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首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >FLUIDIZATION CHARACTERISTICS OF AND PROTEIN ADSORPTION ON FLUORIDE-MODIFIED POROUS ZIRCONIUM OXIDE PARTICLES
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FLUIDIZATION CHARACTERISTICS OF AND PROTEIN ADSORPTION ON FLUORIDE-MODIFIED POROUS ZIRCONIUM OXIDE PARTICLES

机译:氟化物修饰的氧化锆颗粒的流态化和蛋白质吸附

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摘要

Porous zirconia particles cf specific gravity similar to 3.2 g/ml, mean particle sizes of similar to 50 mu m, and terminal settling velocity of similar to 2.8 mm/s in water, were synthesized using an oil emulsion method from 1000 Angstrom colloids and were evaluated for their potential use in expanded bed protein adsorption. Expanded beds of particles were stable even for small volume, shallow beds (settled bed: 10 ml, height to diameter ratio <1.0) and even for fluidization velocities common to much larger particles (210 cm/h for a three-fold bed expansion). When the surface of these particles was modified by fluoride adsorption, the total bed capacity for bovine serum albumin (BSA) adsorption was 42+/-2 mg BSA/ml of settled bed volume at linear velocities of 109-210 cm/h. Residence time distribution studies of several solutes under non-binding conditions were performed to assess the degree of liquid mixing and channeling in the expanded bed as a function of fluidization velocity. Liquid mixing and channeling were also studied, as a function of distributor design. With these very dense particles, the degree of channeling and mixing did not worsen viith the degree of expansion. Elution of adsorbed BSA while the bed was expanded (by a step increase in ionic strength) wits rapid resulting in a narrow peak at high fluidization velocities without resorting to settling of the bed. The dynamic binding capacity of BSA at 5% breakthrough (protein effluent concentration equal to 5% of the inlet concentration) was the same for a two-fold expanded bed as for a settled bed (22+/-2 mg BSA/ml of settled bed volume), though it decreased for higher bed expansions. BSA binding was reproducible following repeated cleaning of the adsorbent with 0.25 M sodium hydroxide. (C) 1997 Elsevier Science B.V
机译:使用油乳液法从1000埃胶体合成比重约3.2 g / ml,平均粒径约50μm,最终沉降速度约2.8 mm / s的多孔氧化锆颗粒。评估了它们在膨胀床蛋白吸附中的潜在用途。即使对于小体积,浅层床(沉降床:10 ml,高径比<1.0),甚至对于较大颗粒常见的流化速度(对于三倍床膨胀为210 cm / h),颗粒的膨胀床也是稳定的。当这些颗粒的表面通过氟化物吸附改性后,在109-210 cm / h的线速度下,牛血清白蛋白(BSA)吸附的总床容量为42 +/- 2 mg BSA / ml沉降床体积。在非结合条件下进行了几种溶质的停留时间分布研究,以评估流化床中液体混合和通道化程度与流化速度的关系。还根据分配器设计对液体混合和通道进行了研究。对于这些非常致密的颗粒,通道化和混合的程度并没有使膨胀度恶化。床膨胀(通过逐步增加离子强度)时,吸附的BSA的洗脱迅速,导致在高流化速度下出现窄峰,而无需依靠床沉降。两倍扩展床的BSA在5%穿透(蛋白质流出物浓度等于入口浓度的5%)时的动态结合能力与沉降床相同(22 +/- 2 mg BSA / ml沉降床)床体积),但随着床扩展的增加而减少。用0.25 M氢氧化钠反复清洗吸附剂后,可重现BSA结合。 (C)1997年Elsevier Science B.V

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