Dragar Črt, Potrč Tanja, Nemec Sebastjan, Roškar Robert, Pajk Stane, Kocbek Petra, Kralj Slavko
Department for Materials Synthesis, Jožef Stefan Institute, 1000 Ljubljana, Slovenia.
Faculty of Pharmacy, University of Ljubljana, 1000 Ljubljana, Slovenia.
Materials (Basel). 2019 Feb 12;12(3):540. doi: 10.3390/ma12030540.
The development of various magnetically-responsive nanostructures is of great importance in biomedicine. The controlled assembly of many small superparamagnetic nanocrystals into large multi-core clusters is needed for effective magnetic drug delivery. Here, we present a novel one-pot method for the preparation of multi-core clusters for drug delivery (i.e., magnetic nanocarriers). The method is based on hot homogenization of a hydrophobic phase containing a nonpolar surfactant into an aqueous phase, using ultrasonication. The solvent-free hydrophobic phase that contained tetradecan-1-ol, γ-Fe₂O₃ nanocrystals, orlistat, and surfactant was dispersed into a warm aqueous surfactant solution, with the formation of small droplets. Then, a pre-cooled aqueous phase was added for rapid cooling and the formation of solid magnetic nanocarriers. Two different nonpolar surfactants, polyethylene glycol dodecyl ether (B4) and our own ¹,¹-dimethyl-²-(tricosan-12-yl)ethane-1,2-diamine (SP11), were investigated for the preparation of MC-B4 and MC-SP11 magnetic nanocarriers, respectively. The nanocarriers formed were of spherical shape, with mean hydrodynamic sizes <160 nm, good colloidal stability, and high drug loading (7.65 wt.%). The MC-B4 nanocarriers showed prolonged drug release, while no drug release was seen for the MC-SP11 nanocarriers over the same time frame. Thus, the selection of a nonpolar surfactant for preparation of magnetic nanocarriers is crucial to enable drug release from nanocarrier.
各种磁响应纳米结构的发展在生物医学中具有重要意义。为了实现有效的磁性药物递送,需要将许多小的超顺磁性纳米晶体可控组装成大型多核簇。在此,我们提出了一种用于制备用于药物递送的多核簇(即磁性纳米载体)的新型一锅法。该方法基于使用超声处理将含有非极性表面活性剂的疏水相热均质化到水相中。将含有十四烷 -1-醇、γ-Fe₂O₃纳米晶体、奥利司他和表面活性剂的无溶剂疏水相分散到温热的水性表面活性剂溶液中,形成小液滴。然后,加入预冷的水相进行快速冷却并形成固体磁性纳米载体。分别研究了两种不同的非极性表面活性剂,聚乙二醇十二烷基醚(B4)和我们自己的1,1-二甲基-2-(二十三烷-12-基)乙烷-1,2-二胺(SP11),用于制备MC-B4和MC-SP11磁性纳米载体。形成的纳米载体呈球形,平均流体动力学尺寸<160 nm,具有良好的胶体稳定性和高载药量(7.65 wt.%)。MC-B4纳米载体显示出药物的持续释放,而在相同的时间范围内,MC-SP11纳米载体未见药物释放。因此,选择用于制备磁性纳米载体的非极性表面活性剂对于实现纳米载体的药物释放至关重要。