Enhanced anti-tumor activity of transferrin/folate dual-targeting magnetic nanoparticles using chemo-thermo therapy on retinoblastoma cancer cells Y79.

Malignant neoplasms are one of the main causes of death, especially in children, on a global scale, despite strenuous efforts made at advancing both diagnostic and therapeutic modalities. In this regard, a new nanocarrier Vincristine (VCR)-loaded Pluronic f127 polymer-coated magnetic nanoparticles conjugated with folic acid and transferrin (PMNP-VCR-FA-TF) were synthesized and characterized by various methods. The cytotoxicity of these nanoparticles was evaluated in vitro and ex vivo conditions. The in vitro anti-tumor effect of the nanoparticles was evaluated by colony formation assay (CFA) and reactive oxygen species (ROS) in Y79 cell line. The results showed that nanoparticles with two ligands conferred greater toxicity toward Y79 cancer cells than ARPE19 normal cells. Under an alternating magnetic field (AMF), these nanoparticles demonstrated a high specific absorption rate. The CFA and ROS results indicated that the AMF in combination with PMNP-VCR-FA-TF conferred the highest cytotoxicity toward Y79 cells compared with other groups (P < 0.05). PMNP-VCR-FA-TF could play an important role in converting externally applied radiofrequency energy into heat in cancer cells. The present study confirmed that dual targeting chemo-hyperthermia using PMNP-VCR-FA-TF was significantly more effective than hyperthermia or chemotherapy alone, providing a promising platform for precision drug delivery as an essential component in the chemotherapy of retinoblastoma.

Self-/Magnetic-Propelled Catalytic Nanomotors Based on a Janus SPION@PEG-Pt/PCL Hybrid Nanoarchitecture: Single-Particle versus Collective Motions.

In this paper, we synthesized superparamagnetic iron oxide nanoparticles (NPs) functionalized with (3-aminopropyl)triethoxysilane (Fe3O4@APTES). The synthesized NPs were coated with succinic anhydride (Fe3O4@COOH) in the next step. Half the surface of the NPs was shielded with wax microparticles via the Pickering emulsion technique, and the unshielded side was covered with poly(ethylene glycol) methyl ether. Platinum nanoparticles (Pt NPs) were deposited between PEG chains by the oxidation-reduction method through an in situ procedure to obtain a metal-polymer composite. These deposited Pt NPs have the potential to catalyze the decomposition of hydrogen peroxide at the surface of Janus nanomotors (JNMs). After de-waxing of the NPs, Irgacure 2959 (as the initiator) was reacted with the bare side of the NPs to provide the opportunity to grow poly(ε-caprolactone) (PCL) chains on the surface of the nanomotors through the "grafting from" method. The diffusion coefficient and velocity of the JNMs (before and after the PCL reaction) in the aqueous solution of 1, 2, 3, 5, and 10% (w/w) hydrogen peroxide and in the presence of different concentrations of NaCl solutions (0, 5, and 10% (w/v)) were investigated by mean square displacement analysis for single-particle or collective motions of JNMs. In addition, the simultaneous effect of an external magnetic field and the NaCl concentration on the movement direction of JNMs was also evaluated in the presence of hydrogen peroxide (10%). Increasing the ionic strength through NaCl addition permits the JNMs to move with relatively lower amounts of fuel [i.e., 2% (w/w)]. The collective motion investigation of the JNMs showed the highest speed in the media with 10% (w/w) hydrogen peroxide and 5% (w/v) NaCl solution (about 1215.78 µm2/s) due to the surfactant effect of the Janus architecture.