43.
    外观设计
    失效

    公开(公告)号:KR3001066940000S

    公开(公告)日:1990-09-24

    申请号:KR3019890006163

    申请日:1989-05-09

    Applicant: 박정극

    Designer: 박정극

    45.
    外观设计
    失效

    公开(公告)号:KR3000745920000S

    公开(公告)日:1987-09-17

    申请号:KR3019860008985

    申请日:1986-06-26

    Applicant: 박정극

    Designer: 박정극

    46.
    外观设计
    失效

    公开(公告)号:KR3000728920000S

    公开(公告)日:1987-07-25

    申请号:KR3019860008986

    申请日:1986-06-26

    Applicant: 박정극

    Designer: 박정극

    신발용 미끄럼 방지구
    47.
    发明公开
    신발용 미끄럼 방지구 有权
    足球防滑设备

    公开(公告)号:KR1020120037750A

    公开(公告)日:2012-04-20

    申请号:KR1020100099397

    申请日:2010-10-12

    Applicant: 박정극

    Inventor: 박정극

    Abstract: PURPOSE: A skid-proof device for shoes is provided to enable users to simply and easily change the location of a spike member before fixing the location by the condition of the road. CONSTITUTION: A skid-proof device for shoes includes a plate(200), a binding band, a supporting axis(300), a spike member(100), a pin(400), a locking lever(600), and a location decision hole(220). The plate is closely attached to the bottom and the side surface of the shoes. The binding band is connected to the upper side of side plates(210). The supporting axis is fixed on the plate. The spike member includes spikes(110) in a blade shape, and axis-combined to the supporting axis. The pin is fixed to both sides of the spike member. The locking lever elastically supports a fixture(610) using a spring(500).

    Abstract translation: 目的:提供防滑装置,使用户能够根据道路状况,在固定位置之前,简单,轻松地更改穗状物的位置。 构成:用于鞋子的防滑装置包括板(200),装订带,支撑轴(300),钉构件(100),销(400),锁定杆(600)和位置 决定孔(220)。 板紧贴在鞋底和侧面上。 装订带连接到侧板(210)的上侧。 支撑轴固定在板上。 尖钉构件包括刀片形状的尖钉(110),并且与支撑轴线轴组合。 销钉固定在钉钉构件的两侧。 锁定杆使用弹簧(500)弹性地支撑固定装置(610)。

    일체형 무균 캡슐 제조장치
    48.
    发明授权
    일체형 무균 캡슐 제조장치 有权
    用于制备无毛囊的集成装置

    公开(公告)号:KR100902781B1

    公开(公告)日:2009-06-12

    申请号:KR1020070100323

    申请日:2007-10-05

    CPC classification number: A61J3/07 B01F13/08

    Abstract: 본 발명은 세포 고정화 캡슐을 무균적으로 제조할 수 있는 일체형 무균 캡슐 제조장치 및 이를 이용한 무균 캡슐 제조방법에 관한 것으로, 본 발명에 따른 제조장치를 이용하여 무균 캡슐을 제조하는 경우 멀티노즐을 통한 현탁액의 적하 및 경화, 캡슐 세척, 크기별 분류, 및 회수 공정을 밀폐된 일체형의 장치 내에서 수행할 수 있어 캡슐의 미생물 오염 가능성을 현저히 낮춤은 물론, 제조에 필요한 설비 및 공정단계를 획기적으로 줄일 수 있으므로, 동물세포 포집 캡슐을 이용하는 인공장기 관련 산업 분야 등에 유용하게 활용될 수 있다.

    겔 비드 충전형 생물반응기를 이용한 생인공 간 시스템
    49.
    发明公开
    겔 비드 충전형 생물반응기를 이용한 생인공 간 시스템 有权
    使用生物反应器包装在凝胶珠的生物肝系统

    公开(公告)号:KR1020080088817A

    公开(公告)日:2008-10-06

    申请号:KR1020070031590

    申请日:2007-03-30

    Abstract: A bio-artificial liver system is provided to prevent channeling and damage of gel beads by circulating plasma downward using height difference between a bioreactor and a plasma storing vessel and to allow removing toxicities in plasma and providing effective proteins more efficiently. A bio-artificial liver system comprises: a fixed layer bioreactor packed with gel beads(1) containing animal hepatocytes, which performs liver-like functions such as removing toxicities and providing effective proteins; a plasma separator(6) to separate plasma from blood, which is located in a place higher than that of the bioreactor and allows plasma circulation by height(pressure) difference; a plasma storing vessel(2); a flow speed controlling pump(5); inflow/outflow tubing(14,15) through which the plasma passes; and a linkage tube(4) connecting between the bioreactor and the plasma.

    Abstract translation: 提供生物人造肝系统以通过使生物反应器和血浆储存容器之间的高度差向下循环血浆以防止血浆中的毒性并且更有效地提供有效的蛋白质来防止凝胶珠的引流和损伤。 生物人造肝系统包括:装有含有动物肝细胞的凝胶珠(1)的固定层生物反应器,其执行肝样功能,例如去除毒性并提供有效的蛋白质; 血浆分离器(6),其将血液与血液分离,所述血液分离器位于比生物反应器高的位置,允许通过高度(压力)差异的血浆循环; 等离子体存储容器(2); 流量调节泵(5); 等离子体通过的流入/流出管道(14,15) 以及连接在生物反应器和等离子体之间的连接管(4)。

    다공성 콜라겐-히아루론산 복합 소재 및 이의 제조방법
    50.
    发明公开
    다공성 콜라겐-히아루론산 복합 소재 및 이의 제조방법 有权
    多孔胶原 - 羟丙酸复合材料及其制备方法

    公开(公告)号:KR1020070089490A

    公开(公告)日:2007-08-31

    申请号:KR1020060019594

    申请日:2006-02-28

    CPC classification number: A61L27/26 A61L27/20 A61L27/24 A61L27/40 A61L27/56

    Abstract: A porous collagen-hyaluronic acid composite material and a manufacturing method thereof are provided to minimize rejection in transplanting the composite material, to secure excellent mechanical property and tissue compatibility, and to make a manufacturing process simple. A porous collagen-hyaluronic acid composite material is produced by forming an aggregate by mixing collagen and hyaluronic acid at pH of 3.0~5.0 and then lyophilizing the aggregate. Atelo collagen or soluble collagen is used. The hyaluronic acid has the molecular weight of 800,000~200,000,000 Daltons. The collagen and hyaluronic acid are mixed at the volume rate of 1:1~2:1. GAG(Glucosaminoglycan) is added at the rate of 1:0.1~1:0.5 for the hyaluronic acid. The GAG is selected from a group comprising chondroitin, chondroitin sulphate, heparin, and heparin sulfate.

    Abstract translation: 提供一种多孔胶原 - 透明质酸复合材料及其制造方法,以最大限度地减少移植复合材料的排斥,确保优异的机械性能和组织相容性,并使制造工艺简单。 通过在3.0〜5.0的pH下混合胶原和透明质酸,然后将骨料冻干而形成骨料,从而制造多孔胶原透明质酸复合材料。 使用Atelo胶原蛋白或可溶性胶原蛋白。 透明质酸的分子量为800,000〜200,000,000道尔顿。 胶原蛋白和透明质酸以1:1〜2:1的体积比混合。 对于透明质酸,加入GAG(葡萄糖胺聚糖)的比例为1:0.1〜1:0.5。 GAG选自软骨素,硫酸软骨素,肝素和硫酸肝素组。

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