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首页> 外文期刊>Journal of Applied Polymer Science >MORPHOLOGY OF MICROPOROUS NEOSEPTA ION-EXCHANGE MEMBRANES AND ITS EFFECT ON SEPARATION OF BIOLOGICAL MIXTURES
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MORPHOLOGY OF MICROPOROUS NEOSEPTA ION-EXCHANGE MEMBRANES AND ITS EFFECT ON SEPARATION OF BIOLOGICAL MIXTURES

机译:微孔Neosepta离子交换膜的形态及其对分离生物混合物的影响

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Specially prepared microporous Neosepta ion-exchange membranes were investigated to establish a correlation between their structural characteristics (pore-size distribution, porosity) and permeability to components of immunoglobulin (Ig) fractions of mouse ascitic fluids. The solutions to be separated contained IgG(1) with specificity to horseradish peroxidase or to the heavy chain of human IgM, some other proteins, and a large amount of ammonium sulfate (0.22-0.35 M). Analysis of the membrane morphology carried out by scanning electron microscopy and mercury porosimetry showed that the membranes possess a polymodal pore-size distribution. There are large open pores (400-600 and 200-300 nm in diameter) on the membrane surfaces, but the void volume of the membranes is a system of connected pores of smaller diameters (from 60-100 to 7-10 nm). The main part of the pores in the membranes displaying the best separation ability was 8-17 nm in diameter. It was found that highly porous charged membranes (relative porosity 58-60%) with low ion-exchange capacity (0.02-0.1 meq/g) made it possible to achieve the desired desalination degree of protein mixture (80-83%) within 5-7 h instead of 5 days needed in the traditional dialysis. Moreover, the amount of separated accompanying proteins reached 25-30% depending on membrane porosity and the quality of specific IgG(1) was considerably improved. (C) 1995 John Wiley & Sons, Inc. [References: 11]
机译:研究了特殊制备的微孔Neosepta离子交换膜,以建立其结构特征(孔径分布,孔隙率)与小鼠腹水免疫球蛋白(Ig)组分的通透性之间的相关性。待分离的溶液包含对辣根过氧化物酶或人IgM重链具有特异性的IgG(1),一些其他蛋白质和大量硫酸铵(0.22-0.35 M)。通过扫描电子显微镜和水银孔隙率法进行的膜形态分析表明,该膜具有多峰孔径分布。膜表面上有大的开孔(直径为400-600和200-300 nm),但膜的空隙体积是较小直径(60-100至7-10 nm)的连通孔的系统。膜中显示出最佳分离能力的孔的主要部分为直径8-17 nm。已经发现,具有低离子交换容量(0.02-0.1meq / g)的高度多孔的带电膜(相对孔隙度为58-60%)使得可以在5之内达到所需的蛋白质混合物的脱盐度(80-83%)。 -7小时,而不是传统透析所需的5天。此外,分离的伴随蛋白的量达到25-30%,具体取决于膜的孔隙率,并且特异性IgG(1)的质量得到了显着提高。 (C)1995 John Wiley&Sons,Inc. [参考:11]

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