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In this study, a new method for preparing macroporous rigid agarose microspheres was developed by one-step pre-crosslinking method with cyclic anhydride. Three different cyclic anhydrides, namely, maleic anhydride, succinic anhydride, and glutaric anhydride, were used to pre-crosslink agarose. The reaction temperature and the amount of cyclic anhydride in the pre-crosslinking process were optimized to endow agarose with stronger cross-linking. Under the optimal cross-linking condition, macroporous rigid agarose microspheres with homogeneous particle size were successfully obtained by adjusting emulsification method. Cryo-scanning electron microscopy was used to characterize the morphology of cross-linked agarose gel and microspheres. The addition of cyclic anhydride increased the gel aperture of cross-linked agarose microspheres, thereby making the macropores in the microspheres more dense and enhancing the mass transfer in the particles. Under low pressure, the cross-linked agarose microsphere column can effectively separate model proteins at linear flow rates three times higher than the agarose microsphere column. These results indicate that the developed agarose microspheres are a promising high-speed chromatographic medium.
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http://dx.doi.org/10.1016/j.ijbiomac.2022.09.146 | DOI Listing |
Sheng Wu Gong Cheng Xue Bao
August 2025
State Key Laboratory of Biopharmaceutical Preparation and Delivery, Institute of Process Engineering, Chinese Academy of Sciences, Beijing 100190, China.
As the need for antibody production rises, there is an urgent need to lower the costs and enhance the efficiency of the separation process. Currently, the chromatographic media used for antibody separation and purification often focus on individual properties of antibodies, such as affinity, hydrophobicity, and charge, leading to issues like low purification efficiency or inadequate adsorption capacity. To address this, an electrostatically coupled polypeptide affinity medium (FD7-3, 5-diaminobenzoic acid n-sepharose, FD7-DA-Sepharose) was developed for rapid purification of antibodies from cell culture supernatant.
View Article and Find Full Text PDFInvest Ophthalmol Vis Sci
August 2025
Department of Ophthalmology, Third Xiangya Hospital, Central South University, Changsha, Hunan, People's Republic of China.
Purpose: Thyroid-associated ophthalmopathy (TAO) is a debilitating autoimmune disorder linked to Graves' disease (GD) that is characterized by inflammation and remodeling of orbital tissues. This study focuses on the use of poly(lactic-co-glycolic) acid (PLGA)-based microspheres (MS) coupled with CD34-specific aptamers to enhance the targeted delivery of Tocilizumab (Toc), an IL-6 receptor monoclonal antibody, to CD34+ orbital fibroblasts, which is a critical cell type implicated in TAO.
Methods: The flow cytometry and aptamer-mediated pull-down assays were applied to detect the affinity of CD34 aptamers (Apts) for CD34+ orbital fibroblasts.
J Chromatogr B Analyt Technol Biomed Life Sci
August 2025
State Key Laboratory of Mariculture Biobreeding and Sustainable Goods, Yellow Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Laboratory for Marine Drugs and Byproducts, Qingdao Marine Science and Technology Center, Qingdao 266071, China; Jiangsu Collaborative Innovation Cente
Recent studies on immunoaffinity chromatography (IAC) columns for aflatoxin B (AFB) have not provided a comprehensive preparation procedure or explored their capacity, reusability, and stability. In this study, we outline a preparation process for an AFB immune affinity column filler (AFB-IAC) for extracting AFB from food sources like rice, peanuts, and soybeans. Using commercially available IAC is often limited due to high costs, low capacity, slow flow rates, and poor reusability.
View Article and Find Full Text PDFInt J Biol Macromol
May 2025
College of Ocean Food and Biological Engineering, Jimei University, Xiamen 361021, PR China; National R&D Center for Red Alga Processing Technology, Xiamen 361021, PR China; Fujian Provincial Engineering Technology Research Center of Marine Functional Food, Xiamen 361021, PR China; Xiamen Key Labora
The spatial configuration and bonding conditions of polysaccharide microspheres make it difficult to distinguish molecules with similar hydrophobic properties in practical applications. Fortunately, medium modification offers more flexible chromatography conditions and higher selectivity, providing new solutions for complex purification environments. We synthesized hydrophobic composite core-shell agarose microspheres equipped with hydrophobic ligands and investigated the effects of hydrophobic ligand coupling on the morphology, particle size, pressure resistance, functional group change and protein adsorption capacity of microspheres.
View Article and Find Full Text PDFAnal Chem
April 2025
State Key Laboratory of Medical Proteomics, National Chromatographic R&A Center, CAS Key Laboratory of Separation Science for Analytical Chemistry, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, China.
Protein N-phosphorylation has been garnering increasing attention owing to its unique biological functions. The large-scale identification of protein N-phosphorylation serves as the foundation for exploring a novel function. Despite the advancements in enrichment methods under neutral conditions, persistently low enrichment efficiency has long hindered the progress of this field.
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