Huang Yanqi, Verduijn Joost, Coenye Tom, Liu Pengfei, Skirtach Andre G, Parakhonskiy Bogdan V
Nano-Biotechnology Group, Faculty of Bioscience Engineering, Ghent University, 9000 Ghent, Belgium.
LPM Laboratory of Pharmaceutical Microbiology, Ghent University, 9000 Ghent, Belgium.
Int J Biol Macromol. 2025 May;305(Pt 1):141047. doi: 10.1016/j.ijbiomac.2025.141047. Epub 2025 Feb 16.
Porous vaterite particles exhibit good biocompatibility, degradability, and favorable physical and chemical properties, making them promising candidates for drug carriers. However, challenges such as low loading capacity, burst release effect and limited antibacterial properties hinder their practical applications. Herein, submicron vaterite particles were synthesized at low temperature and modified by stearic acid, and the resulting modified vaterite particles (Vc) possess exceptional loading capacity towards a typical anticancer drug - doxorubicin. Quaternary ammonium chitosan (QCS) with antibacterial properties was synthesized by chemically modifying chitosan and was coated onto the surface of Vc/Dox through electrostatic adsorption. AgCO nanoparticles were uniformly deposited on the surface of Vc/Dox/QCS through the reaction between Ag and CO, while a small amount of Ag nanoparticles was generated through the reduction of adsorbed Ag, which was attributed to the reducing properties of -NH and aldehyde groups. Aldehyde functionalized hyaluronic acid was adsorbed on the outermost layer as a targeting polymer with the ability to induce cellular interaction. The composite (Vc/Dox/QCS/Ag/AHA) showed excellent sustained release and pH responsiveness, and the presence of QCS, Ag, and AgCO nanoparticles provided good antibacterial properties for the composite particles. In addition, cell experiments confirmed the almost no-cytotoxic properties and effective cellular interaction of the composite particles treated by low Ag concentration solutions. Compared with various micro-nanoparticles, this study ingeniously employed multifunctional polymers, Layer-by-Layer (LbL) technique, and modified inorganic nanoparticles to address the limitations of vaterite particles, paving the way for enhanced drug delivery applications and inspiring the development of multifunctional targeted drug capsules.
多孔球霰石颗粒具有良好的生物相容性、可降解性以及优良的物理和化学性质,使其成为药物载体的有潜力候选者。然而,诸如低载药量、突释效应和有限的抗菌性能等挑战阻碍了它们的实际应用。在此,通过低温合成了亚微米级球霰石颗粒并用硬脂酸进行修饰,所得的修饰球霰石颗粒(Vc)对典型抗癌药物阿霉素具有优异的载药量。通过对壳聚糖进行化学修饰合成了具有抗菌性能的季铵化壳聚糖(QCS),并通过静电吸附将其包覆在Vc/Dox表面。通过Ag与CO之间的反应,AgCO纳米颗粒均匀沉积在Vc/Dox/QCS表面,同时通过吸附的Ag的还原产生少量Ag纳米颗粒,这归因于-NH和醛基的还原性能。醛基官能化的透明质酸作为具有诱导细胞相互作用能力的靶向聚合物吸附在最外层。该复合材料(Vc/Dox/QCS/Ag/AHA)表现出优异的缓释性能和pH响应性,并且QCS、Ag和AgCO纳米颗粒的存在为复合颗粒提供了良好的抗菌性能。此外,细胞实验证实了低Ag浓度溶液处理的复合颗粒几乎无细胞毒性且具有有效的细胞相互作用。与各种微纳米颗粒相比,本研究巧妙地采用多功能聚合物、层层(LbL)技术和修饰的无机纳米颗粒来解决球霰石颗粒的局限性,为增强药物递送应用铺平了道路,并激发了多功能靶向药物胶囊的开发。