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Surface modified polymeric nanoparticles for immunisation against equine strangles.

机译:表面修饰的聚合物纳米颗粒,可针对马勒死情况进行免疫接种。

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The successful development of particulate vaccines depends on the understanding of their physicochemical and biological characteristics. Therefore, the main purpose of this study was to develop and characterise stable surface modified poly(lactic acid) (PLA) nanoparticles, using polyvinyl alcohol (PVA), alginate (ALG) and glycolchitosan (GCS) containing a Streptococcus equi enzymatic extract adsorbed onto the surface. The characterisation of the preparations and a physicochemical study of the adsorption process were performed. The adsorption of S. equi proteins is a rapid process reaching, within 1h, maximum adsorption efficiency values of 75.2+/-1.9% (w/w) for PLA-PVA, 84.9+/-0.2% (w/w) for PLA-GCS and 78.1+/-0.4% (w/w) for PLA-ALG nanoparticles. No protein degradation was detected throughout the formulation procedures. As expected from a complex mixture of proteins, adsorption data suggest a Freundlich-type of equilibrium with regression coefficients (r(2)) of 0.9958, 0.9839 and 0.9940 for PLA-PVA, PLA-GCS and PLA-ALG, respectively. Desorption studies revealed a burst release within the first 6h, for all formulations, followed by a sustained release profile. Nanoparticle surface modification with GCS improved the sustained release profile, as 20% of protein remained attached to the particle surface after 30 days. The results show that adsorption is an alternative method for the production of S. equi antigen carriers for vaccination purposes.
机译:颗粒疫苗的成功开发取决于对它们的理化和生物学特性的了解。因此,本研究的主要目的是开发和表征稳定的表面改性的聚乳酸(PLA)纳米颗粒,方法是使用聚乙烯醇(PVA),藻酸盐(ALG)和糖壳聚糖(GCS)包含吸附在其上的链球菌等酶提取物表面。进行了制剂的表征和吸附过程的理化研究。马链球菌蛋白的吸附是一个快速过程,在1小时内达到最大吸附效率值,PLA-PVA为75.2 +/- 1.9%(w / w),PLA-PVA为84.9 +/- 0.2%(w / w) -GCS和PLA-ALG纳米粒子的78.1 +/- 0.4%(w / w)。在整个配制过程中未检测到蛋白质降解。正如从复杂的蛋白质混合物中所预期的那样,吸附数据表明,PLA-PVA,PLA-GCS和PLA-ALG的Freundlich型平衡的回归系数(r(2))分别为0.9958、0.9839和0.9940。解吸研究表明,对于所有制剂,在最初的6h内会突然释放,然后是持续释放。用GCS进行的纳米粒子表面修饰改善了缓释特性,因为30天后20%的蛋白质仍附着在粒子表面。结果表明,吸附是生产用于疫苗接种的马链球菌抗原载体的替代方法。

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