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首页> 外文期刊>The international journal of artificial organs >In vitro and in vivo evaluation of a new polysulfone membrane for hemodialysis. Reference methodology and clinical results. (Part 1: in vitro study).
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In vitro and in vivo evaluation of a new polysulfone membrane for hemodialysis. Reference methodology and clinical results. (Part 1: in vitro study).

机译:用于血液透析的新型聚砜膜的体外和体内评估。参考方法和临床结果。 (第1部分:体外研究)。

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摘要

Different high flux membranes have been recently developed. The present study is aimed at describing the technical features and the clinical performances of a new high flux polysulfone membrane (T-sulfone, Toray, Japan). The study has been carried out on two different dialyzers (surface area = 1.3 and 1.8 m2). The filters have been tested in vitro under definite experimental conditions. The hydraulic flow resistance, the pressure drop in the blood compartment and the hydraulic permeability have been determined in a wide range of in vitro experimental conditions. The in vitro sieving coefficients for various solutes have also been determined utilizing human blood. Hydraulic permeability was found in the range of 28.4 ml/h/mm Hg/m2 and sieving coefficients were between 0.96 and 1.0 for all low molecular weight solutes. The sieving coefficient for inulin was 0.95. The pressure drop in the filter at 300 ml/min of blood flow was 95 mm Hg for the 1.3 m2 and 57 mm Hg for the 1.8 m2. The filters are then designed to operate in the presence of high blood flows without excessive resistance in the blood compartment. The blood compartment analyzed by means of a special radiological sequence obtained with a helical scanner after dye injection confirmed the homogeneous distribution of the blood flow in several cross sections of the bundle. Adequate distribution of dialysate was confirmed with a similar method applied to the dialysate compartment. The new imaging techniques utilized were greatly helpful to determine adequacy of filter design and flows distribution.
机译:最近已经开发了不同的高通量膜。本研究旨在描述新型高通量聚砜膜(T-砜,Toray,日本)的技术特征和临床性能。该研究是在两种不同的透析仪上进行的(表面积分别为1.3和1.8 m2)。过滤器已经在确定的实验条件下进行了体外测试。在广泛的体外实验条件下已经确定了水力流动阻力,血液室中的压降和水力渗透性。还已经利用人血确定了各种溶质的体外筛选系数。发现所有低分子量溶质的水力渗透性在28.4 ml / h / mm Hg / m2的范围内,筛分系数在0.96至1.0之间。菊粉的筛分系数为0.95。血液流量为300 ml / min时,过滤器中的压降对于1.3平方米为95毫米汞柱,对于1.8平方米为57毫米汞柱。然后将过滤器设计为在高血流量的情况下运行,而不会在血室中产生过多阻力。注射染料后,通过使用螺旋扫描仪获得的特殊放射学序列分析的血液室,证实了血流在束的多个横截面中的均匀分布。透析液的充分分配是通过将类似的方法应用于透析液室来确认的。所采用的新成像技术对确定过滤器设计和流量分配的充分性非常有帮助。

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