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电泳迁移率作为从皂树(Quillaja saponaria Molina)中分离免疫佐剂皂苷的一种工具。

Electrophoretic mobility as a tool to separate immune adjuvant saponins from Quillaja saponaria Molina.

作者信息

Gilabert-Oriol Roger, Weng Alexander, von Mallinckrodt Benedicta, Stöshel Anja, Nissi Linda, Melzig Matthias F, Fuchs Hendrik, Thakur Mayank

机构信息

Institut für Laboratoriumsmedizin, Klinische Chemie und Pathobiochemie, Charité-Universitätsmedizin Berlin, Campus Virchow-Klinikum, Augustenburger Platz 1, D-13353 Berlin, Germany.

Institut für Pharmazie-Pharmazeutische Biologie, Freie Universität Berlin, Königin-Luise-Straße 2+4, D-14195 Berlin, Germany.

出版信息

Int J Pharm. 2015 Jun 20;487(1-2):39-48. doi: 10.1016/j.ijpharm.2015.03.063. Epub 2015 Mar 31.

Abstract

Quillaja saponins are used as adjuvants in animal vaccines but their application in human vaccination is still under investigation. Isolation and characterization of adjuvant saponins is very tedious. Furthermore, standardization of Quillaja saponins is critical pertaining to its application in humans. In this study, a convenient method based on agarose gel electrophoresis was developed for the separation of Quillaja saponins. Six different commercial Quillaja saponins were segregated by size/charge into numerous fractions. Each of the fractions was characterized by ESI-TOF-MS spectroscopy and thin layer chromatography. Real-time impedance-based monitoring and red blood cell lysis assay were used to evaluate cytotoxicity and hemolytic activities respectively. Two specific regions in the agarose gel (delimited by specific relative electrophoretic mobility values) were identified and characterized by exclusive migration of acylated saponins known to possess immune adjuvant properties (0.18-0.58), and cytotoxic and hemolytic saponins (0.18-0.94). In vivo experiments in mice with the isolated fractions for evaluation of adjuvant activity also correlated with the relative electrophoretic mobility. In addition to the separation of specific Quillaja saponins with adjuvant effects as a pre-purification step to HPLC, agarose gel electrophoresis stands out as a new method for rapid screening, separation and quality control of saponins.

摘要

皂树皂苷在动物疫苗中用作佐剂,但其在人类疫苗接种中的应用仍在研究中。佐剂皂苷的分离和表征非常繁琐。此外,皂树皂苷的标准化对于其在人类中的应用至关重要。在本研究中,开发了一种基于琼脂糖凝胶电泳的简便方法用于皂树皂苷的分离。六种不同的市售皂树皂苷按大小/电荷分离成多个组分。每个组分通过电喷雾电离飞行时间质谱(ESI-TOF-MS)光谱和薄层色谱进行表征。基于实时阻抗的监测和红细胞裂解试验分别用于评估细胞毒性和溶血活性。在琼脂糖凝胶中确定了两个特定区域(由特定的相对电泳迁移率值界定),并通过已知具有免疫佐剂特性的酰化皂苷(0.18 - 0.58)以及细胞毒性和溶血皂苷(0.18 - 0.94)的专属迁移进行了表征。在小鼠体内用分离的组分进行佐剂活性评估的实验也与相对电泳迁移率相关。除了作为高效液相色谱(HPLC)预纯化步骤分离具有佐剂作用的特定皂树皂苷外,琼脂糖凝胶电泳作为一种用于皂苷快速筛选、分离和质量控制的新方法脱颖而出。

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