Lactam terpolymer membranes, and their use in a process for dialyzing blood

    公开(公告)号:EP0006030A3

    公开(公告)日:1980-01-02

    申请号:EP79301052

    申请日:1979-06-04

    申请人: MONSANTO COMPANY

    IPC分类号: B01D13/04 A61M01/03 C08G69/44

    摘要: Permselective membranes are provided consisting of lactam-polyol-polyacyl lactam block terpolymers having from 35 to 75% by weight polylactam blocks and 25 to 65% by weight polyalkylene ether blocks. The membranes are particularly suitable as blood dialysis membranes having improved permeability to solutes in the medium range of molecular weights while maintaining acceptable ultrafiltration rates and permeability to low molecular weight solutes. The membranes are provided both as planar films and hollow fibers, have high hydrolytic stability under hot wet sterilization conditions and good mechanical properties under hemodialysis conditions.

    Dialysis composition and method for removing uremic substances from blood
    44.
    发明公开
    Dialysis composition and method for removing uremic substances from blood 失效
    用于从血液中去除尿素的DIALYSIS组合物和方法

    公开(公告)号:EP0003914A3

    公开(公告)日:1979-09-19

    申请号:EP79300293

    申请日:1979-02-26

    IPC分类号: A61M01/03 B01D13/00 B01D15/00

    摘要: A dialysis composition for adsorption of uremic substances in an artificial kidney is described, comprising a cation exchanger suspended in a suspending agent, A more particular example of such a composition comprises a surface adsorptive agent capable of adsorption of uremic substances; an enzyme to serve as a catalyst for urea degradation; a suspending agent; and a cation exchanger capable of being suspended in said suspending agent. A method for removing uremic substances from blood during hemodialysis with the above dialysis compositions is also described.

    Immune complex removal and tumor specific antibody generation by immobilized protein a perfusion and postperfusion drug infusion
    45.
    发明公开
    Immune complex removal and tumor specific antibody generation by immobilized protein a perfusion and postperfusion drug infusion 失效
    免疫复合物去除和肿瘤特异性抗体产生由固定化蛋白质灌注和放射性药物输注

    公开(公告)号:EP0079221A3

    公开(公告)日:1986-01-22

    申请号:EP82305913

    申请日:1982-11-05

    CPC分类号: A61M1/3472 A61M1/3486

    摘要: Significantly increased removal of immunal complexes and tumor specific antibody generation are achieved by extracorporeal plasma perfusion over a therapeutic immobilized protein A (staphylococcal). SPA. The perfused plasma is returned to the host or can be taken off one person and used to treat another and stored in perfused plasma banks. Immobilized protein A quantities, volumes of plasma perfused and the rate of administration based on clinical and toxicity evaluations are set forth. A non-toxic drug infusion, such as cytosine arabinoside, during the immediate postperfusion period obtains an observed tumoricidal response far exceeding those due to the extracorporeal plasma perfusion or drug infusion alone representing an in vivo synergism between tumor specific antibody and the drug. Also disclosed are the therapeutic protein A cartridge, its loading and delivery system, a miniaturized immunoabsorbent apparatus enabling the processing of serum samples for testing small quanitities of plasma, and a radioimmuno-assay for detecting and measuring tumor specific antibodies in the serum samples for profiling and screening of patients for treatment and assessment. The United States government has rights in these inventions pursuant to U.S. Public Health Service Grants or Awards 5K04A100302 and 5R01GM23517.

    摘要翻译: 通过在治疗性固定化蛋白A(葡萄球菌),SPA上的体外血浆灌注实现显着增加的免疫复合物的去除和肿瘤特异性抗体产生。 将灌注的血浆返回主体,或者将其从一个人中取出并用于治疗另一个并存储在灌注的血浆库中。 固定化蛋白质A量,血浆灌注体积和基于临床和毒性评估的给药速率。 在直接灌注后期间,无毒药物输注如阿糖胞苷获得了远远超过体外等离子体灌注或药物输注的观察到的杀肿瘤反应,代表肿瘤特异性抗体与药物之间的体内协同作用。 还公开了治疗性蛋白A盒,其装载和递送系统,能够处理血清样品以测试血浆的小量的微型免疫吸收装置,以及用于检测和测量血清样品中的肿瘤特异性抗体的放射免疫分析 并筛查患者的治疗和评估。 美国政府根据美国公共卫生服务补助金或奖励5K04AI00302和5R01GM23517对这些发明有权利。

    Single needle blood fractionation system having adjustable recirculation through filter
    46.
    发明公开
    Single needle blood fractionation system having adjustable recirculation through filter 失效
    具有通过过滤器进行可调节再生的单针血液分离系统

    公开(公告)号:EP0128683A3

    公开(公告)日:1986-01-15

    申请号:EP84303509

    申请日:1984-05-24

    IPC分类号: A61M01/03

    摘要: A single needle batch-type blood fractionation system for separating plasma from whole blood includes a disposable flow system having a single-lumen phlebotomy needle and associated donor conduit, a flow-through plasma separation filter, and an in-process fluid reservoir. During an initial draw cycle whole blood is pumped through the filter to the in-process reservoir by a peristaltic-type inlet pump operating at a predetermined draw rate. When a predetermined volume of filtered plasma-deficient blood has been collected in the reservoir, as sensed by the weight of the reservoir the system reverts to a return cycle wherein a portion of the plasma deficient blood in the reservoir is pumped back to the donor conduit by a peristaltic-type return pump operating at a predetermined return rate higher than the draw rate of the inlet pump. Depending on the relative operating speeds of the inlet and return pumps, an operator-controlfable portion of the plasma-deficient blood from the in-process reservoir is returned to the donor through the phlebotomy needle, and the remaining portion is recirculated through the filter. The partial recirculation of plasma-deficient blood through the filter during the return mode reduces the processing time of the system, provides for improved accommodation of whole blood of unusually high or low hematocrit, and enables the use of a smaller and less expensive filter.

    An arrangement for the removal of one or more fractions out of whole blood, plasma or other similar body fluids
    47.
    发明公开
    An arrangement for the removal of one or more fractions out of whole blood, plasma or other similar body fluids 失效
    从全血,等离子体或其他类似身体流体中去除一个或多个部分的安排

    公开(公告)号:EP0111696A3

    公开(公告)日:1984-07-25

    申请号:EP83110796

    申请日:1983-10-28

    申请人: Gambro Lundia AB

    IPC分类号: A61M01/03

    摘要: An arrangement forthe removal of one or more fractions out of whole blood, plasma or other similar body fluids with the help of adsorption on an adsorption column (23,24) comprising means for the feed of the said fluid of the column and means for the removal of the same. In accordance with the invention the said means for the removal of the fluid comprise at least one analysing device (31,32) for the coarse analysis of the fluid and a valve device (33,34) which is adapted so as to conduct the fluid flow from the column (23,24) as a function of the analysis carried out either to a second analysing device (38,46,47) for the fine analysis of the fluid or back to the source (1) of the same, e.g. a patient, or to a drain (36). The arrangement can be eluated with the help of a regenerating liquid which is adapted so as to tower the pH of the column gradually during a certain period. Preferably means are adapted so that at the start of the period a rapid loweing is achieved so as to accelerate the starting of the regeneration, whereupon the lowering is adapted so as to occur slowly during the actual regeneration, and appropriately to be terminated rapidly during the finish of the said period.

    Filtration membrane and process for producing the membrane
    50.
    发明公开
    Filtration membrane and process for producing the membrane 失效
    过滤膜和生产膜的方法

    公开(公告)号:EP0098392A3

    公开(公告)日:1984-03-07

    申请号:EP83105534

    申请日:1983-06-06

    IPC分类号: B01D13/04 A61M01/03

    摘要: Filtration membrane, especially adapted for use in hemofiltration as well as filtration of infusion solutions. The membrane, preferably in the form of a hollow fiber, is made of a polymer which is soluble in a polar, non-protonic organic solvent. The most preferred polymer for the membrane material is polyamide. Characterizing for the membrane is high ultrafiltration rates (permeabilities to water) of up to 500 x 10- 4 ml/sec. x cm2 x atm., and impermeability to albumin (M w 68,000). The membrane is prepared by extruding a polymer solution with a center liquid under conditions such that the volume of polymer solution to volume of center liquid ratio is within the range of from 2 : 1 to 4 : 1. Simultaneously, the inner diameter to wall thickness ratio of the hollow fiber is preferably correlated to the polymer concentration and is set to 150:75 to 280:75 at a polymer concentration of 5-20%. The most preferred such correlation is 220 : 75 at a polymer concentration of 11 %.