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    • 45. 发明申请
    • SYSTEM AND METHOD FOR PARALLEL IMAGING OPTICAL COHERENCE TOMOGRAPHY
    • 用于平行成像光学相干坐标系统和方法
    • WO2014089504A1
    • 2014-06-12
    • PCT/US2013/073704
    • 2013-12-06
    • LEHIGH UNIVERSITY
    • ZHOU, Chao
    • G01B9/02
    • G01B9/02012G01B9/02027G01B9/02091G01N21/4795
    • A parallel imaging optical coherence tomography system. In one embodiment, the system includes a light source, a movable scan unit, and an interferometer comprising a reference arm and a sample arm. The scan unit includes a plurality of apertures illuminated by incident light from the light source. The scan unit produces a plurality of light beams transmitted to the interferometer. The light beams are each split producing a plurality of reference and sampling beams. The sampling beams are scanned onto a sample and return reflected sampling light signals through the sample arm which are combined with reflected, reference light signals from the reference arm An interference pattern is formed which Is detected by an image sensor and processed to generate a digital image of the sample. In some embodiments, the scan unit may include a microlens array, A related scanning method is also provided.
    • 平行成像光学相干断层扫描系统。 在一个实施例中,系统包括光源,可移动扫描单元和包括参考臂和样本臂的干涉仪。 扫描单元包括由来自光源的入射光照射的多个孔。 扫描单元产生传输到干涉仪的多个光束。 光束每个分割产生多个参考和采样光束。 采样光束被扫描到样品上,并通过样品臂返回反射的采样光信号,该信号与来自参考臂的反射的参考光信号组合。形成由图像传感器检测并被处理以产生数字图像的干涉图案 的样品。 在一些实施例中,扫描单元可以包括微透镜阵列,还提供了相关的扫描方法。
    • 50. 发明申请
    • NANO/MACROPOROUS BIOACTIVE GLASSES MADE BY MELT-QUENCH METHODS
    • NANO /通过熔融法制造的大面积生物玻璃
    • WO2008101011A1
    • 2008-08-21
    • PCT/US2008/053851
    • 2008-02-13
    • LEHIGH UNIVERSITYJAIN, HimanshuMOAWAD, Hassan, Mohamady, Mohamed
    • JAIN, HimanshuMOAWAD, Hassan, Mohamady, Mohamed
    • B82B3/00
    • A61L27/10A61L27/56
    • The methods and materials described herein provide novel and simple procedures for the preparation of nano/macroporous glasses, in which the pore structure is characterized by interconnected pores of, e.g., both hundreds of micrometers and several to tens of nanometers in size. Such materials may be used for enhanced bone regeneration, bioscaffolds, drug delivery devices, and filtration media, among other uses. For example, silica-based bone tissue scaffolds are made with a controlled nano/macroporosity, which enhances bone regeneration performance. Also provided herein are new biocompatible CaO-Na 2 O-P 2 O 5 -S i O 2 glasses prepared by thermal melt-quench methods that result in spinodal phase separation and crystallization of phases at very different length scales. Selective chemical leaching of these phases causes formation of interconnected multi-modal porosity, with pore sizes ranging from several nanometers to tens of micrometers.
    • 本文所述的方法和材料提供了用于制备纳米/大孔玻璃的新颖且简单的方法,其中孔结构的特征在于尺寸为几百微米和数十纳米的互连孔。 除了其它用途之外,这种材料可用于增强骨再生,生物支架,药物递送装置和过滤介质。 例如,二氧化硅基骨组织支架用受控的纳米/大孔隙度制成,这增强了骨再生性能。 本文还提供了新的生物相容性CaO-Na 2 O 2 O 2 O 2 -Si O 2 通过热熔融淬火方法制备的玻璃杯,其导致相分离并在非常不同的长度尺度下结晶相。 这些相的选择性化学浸出导致互连的多模式孔隙的形成,其孔径范围从几纳米到几十微米。