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The composite materials combining quantum dots (QDs) and photonic crystals (PCs) could produce complex and high-dimensional anti-counterfeiting patterns, which solves the problems of simple coding information and low anti-counterfeiting level...

Novel approach has been constructed for preparing the amphiphilic star copolymer pH/reduction stimuli-responsive cross-linked micelles (SCMs) as a smart drug delivery system for the well-controlled anti-tumor drug doxorubicin (DOX) release. The SCMs had a low CMC value of 5.3 mg/L. The blank and DOX-loaded SCMs both had a spherical shape with sizes around 100–180 nm. In addition, the good stability and well pH/reduction-sensitivity of the SCMs were determined by dynamic light scattering (DLS) as well. The SCMs owned a low release of DOX in bloodstream and normal tissues while it had a fast release in tumor higher glutathione (GSH) concentration and/or lower pH value conditions, which demonstrates their pH/reduction dual-responsiveness. Furthermore, we conducted the thermodynamic analysis to study the interactions between the DOX and polymer micelles in the DOX release process. The values of the thermodynamic parameters at pH 7.4 and at pH 5.0 conditions indicated that the DOX release was endothermic and controlled mainly by the forces of an electrostatic interaction. At pH 5.0 with 10 mM GSH condition, electrostatic interaction, chemical bond, and hydrophobic interactions contributed together on DOX release. With the low cytotoxicity of blank SCMs and well cytotoxicity of DOX-loaded SCMs, the results indicated that the SCMs could form a smart cancer microenvironment-responsive drug delivery system. The release kinetic and thermodynamic analysis offer a theoretical foundation for the interaction between drug molecules and polymer matrices, which helps provide a roadmap for the oriented design and control of anti-cancer drug release for cancer therapy.

Gold nanoparticles (GNPs), usually fabricated through reduction and stabilization two steps, have been widely used in biomedical field. Here, the six-armed star copolymer was synthesized and self-assembled into crosslinked micelles for the in-situ preparation of GNPs in one-step without external reductant.The copolymer and their precursors were synthesized by a combination of ring-opening polymerization (ROP), activators regenerated by electron transfer atom transfer radical polymerization (ARGET ATRP), and Michael addition reaction. Their molecular weights and structures were measured by gel permeation chromatography (GPC) and 1 H NMR. The diselenide bond of crosslinked micelles reduced AuCl 4 À to GNPs, and the crosslinked micelles stabilized the GNPs in-situ. Through increasing AuCl 4 À concentration, the collision probability between the GNPs increased, with particle diameters of 1.5, 2.3, and 3.0 nm. Moreover, the GNPs showed good stability, and the wavelength of maximum absorbance (λ max ) did not change under different dilution, temperature, and storage conditions. Furthermore, integrating dissipative particle dynamics (DPD) simulations and scripts with experiments, the formation process of crosslinked micelles, the stabilization process, and the size regulation of GNPs at mesoscopic scale were revealed. Therefore, this stable crosslinked micelles/GNPs hybrid material is expected to be used as a nanocarrier in an integrated diagnosis and treatment system.