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1. 发明申请

WO2007046757A1 EXTRACORPOREAL BLOOD CLEANING 审中-公开
标题翻译：超声波清洗
公开(公告)号：WO2007046757A1
公开(公告)日：2007-04-26
申请号：PCT/SE2006/050349
申请日：2006-09-25
申请人： GAMBRO LUNDIA AB , STERNBY, Jan , WIESLANDER, Anders , KJELLSTRAND, Per , LINDÉN, Torbjörn
发明人： STERNBY, Jan , WIESLANDER, Anders , KJELLSTRAND, Per , LINDÉN, Torbjörn
IPC分类号： A61M1/34 , A61M1/16 , A61M1/36
CPC分类号： A61M1/3472 , A61M1/3479 , A61M1/3482 , A61M1/3486 , A61M1/3686 , A61M1/3687 , A61M1/369 , A61M2205/055 , A61M2205/058
摘要： An apparatus (100) for extracorporeal blood cleaning includes a separation unit (110), at least two processing branches (120; 130) and a mixing unit (140). The separation unit (110) receives 5 incoming blood (B A ) and divides off a first fraction (f C ) from this blood. The first fraction (f C ) contains predominantly blood cells. The separation unit (110) also divides off at least one second fraction (f P ) , which contains predominantly blood plasma. A first processing branch (120) processes the first fraction (f C ) accor- 10 d i n g to a first cleaning process, in which cell-bound substances are removed from the blood cells. As a result, a first cleaned fraction (f C c ) containing washed blood cells is produced. A second processing branch (130) processes the second fraction (f P ) according to a second cleaning process in which toxins bound on proteins within the plasma and/or toxins dissolved in 15 the plasma are removed, and a second cleaned fraction (f P c ) is produced. The second cleaning process is different from the first cleaning process. Thereby each process can be tailored for the requirements of the respective fraction (f C , f P ) . The mixing unit 20 (140) receives the first and second cleaned fractions (f C c , f P c ) , combines these fractions (f C c , f P c ) , and outputs cleaned whole blood (B V ).
摘要翻译：用于体外血液清洁的装置（100）包括分离单元（110），至少两个处理分支（120; 130）和混合单元（140）。分离单元（110）接收5个进入的血液（B A），并从该血液中分离出第一部分（f _{C）。第一级分（f C C）主要含有血细胞。分离单元（110）还分离出主要含有血浆的至少一个第二级分（f SUB P）。第一处理分支（120）将第一分数（f C C C）进行处理，其中细胞结合物质从血细胞中移除。结果，第一清洗部分（f C）}

2. 发明申请

WO2005082378A1 A MEDICAL SOLUTION, A METHOD FOR PRODUCING SAID MEDICAL SOLUTION AND USE THEREOF 审中-公开
标题翻译：医疗解决方案，生产医疗解决方案的方法及其用途
公开(公告)号：WO2005082378A1
公开(公告)日：2005-09-09
申请号：PCT/SE2005/000238
申请日：2005-02-22
申请人： GAMBRO LUNDIA AB , CARLSSON, Ola , ERIXON, Martin , FORSBÄCK, Gunita , KJELLSTRAND, Per , LINDÉN, Torbjörn , WIESLANDER, Anders
发明人： CARLSSON, Ola , ERIXON, Martin , FORSBÄCK, Gunita , KJELLSTRAND, Per , LINDÉN, Torbjörn , WIESLANDER, Anders
IPC分类号： A61K31/7004
CPC分类号： A61K31/7004
摘要： The present invention relates to a medical solution comprising a first single solution containing glucose and/or glucose-like compound. According to the present invention said first single solution has a pH in the range of 1.8-2.6. The present invention further relates to a method for producing said medical solution as well as use thereof.
摘要翻译：本发明涉及包含含有葡萄糖和/或葡萄糖样化合物的第一单一溶液的医用溶液。根据本发明，所述第一单溶液的pH在1.8-2.6的范围内。本发明还涉及一种生产所述医用溶液的方法及其用途。

3. 发明授权

EP1951337B1 EXTRACORPOREAL BLOOD CLEANING 有权
公开(公告)号：EP1951337B1
公开(公告)日：2018-08-01
申请号：EP06799812.0
申请日：2006-09-25
申请人： Gambro Lundia AB
发明人： STERNBY, Jan , WIESLANDER, Anders , KJELLSTRAND, Per , LINDÉN, Torbjörn
IPC分类号： A61M1/34 , A61M1/16 , A61M1/36
CPC分类号： A61M1/3472 , A61M1/3479 , A61M1/3482 , A61M1/3486 , A61M1/3686 , A61M1/3687 , A61M1/369 , A61M2205/055 , A61M2205/058
摘要： An apparatus (100) for extracorporeal blood cleaning includes a separation unit (110), at least two processing branches (120; 130) and a mixing unit (140). The separation unit (110) receives 5 incoming blood (B A) and divides off a first fraction (fC) from this blood. The first fraction (fC) contains predominantly blood cells. The separation unit (110) also divides off at least one second fraction (fP), which contains predominantly blood plasma. A first processing branch (120) processes the first fraction (fC) according to a first cleaning process, in which cell-bound substances are removed from the blood cells. As a result, a first cleaned fraction (fC c) containing washed blood cells is produced. A second processing branch (130) processes the second fraction (fP) according to a second cleaning process in which toxins bound on proteins within the plasma and/or toxins dissolved in 15 the plasma are removed, and a second cleaned fraction (fP c) is produced. The second cleaning process is different from the first cleaning process. Thereby each process can be tailored for the requirements of the respective fraction (fC, fP). The mixing unit 20 (140) receives the first and second cleaned fractions (fC c, fP c, combines these fractions (fC c, fP c, and outputs cleaned whole blood (BV).

4. 发明公开

EP1951337A1 EXTRACORPOREAL BLOOD CLEANING 有权
标题翻译：体外血液净化
公开(公告)号：EP1951337A1
公开(公告)日：2008-08-06
申请号：EP06799812.0
申请日：2006-09-25
申请人： Gambro Lundia AB
发明人： STERNBY, Jan , WIESLANDER, Anders , KJELLSTRAND, Per , LINDÉN, Torbjörn
IPC分类号： A61M1/34 , A61M1/16 , A61M1/36
CPC分类号： A61M1/3472 , A61M1/3479 , A61M1/3482 , A61M1/3486 , A61M1/3686 , A61M1/3687 , A61M1/369 , A61M2205/055 , A61M2205/058
摘要： An apparatus (100) for extracorporeal blood cleaning includes a separation unit (110), at least two processing branches (120; 130) and a mixing unit (140). The separation unit (110) receives 5 incoming blood (B A ) and divides off a first fraction (f C ) from this blood. The first fraction (f C ) contains predominantly blood cells. The separation unit (110) also divides off at least one second fraction (f P ) , which contains predominantly blood plasma. A first processing branch (120) processes the first fraction (f C ) accor- 10 d i n g to a first cleaning process, in which cell-bound substances are removed from the blood cells. As a result, a first cleaned fraction (f C c ) containing washed blood cells is produced. A second processing branch (130) processes the second fraction (f P ) according to a second cleaning process in which toxins bound on proteins within the plasma and/or toxins dissolved in 15 the plasma are removed, and a second cleaned fraction (f P c ) is produced. The second cleaning process is different from the first cleaning process. Thereby each process can be tailored for the requirements of the respective fraction (f C , f P ) . The mixing unit 20 (140) receives the first and second cleaned fractions (f C c , f P c ) , combines these fractions (f C c , f P c ) , and outputs cleaned whole blood (B V ).

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