Data were expressed as average ± SD (n = 3). CLSM observation Confocal laser scanning microscopy (CLSM, Zeiss, LSM 510, Oberkochen,

Germany) was employed selleck inhibitor to examine the intracellular distribution of DOX. HepG2 cells were seeded on slides on a 6-well plate at a density of 4 × 105 cells/well in 2 mL of DMEM and were cultured for 24 h at 37°C in 5% CO2 atmosphere. The cells were then incubated with free DOX and DOX-loaded micelles at a final DOX concentration of 50 μg/mL in DMEM for 4 or 24 h at 37°C. At each predetermined time, the culture media were removed and the cells were washed with PBS (1 min × 3) to remove the DOX-loaded micelles that were not ingested by the cells. Subsequently, the cells were fixed with 4% (w/v) paraformaldehyde aqueous solution for 30 min at room temperature. The slides were then rinsed with PBS (2 min × 3). Finally, the cells were stained with Hoechst 33324 (5 mg/mL in PBS) at 37°C for 15 min, and the slides were rinsed with PBS (2 min × 3). The prepared slides were obtained by CLSM. Characterization 1H NMR spectra measurements were examined in d 6-DMSO and CDCl3 at 25°C using Bruker AVANCE ΙΙΙ 400 (Madison, WI, USA) operating at 400 MHz. The number average molecular weight (M n) and polydispersity index (M w/M n) were determined

by gel permeation chromatography (GPC) adopting an Agilent 1200 series GPC system (Santa Clara, CA, USA) equipped with a LC quant pump, PL gel 5 mm 500, 104, and 105 Å columns in series, and RI detector. The column system was calibrated NCT-501 ic50 with a set of monodisperse polystyrene standards using HPLC grade THF as mobile phase with a flow rate of 1.0 mL/min at 30°C. Fluorescence spectra were recorded using a fluorescence spectrophotometer (F-4500, Hitachi, Chiyoda-ku, Japan). The hydrodynamic diameter (D h) and distribution (PDI) of micelles were measured by dynamic

light scattering (DLS, Malvern Zetasizer Nano S, Malvern, WR, UK). Morphologies of micelles were investigated by transmission electron microscopy (TEM, Hitachi H-7650) operating at 80 kV. Results and discussion Synthesis and characterization of (PCL)2(PDEA-b-PPEGMA)2 A2(BC)2 miktoarm star polymers (PCL)2(PDEA-b-PPEGMA)2 were synthesized by using the difunctional initiator for HDAC inhibitor sequential ROP of ϵ-CL and continuous ARGET ATRP of DEA and PEGMA, Rucaparib purchase as illustrated in Figure 1. Representative 1H NMR spectra of (PCL)2-Br2 and (PCL)2(PDEA-b-PPEGMA)2 were depicted in Figure 2, and all of the peaks corresponding to characteristic hydrogen atoms were labeled. In Figure 2A, the characteristic signals at 1.96, 3.65, and 4.31 ppm were assigned, respectively, to -C(CH3)2-Br, −O-CH2-, and -COO-CH2- in the pentaerythritol unit, whereas the characteristic signals at 1.40, 1.66, 2.33, and 4.10 ppm were from -CH2- protons of PCL backbone. In Figure 2B, the signals at 0.90 and 1.82 to 1.92 ppm are assigned respectively to -CCH3 and -CH2- of methacrylate backbone.