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13 条记录 (耗时 0.012 秒)

    Process for determining tissue product break-through
    1.
    发明授权
    Process for determining tissue product break-through 有权
    确定组织产品突破的方法

    公开(公告)号：US08127601B2

    公开(公告)日：2012-03-06

    申请号：US12481680

    申请日：2009-06-10

    申请人： Kevin Mitchell Wiwi ,  Gregg Thomas Weaver ,  Michael Scott Prodoehl ,  LaTisha Evette Salaam

    发明人： Kevin Mitchell Wiwi ,  Gregg Thomas Weaver ,  Michael Scott Prodoehl ,  LaTisha Evette Salaam

    IPC分类号： G01L5/04 ,  G01N1/00 ,  G01N17/00

    CPC分类号： G01N33/346 ,  Y10S530/836

    摘要： A method for testing the break-through strength of a tissue product is disclosed. The method entails the steps of: a) observing a first condition of the tissue product; b) disposing the tissue product between a lower platen and an upper platen; c) disposing at least a portion of the tissue product within an aperture disposed within the lower platen and an aperture disposed within the upper platen; d) providing a simulated mucous composition; e) directing the simulated mucous composition toward the tissue product disposed within the aperture disposed within the lower platen and the aperture disposed within the upper platen; f) after step d), observing a second condition of the tissue product; and, g) comparing the first and the second conditions of the tissue product.

    摘要翻译： 公开了一种用于测试纸巾产品的穿透强度的方法。 该方法包括以下步骤：a）观察组织产品的第一条件; b）将纸巾产品放置在下压板和上压板之间; c）将所述纸巾产品的至少一部分设置在设置在所述下压板内的孔内，以及设置在所述上​​压板内的孔; d）提供模拟的粘液组合物; e）将模拟的粘液组合物引导到设置在设置在下压板内的孔内的组织产品和设置在上压板内的孔; f）在步骤d）之后，观察组织产品的第二条件; 以及g）比较所述纸巾产品的第一和第二条件。

    PROCESS FOR DETERMINING TISSUE PRODUCT BREAK-THROUGH
    6.
    发明申请
    PROCESS FOR DETERMINING TISSUE PRODUCT BREAK-THROUGH 有权
    确定组织产品的方法

    公开(公告)号：US20100313649A1

    公开(公告)日：2010-12-16

    申请号：US12481680

    申请日：2009-06-10

    申请人： Kevin Mitchell Wiwi ,  Gregg Thomas Weaver ,  Michael Scott Prodoehl ,  LaTisha Evette Salaam

    发明人： Kevin Mitchell Wiwi ,  Gregg Thomas Weaver ,  Michael Scott Prodoehl ,  LaTisha Evette Salaam

    IPC分类号： G01N33/34

    CPC分类号： G01N33/346 ,  Y10S530/836

    摘要： A method for testing the break-through strength of a tissue product is disclosed. The method entails the steps of: a) observing a first condition of the tissue product; b) disposing the tissue product between a lower platen and an upper platen; c) disposing at least a portion of the tissue product within an aperture disposed within the lower platen and an aperture disposed within the upper platen; d) providing a simulated mucous composition; e) directing the simulated mucous composition toward the tissue product disposed within the aperture disposed within the lower platen and the aperture disposed within the upper platen; f) after step d), observing a second condition of the tissue product; and, g) comparing the first and the second conditions of the tissue product.

    摘要翻译： 公开了一种用于测试纸巾产品的穿透强度的方法。 该方法包括以下步骤：a）观察组织产品的第一条件; b）将纸巾产品放置在下压板和上压板之间; c）将所述纸巾产品的至少一部分设置在设置在所述下压板内的孔内，以及设置在所述上​​压板内的孔; d）提供模拟的粘液组合物; e）将模拟的粘液组合物引导到设置在设置在下压板内的孔内的组织产品和设置在上压板内的孔; f）在步骤d）之后，观察组织产品的第二条件; 以及g）比较所述纸巾产品的第一和第二条件。

    Method of purifying intrinsic factor
    8.
    发明授权
    Method of purifying intrinsic factor 失效
    净化内在因素的方法

    公开(公告)号：US3591678A

    公开(公告)日：1971-07-06

    申请号：US3591678D

    申请日：1969-09-05

    申请人： AMERICAN CYANAMID CO

    发明人： ELLENBOGEN LEON ,  HIGHLEY DEREK ROWLAND

    IPC分类号： A61K35/38 ,  A61K27/00

    CPC分类号： A61K35/38 ,  Y10S530/836 ,  Y10S530/843 ,  Y10S530/844

    摘要： A PROCESS FOR PURIFYING INTRINSIC FACTOR BY A BATCH CHROMATOGRAPHY PROCESS WHICH UTILIZES AN ION EXCHANGE RESIN; AND THE RESULTANT HIGH PURITY INTRINSIC FACTOR. TYPICALLY, IMPURE INTRINSIC FACTOR IS DISSOLVED IN A BUFFER SOLUTION HAVING RELATIVELY LOW PH AND IONIC STRENGTH, AND THE RESULTANT SOLUTION IS CONTACTED WITH A CELLULOSIC EXCHANGE RESIN. THE RESIN IS SEPARATED FROM THE SOLUTION AND THE PURIFIED INTRINSIC FACTOR IS ELUTED THEREFROM WITH A BUFFER SOLUTION HAVING A HIGHER PH AND IONIC STRENGTH THAN THE BUFFER SOLUTION IN WHICH THE IMPURE INTRINSIC FACTOR WAS DISSOLVED. THE PRODUCT IS RECOVERED FROM THE ELUATE BY EVAPORATING THE LIQUID SOLVENT. THE RESIDUE, WHICH IS THE PURIFIED PRODUCT, HAS A POTENCY OF AT LEAST 1 N.F. UNIT IN AMOUNTS AS LOW AS 0.5 MG.