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    Submerged type hollow fiber membrane module and method for manufacturing the same
    1.
    发明授权
    Submerged type hollow fiber membrane module and method for manufacturing the same 有权
    淹没式中空纤维膜组件及其制造方法

    公开(公告)号：US09409130B2

    公开(公告)日：2016-08-09

    申请号：US12581495

    申请日：2009-10-19

    申请人： Moo-Seok Lee ,  Sung-Hak Choi

    发明人： Moo-Seok Lee ,  Sung-Hak Choi

    IPC分类号： B01D63/02

    CPC分类号： B01D63/022 ,  B01D63/023 ,  B01D63/024 ,  B01D2315/06 ,  Y10T156/10

    摘要： A submerged-type hollow fiber membrane module and a method for manufacturing the same are disclosed, which is capable of realizing a great sealing strength between a module case and a bundle of hollow fiber membranes without an additional centrifugal molding apparatus. The method includes forming a bundle of hollow fiber membranes held together and fixed by a first potting material, wherein one end of each of the hollow fiber membranes is open; putting the bundle of hollow fiber membranes in a module case and fixing the bundle of hollow fiber membranes in the module case by forming a second potting material on the first potting material.

    摘要翻译： 公开了一种浸没式中空纤维膜组件及其制造方法，其能够在没有附加的离心成型装置的情况下实现模块壳体与一束中空纤维膜之间的极大的密封强度。 所述方法包括形成一束中空纤维膜，所述一束中空纤维膜保持在一起并由第一灌封材料固定，其中每个中空纤维膜的一端是开放的; 将一束中空纤维膜放入模块外壳中，并在第一灌封材料上形成第二灌封材料将中空纤维膜束固定在模块外壳中。

    Oxazolidinone derivatives
    2.
    发明授权
    Oxazolidinone derivatives 有权
    恶唑烷酮衍生物

    公开(公告)号：US07816379B2

    公开(公告)日：2010-10-19

    申请号：US10596412

    申请日：2004-12-17

    申请人： Jae Keol Rhee ,  Weon Bin Im ,  Chong Hwan Cho ,  Sung Hak Choi ,  Tae Ho Lee

    发明人： Jae Keol Rhee ,  Weon Bin Im ,  Chong Hwan Cho ,  Sung Hak Choi ,  Tae Ho Lee

    IPC分类号： A61K31/4439 ,  C07D413/14

    CPC分类号： A61K31/4439 ,  A61K31/675 ,  C07D263/32 ,  C07D413/14 ,  C07D417/10 ,  C07D417/14 ,  C07F9/653 ,  C07F9/65583

    摘要： The present invention relates to novel derivatives of oxazolidinone, a method thereof and pharmaceutical compositions comprising the derivatives for use in an antibiotic. The oxazolidinone derivatives of the present invention show inhibitory activity against a broad spectrum of bacteria and lower toxicity. The prodrugs, prepared by reacting the compound having hydroxyl group with amino acid or phosphate, have an excellent efficiency on solubility thereof against water. Further, the derivatives of the present invention may exert potent antibacterial activity versus various human and animal pathogens, including Gram-positive bacteria such as Staphylococi, Enterococci and Streptococi, anaerobic microorganisms such as Bacteroides and Clostridia, and acid-resistant microorganisms such as Mycobacterium tuberculosis and Mycobacterium avium. Accordingly, the compositions comprising the oxazolidinone are used in an antibiotic.

    摘要翻译： 本发明涉及恶唑烷酮的新衍生物，其方法和药物组合物，其包含用于抗生素的衍生物。 本发明的恶唑烷酮衍生物显示出对广谱细菌的抑制活性和较低的毒性。 通过使具有羟基的化合物与氨基酸或磷酸酯反应制备的前药在对水的溶解性方面具有优异的效果。 此外，本发明的衍生物可以相对于各种人和动物病原体，包括葡萄球菌，肠球菌和链球菌等革兰阳性菌，拟杆菌和梭菌等厌氧菌，耐结核菌如结核分枝杆菌 和鸟分枝杆菌。 因此，包含恶唑烷酮的组合​​物用于抗生素中。

    Oxazolidinone derivatives
    4.
    发明授权
    Oxazolidinone derivatives 有权
    恶唑烷酮衍生物

    公开(公告)号：US08420676B2

    公开(公告)日：2013-04-16

    申请号：US12211655

    申请日：2008-09-16

    申请人： Jae Keol Rhee ,  Weon Bin Im ,  Chong Hwan Cho ,  Sung Hak Choi ,  Tae Ho Lee

    发明人： Jae Keol Rhee ,  Weon Bin Im ,  Chong Hwan Cho ,  Sung Hak Choi ,  Tae Ho Lee

    IPC分类号： A61K31/4439 ,  C07D413/14

    CPC分类号： A61K31/4439 ,  A61K31/675 ,  C07D263/32 ,  C07D413/14 ,  C07D417/10 ,  C07D417/14 ,  C07F9/653 ,  C07F9/65583

    摘要： The present invention relates to novel derivatives of oxazolidinone, a method thereof and pharmaceutical compositions comprising the derivatives for use in an antibiotic. The oxazolidinone derivatives of the present invention show inhibitory activity against a broad spectrum of bacteria and lower toxicity. The prodrugs, prepared by reacting the compound having hydroxyl group with amino acid or phosphate, have an excellent efficiency on solubility thereof against water. Further, the derivatives of the present invention may exert potent antibacterial activity versus various human and animal pathogens, including Gram-positive bacteria such as, Staphylococci, Enterococci and Streptococci anaerobic microorganisms such as Bacteroides and Clostridia, and acid-resistant microorganisms such as Mycobacterium tuberculosis and Mycobacterium avium. Accordingly, the compositions comprising the oxazolidinone are used in an antibiotic.

    摘要翻译： 本发明涉及恶唑烷酮的新衍生物，其方法和药物组合物，其包含用于抗生素的衍生物。 本发明的恶唑烷酮衍生物显示出对广谱细菌的抑制活性和较低的毒性。 通过使具有羟基的化合物与氨基酸或磷酸酯反应制备的前药在对水的溶解性方面具有优异的效果。 此外，本发明的衍生物相对于各种人和动物病原体，包括革兰氏阳性菌如葡萄球菌，肠球菌和链球菌厌氧微生物如拟杆菌和梭菌，以及耐酸微生物如结核分枝杆菌 和鸟分枝杆菌。 因此，包含恶唑烷酮的组合​​物用于抗生素中。

    Tubular braid and composite hollow fiber membrane using the same
    6.
    发明授权
    Tubular braid and composite hollow fiber membrane using the same 有权
    管状编织物和复合中空纤维膜使用相同

    公开(公告)号：US08201485B2

    公开(公告)日：2012-06-19

    申请号：US12518557

    申请日：2008-02-05

    申请人： Moo-Seok Lee ,  Joon-Khee Yoon ,  Sung-Hak Choi ,  Yong-Cheol Shin

    发明人： Moo-Seok Lee ,  Joon-Khee Yoon ,  Sung-Hak Choi ,  Yong-Cheol Shin

    IPC分类号： D04C1/06

    CPC分类号： B01D69/087 ,  B01D69/10 ,  B01D69/12 ,  B01D71/34 ,  B01D71/68 ,  B01D2325/40

    摘要： A tubular braid and a composite hollow fiber membrane using the same are disclosed. The tubular braid is made by braiding yarns, the yarn made by combining thin filament and thick filament, wherein the thin filament is comprised of a plurality of monofilament having a fineness of 0.01 to 0.4 denier, and the thick filament is comprised of at least one monofilament having a fineness of 3 to 50 denier. Also, the composite hollow fiber membrane using the tubular braid of the present invention can realize excellent water permeability, high mechanical strength, good filtration reliability, great peeling strength, low dope permeation, and high stiffness.

    摘要翻译： 公开了一种管状编织物和使用其的复合中空纤维膜。 管状编织物通过编织纱线制成，纱线通过组合细长丝和粗细丝而制成，其中细丝由多根细丝为0.01至0.4旦尼尔的单丝组成，并且粗丝由至少一个 单丝的细度为3〜50旦。 此外，使用本发明的管状编织物的复合中空纤维膜可以实现优异的透水性，高机械强度，良好的过滤可靠性，高剥离强度，低涂料透过性和高刚度。

    SUBMERGED TYPE HOLLOW FIBER MEMBRANE MODULE AND METHOD FOR MANUFACTURING THE SAME
    9.
    发明申请
    SUBMERGED TYPE HOLLOW FIBER MEMBRANE MODULE AND METHOD FOR MANUFACTURING THE SAME 有权
    中空型中空纤维膜模块及其制造方法

    公开(公告)号：US20100038301A1

    公开(公告)日：2010-02-18

    申请号：US12581495

    申请日：2009-10-19

    申请人： Moo-Seok LEE ,  Sung-Hak Choi

    发明人： Moo-Seok LEE ,  Sung-Hak Choi

    IPC分类号： B01D63/02 ,  B29C65/00

    CPC分类号： B01D63/022 ,  B01D63/023 ,  B01D63/024 ,  B01D2315/06 ,  Y10T156/10

    摘要： A submerged-type hollow fiber membrane module and a method for manufacturing the same are disclosed, which is capable of realizing a great sealing strength between a module case and a bundle of hollow fiber membranes without an additional centrifugal molding apparatus. The method includes forming a bundle of hollow fiber membranes held together and fixed by a first potting material, wherein one end of each of the hollow fiber membranes is open; putting the bundle of hollow fiber membranes in a module case and fixing the bundle of hollow fiber membranes in the module case by forming a second potting material on the first potting material.

    摘要翻译： 公开了一种浸没式中空纤维膜组件及其制造方法，其能够在没有附加的离心成型装置的情况下实现模块壳体与一束中空纤维膜之间的极大的密封强度。 所述方法包括形成一束中空纤维膜，所述一束中空纤维膜保持在一起并由第一灌封材料固定，其中每个中空纤维膜的一端是开放的; 将一束中空纤维膜放入模块外壳中，并在第一灌封材料上形成第二灌封材料将中空纤维膜束固定在模块外壳中。

    NOVEL OXAZOLIDINONE DERIVATIVES
    10.
    发明申请
    NOVEL OXAZOLIDINONE DERIVATIVES 有权
    新型氧杂环丁酮衍生物

    公开(公告)号：US20090192197A1

    公开(公告)日：2009-07-30

    申请号：US12211655

    申请日：2008-09-16

    申请人： Jae Keol Rhee ,  Weon Bin Im ,  Chong Hwan Cho ,  Sung Hak Choi ,  Tae Ho Lee

    发明人： Jae Keol Rhee ,  Weon Bin Im ,  Chong Hwan Cho ,  Sung Hak Choi ,  Tae Ho Lee

    IPC分类号： A61K31/4439 ,  C07D413/14 ,  A61P3/04

    CPC分类号： A61K31/4439 ,  A61K31/675 ,  C07D263/32 ,  C07D413/14 ,  C07D417/10 ,  C07D417/14 ,  C07F9/653 ,  C07F9/65583

    摘要： The present invention relates to novel derivatives of oxazolidinone, a method thereof and pharmaceutical compositions comprising the derivatives for use in an antibiotic. The oxazolidinone derivatives of the present invention show inhibitory activity against a broad spectrum of bacteria and lower toxicity. The prodrugs, prepared by reacting the compound having hydroxyl group with amino acid or phosphate, have an excellent efficiency on solubility thereof against water. Further, the derivatives of the present invention may exert potent antibacterial activity versus various human and animal pathogens, including Gram-positive bacteria such as Staphylococi, Enterococci and Streptococi, anaerobic microorganisms such as Bacteroides and Clostridia, and acid-resistant microorganisms such as Mycobacterium tuberculosis and Mycobacterium avium. Accordingly, the compositions comprising the oxazolidinone are used in an antibiotic.

    摘要翻译： 本发明涉及恶唑烷酮的新衍生物，其方法和药物组合物，其包含用于抗生素的衍生物。 本发明的恶唑烷酮衍生物显示出对广谱细菌的抑制活性和较低的毒性。 通过使具有羟基的化合物与氨基酸或磷酸酯反应制备的前药在对水的溶解性方面具有优异的效果。 此外，本发明的衍生物可以相对于各种人和动物病原体，包括葡萄球菌，肠球菌和链球菌等革兰阳性菌，拟杆菌和梭菌等厌氧菌，耐结核菌如结核分枝杆菌 和鸟分枝杆菌。 因此，包含恶唑烷酮的组合​​物用于抗生素中。