Bioartificial devices for treatment of neurologic diseases
Bioartificial devices for treatment of neurologic diseases
批准号:
10838016
负责人:
IWATA Hiroo
金额:
$2.11万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (C)
财政年份:
1998
资助国家:
日本
项目状态:
已结题
起止时间:
1998 至 2000
中文摘要
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英文摘要
It has been reported that Parkinson's disease can be treated by transplantation of dopamine releasing cells and sever pain of end stage cancer patients can be alleviated by transplanting morphine releasing cells. Immunological reactions are most likely to be the reason for failure when transplanting allogeneic and xenogeneic cells. To overcome this problem, cells are transplanted after they are enclosed into a semipermeable polymer membrane, which must be permeable to small molecules such as oxygen, nutrients and bioactive substances, but impermeable to lymphocytes and immunoglobulins and complement proteins. In addition, it is difficult to find space for a large volume of transplant in central nerve system. Therefore, cen trifugal microencapsulation of cell aggregates was examined to solve these problems. Spherical cell aggregates were suspended into the alginate solution. 0.4 ml of the suspension was over-layed on the top of three layers composed of a 2.5 ml layer of 7 wt% dextran, a 0.5 ml layer of BaCl2 solution and a 0.5 ml layer Of 13 wt% dextran from the top in a 12 ml glass test-tube of 14 mm inner diameter. The test-tube was centrifuged at 170 x g for 10 min to spin the aggregates to the bottom of the tube. This procedure can effectively enclose cell aggregates in microcapsules with a very thin wall without contamination of empty microcapsules.The test-tube method can't be applied to microencapsulation of a large number of cell aggregates. A special centrifuge was developed. It can easily be operate and effectively microencapsulate a large number of cell aggregates, but there is a problem to solve in collecting microencapsulated aggregates from the centrifuge.
期刊论文(8)
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N.Hisano: "Entrapment of islets into Reversible Disulfide Hydrogels"J.Biomed.Mater.Res.. 40. 115-123 (1998)
N.Hisano:“将胰岛捕获到可逆二硫化物水凝胶中”J.Biomed.Mater.Res.. 40. 115-123 (1998)
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H.Iwata: "Encapsulation of spheroids into agarose based microbeads"Academic Press (in press).
H.Iwata:“将球体封装到基于琼脂糖的微珠中”学术出版社(正在出版)。
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岩田博夫: "蛋白質核酸酵素9月号増刊"再生医学と生命科学""共立出版. 368 (2000)
岩田宽夫:“蛋白质核酸酶九月号特刊‘再生医学和生命科学’”Kyoritsu Shuppan 368(2000)。
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I.Hirata: "Study of complement activation on well-defined surfaces using surface plasmon resonance"Colloids and Surfaces B : Biointerfaces. 18. 285-292 (2000)
I.Hirata:“使用表面等离子体共振研究明确表面上的补体激活”胶体和表面 B:生物界面。
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Y.G.Park: "Microencapsulation of islets and Model Beads with a Thin Alginate-Ba2+ Gel Layer Using Centrifugation"Polym.Adv.Technol.. 9. 734-739 (1998)
Y.G.Park:“使用离心法用薄藻酸盐-Ba2 凝胶层对胰岛和模型珠进行微囊化”Polym.Adv.Technol.. 9. 734-739 (1998)
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