Institute of Theoretical and Experimental Biophysics, Russian Academy of Science, Institutskaya St., 3, 142290, Puschino, Moscow Region, Russia.
Sci Rep. 2022 Mar 7;12(1):4032. doi: 10.1038/s41598-022-08054-x.
Polyelectrolyte microcapsules can be applied as microcontainers for the delivery of a wide range of substances, and it is important to search for new methods for capsule destruction and releasing substances from them. In this work, we studied the possibility of using sodium dodecyl sulfonate (SDS) for the release of fluorescein isothiocyanate-dextran from six-layer microcapsules composed of PAH and PSS. It was shown that the presence of SDS in the medium, at a concentration of 3000 μg/ml, leads to the destruction of polyelectrolyte microcapsules and the release of the substance from them (54% of the amount of the encapsulated substance), while the main part of the FITC-dextran released during the first hours of incubation. At an SDS concentration of 100 μg/ml, the substance released is uniform and is 44% in 24 h. At SDS concentrations from 50 to 100 μg/ml, the process of destruction of microcapsules proceeds more slowly. At SDS concentrations from 10 to 50 μg/ml, microcapsules are not degraded.
聚电解质微胶囊可用作广泛物质的递送微容器,寻找破坏胶囊并从中释放物质的新方法非常重要。在这项工作中,我们研究了使用十二烷基硫酸钠(SDS)从由 PAH 和 PSS 组成的六层微胶囊中释放荧光素异硫氰酸酯-葡聚糖的可能性。结果表明,在介质中存在 SDS(浓度为 3000μg/ml)会导致聚电解质微胶囊的破坏,并从其中释放出物质(包裹物质的 54%),而在孵育的最初几个小时内,主要部分的 FITC-葡聚糖被释放出来。在 SDS 浓度为 100μg/ml 时,释放的物质均匀,24 小时内释放 44%。在 SDS 浓度为 50 至 100μg/ml 时,微胶囊的破坏过程进行得更慢。在 SDS 浓度为 10 至 50μg/ml 时,微胶囊不会降解。