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Optimization methods are presented to design Halbach arrays to maximize the forces applied on magnetic nanoparticles at deep tissue locations. In magnetic drug targeting, where magnets are used to focus therapeutic nanoparticles to disease locations, the sharp fall off of magnetic fields and forces with distances from magnets has limited the depth of targeting. Creating stronger forces at a depth by optimally designed Halbach arrays would allow treatment of a wider class of patients, e.g. patients with deeper tumors. The presented optimization methods are based on semi-definite quadratic programming, yield provably globally optimal Halbach designs in 2 and 3-dimensions, for maximal pull or push magnetic forces (stronger pull forces can collect nanoparticles against blood forces in deeper vessels; push forces can be used to inject particles into precise locations, e.g. into the inner ear). These Halbach designs, here tested in simulations of Maxwell's equations, significantly outperform benchmark magnets of the same size and strength. For example, a 3-dimensional 36 element 2000 cm3 volume optimal Halbach design yields a 5× greater force at a 10 cm depth compared to a uniformly magnetized magnet of the same size and strength. The designed arrays should be feasible to construct, as they have a similar strength (≤1 T), size (≤2000 cm3), and number of elements (≤36) as previously demonstrated arrays, and retain good performance for reasonable manufacturing errors (element magnetization direction errors ≤5°), thus yielding practical designs to improve magnetic drug targeting treatment depths. 相似文献
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运用金属有机物化学气相沉积法(MOCVD),在LaAlO3(LAO)单晶上沉积YBa2Cu3O7-x(YBCO)超导薄膜。通过使用优化的进液装置,使金属有机源连续、稳定地输送至蒸发皿进行闪蒸。通过优化总气压、氧分压等生长条件,获得高质量的YBCO薄膜。在固定的温度条件下,调节反应总气压和氧分压,在总压为380Pa,氧分压为180Pa获得YBCO薄膜临界电流密度Jc=0.6MA/cm2。随着氧分压增大,YBCO薄膜产生a轴取向,(005)峰向左偏移,且薄膜中的Cu/Ba由1.0变化至1.63。在Cu/Ba=1.48时,YBCO薄膜结构与性能较优。 相似文献
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