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The preparation of environment-friendly and efficient superhydrophobic filter screen still faces great challenges. Herein, a compact, solid cerium stearate superhydrophobic-coated stainless steel mesh (SSSM) was prepared by a simple, efficient, and environmentally friendly one-step electrodeposition process. Fourier transform infrared (FTIR) spectroscopy, energy-dispersive X-ray spectroscopy (EDS), scanning electron microscopy (SEM), and contact angle measurement were used to characterize the surface coating (composition, morphology, and contact angle) of SSSM. The results show that the SSSM surface is a dense mastoid cerium stearate micronanostructure coating, and its static contact angle with water can reach 162.73°. In addition, it has excellent self-cleaning performance for conventional simulated pollutants, and the contact angle can still reach 161° after 28 days of storage. In the wear resistance and corrosion resistance tests, the contact angle can still be kept above 150° after 600 mm abrasion under the load of 19.6 kPa, the corrosion current of SSSM is reduced by two orders of magnitude, and its corrosion inhibition efficiency reaches 99.74%. In addition, the oil/water separation performance of SSSM is also very good, and the separation efficiency for different oil/water mixtures exceeds 97%. This study will provide important data support and method reference for the preparation of metal anticorrosion superhydrophobic material coating and the development of environment-friendly and efficient oil–water separation materials. [ABSTRACT FROM AUTHOR]

The formation of nanoparticles (NPs) and surface properties such as size and charge are affected by the amphiphilic property of polymer, which is vital for evaluating their function. Here, we synthesized cholesteryl-modified aminated pullulan polymers (CHPNs) with different amounts of cholesterol succinate (CHS). We characterized the three hydrophobically modified polymers (CHPN1, CHPN2, and CHPN3) (CHS: Pu ‐ N H 2 = 1 / 5 , 2 / 5 , 3 / 5) by Fourier transform infrared spectrometry. Dynamic light scattering (DLS) was used to measure particle size and zeta potential of CHPN NPs. The particle sizes of the three NPs CHPN1, CHPN2, and CHPN3 were 178.0, 144.4, and 97.8 nm, respectively. The particle size was related to the cholesteryl substitution of polymers to a certain extent: the stronger the hydrophobicity, the smaller the particle size. In 48 h, the drug release for CHPN3 and CHPN1 NPs was 57.8% and 72.7%. Thus, the NPs showed good sustained drug release: the greater the degree of hydrophobic substitution, the better the sustained release. The cytotoxicity findings were reversed: CHPN1 NPs, with low hydrophobic substitution, showed the best inhibition of Lewis lung cancer cells. [ABSTRACT FROM AUTHOR]

To clarify nanoparticle-protein interaction and their action characteristics, the interactions between MTO-CHP NPs and human serum albumin (HSA) were studied by isothermal titration calorimetry (ITC), fluorescence spectroscopy, dynamic light scattering (DLS), and circular dichroism spectroscopy (CD). Hydrophobically modified pullulan (CHP) nanoparticles (NPs) loaded with mitoxantrone (MTO) were prepared (MTO-CHP NPs) with size 166.9 nm. The spherical shape was verified by transmission electron microscopy (TEM). The ITC results demonstrated an interaction between MTO-CHP NPs mainly by hydrophobic interaction force, electrostatic force, and hydrogen bonding. The mean binding constant KA was 0.832×104 M−1 and mean HSA coverage 0.939±0.302. MTO-CHP NPs could quench the fluorescence intensity of HSA, which gradually decreased to be balanced in 9 h and indicated the completion of the complexation. The size and zeta potential changes of the combined particle were dynamically detected with DLS at 0, 3, 6, 9, 12, 15, and 18 h. When the reaction was completed at 9 h, the particle size and potential remained stable, accompanied by a size change from 89.91 to about 145 nm and potential change from -15 to -3 mV, respectively. The results of CD measurement showed that the change in ellipticity of HSA at 208 nm was similar to the fluorescence spectra and DLS measurements with MTO-CHP NPs combined with HSA. At the beginning of the reaction, the proportion of α-helix was 52.3% to 43.7%, which decreased by 39.1% at compound stabilization. The release of MTO from MTO-CHP NPs at pH=5.6 was significantly accelerated, whereas that of MTO from HSA-MTO-CHP NPs was significantly reduced, and the drug release was significantly slowed down even under acidic conditions, which indicates the beneficial effect of HSA on the persistence and stability of the HSA-MTO-CHP NP compound. [ABSTRACT FROM AUTHOR]