This research may spur the use of enzyme-activatable fluorescent probes for the progress of tumor diagnosis and image-guided surgery (IGS).Diarrheal illnesses from enteric pathogens are a leading cause of death in children under five in low- and middle-income countries (LMICs). Sanitation is one way to reduce the spread of enteric pathogens in the environment; however, few studies have investigated the effectiveness of sanitation in rural LMICs in reducing pathogens in the environment. In this study, we measured the impact of a sanitation intervention (dual-pit latrines, sani-scoops, child potties delivered as part of a randomized control trial, WASH Benefits) in rural Bangladeshi household compounds by assessing prevalence ratios, differences, and changes in the concentration of pathogen genes and host-specific fecal markers. We found no difference in the prevalence of pathogenic Escherichia coli, norovirus, or Giardia genes in the domestic environment in the sanitation and control arms. The prevalence of the human fecal marker was lower on child hands and the concentration of animal fecal marker was lower on mother hands in the sanitation arm in adjusted models, but these associations were not significant after correcting for multiple comparisons. In the subset of households with ≥10 individuals per compound, the prevalence of enterotoxigenic E. coli genes on child hands was lower in the sanitation arm. Incomplete removal of child and animal feces or the compound (versus community-wide) scale of intervention could explain the limited impacts of improved sanitation.Cellulose nanofibrils (CNFs) prepared from wood biomass are promising candidates to replace oil-based materials in, for example, packaging applications. However, CNFs' affinity for water combined with their small size leads to very slow and energy-demanding processes for handling and removal of water. To a large extent, this is the major roadblock that prevents a feasible production of dry CNF-based materials on an industrial scale. In this work, self-fibrillating fibers (SFFs) from wood, where the fibrils can be liberated by external stimuli, were prepared via sequential TEMPO and periodate oxidation reactions. Papers made from these modified fibers using conventional laboratory papermaking methods were then in situ nanofibrillated via a modest pH increase. With a dewatering time of less than 10 s for a 3 g/L dispersion, SFFs represent a major improvement over conventional CNF nanopapers that take approximately 6 h to dewater. Moreover, 100 g/m2 nanopapers obtained through in situ fibrillation exhibited comparable, if not superior, properties to those reported for conventionally made CNF films. A tensile strength of 184 MPa, a Young's modulus of 5.2 GPa, a strain at break of 4.6%, 90% optical transmittance, and an oxygen permeability of 0.7 cm3 μm m-2 d-1 kPa-1 at 50% RH were measured for SFF nanopapers. Furthermore, in situ nanofibrillation of the SFFs can also be achieved from already dried papers, facilitating numerous possibilities in terms of logistics and handling for an industrial scale-up and transportation of nanomaterials. Overall, stimuli-induced SFFs indeed enable a rapid production of strong, transparent, gas barrier nanopapers, which likely can be industrially scaled up and eventually compete with the oil-based plastics in the market for packaging materials.In this work, a cleancap-regulated aggregation-induced emission (AIE) strategy based on copper nanoclusters (CuNCs) was developed with stepwise recognition for highly specific analysis of the enzyme. The dissolved CuNCs with AIE characteristics in alkaline solution were prepared by using p-mercaptophenylboronic acid as the reducing agent and the stabilizing ligand. The prepared CuNCs can specifically conjugate with glucose (Glu) to connect with each other via the rapid boronate esters formation between boronic acids of CuNCs and a pair of cis-diols on Glu. selleck The cleancap-regulated AIE strategy was further identified by modification of CuNCs with d-glucose 6-phosphate (P-Glu) as the capper and substrate. Introduction of alkaline phosphatase to the P-Glu/CuNCs complex can induce the cleavage of phosphate group to activate the 5,6-diol of Glu on the CuNCs. The decapped complexes could be aggregated through further conjugation between 5,6-diol and boronic acid of two CuNCs, resulting in strong red AIE luminescence. The dual recognitions of enzymatic cleavage and cis-diols/boronic acid conjugation endow the designed method with highly specific detection and cell imaging of enzymatic activity. The cleancap-regulated AIE strategy provides a universal tool for regulation of AIE phenomenon in trace analysis.Supramolecular systems are intrinsically dynamic and sensitive to changes in molecular structure and external conditions. Because of these unique properties, strategies to control polymer length, composition, comonomer sequence, and morphology have to be developed for sufficient control over supramolecular copolymerizations. We designed photoresponsive, mono acyl hydrazone functionalized benzene-1,3,5-tricarboxamide (m-BTA) monomers that play a dual role in the coassembly with achiral alkyl BTAs (a-BTA). In the E isomer form, the chiral m-BTA monomers intercalate into stacks of a-BTA and dictate the chirality of the helices. Photoisomerization to the Z isomer transforms the intercalator into a chain capper, allowing dynamic shortening of chain length in the supramolecular aggregates. We combine optical spectroscopy and light-scattering experiments with theoretical modeling to show the reversible decrease in length when switching from the E to Z isomer of m-BTA in the copolymer with inert a-BTA. With a mass-balance thermodynamic model, we gain additional insights into the composition of copolymers and length distributions of the species over a broad range of concentrations and mixing ratios of a-BTA/m-BTA. Moreover, the model was used to predict the impact of an additive (chain capper and intercalator) on the chain length over a range of concentrations, showing a remarkable amplification of efficiency at high concentrations. By employing a stimuli-responsive comonomer in a mostly inert polymer, we can cooperatively amplify the effect of the switching and obtain photocontrol of polymer length. Moreover, this dynamic decrease in chain length causes a macroscopic gel-to-sol phase transformation of the copolymer gel, although 99.4% of the organogel is inert to the light stimulus.selleck