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Nuclear magnetic resonance flow imaging (MRFI) was used to measure fluid flow noninvasively in the extracapillary space (ECS) of a hollow-fiber bioreactor without cells. Agreement between these axial flow measurements in a single hollow-fiber module and predicted axial velocity contour plots at various image planes along the path length was good.Flow in a solid-wall tube (phantom) was first used to calibrate pixel intensities with axial velocities. Flow images at several locations along the permeable hollow fiber length were then obtained in order to observe the well-known leakage or Starling flow in the ECS. These quantitative spatially dependent velocity measurements were then compared to theoretically derived velocities obtained from a solution of Poisson's equation with a constant pressure gradient and no slip at the solid surfaces. A mathematical transformation was used to simplify the numerical methods. Leakage flow through the ECS of a multifiber bioreactor (40 fibers) was also measured by MRFI, illustrating the applicability of this method for optimizing operational procedures and design of membrane bioreactors and filtration devices.

A new group-specific affinity membrane using metal chelates as ligands and inorganic glass hollow fiber microfiltration membranes as support matrices is developed and tested. The study focused on developing the optimum activation and coupling procedures to bind the chelating agent (iminodiacetic acid, IDA) to the surface of the microporous glass hollow fiber membrane and testing the resultant affinity membrane. Starting with three different glass surfaces, five modification reactions were evaluated. All the modified "active surfaces" were first tested for their protein adsorptive properties in batch mode with suspended microporous glass grains using model proteins with known binding characteristics with Cu-IDA systems. The metal loading capacities of the surfaces exhibiting favorable fractionation were then measured by atomic absorption spectroscopy.The results were compared with the results obtained with a commercial material used in immobilized metal affinity column chromatography. The protein binding characteristics of the hollow fiber affinity membranes were also evaluated under conditions of convective flow. This was performed by flowing single solute protein solutions through the microporous membrane at different flow rates. These results were then used to estimate the optimum loading and elution times for the process. A mathematical model incorporating radial diffusion was solved using a finite difference discretization method. Comparison between model predictions and experimental results was performed for four different proteins at one flow rate. These results suggested that the kinetics of adsorption was concentration dependent. Finally, the hollow fiber affinity membranes were challenged with two component mixtures to test their ability to fractionate mixed protein solutions. Efficient separation and good purity were obtained.The results presented here represent the development of a new fast flow affinity membrane process-immobilized metal affinity membranes (IMAM). (c) 1994 John Wiley & Sons, Inc.

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