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Hydrolytic Cationic Ester Microparticles for Highly Efficient DNA Vaccine Delivery

机译:水解阳离子酯微粒,可高效递送DNA疫苗

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DNA vaccination holds great potential to be a safer and more efficient alternative to traditional vaccination strategies, but the current lack of nontoxic and effective delivery systems is the greatest impediment to its clinical implementation. In this work, a convenient one-step method is used to prepare a degradable “microgel” delivery platform, featuring hydrolytic esters. Prior to hydrolysis, these micrometer-sized gel particles can effectively condense DNA due to their positive surface charge. Upon entering antigen-presenting cells (APCs), the microgels can be hydrolyzed to nontoxic zwitterionic polymers, consequently releasing the DNA and inducing phagosomal escape. Surface charge, DNA loading, cytotoxicity, and gene transfection efficiency of the hydrolysable microparticles with different tertiary to quaternary amine ratios are systematically studied. Nonhydrolysable counterparts and commercially developed PLGA-CTAB particles are used as the control. The passive targeting effect is further evaluated by blocking the phagocytosis pathway of the cells. The hydrolytic microgels prepared in this study possess great potential to become a platform for DNA vaccine delivery.
机译:DNA疫苗具有巨大的潜力,可以替代传统的疫苗接种策略,从而成为一种更安全,更有效的方法,但是目前缺乏无毒且有效的递送系统是其临床实施的最大障碍。在这项工作中,一种方便的一步方法用于制备具有水解酯的可降解“微凝胶”递送平台。在水解之前,这些微米级的凝胶颗粒由于其正表面电荷而可以有效地凝聚DNA。进入抗原呈递细胞(APC)后,微凝胶可水解成无毒的两性离子聚合物,从而释放DNA并诱导吞噬体逃逸。系统研究了具有不同叔胺和季胺比率的可水解微粒的表面电荷,DNA负载,细胞毒性和基因转染效率。不可水解的对应物和商业开发的PLGA-CTAB颗粒用作对照。通过阻断细胞的吞噬作用途径进一步评估了被动靶向作用。在这项研究中制备的水解微凝胶具有巨大的潜力,可以成为DNA疫苗输送的平台。

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