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设计用作稳定免疫吸附剂的微孔微粒。

Microporous microparticles designed as stable immunoadsorbents.

作者信息

Ubrich N, Rivat C, Vigneron C, Maincent P

机构信息

Laboratoire de Pharmacie Galénique et Biopharmacie, Faculté des Sciences Pharmaceutiques et Biologiques, 5, rue Albert Lebrun B.P. 403, 54001 Nancy-Cedex, France.

出版信息

Biotechnol Bioeng. 1998 Jun 20;58(6):581-6.

Abstract

We have developed a solid-phase immunoadsorbent based on encapsulated goat anti-apolipoprotein B polyclonal antibodies previously crosslinked with a 0.25% glutaraldehyde solution, and designed to remove by immunoaffinity the excess of apolipoproteins B from the plasma of patients affected by familial hypercholesterolemia. Compared to a classical immunoadsorbent prepared by activation of Sepharose CL-4B with cyanogen bromide, the resulting immunoadsorbent exhibits both optimal adsorption capacity and stability over the entire range of chemical and biochemical conditions during its practical handling. This approach will serve as a model system to demonstrate the applicability of microparticles as immunoadsorbents, which can be achieved for other encapsulated crosslinked proteins.

摘要

我们开发了一种基于包封的山羊抗载脂蛋白B多克隆抗体的固相免疫吸附剂,该抗体先前已与0.25%的戊二醛溶液交联,旨在通过免疫亲和作用从家族性高胆固醇血症患者的血浆中去除过量的载脂蛋白B。与通过溴化氰活化琼脂糖凝胶CL-4B制备的传统免疫吸附剂相比,所得的免疫吸附剂在实际操作过程中的整个化学和生化条件范围内均表现出最佳的吸附能力和稳定性。这种方法将作为一个模型系统,以证明微粒作为免疫吸附剂的适用性,这对于其他包封的交联蛋白也可以实现。

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