首页> 外文期刊>International Journal of Pharmaceutics >Quillaja saponaria extract as mucosal adjuvant with chitosan functionalized gold nanoparticles for mucosal vaccine delivery: Stability and immunoefficiency studies
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Quillaja saponaria extract as mucosal adjuvant with chitosan functionalized gold nanoparticles for mucosal vaccine delivery: Stability and immunoefficiency studies

机译:Quillaja saponaria提取物作为粘膜佐剂与壳聚糖功能化金纳米颗粒用于粘膜疫苗的递送:稳定性和免疫效率研究

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Carrier mediated delivery of vaccines along with adjuvants can possibly address the issue related to oral vaccines like inadequate immune potentiation. In this study, chitosan functionalized gold nanoparticles (CsAuNPs) were used as a carrier for the model antigen tetanus toxoid (TT) along with immunostimulant Quillaja saponaria extract (QS). Physicochemical properties (size, zeta potential, pH value) of formulation were investigated as stability indicating parameters. The synthesized CsAuNPs were spherical in shape, around 40 nm in size, positively charged (around +35 mV) and had TT and QS payload of 65% and 0.01%, respectively. Formulation parameters did not alter the secondary structure of TT, as determined by FTIR, fluorescence and CD spectroscopy. Antigen specificity, determined by an ELISA, was also not compromised. The CsAuNPs conferred protection to TT against gastric hydrolysis as studied in vitro. TT-QS-CsAuNPs induced up to 28-fold immune responses compared to control formulations (TT, TT-QS) after oral administration of formulations in BALB/c mice. The immune responses were quantified by measuring the TT-specific IgG and IgA titers using ELISA. Findings herein demonstrate that co-delivery of TT and QS with functionalized CsAuNPs promotes better systemic and local immune responses and hence can be considered as a sound approach for oral vaccine delivery. ? 2012 Elsevier B.V. All rights reserved.
机译:疫苗与佐剂一起由载体介导的传递可能可以解决与口服疫苗相关的问题,例如免疫增强作用不足。在这项研究中,壳聚糖功能化的金纳米颗粒(CsAuNPs)与模型免疫破伤风提取物(Quillaja saponaria)提取物(QS)一起用作模型抗原破伤风类毒素(TT)的载体。研究了制剂的理化性质(大小,ζ电位,pH值)作为稳定性指示参数。合成的CsAuNPs呈球形,大小约为40 nm,带正电(约+35 mV),TT和QS有效载荷分别为65%和0.01%。通过FTIR,荧光和CD光谱确定,配方参数不会改变TT的二级结构。通过ELISA确定的抗原特异性也没有受到损害。体外研究表明,CsAuNPs可保护TT抵抗胃液水解。在BALB / c小鼠中口服制剂后,与对照制剂(TT,TT-QS)相比,TT-QS-CsAuNPs诱导的免疫应答高达28倍。通过使用ELISA测量TT特异性IgG和IgA滴度来定量免疫反应。本文的发现表明,TT和QS与功能化的CsAuNP的共同递送促进了更好的全身和局部免疫应答,因此可以被认为是口服疫苗递送的合理方法。 ? 2012 Elsevier B.V.保留所有权利。

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