首页> 外文期刊>Biologicals: Journal of the International Association of Biological Standardization >A novel Enzyme-Linked Immuno-Sorbent Assay (ELISA) for the quantification of total and free polysaccharide in Haemophilus influenzae b-Tetanus toxoid conjugate vaccines in monovalent and combined vaccine formulations
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A novel Enzyme-Linked Immuno-Sorbent Assay (ELISA) for the quantification of total and free polysaccharide in Haemophilus influenzae b-Tetanus toxoid conjugate vaccines in monovalent and combined vaccine formulations

机译:一种新颖的酶联免疫吸附测定(ELISA)方法,用于定量单价和组合疫苗制剂中的流感嗜血杆菌b-破伤风类毒素结合疫苗中的总多糖和游离多糖

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摘要

Current Haemophilus influenzae b conjugate vaccines (Hib), which are made of purified capsular polysaccharide (poly-ribosyl-ribitol-phosphate; PRP) conjugated to a carrier protein, are almost completely evaluated by physico-chemical methods to ensure the integrity and stability of the vaccine and consistency of manufacture of batches. The absence of a potency assay makes the quantification of total PRP content (in SI units) and of % free polysaccharide in final fills or bulk components of Hib vaccines critical release tests for both manufacturers and national control authorities. Here we describe a simple and sensitive Enzyme-Linked Immuno-sorbent Assay (ELISA) which has been developed to quantify total and free PRP content in Hib-TT vaccine alone or when in combination with other vaccines. The assay is robust, specific and highly sensitive.
机译:目前的流感嗜血杆菌b结合疫苗(Hib)由结合了载体蛋白的纯化荚膜多糖(聚核糖基核糖醇-磷酸盐; PRP)制成,几乎已通过理化方法进行了全面评估,以确保其完整性和稳定性。疫苗和批次生产的一致性。缺乏效价测定的方法,对于制造商和国家控制机构而言,Hib疫苗最终填充物或散装成分中总PRP含量(以SI单位)和游离多糖%的定量至关重要。在这里,我们描述了一种简单而灵敏的酶联免疫吸附测定(ELISA),该测定已被开发用于定量单独或与其他疫苗组合使用的Hib-TT疫苗中的总PRP和游离PRP含量。该测定是鲁棒的,特异性的和高度敏感的。

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