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In vitro performance of lipid-PLGA hybrid nanoparticles as an antigen delivery system: lipid composition matters

机译:脂质-PLGA杂化纳米颗粒作为抗原递送系统的体外性能:脂质组成很重要

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摘要

Due to the many beneficial properties combined from both poly(lactic-co-glycolic acid) (PLGA) nanoparticles (NPs) and liposomes, lipid-PLGA hybrid NPs have been intensively studied as cancer drug delivery systems, bio-imaging agent carriers, as well as antigen delivery vehicles. However, the impact of lipid composition on the performance of lipid-PLGA hybrid NPs as a delivery system has not been well investigated. In this study, the influence of lipid composition on the stability of the hybrid NPs and in vitro antigen release from NPs under different conditions was examined. The uptake of hybrid NPs with various surface charges by dendritic cells (DCs) was carefully studied. The results showed that PLGA NPs enveloped by a lipid shell with more positive surface charges could improve the stability of the hybrid NPs, enable better controlled release of antigens encapsulated in PLGA NPs, as well as enhance uptake of NPs by DC.
机译:由于聚乳酸-乙醇酸(PLGA)纳米颗粒(NPs)和脂质体具有许多有益的特性,脂质-PLGA杂化NP已被广泛研究作为癌症药物输送系统,生物成像剂载体,以及抗原递送载体。然而,尚未充分研究脂质组成对脂质-PLGA杂化NP作为递送系统的性能的影响。在这项研究中,研究了脂质组成对杂合NPs稳定性和在不同条件下从NPs释放体外抗原的影响。仔细研究了树突状细胞(DC)对具有各种表面电荷的杂化NP的吸收。结果表明,脂质壳包裹的具​​有更多正表面电荷的PLGA NP可以提高杂化NP的稳定性,可以更好地控制PLGA NP中封装的抗原的释放,并增强DC对NP的吸收。

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