and is stored in a memory, the compressed image data is expanded by the image processor for printing as it is, is converted only in the case of the image data in the first color space and is supplied to the print engine as the expanded image data in the second color space.
摘要:
An airbag apparatus has an airbag, an inflator, a cover and an opening mechanism. When an impact the magnitude of which is greater than a predetermined value is applied to the vehicle, the inflator supplies gas to the airbag. The cover covers the airbag. The opening mechanism opens the cover prior to inflation of the airbag.
摘要:
The present invention provides an insulin-administering device enabling the effective administration of insulin via a percutaneous or submucous administration route. The present device is used to percutaneously or transmucosally administer an insulin lispro represented by the structural formula indicated below, or a pharmaceutically acceptable salt thereof, using iontophoresis and electroporation.
摘要:
An electrode structure is provided which is capable of efficiently using a material that can be a non-polarized electrode component, allowing the material to fully demonstrate the effect as the non-polarized electrode and maintaining the performance. This electrode structure comprises an insulating base (13), a polarized component layer (first layer) (12) laminated on the insulating base so as not to penetrate the insulating base, the polarized component layer comprising a conductive paste or metallic foil which is predominantly made of a component that can be a polarized electrode, and a non-polarized component layer (second layer) (11) provided on the polarized component layer, the non-polarized component layer comprising a conductive paste which is predominantly made of a component that can be a non-polarized electrode.
摘要:
An image forming system including multiple photoconductors arranged in a line extending in a vertical direction and forming one body as one unit, and multiple development devices and multiple exposure devices arranged on one side of the line of the multiple photoconductors. An image is transferred to a recording medium on an other side of the line of the multiple photoconductors.
摘要:
An image forming system having multiple photoconductors arranged in a line and forming one body as one unit, multiple development devices and multiple exposure devices arranged on one side of the line of the multiple photoconductors, an intermediate transfer device arranged on the other side of the line of the multiple photoconductors and a form cassette arranged below the line of the multiple photoconductors. The image forming system further includes a transfer device and a fusing device arranged at an opposite side of the intermediate transfer device with respect to the line of the multiple photoconductors.
摘要:
Compression and encoding sections (311 (1), 311 (2) and 311 (3) compress and encode input signals VS, AS and SS separately to generate compressed data. A SCSI interface (32) outputs the compressed data to a DSM (50). Output buffers (312 (1), 312 (2) and 312 (3)), a stream interface (34) and an input buffer (33) transfer the compressed data generated at the compression and encoding sections (311 (1), 311 (2) and 311 (3)) to the SCSI interface (32) through data transfer buses (38(1), 38 (2), 38 (3), 39 and 40). A CPU (35), a RAM (36) and a ROM (37) control data transfer through a CPU bus (42).