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    • 2. 发明授权
    • Technique for enabling a plurality of software components to communicate in a software component matrix environment
    • 用于使多个软件组件能够在软件组件矩阵环境中进行通信的技术
    • US08086665B1
    • 2011-12-27
    • US10224417
    • 2002-08-21
    • Martin SoukupGregory HughesMichael Heffernan
    • Martin SoukupGregory HughesMichael Heffernan
    • G06F15/16
    • H04L67/16G06F9/541G06F9/547H04L67/42
    • A technique for enabling a plurality of software components to communicate in a software component matrix environment is disclosed. In one particular exemplary embodiment, the technique may be realized by a method for enabling a plurality of software components to communicate in a software component matrix environment comprising the steps of encoding a request at a client side; communicating the request to a server at a server side via a communication interface; comparing the request to a plurality of operations supported at the server side; determining whether a function match exists at the server side; and returning a response comprising the function match to the client side in response to the request via the communication interface wherein the response is mapped to a data model of a client.
    • 公开了一种使多个软件组件能够在软件组件矩阵环境中进行通信的技术。 在一个特定示例性实施例中,该技术可以通过使多个软件组件能够在软件组件矩阵环境中进行通信的方法来实现,该方法包括以下步骤:在客户端侧对请求进行编码; 通过通信接口将请求传送到服务器端的服务器; 将所述请求与在所述服务器侧支持的多个操作进行比较; 确定服务器端是否存在功能匹配; 以及响应于经由所述通信接口的所述请求,将包括所述功能匹配的响应返回给所述客户端,其中所述响应被映射到客户端的数据模型。
    • 4. 发明申请
    • SYSTEM AND METHOD FOR BALANCING A TIRE AND RIM ASSEMBLY
    • 用于平衡轮胎和轮胎组件的系统和方法
    • US20080135146A1
    • 2008-06-12
    • US11928946
    • 2007-10-30
    • Michael HeffernanRussell J. Freeman
    • Michael HeffernanRussell J. Freeman
    • F16F15/36B23P17/00
    • F16F15/363Y10T29/49494
    • A self-balancing wheel assembly includes a rim, a tire mounted to the rim and defining an inflatable chamber between the rim and the tire, and a valve mounted to the rim for inflating and deflating the tire. The valve includes a housing having a channel therein extending between an outer surface of the housing and the chamber. The valve includes a stopper movable within the channel between an open and a closed position for allowing and blocking fluid flow through the channel, the stopper being narrower in width than the channel. The assembly further includes balancing media in the chamber, the balancing media comprising solid particles sized sufficiently large to inhibit passage of the solid particles past the stopper. The assembly can be used in wheels having integral TPMS modules, and having aluminum valve stems connected to the modules and short, nickel plated valve cores mounted in the stems.
    • 自平衡轮组件包括轮辋,安装到轮辋并且限定轮辋和轮胎之间的可充气室的轮胎和安装到轮辋上的用于使轮胎充气和放气的阀。 阀包括壳体,该壳体具有在壳体的外表面和腔室之间延伸的通道。 该阀包括可在通道内在打开和关闭位置之间移动的止动件,用于允许和阻止流体流过通道,止动器的宽度比通道窄。 组件还包括室中的平衡介质,平衡介质包括固体颗粒,其尺寸足够大以阻止固体颗粒通过塞子。 该组件可用于具有整体TPMS模块的车轮中,并且具有连接到模块的铝阀杆和安装在杆中的短的镀镍阀芯。
    • 5. 发明申请
    • Modified release compositions of milnacipran
    • 米那普仑的改性释放组合物
    • US20060024366A1
    • 2006-02-02
    • US11192885
    • 2005-07-29
    • Jane HirshRoman RariyShubha ChungiSrinivas RaoMichael Heffernan
    • Jane HirshRoman RariyShubha ChungiSrinivas RaoMichael Heffernan
    • A61K9/22
    • A61K9/2054A61K9/2846
    • A once-a-day oral milnacipran modified release formulation has been developed. The formulation comprises an extended release dosage unit (optionally containing the immediate release portion) coated with delayed release coating. The milnacipran composition, when administered orally, first passes through the stomach releasing from zero to less than 10% of the total milnacipran dose and then enters the intestines where drug is released slowly over an extended period of time. The release profile is characterized by a 0.05-4 hours lag time period during which less than 10% of the total milnacipran dose is released followed by a slow or extended release of the remaining drug over a defined period of time. The composition provides in vivo drug plasma levels characterized by Tmax at 4-10 hours and an approximately linear drop-off thereafter and Cmax below 3000 ng/ml, preferably below 2000 ng/ml, and most preferably below 1000 ng/ml. The composition provides a therapeutic effect over approximately 24 hours, when administered to a patient in need, resulting in diminished incidence or decreased intensity of common milnacipran side effects such as sleep disturbance, nausea, vomiting, headache, tremulousness, anxiety, panic attacks, palpitations, urinary retention, orthostatic hypotension, diaphoresis, chest pain, rash, weight gain, back pain, constipation, vertigo, increased sweating, agitation, hot flushes, tremors, fatigue, somnolence, dyspepsia, dysoria, nervousness, dry mouth, abdominal pain, irritability, and insomnia.
    • 已经开发了一天一次的口服米那普仑改性释放制剂。 该制剂包含用延迟释放包衣涂覆的延长释放剂量单位(任选地含有速释部分)。 当口服给药时,米那普仑组合物首先通过胃从零释放至总的米那普仑剂量的10%,然后进入肠道,药物在较长时间内缓慢释放。 释放曲线的特征在于0.05-4小时的滞后时间,在此期间,释放总的米那普仑总量的不到10%,然后在规定的时间段内缓慢或延长释放剩余的药物。 该组合物在4-10小时时提供特征为T max max的体内药物血浆水平,此后大约线性下降,低于3000ng / ml,优选低于 2000ng / ml,最优选低于1000ng / ml。 当给予需要的患者时,该组合物在约24小时内提供治疗效果,导致常见的米那普仑副作用的发生率降低或强度降低,例如睡眠障碍,恶心,呕吐,头痛,惊恐,焦虑,惊恐发作,心悸 ,尿潴留,直立性低血压,尿频,胸痛,皮疹,体重增加,背痛,便秘,眩晕,出汗增加,激动,潮红,震颤,疲劳,嗜睡,消化不良,呕吐,紧张,口干,腹痛, 烦躁不安和失眠。