The efficient delivery of biopharmaceutical drugs such as proteins and peptides into the cytosol of target cells poses substantial challenges owing to their large size and susceptibility to degradation. Current protein delivery vehicles have limitations such as the need for protein modification, insufficient delivery of large-size proteins or small peptides, and loss of protein function after the delivery. Here, we adopted a rational approach to design a polymer with robust efficacy for intracellular protein and peptide delivery. The polymer is composed of a dendrimer scaffold, a hydrophobic membrane-disruptive region, and a multivalent protein binding surface. It allows efficient protein/peptide binding, endocytosis, and endosomal disruption and is capable of efficiently delivering various biomacromolecules including bovine serum albumin, R-phycoerythrin, p53, saporin, β-galactosidase, and peptides into the cytosol of living cells. Transduction of apoptotic proteins and peptides successfully induces apoptosis in cancer cells, suggesting that the activities of proteins and peptides are maintained during the delivery. This technology represents an efficient and useful tool for intracellular protein and peptide delivery and has broad applicability for basic research and clinical applications.

Multiwall carbon nanotubes were dispersed in Nafion (MWCNTs-NA) solution and used in combination with bismuth (MWCNTs-NA/Bi) for fabricating composite sensors to determine trace Pb(II) and Cd(II) by differential pulse anodic stripping voltammetry (DPASV). The electrochemical properties of the MWCNTs-NA/Bi composites film modified glassy carbon electrode (GCE) were evaluated. The synergistic effect of MWCNTs and bismuth composite film was obtained for Pb(II) and Cd(II) detection with improved sensitivity and reproducibility. Linear calibration curves ranged from 0.05 to 100 mg/L for Pb(II) and 0.08 to 100 mg/L for Cd(II). The determination limits (S/N ¼ 3) were 25 ng/L for Pb and 40 ng/L for Cd, which compared favorably with previously reported methods in the area of electrochemical Pb(II) and Cd(II) detection. The MWCNTs-NA/Bi composite film electrodes were successfully applied to determine Pb(II) and Cd(II) in real sample, and the results of the present method agreed well with those of atomic absorption spectroscopy.

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Multistimuli‐responsive hydrogels with specific functions have attracted great interest for biomedical applications; however, these smart hydrogels usually require the presynthesis of macromolecular building blocks with multiple ligands and the integration of bioactive cargoes into the gels. Here, a multistimuli‐responsive hydrogel with potent antibacterial activity by a combination of supramolecular assembly and iminoboronate chemistry is reported. The hydrogel consists of all‐small‐molecule building blocks including aminoglycoside, guanosine, potassium ion, and a bifunctional anchor bearing both boronic acid and aldehyde groups. Guanosines form quadruplexes in the presence of potassium ions via supramolecular assembly, and the bifunctional anchor connects aminoglycosides, a class of potent antibiotics to cis‐diol groups on quadruplexes via dynamic iminoboronate chemistry, yielding a smart hydrogel containing abundant antibiotics. The hydrogel is sensitive to multistimuli such as heat, acids, oxidants, glucose and crown ether, which promote the release of antibiotics from the gels. Moreover, the prepared hydrogels show potent antibacterial activities both in vitro and in vivo. The results provide a new option to prepare antibacterial hydrogels with multistimuli responsiveness via facile chemistry using all‐small‐molecule building blocks.

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