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Influence of the nature of coupling agents on insulin adsorption on supports grafted with sialic acid for high-performance affinity chromatography
Institution:1. Department of Chemistry, Post-Graduation Studies, Vijaya College (Affiliated to Bangalore University), Basavanagudi, Bengaluru 560004, Karnataka, India;2. Department of Chemistry, School of Engineering and Technology, CMR University, Bengaluru 562149, Karnataka, India;1. Chair of Environmental Chemistry and Bioanalytics, Faculty of Chemistry, Nicolaus Copernicus University in Toruń, Gagarina 7, 87-100 Toruń, Poland;2. Interdisciplinary Centre of Modern Technologies, Nicolaus Copernicus University in Toruń, Wileńska 4, 87-100 Toruń, Poland;1. Laboratory of Applied Chemistry, Faculty of Sciences and Techniques of Fez, Sidi Mohammed Ben Abdellah University, BP 2202 – Route Imouzzer, Fez, Morocco;2. Aix-Marseille University, Laboratory of Environment Chemistry, Équipe MPO, Europôle de l’Arbois, Bât. Villemin BP 80, 13545 Aix en Provence Cedex 4, France;3. Universidade Nova de Lisboa, FCT, Centro de Física Atómica, 2829-516 Caparica, Portugal;1. Southern Federal University, Rostov-on-Don, 344090, Russia;2. Department of Botany and Microbiology, College of Science, King Saud University, Riyadh, 11451, Saudi Arabia
Abstract:Porous silica exhibits excellent mechanical properties for use as a stationary phase for high-performance liquid chromatography. However, negative surface charges make it unusable in its native state. For this reason, silica beads are coated with dextran polymers carrying a calculated amount of diethylaminoethyl groups. Both the minimization of non-specific interactions and the hydrophilic character of such supports allow their functionalization with biospecific ligands and finally their use in high-performance affinity chromatography of biological products. The use of these modified supports in high-performance affinity chromatography requires a better understanding of various characteristics of stationary phases. For this purpose, several techniques were utilized, in particular, size-exclusion chromatography and adsorption of radiolabelled albumin. These methods provided complementary information on the structure of these supports. Coated silica-based supports were functionalized with sialic acid by means of different coupling agents. The affinity of these supports for insulin was determined by the establishment of adsorption isotherms and by high-performance affinity chromatography, to evidence the relationships between structural characteristics of the supports and their separation properties. The study of interactions between these supports and insulin allowed us to show the importance of the coupling method on the performances of supports in affinity chromatography.
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