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External light-independent antitumor PDT is successfully realized with a covalent organic framework (COF)-based host–guest nanosystem. Its highly effective antitumor behavior is fully demonstrated by both H2O2-overexpressed 4T1 and H2O2-less expressed HCT116 and MCF-7 xenograft models. [ABSTRACT FROM AUTHOR]

Herin, we report a Cu(II)-porphyrin-derived nanoscale COF, which can be triggered by endogenous H2S via an intracellular sulfidation reaction to generate a metal-free COF-photosensitizer for PDT against H2S-enriched colon tumors with controllable singlet oxygen release; meanwhile in situ generated CuS can be synchronously used as a photothermal agent for PTT. [ABSTRACT FROM AUTHOR]

Multifunctional drug delivery systems combining two or more therapies have a wide-range of potential for high efficacy tumor treatment. Herein, we designed a novel hollow mesoporous Prussian blue nanoparticles (HMPBs)-based platform for targeted and synergetic chemo-photothermal treatment of acute myeloid leukemia (AML). The HMPBs were first loaded with the anticancer drugs daunorubicin (DNR) and cytarabine (AraC), and were subsequently coated with polyethylenimine (PEI) through electrostatic adsorption. Then, zwitterionic sulfobetaine (ZS) and CXCR4 antagonist peptide E5 were modified onto the surface of the nanoparticles via covalent bonding to fabricate a nanoplatform (denoted as HMPBs(DNR + AraC)@PEI-ZS-E5). The nanoplatform showed excellent photothermal effects, superior photothermal stability, reduced nonspecific protein adsorption, efficient targeting capability, a constant hydrodynamic diameter and good biocompatibility. Additionally, a laser-responsive drug release pattern was observed. In vitro results indicated that the nanoplatform could achieve active targeting and remarkable chemo-photothermal synergetic therapeutic effects, showcasing its great potential in AML treatment. [ABSTRACT FROM AUTHOR]

Salmonella spp. are zoonotic pathogens of substantial public health concern. To enable detection in the field or under instrument-free conditions, we developed a rapid and robust lateral flow fluorescent immunoassay based on strand exchange amplification (SEA-LFIA) for the quantitative detection of Salmonella spp. As far as we know, this work is the first report regarding the use of Bst DNA polymerase-assisted SEA for fluorescence sensing to detect Salmonella spp. The SEA method was further confirmed by enzymatic digestion and Sanger dideoxy sequencing. The specificity of SEA-LFIA assay was verified by 89 Salmonella strains (18 Salmonella reference strains and 71 clinical isolates) and 15 non-Salmonella reference strains (different genera). The sensitivity of SEA-LFIA assay was 6 × 100 CFU mL−1 of Salmonella pure culture or 3 × 104 CFU 25 g−1 of artificially spiked raw chicken meat. Using this assay, it was found that 37 (16%) of the 236 samples collected were positive, which was consistent with the results of conventional PCR. The cutoff value is 15 and SEA-LFIA assay only takes ∼30 min without high equipment and reagent cost. In addition, the proposed strategy can be easily extended by redesigning the corresponding amplification primers to detect target analytes. In conclusion, the optimized SEA-LFIA assay is an efficient and specific method for the detection of Salmonella spp., and can potentially serve as a new on-site diagnostic tool in life sciences. [ABSTRACT FROM AUTHOR]

A visible light triggered protein delivery system has been assembled through hydroxyl coordinated onto titania nanoparticles. Biomolecules such as hemoglobin (Hb) can be controlled-released from the hybrid material TiO2–DB–Hb by switching visible light on/off. The released Hb not only retains its senior structure but also can fulfil the enzymatic bioactivity. Controlled delivery of Hb stems from the scission of the Ti–O coordination bond with the aid of photo-inducing electron transfer property of titania. [ABSTRACT FROM AUTHOR]

Herin, we report a Cu(ii)-porphyrin-derived nanoscale COF, which can be triggered by endogenous H 2 S via an intracellular sulfidation reaction to generate a metal-free COF-photosensitizer for PDT against H 2 S-enriched colon tumors with controllable singlet oxygen release; meanwhile in situ generated CuS can be synchronously used as a photothermal agent for PTT.

A N-O bond is introduced into hyperbranched polyimide photocatalysts for the first time to change their polarity and modulate electronic structure. Both of the changes help improve the photocatalytic ability of the polyimide. This strategy shows great prospect for synthesizing effective organic photocatalysts., (This journal is © The Royal Society of Chemistry 2012)