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含有绵羊布鲁氏菌抗原的聚(ε-己内酯)微粒作为抗布鲁氏菌病疫苗递送系统的稳定性

Stability of poly(epsilon-caprolactone) microparticles containing Brucella ovis antigens as a vaccine delivery system against brucellosis.

作者信息

Estevan Maite, Gamazo Carlos, Martínez-Galan Fernando, Irache Juan M

机构信息

Immunoadjuvant Unit, Department of Microbiology, University of Navarra, 31008, Pamplona, Spain.

出版信息

AAPS PharmSciTech. 2008;9(4):1063-9. doi: 10.1208/s12249-008-9149-2. Epub 2008 Oct 16.

Abstract

In previous works, our research group has successfully proved the use of subcellular vaccines based on poly(epsilon-caprolactone) (PEC) microparticles containing an antigenic extract of Brucella ovis (HS) against experimental brucellosis in both mice and rams. However, the successful exploitation of pharmaceutical products, and therefore of this product as veterinary vaccine, requires preservation of both biological activity and native structure in all steps of development from purification to storage. In this context, we have carried out an accelerated stability study to evaluate the relative stability of HS when loading in PEC microparticles. For this purpose, freeze-dried microparticles were stored at 40 +/- 1 degrees C and 75% RH as a preliminary analysis of a stability testing. The results showed that both physico-chemical (size, morphology, antigen content, release profile) and biological (integrity and antigenicity of the HS) properties were preserved after 6 months of storage. On the contrary, after 1 year of storage, the HS release profile was dramatically affected probably due to a progressive loss of the polymer microstructure. In addition, the degradation and loss of the antigenicity of the HS components was also evident by SDS-PAGE and immunoblotting analysis. In fact, after 12 months of storage, only the integrity and antigenicity of two of the major protective proteins of the HS antigenic complex were preserved.

摘要

在之前的研究中,我们的研究小组已成功证明,基于聚(ε-己内酯)(PEC)微粒且含有绵羊布鲁氏菌(HS)抗原提取物的亚细胞疫苗,对小鼠和公羊的实验性布鲁氏菌病有效。然而,要成功开发药品,进而将该产品开发为兽用疫苗,需要在从纯化到储存的所有开发步骤中都保持生物活性和天然结构。在此背景下,我们开展了一项加速稳定性研究,以评估HS负载于PEC微粒中的相对稳定性。为此,作为稳定性测试的初步分析,将冻干微粒储存在40±1℃和75%相对湿度的环境中。结果显示,储存6个月后,物理化学性质(尺寸、形态、抗原含量、释放曲线)和生物学性质(HS的完整性和抗原性)均得以保留。相反,储存1年后,HS的释放曲线受到显著影响,这可能是由于聚合物微观结构逐渐丧失所致。此外,通过SDS-PAGE和免疫印迹分析也明显看出HS成分的降解和抗原性丧失。事实上,储存12个月后,HS抗原复合物中只有两种主要保护性蛋白的完整性和抗原性得以保留。

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