Dendritic Mesoporous Silica Nanoparticles (DMSNs) are considered superior in the adsorption of unfavorable chemical compounds and biological pollutants. Herein, we have synthesized folic acid-terminated dendritic mesoporous silica nanoparticles (FA-DMSN) for the removal of cationic dyes, methylene blue (MB), from aqueous solutions. The structural, morphological, functional, specific surface area, pore size distribution, and thermal properties of the synthesized DMSNs were identified using a scanning electron microscope (SEM), a transmission electron microscope (TEM), Fourier transform infrared spectroscopy (FTIR), dynamic light scattering (DLS), Brunauer−Emmett−Teller (BET), and Thermogravimetric Analyzer (TGA). The synthesized DMSNs exhibited a high surface area (521 m^{2 −1}) and pore volume (1.2 cm³ g⁻¹). In addition, it features both wide pore size and narrow distributions, which strongly affect the adsorption performance in terms of the equilibrium uptake time. Moreover, the impact of pH, contacting time, and dye’s initial concentration on the removal efficiency of MB was studied. The extraction efficiency of FA-DMSN was found to be three times more effective than the bare DMSN materials. Langmuir isotherm fitted the experimental data very well with a correlation coefficient value of 0.99. According to the Langmuir model, the maximum adsorption capacity was 90.7 mg/g. Furthermore, the intra−particle diffusion model revealed a significantly fast intra-particle diffusion which can be attributed to the presence of the large pore’s channels. Finally, the fast adsorption of MB molecules, reaching their equilibrium capacity within tens of seconds, as well as the low cost and ease of FA-DMSN fabrication, makes the developed material an effective adsorbent for water remediations.

In this paper, a new pH-responsive nanosystem based on mesoporous silica nanoparticles (MSNs) was developed for cancer therapy. Poly(2-(diethylamino) ethyl methacrylate) (PDEAEMA) was grafted on their outer surface and acts as a gatekeeper, followed by subsequent modification of the polymer by cysteine (MSN-PDEAEMA-Cys) and poly(oligo(ethylene glycol) methyl ether methacrylate) (MSN-PDEAEMA-Cys-POEGMEMA). The physicochemical properties of these nanocarriers were characterized using scanning and transmission electron microscopies (SEM and TEM), Fourier-transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), and dynamic light scattering (DLS). The synthesized nanoparticles were well-dispersed with a diameter of ca. 200 nm. The obtained XPS results confirm the successful modification of MSN-PDEAEMA with Cys and POEGMEMA by increasing the peak intensity of C–O and C=O groups at 286.5 and 288.5 eV, respectively. An anti-cancer drug, doxorubicin (DOX), was encapsulated into the fabricated nanoplatform. The DOX release amount at physiological pH of 7.4 was limited (10%), while an accumulation drug release of ca. 35% was accomplished after 30 h in acidic media. The MTT cell line was used to assess the cytotoxicity of the unloaded and DOX-loaded fabricated nanoplatforms. Upon loading of DOX on these nanomaterials, they showed significant toxicity to human liver cancer cells. These results suggest that the prepared nano-structured materials showed good biocompatibility as well, and they can serve as nanocarriers for the delivery of anti-cancer drugs.

Magnetic mesoporous silica nanoparticles (Fe₃O₄-MSNs) were successfully synthesized with a relatively high surface area of 568 m²g⁻¹. Fe₃O₄-MSNs were then modified with poly(2-diethyl aminoethyl methacrylate) (PDEAEMA) brushes using surface-initiated ARGET atom transfer radical polymerization (ATRP) (Fe₃O₄@MSN-PDMAEMA). Since the charge of PDEAEMA is externally regulated by solution pH, tertiary amines in the polymer chains were quaternized using 2-iodoethanol to obtain cationic polymer chains with a permanent positive charge (Fe₃O₄@MSN-QPDMAEMA). The intensity of the C−O peak in the C1s X-ray photoelectron spectrum increased after reaction with 2-iodoethanol, suggesting that the quaternization process was successful. The applicability of the synthesized materials on the removal of methyl orange (MO), and sunset yellow (E110) dyes from an aqueous solution was examined. The effects of pH, contact time, and initial dyes concentrations on the removal performance were investigated by batch experiments. The results showed that the Fe₃O₄@MSN-PDMAEMA sample exhibited a weak adsorption performance toward both MO and E110, compared with Fe₃O₄@MSN-QPDMAEMA at a pH level above 5. The maximum adsorption capacities of MO and E110 using Fe₃O₄@MSN-QPDMAEMA were 294 mg g⁻¹ and 194.8 mg g⁻¹, respectively.