Xuan Mingjun, Shao Jingxin, Lin Xiankun, Dai Luru, He Qiang
State Key Lab of Urban Water Resource and Environment, Micro/Nanotechnology Research Centre, Harbin Institute of Technology, Harbin 150080 (P.R. China).
Chemphyschem. 2014 Aug 4;15(11):2255-60. doi: 10.1002/cphc.201402111. Epub 2014 Apr 16.
The synthesis of an innovative self-propelled Janus nanomotor with a diameter of about 75 nm that can be used as a drug carrier is described. The Janus nanomotor is based on mesoporous silica nanoparticles (MSNs) with chromium/platinum metallic caps and propelled by decomposing hydrogen peroxide to generate oxygen as a driving force with speeds up to 20.2 μm s(-1) (about 267 body lengths per second). The diffusion coefficient (D) of nanomotors with different H2 O2 concentrations is calculated by tracking the movement of individual particles recorded by means of a self-assembled fluorescence microscope and is significantly larger than free Brownian motion. The traction of a single Janus MSN nanomotor is estimated to be about 13.47×10(-15) N. Finally, intracellular localization and drug release in vitro shows that the amount of Janus MSN nanomotors entering the cells is more than MSNs with same culture time and particle concentrations, meanwhile anticancer drug doxorubicin hydrochloride loaded in Janus MSNs can be slowly released by biodegradation of lipid bilayers in cells.
本文描述了一种创新的自驱动 Janus 纳米马达的合成,其直径约为 75 纳米,可用作药物载体。该 Janus 纳米马达基于带有铬/铂金属帽的介孔二氧化硅纳米颗粒(MSN),通过分解过氧化氢产生氧气作为驱动力来推动,速度高达 20.2 μm·s⁻¹(约每秒 267 个体长)。通过跟踪自组装荧光显微镜记录的单个颗粒的运动,计算了不同过氧化氢浓度下纳米马达的扩散系数(D),其明显大于自由布朗运动。单个 Janus MSN 纳米马达的牵引力估计约为 13.47×10⁻¹⁵ N。最后,体外细胞内定位和药物释放表明,在相同培养时间和颗粒浓度下,进入细胞的 Janus MSN 纳米马达数量多于 MSN,同时负载在 Janus MSN 中的抗癌药物盐酸多柔比星可通过细胞内脂质双层的生物降解缓慢释放。