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首页> 外文期刊>Langmuir: The ACS Journal of Surfaces and Colloids >Supramolecular Organization and siRNA Binding of Hyaluronic Acid-Coated Lipoplexes for Targeted Delivery to the CD44 Receptor
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Supramolecular Organization and siRNA Binding of Hyaluronic Acid-Coated Lipoplexes for Targeted Delivery to the CD44 Receptor

机译:透明质酸涂层脂复合物的超分子组织和siRNA结合用于靶向递送至CD44受体。

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摘要

The dynamics of the formation of siRNA-lipoplexes coated with hyaluronic acid (HA) and the parameters influencing their supramolecular organization were studied. The insertion of a HA-dioleylphosphatidylethanolamine (DOPE) conjugate in the liposome structure as well as subsequent complexation with siRNA increased the liposome size. Lipoplexes were around 110 nm at high +/- charge ratios with a zeta potential around +50 mV and around 230 nm at low +/- ratios, with a zeta potential that decreased to negative values, reaching -45 mV. The addition of the conjugate did not compromise siRNA binding to liposomes, although these nucleic acids induced a displacement of part of the HA-DOPE conjugate upon lipoplex formation, as confirmed by capillary electrophoresis. Isothermal titration calorimetry, X-ray diffraction studies, and cryo-TEM microscopy demonstrated that in addition to electrostatic interactions with siRNA a rearrangement of the lipid bilayers takes place, resulting in condensed oligolamellar vesicles. This phenomenon is dependent on the number of siRNA molecules and the degree of modification with HA. Finally, the suitable positioning of HA on the lipoplex surface and its ability to bind specifically to the CD44 receptors in a concentration-dependent manner was demonstrated by surface plasmon resonance analysis.
机译:研究了透明质酸(HA)包被的siRNA-脂质复合物的形成动力学及其影响其超分子组织的参数。在脂质体结构中插入HA-二醇基磷脂酰乙醇胺(DOPE)缀合物以及随后与siRNA的络合增加了脂质体的大小。脂质体在高+/-电荷比下约为110 nm,ζ电位约为+50 mV,在低+/-比率下约为230 nm,ζ电位降低至负值,达到-45 mV。偶联物的添加并没有损害siRNA与脂质体的结合,尽管这些核酸在脂质复合物形成后诱导了HA-DOPE偶联物的一部分被毛细管电泳所证实。等温滴定量热法,X射线衍射研究和低温TEM显微镜显示,除了与siRNA的静电相互作用外,脂质双层的重排也发生了,从而导致了寡层囊泡的浓缩。这种现象取决于siRNA分子的数量和HA修饰的程度。最后,通过表面等离振子共振分析证明HA在脂质复合物表面上的合适定位及其以浓度依赖性方式特异性结合CD44受体的能力。

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