McCreath G E, Chase H A, Purvis D R, Lowe C R
Department of Chemical Engineering, University of Cambridge, UK.
J Chromatogr. 1993 Jan 22;629(2):201-13. doi: 10.1016/0021-9673(93)87034-j.
Perfluorocarbon affinity emulsions are generated by the homogenisation of a perfluorocarbon oil with a polymeric fluorosurfactant previously derivatised with an affinity ligand and subsequently cross-linked in situ. This procedure gives rise to a novel liquid affinity adsorbent that can be used for continuous protein purification. Discrete emulsion droplets were found to be unstable when pumped for prolonged periods; however, when flocculated, the emulsion floccules with diameters of around 125 microns, were very stable and sedimented faster. A four-stage reactor unit (perfluorocarbon emulsion reactor for continuous affinity separations, PERCAS) was designed and constructed to carry out continuous separations, and exploited the unusual properties of the absorbent, i.e. liquid nature and high density. Each of the four stages of PERCAS consisted of a mixing tank, for contacting between emulsion phase and aqueous phase, adjacent to a settling tank for the subsequent separation of emulsion from the aqueous phase. Using PERCAS adsorption, washing, elution and re-equilibration of the emulsion could be carried out continuously with emulsion recycle. Using single-component adsorption of human serum albumin to a perfluorocarbon affinity emulsion derivatised with the triazine dye C.I. Reactive Blue 2, PERCAS was optimised with respect to flow-rates and input concentrations. The work was then extended to the continuous purification of essentially homogeneous human serum albumin from blood plasma.
全氟碳亲和乳液是通过将全氟碳油与预先用亲和配体衍生化并随后原位交联的聚合氟表面活性剂进行均质化而生成的。该过程产生了一种新型液体亲和吸附剂,可用于连续蛋白质纯化。发现离散的乳液滴在长时间泵送时不稳定;然而,絮凝后,直径约125微米的乳液絮凝物非常稳定且沉降更快。设计并构建了一个四级反应器单元(用于连续亲和分离的全氟碳乳液反应器,PERCAS)以进行连续分离,并利用了吸附剂的特殊性质,即液体性质和高密度。PERCAS的四个阶段中的每个阶段都由一个混合罐组成,用于乳液相和水相之间的接触,与一个沉降罐相邻,用于随后从水相中分离乳液。使用PERCAS,可以通过乳液循环连续进行乳液的吸附、洗涤、洗脱和再平衡。使用人血清白蛋白对用三嗪染料C.I.活性蓝2衍生化的全氟碳亲和乳液进行单组分吸附,对PERCAS的流速和输入浓度进行了优化。然后将这项工作扩展到从血浆中连续纯化基本均质的人血清白蛋白。