Departamento de Química Física, Facultad de Ciencias Químicas, Universidad Complutense de Madrid, Ciudad Universitaria s/n, Madrid 28040, Spain.
Instituto Pluridisciplinar, Universidad Complutense de Madrid, Paseo Juan XXIII 1, Madrid 28040, Spain.
Langmuir. 2021 May 25;37(20):6189-6200. doi: 10.1021/acs.langmuir.1c00341. Epub 2021 May 4.
This work presents a simple methodology for coating small unilamellar liposomes bearing different degrees of positive charge with polyelectrolyte multilayers using the sequential layer-by-layer deposition method. The liposomes were made of mixtures of 1,2-dioleyl--glycero-3-phosphocoline and dimethyl dioctadecyl ammonium bromide (DODAB) and coated by alternated layers of the sodium salt of poly(4-styrenesulfonate) (PSS) and poly(allylamine) (PAH) as polyanions and polycations, respectively. The results show that the zeta potential of the liposomes was not very sensitive to the mole fraction of DODAB in the membrane, , in the range 0.3 ≤ ≤ 0.8. We were able to coat the liposomes with up to four polymer bilayers. The growth of the capsule size was followed by dynamic light scattering, and in some cases, by cryo-transmission electron microscopy, with good agreement between both techniques. The thickness of the layers, measured from the hydrodynamic radius of the coated liposome, depends on the polyelectrolyte used, so that the PSS layers adopt a much more packaged conformation than the PAH layers. An interesting finding is that the PSS amount needed to reach the isoelectric point of the capsules increases linearly with the charge density of the bare liposomes, whereas the amount of PAH does not depend on it. As expected, the preparation of the multilayers has to be done in such a way that when the system is close to the isoelectric point, the capsules do not aggregate. For this, we dropped the polyelectrolyte solution quickly, stirred it fast, and used dilute liposome suspensions. The method is very flexible and not limited to liposomes or polyelectrolyte multilayers; also, coatings containing charged nanoparticles can be easily made. Once the liposomes have been coated, lipids can be easily eliminated, giving rise to polyelectrolyte nanocapsules (polyelectrosomes) with potential applications as drug delivery platforms.
本文提出了一种简单的方法,用于使用逐层沉积法将具有不同正电荷程度的小单层脂质体用聚电解质多层包覆。脂质体由 1,2-二油酰基-sn-甘油-3-磷酸胆碱和二甲基十八烷基溴化铵(DODAB)的混合物制成,并通过交替的聚 4-苯乙烯磺酸钠(PSS)和聚烯丙胺(PAH)的钠盐层作为聚阴离子和聚阳离子进行包覆。结果表明,脂质体的 ζ 电位对膜中 DODAB 的摩尔分数, ,在 0.3 ≤ ≤ 0.8 的范围内不是很敏感。我们能够用多达四个聚合物双层包覆脂质体。通过动态光散射跟踪胶囊尺寸的生长,在某些情况下,通过冷冻传输电子显微镜进行跟踪,两种技术之间具有良好的一致性。从包覆脂质体的水动力半径测量得到的层厚度取决于所使用的聚电解质,因此 PSS 层比 PAH 层采用更封装的构象。一个有趣的发现是,达到胶囊等电点所需的 PSS 量与裸脂质体的电荷密度呈线性关系,而 PAH 的量则与其无关。正如预期的那样,必须以这样的方式制备多层,使得当系统接近等电点时,胶囊不会聚集。为此,我们快速滴加聚电解质溶液,快速搅拌并使用稀脂质体悬浮液。该方法非常灵活,不仅限于脂质体或聚电解质多层;还可以轻松制备含有带电纳米颗粒的涂层。一旦脂质体被包覆,就可以很容易地去除脂质,从而产生具有潜在应用的聚电解质纳米胶囊(聚电介质体)作为药物输送平台。