An autonomously ultrafast self-healing, highly colourless, tear-resistant and compliant elastomer tailored for transparent electromagnetic interference shielding films integrated in flexible and optical electronics.

Considering the operation reliability of flexible and optical electronics (FOEs) in dynamic and real-world environments, autonomous self-healing electromagnetic interference (EMI) shielding materials with high transparency, good stretchability and excellent tear-resistance are urgently required but always difficult to achieve due to the poor dynamics of their elastic substrates. Herein, we propose a facile strategy to design a highly dynamic polyurea elastomer (PDMS-MPI-HDI) featuring with ultrahigh optical transparency (>94%), ultralow elastic modulus (<1 MPa), high tear-resistant stretchability (800%), and ultrafast autonomous self-healing (100 s for scratch-healing). Taking PDMS-MPI-HDI as a substrate for embedding silver nanowires (Ag NWs), the first transparent, stretchable and self-healable EMI shielding materials (Ag NWs/PDMS-MPI-HDI) are presented.

A Cell Membrane-Targeting Self-Delivery Chimeric Peptide for Enhanced Photodynamic Therapy and In Situ Therapeutic Feedback.

Nowadays, cell membrane-targeted therapy, which owns high antitumor efficacy by avoiding cell barriers, has received great attention. Here, a cell membrane-targeted self-delivery theranostic chimeric peptide CMP-PpIX is designed for simultaneously targeted photodynamic therapy (PDT) of tumor and real-time therapeutic feedback. Self-assembled CMP-PpIX nanoparticles can effectively accumulate in tumor by enhanced permeability and retention effect without additional vector.

Synthesis and in vitro cytotoxic evaluation of new 1H-benzo[d]imidazole derivatives of dehydroabietic acid.

A series of new 1H-benzo[d]imidazole derivatives of dehydroabietic acid were designed and synthesized as potent antitumor agents. Structures of the target molecules were characterized using MS, IR, H NMR, C NMR and elemental analyses. In the in vitro cytotoxic assay, most compounds showed significant cytotoxic activities against two hepatocarcinoma cells (SMMC-7721 and HepG2) and reduced cytotoxicity against noncancerous human hepatocyte (LO2).