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Comparative stability study of lyophilised aluminium hydroxide adjuvanted vaccine formulations containing a monoclonal antibody as a model antigen and methods used for their characterisation

机译:含有单克隆抗体作为模型抗原的冻干氢氧化铝佐剂疫苗制剂的比较稳定性研究及其表征方法

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This study evaluates the stability of lyophilised aluminium hydroxide adjuvanted vaccine formulations during stress testings at elevated temperatures. Trehalose, dextran, HES, PVP, saccharose and sorbitol were used as excipients to protect both vaccine components - protein/antigen and an adjuvant - during lyophilisation from freezing- and dehydration stresses. Exemplary vaccine components were abagovomab, a monoclonal anti idiotypic antibody developed as an immuno-vaccine for the treatment of ovarian cancer and aluminium hydroxide adjuvant. All six excipients protected the monoclonal antibody abagovomab from denaturation and loss in potency as detected with sodium dodecylsulfate polyacrylamide gel electrophoresis (SIDS-PAGE). Enzyme-linked immunosorbent assay (ELISA) could show maintenance of abagovomab potency within the lyophilised samples throughout the stress testings as could also be shown for stress tested drug substance. Particle size analysis, sedimentation assay and wide angle Xray diffraction (WAXD) revealed that dextran, hydroxyethyl starch (HES) and polyvinyl pyrrolidone K 25 (PVP) particularly enhanced stability of the adjuvant within a vaccine formulation during stress testing. The present study could further demonstrate the applicability of Nile Red fluorescence microscopy and adsorption studies for in-depth characterisation of freeze dried vaccine formulations.
机译:这项研究评估了高温下压力测试期间冻干的氢氧化铝佐剂疫苗制剂的稳定性。海藻糖,右旋糖酐,HES,PVP,蔗糖和山梨糖醇用作赋形剂,可在冻干过程中保护两种疫苗成分-蛋白质/抗原和佐剂-免受冷冻和脱水压力的影响。示例性疫苗成分是abagovomab,它是一种单克隆抗独特型抗体,被开发为用于治疗卵巢癌和氢氧化铝佐剂的免疫疫苗。通过十二烷基硫酸钠聚丙烯酰胺凝胶电泳(SIDS-PAGE)检测,所有六种赋形剂均能保护单克隆抗体abagovomab免受变性和效能损失的影响。酶联免疫吸附试验(ELISA)可以显示在整个压力测试过程中冻干样品中的abagovomab药效保持不变,这也可以用于压力测试的药物。粒度分析,沉降测定和广角X射线衍射(WAXD)显示,葡聚糖,羟乙基淀粉(HES)和聚乙烯吡咯烷酮K 25(PVP)在压力测试过程中特别增强了佐剂在疫苗制剂中的稳定性。本研究可以进一步证明尼罗红荧光显微镜和吸附研究对冷冻干燥疫苗制剂的深入表征的适用性。

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