School of Chemical Engineering , University of Birmingham , Birmingham , U.K.
Formulation Technology Group , Syngenta Ltd, Jealott's Hill International Research Centre , Bracknell , Berkshire , U.K.
Langmuir. 2018 Apr 3;34(13):3934-3948. doi: 10.1021/acs.langmuir.7b04315. Epub 2018 Mar 19.
Aside from single active microencapsulation, there is growing interest in designing structures for the coencapsulation and codelivery of multiple species. Although currently achievable within solid systems, significant challenges exist in realizing such functionality in liquid formulations. The present study reports on a novel microstructural strategy that enables the coencapsulation and corelease of two actives from oil-in-water emulsions. This is realized through the fabrication of sodium caseinate/chitosan (NaCAS/CS) complexes that in tandem function as encapsulants of one active (hydrophilic) but also as ("Pickering-like") stabilizers to emulsion droplets containing a secondary active (hydrophobic). Confocal microscopy confirmed that the two coencapsulated actives occupied distinct emulsion microstructure regions; the hydrophilic active was associated with the NaCAS/CS complexes at the emulsion interface, while the hydrophobic active was present within the oil droplets. Aided by their segregated coencapsulation, the two actives exhibited markedly different corelease behaviors. The hydrophilic active exhibited triggered release that was promoted by changes to pH, which weakened the protein-polysaccharide electrostatic interactions, resulting in particle swelling. The hydrophobic secondary active exhibited sustained release that was impervious to pH and instead controlled by passage across the interfacial barrier. The employed microstructural approach can therefore lead to the segregated coencapsulation and independent corelease of two incompatible actives, thus offering promise for the development of liquid-emulsion-based formulations containing multiple actives.
除了单一活性微胶囊化外,人们对设计用于共包封和共递送多种物质的结构越来越感兴趣。尽管在固体系统中目前可以实现,但在实现液体制剂中的这种功能方面仍然存在重大挑战。本研究报告了一种新颖的微结构策略,该策略能够从水包油乳液中共包封和共释放两种活性物质。这是通过制备酪蛋白酸钠/壳聚糖(NaCAS/CS)复合物来实现的,该复合物既可以作为一种活性物质(亲水性)的包封剂,也可以作为含有第二种活性物质(疏水性)的乳液滴的(类“Pickering”)稳定剂。共聚焦显微镜证实,两种共包封的活性物质占据了不同的乳液微结构区域;亲水性活性物质与乳液界面处的 NaCAS/CS 复合物相关联,而疏水性活性物质则存在于油滴中。借助于它们的分离共包封,两种活性物质表现出明显不同的释放行为。亲水性活性物质表现出触发释放,这是由 pH 值变化促进的,这削弱了蛋白质-多糖静电相互作用,导致颗粒溶胀。疏水性次级活性物质表现出持续释放,不受 pH 值影响,而是由穿过界面屏障的控制。因此,所采用的微观结构方法可以导致两种不相容的活性物质的分离共包封和独立释放,从而为开发含有多种活性物质的液体乳液制剂提供了希望。