Arslanov Vladimir V, Krylov Daniil I
Frumkin Institute of Physical Chemistry and Electrochemistry, Russian Academy of Sciences, Leninsky Pr. 31-4, Moscow 119071, Russia.
J Colloid Interface Sci. 2024 May 15;662:342-356. doi: 10.1016/j.jcis.2024.02.035. Epub 2024 Feb 9.
This paper presents, for the first time, evidence for vesicle destruction and payload loss at the stage of purification of niosome dispersions by centrifugation, an important operation in the assembly of vesicular materials. The ability of niosomes of different compositions to reassemble, i.e., to restore the vesicular structure after destruction in the field of centrifugal forces, was demonstrated by dynamic light scattering and fluorescence spectroscopy. The kinetics of reassembly of vesicular structures is determined by the strength of the centrifugal field and the composition of niosomes. In contrast to ternary compositions, where particle size and modality are essentially unchanged after redispersion of the precipitate resulting from centrifugation, niosome dispersions containing anionic dicetyl phosphate includes micron-sized particles after redispersion, which vary in size over a wide range throughout the observation period. The reassembly process is complicated by the presence of charge on the surface of the niosomes. Elastic niosomes - ethosomes have been synthesised which, due to the high deformability of the shells, are less susceptible to destruction in the centrifugal field and retain the contents of the aqueous core. Using the "energy landscape" approximation, it is shown that vesicular structures assembled during hydration and reassembled after their centrifugation occupy different positions in the energetic pathway of their preparation. The results obtained should also be taken into account when determining the entrapment efficiency, since this procedure uses centrifugation to separate the load. It is important to note that the physical stability of niosomes, which is usually considered in terms of the functional activity of particles, is manifest and should be considered at the material preparation stage.
本文首次提供了证据,表明在通过离心法纯化囊泡分散体的阶段会发生囊泡破坏和载药量损失,离心法是囊泡材料组装过程中的一项重要操作。通过动态光散射和荧光光谱法证明了不同组成的囊泡能够重新组装,即在离心力场中被破坏后恢复囊泡结构。囊泡结构的重新组装动力学取决于离心场的强度和囊泡的组成。与三元组合物不同,三元组合物离心后产生的沉淀物重新分散后粒径和模态基本不变,而含有阴离子型磷酸二鲸蜡酯的囊泡分散体重新分散后包含微米级颗粒,在整个观察期内粒径变化范围很广。囊泡表面电荷的存在使重新组装过程变得复杂。已经合成了弹性囊泡——醇质体,由于其外壳具有高可变形性,在离心场中不易被破坏,并保留了水相核心的内容物。使用“能量景观”近似法表明,在水合过程中组装并在离心后重新组装的囊泡结构在其制备的能量途径中占据不同位置。在确定包封效率时也应考虑所得结果,因为该过程使用离心法分离负载物。需要注意的是,囊泡的物理稳定性通常从颗粒的功能活性方面考虑,在材料制备阶段就很明显且应予以考虑。