Gerasimovich Evgeniia, Kriukova Irina, Shishkov Vsevolod V, Efremov Yuri M, Timashev Peter S, Karaulov Alexander, Nabiev Igor, Sukhanova Alyona
Life Improvement by Future Technologies (LIFT) Center, 143025 Moscow, Russian Federation.
Laboratory of Nano-Bioengineering, National Research Nuclear University MEPhI (Moscow Engineering Physics Institute), 115522 Moscow, Russian Federation.
ACS Omega. 2024 Jun 28;9(27):29739-29750. doi: 10.1021/acsomega.4c03307. eCollection 2024 Jul 9.
Polyelectrolyte microparticles (MPs) synthesized on calcium carbonate cores are considered a promising basis for new drug delivery systems. It is known that microparticles entering a physiological environment absorb proteins on their surface, which can change the properties of the microparticles and alter their functional activity. This study aimed to compare the compositions of the adsorbed protein layer formed on microparticles with the core/shell and shell structures obtained by layer-by-layer deposition. The difference in the microparticle structure was associated with changes in their surface topography and ζ-potential. These microparticles were incubated with human serum or plasma at 37°C for 24 h. The adsorbed proteins were eluted and analyzed by means of SDS-PAGE. The protein composition of the eluates was determined by liquid chromatography-tandem mass spectrometry (LC-MS/MS); a total of 357 proteins were identified, and 183 of them were detected in all samples. Our results demonstrate that the relative abundance of proteins of different functional groups (immunoglobulins, complement proteins, and apolipoproteins) varied depending on the structure and surface characteristics of the polyelectrolyte microparticles and the incubation medium. Our findings expand the understanding of the influence of the physicochemical properties of the microparticles on their interaction with proteins, which can help to improve the design of microparticles for drug delivery.
在碳酸钙核上合成的聚电解质微粒(MPs)被认为是新型药物递送系统的一个有前景的基础。已知进入生理环境的微粒会在其表面吸附蛋白质,这会改变微粒的性质并改变其功能活性。本研究旨在比较在具有核/壳和通过层层沉积获得的壳结构的微粒上形成的吸附蛋白层的组成。微粒结构的差异与它们的表面形貌和ζ电位的变化有关。将这些微粒在37°C下与人血清或血浆孵育24小时。洗脱吸附的蛋白质并通过SDS-PAGE进行分析。通过液相色谱-串联质谱(LC-MS/MS)测定洗脱液的蛋白质组成;共鉴定出357种蛋白质,其中183种在所有样品中均被检测到。我们的结果表明,不同功能组(免疫球蛋白、补体蛋白和载脂蛋白)的蛋白质相对丰度因聚电解质微粒的结构和表面特性以及孵育介质而异。我们的发现扩展了对微粒物理化学性质对其与蛋白质相互作用影响的理解,这有助于改进用于药物递送的微粒设计。