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Smart antenna arrays are used in a variety of wireless communication applications. An antenna array can be used to form a smart antenna that gathers multiple types of signal information in its operating bandwidth. An example of a smart antenna for a code division multiple access (CDMA) system is a linear, two dimensional, planar configuration that is implemented by a two dimensional array of electrically small antenna elements. This arrangement is referred to as a smart antenna because it is an array of antenna elements used as a group to form a virtual antenna that can optimize signal communication performance for the application. A smart antenna array can improve the isolation between signals received or transmitted by the array from or to multiple users within the coverage area. This is especially true for a cellular telephone system where increasing the cell capacity allows more users within the cell. Smart antenna arrays can improve the quality and reliability of a given service by identifying and demodulating signals for multiple users.
A smart antenna can be thought of as a diversity antenna that is used for improved system performance. This performance can be further enhanced by using three or more antennas where one of the antennas is selected based on its signal strength for use as the “best” or “high quality” antenna. The other antennas are used as “degraded” antennas that can provide complementary performance. This may provide performance improvement over using two antennas with the antennas independently selected as the best and the worst antennas.
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Welcome to Catia.

Catia is a product lifecycle management software and design-automation software offering BOM (bill of materials) products, 3D assembly and stamping data-processing products, and welding and support products.Impact of sirolimus on the expression of drug transporters in rats during acute renal toxicity.
Sirolimus (SRL) is used as an immunosuppressant in the prevention of organ transplant rejection and in the treatment of autoimmune diseases. It is also one of the most widely-administered immunosuppressants in animal models of human diseases. However, the inhibitory effect of SRL on drug transporter function has recently been reported. In this study, the effects of SRL on renal drug transporter expression and function were investigated using the drug-induced nephrotoxicity model. Rats were injected i.v. with phenacetin, probenecid, isradipine, or fluvastatin once daily for 3 consecutive days. At 0.5, 1, 2, and 4 h after the last injection, blood and renal tissue samples were collected. P-glycoprotein (P-gp) expression was evaluated using immunoblotting. Urinary and fractional excretion (FE) of phenacetin, probenecid, and fluvastatin were measured at 0, 4, and 8 h. In addition, renal blood flow (RBF) and glomerular filtration rate (GFR) were measured in anesthetized rats. The renal expression of OAT1, MRP2, BCRP and OATP1A2 proteins was also analyzed using immunoblotting. In addition, renal uptake of phenacetin and fluvastatin was measured using in situ perfusion at 0, 30, and 60 min. The urinary excretion of probenecid and fluv

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