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    • 1. 发明授权
    • Indium bump hybrid bonding method and system
    • 铟凸块混合键合方法及系统
    • US4573627A
    • 1986-03-04
    • US684223
    • 1984-12-20
    • Brian S. MillerAubrey J. Dunn
    • Brian S. MillerAubrey J. Dunn
    • B23K20/02H01L21/98B23K20/00B23K31/02
    • H01L25/50B23K20/02H01L2924/0002
    • In order to ensure total bonding together of two-dimensional arrays of inm bumps on circuit boards, additional bumps are placed on each board in a triangular pattern which contains the array of that board. Opposing sets of thrusters are used to move the boards and their bumps toward each other, after the arrays are aligned with the boards juxtaposed and substantially parallel to each other. As corresponding sets of additional bumps touch each other, the set of thrusters moving the boards at those points hold their positions, until all sets of additional bumps are in touch; all of the thrusters of at least one board are then simultaneously energized until a predetermined pressure is achieved between the boards.
    • 为了确保电路板上的铟凸块的二维阵列的全部结合在一起,附加的凸块以包含该板的阵列的三角形图案放置在每个板上。 在将阵列与彼此并置并且基本上彼此平行的板对准之后,相反的推进器组被用于将板和它们的凸起朝向彼此移动。 当相应的附加凸块相互接触时,在那些位置移动板的推进器组保持它们的位置,直到所有的附加凸块组合在一起; 然后至少一个板的所有推进器同时通电,直到板之间达到预定的压力。
    • 3. 发明授权
    • Sustained release of antiinfectives
    • 持续释放抗感染药
    • US07718189B2
    • 2010-05-18
    • US11185448
    • 2005-07-19
    • Lawrence T. BoniBrian S. MillerVladimir MalininXingong Li
    • Lawrence T. BoniBrian S. MillerVladimir MalininXingong Li
    • A61K9/127
    • A61K47/28A61K9/0078A61K9/127A61K9/1277A61K31/407A61K31/4709A61K31/496A61K31/545A61K31/7036A61K31/704A61K45/06Y02A50/473
    • Provided are lipid antiinfective formulations substantially free of anionic lipids with a lipid to antiinfective ratio is about 1:1 to about 4:1, and a mean average diameter of less than about 1 μm. Also provided is a method of preparing a lipid antiinfective formulation comprising an infusion process. Also provided are lipid antiinfective formulations wherein the lipid to drug ratio is about 1:1 or less, about 0.75:1 or less, or about 0.50:1 or less prepared by an in line fusion process. The present invention also relates to a method of treating a patient with a pulmonary infection comprising administering to the patient a therapeutically effective amount of a lipid antiinfective formulation of the present invention. The present invention also relates to a method of treating a patient for cystic fibrosis comprising administering to the patient a therapeutically effective amount of a lipid antiinfective formulation of the present invention.
    • 提供基本上不含阴离子脂质的脂质抗感染制剂,其脂质与抗感染比为约1:1至约4:1,平均平均直径小于约1μm。 还提供了制备包含输注方法的脂质抗感染制剂的方法。 还提供了脂质抗感染制剂,其中通过在线融合方法制备的脂质与药物的比例为约1:1或更低,约0.75:1或更低,或约0.50:1或更低。 本发明还涉及治疗患有肺部感染的患者的方法,其包括向患者施用治疗有效量的本发明的抗脂质抗感染药物。 本发明还涉及一种治疗患者囊性纤维化的方法,其包括向患者施用治疗有效量的本发明的抗脂质抗感染制剂。
    • 6. 发明申请
    • CONTROL OF EQUIPMENT USING REMOTE DISPLAY
    • 使用远程显示控制设备
    • US20080229409A1
    • 2008-09-18
    • US12041168
    • 2008-03-03
    • Brian S. MillerJack VaughanOscar A. LedriereGino DiSimone
    • Brian S. MillerJack VaughanOscar A. LedriereGino DiSimone
    • G06F21/00
    • G06F21/32
    • An example display unit for facilitating operation of equipment includes a housing, an electronic display supported by the housing, and an electronic circuit located within the housing. The display unit may include one or more data receivers, such as a wireless receiver and/or an electrical interface. A biometric scanner, including a biometric sensor and proving an authorization signal when an authorized biometric input is detected by the biometric sensor, may be configured to electrically (and optionally mechanically) interconnect to the display unit. The example display unit receives an authorization status for operation of the equipment from the biometric scanner, and displays the authorization status and operational parameters relating to equipment use on the electronic display.
    • 用于便于设备操作的示例性显示单元包括壳体,由壳体支撑的电子显示器和位于壳体内的电子电路。 显示单元可以包括一个或多个数据接收器,诸如无线接收器和/或电接口。 当生物特征传感器检测到授权的生物测定输入时,包括生物测定传感器和验证授权信号的生物测定扫描仪可以被配置为电连接(并且可选择地机械地)互连到显示单元。 示例显示单元从生物识别扫描器接收设备操作的授权状态,并在电子显示器上显示与设备使用相关的授权状态和操作参数。
    • 7. 发明申请
    • Platinum Aggregates and Process for Producing the Same
    • 白金聚集体及其生产方法
    • US20080187578A1
    • 2008-08-07
    • US12027752
    • 2008-02-07
    • Jin K. LeeBrian S. MillerFangjun WuLawrence T. BoniVladimir Malinin
    • Jin K. LeeBrian S. MillerFangjun WuLawrence T. BoniVladimir Malinin
    • A61K9/127A61K33/24A61K31/28
    • A61K9/127A61K9/0078A61K9/1277A61K31/28A61K33/24A61K47/544A61K47/554
    • One aspect of the disclosure relates to a new form of lipid-complexed active platinum compound, which allows for high concentrations of platinum compound in the composition. For example, the concentration of cisplatin in the composition is higher at room temperature, e.g., about greater than 1.2 mg/mL, compared to 1 mg/mL in aqueous solution. In one embodiment, the present invention is directed to a composition comprising a lipid-complexed active platinum compound, wherein the complex has a lipid to drug (L/D) ratio of less than about 1 by weight, e.g. about 0.10 to 1, wherein the lipid-complexed active platinum compound comprises at least one lipid and at least one active platinum compound. In other embodiments, wherein lipid-complexed active platinum compound has an average volume-weighted diameter of about 0.5 to about 20 microns. In still other embodiments, the composition further comprises a liposome. The liposome may comprise at least one lipid, and may further comprise at least one active platinum compound. The disclosure also relates to a pharmaceutical formulation comprising a lipid complexed active platinum compound and a pharmaceutically acceptable carrier or diluent. The pharmaceutical formulation may be formulated for inhalation or injection.
    • 本公开的一个方面涉及脂质复合的活性铂化合物的新形式,其允许组合物中高浓度的铂化合物。 例如,与1mg / mL的水溶液相比,组合物中顺铂的浓度在室温较高,例如大于1.2mg / mL。 在一个实施方案中,本发明涉及包含脂质复合的活性铂化合物的组合物,其中所述复合物具有小于约1重量比的脂质与药物(L / D)比例,例如。 约0.10至1,其中所述脂质复合的活性铂化合物包含至少一种脂质和至少一种活性铂化合物。 在其它实施方案中,其中脂质配合的活性铂化合物的平均体积加权直径为约0.5至约20微米。 在其它实施方案中,组合物还包含脂质体。 脂质体可以包含至少一种脂质,并且还可以包含至少一种活性铂化合物。 本公开还涉及包含脂质复合的活性铂化合物和药学上可接受的载体或稀释剂的药物制剂。 药物制剂可以配制用于吸入或注射。