Doxorubicin conjugates: a practical approach for its cardiotoxicity alleviation.

INTRODUCTION: Doxorubicin (DOX) emerges as a cornerstone in the arsenal of potent chemotherapeutic agents. Yet, the clinical deployment of DOX is tarnished by its proclivity to induce severe cardiotoxic effects, culminating in heart failure and other consequential morbidities. In response, a panoply of strategies has undergone rigorous exploration over recent decades, all aimed at attenuating DOX's cardiotoxic impact. The advent of encapsulating DOX within lipidic or polymeric nanocarriers has yielded a dual triumph, augmenting DOX's therapeutic efficacy while mitigating its deleterious side effects. AREAS COVERED: Recent strides have spotlighted the emergence of DOX conjugates as particularly auspicious avenues for ameliorating DOX-induced cardiotoxicity. These conjugates entail the fusion of DOX through physical or chemical bonds with diminutive natural or synthetic moieties, polymers, biomolecules, and nanoparticles. This spectrum encompasses interventions that impinge upon DOX's cardiotoxic mechanism, modulate cellular uptake and localization, confer antioxidative properties, or refine cellular targeting. EXPERT OPINION: The endorsement of DOX conjugates as a compelling stratagem to mitigate DOX-induced cardiotoxicity resounds from this exegesis, amplifying safety margins and the therapeutic profile of this venerated chemotherapeutic agent. Within this ambit, DOX conjugates stand as a beacon of promise in the perpetual pursuit of refining chemotherapy-induced cardiac compromise.

Room-Temperature Synthesis of Thioether-Stabilized Ruthenium Nanocubes and Their Optical Properties.

Controlling the nucleation and growth processes for nanoparticle synthesis allows the development of well-defined structures that offer unique chemical and physical properties. Here, we report a wet chemical reduction method for synthesizing ruthenium nanocubes (Ru NCs) that display plasmonic properties at room temperature (RT). The growth of the particles to form nanostructured cubes was established by varying the carbon chain length of the thioether stabilizing ligands and the reaction time to produce stable and controlled growth. In this study, we found that the longer the thioether chain length, the less isotropic the shape of the particles. Short chain lengths of thioethers (ethyl sulfide and butyl sulfide) produced spherical nanoparticles, whereas longer chain lengths (hexyl sulfide and octyl sulfide) produced cubic nanoparticles. In addition, parameters such as the ligand to precursor ratio also played an important role in the homogeneity of the nanocubes. The Ru NCs were characterized by UV-visible absorbance spectroscopy, transmission electron microscopy (TEM), X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS), which supported a face-centered cubic (fcc) structure. Moreover, to demonstrate catalytic efficiency, we studied their ability to reduce benzaldehyde to benzyl alcohol, and the Ru NCs demonstrated an overall 78% efficiency at room temperature.

Recent Advances of Enzyme-Free Electrochemical Sensors for Flexible Electronics in the Detection of Organophosphorus Compounds: A Review.

Emerging materials integrated into high performance flexible electronics to detect environmental contaminants have received extensive attention worldwide. The accurate detection of widespread organophosphorus (OP) compounds in the environment is crucial due to their high toxicity even at low concentrations, which leads to acute health concerns. Therefore, developing rapid, highly sensitive, reliable, and facile analytical sensing techniques is necessary to monitor environmental, ecological, and food safety risks. Although enzyme-based sensors have better sensitivity, their practical usage is hindered due to their low specificity and stability. Therefore, among various detection methods of OP compounds, this review article focuses on the progress made in the development of enzyme-free electrochemical sensors as an effective nostrum. Further, the novel materials used in these sensors and their properties, synthesis methodologies, sensing strategies, analytical methods, detection limits, and stability are discussed. Finally, this article summarizes potential avenues for future prospective electrochemical sensors and the current challenges of enhancing the performance, stability, and shelf life.

Addressing Short-Chain PFAS Contamination in Water with Nanofibrous Adsorbent/Filter Material from Electrospinning.

ConspectusPer- and polyfluoroalkyl substances (PFAS) stand for thousands of fully/highly fluorinated aliphatic chemicals, which have been widely manufactured and used in consumer products. Due to easy deprotonation of headgroups and high strength of C-F bonds in their molecules, PFAS are water-soluble and extremely stable in our environment. Significant accumulation of PFAS in water bodies started as early as the beginning of their production in the late 1940s. Recent studies confirmed the occurrence and accumulation of PFAS in all human tissues as well as their harmful health effects. Upon environmental regulations and health advisories, the PFAS industry quickly shifted to short-chain PFAS, e.g., hexafluoropropylene oxide dimer acid and its ammonium salt (GenX), to replace traditional long-chain PFAS. According to the recent fact sheet by the U.S. Environmental Protection Agency (EPA) in October 2021, however, GenX turned out to be more toxic than people originally thought and has shown health effects on liver, kidney, immune system, and so forth upon animal tests. On June 15, 2022, the EPA released the final health advisory for GenX, which is just 10 ppt. Thus, there is an urgent need of novel adsorbents for highly effective GenX remediation from water.Until now, there have been just a few reports on the remediation of GenX from water despite its popular use. In this Account, we reviewed current technology on PFAS remediation and illustrated our research on how to use polyacrylonitrile (PAN), a common and economic polymer for water filtration, in the form of nanofibrous membrane with handy chemical surface modification to develop innovative adsorbent/filter material for effective and scalable GenX remediation from water at the largest HBCU in the nation together with opportunities and challenges that are associated with this research. For the first time, we compared the GenX removal capability of electrospun PAN (ESPAN) nanofibrous membrane and amidoxime surface-functionalized ESPAN (ASFPAN) nanofibrous membrane. By modifying the surface of ESPAN nanofibrous membrane and introducing amidoxime functional group, the maximum GenX removal capacity (weight-normalized GenX removal) was almost doubled and reached ∼0.6 mmol/g at pH 4, which is higher than or comparable to that of most reported adsorbents for GenX removal. Hydrophobic interaction and dipole-dipole interaction could be the GenX adsorption mechanism on the ESPAN nanofibrous membrane while surface hydrophilicity and electrostatic interaction play major roles in GenX adsorption on the ASFPAN nanofibrous membrane. Our research shed light on understanding the GenX adsorption mechanism and developing new adsorbent/filter materials for practical short-chain PFAS remediation from water.

Development of a nanocopper-decorated laser-scribed sensor for organophosphorus pesticide monitoring in aqueous samples.

Organophosphorus pesticides are widely used in industrial agriculture and have been associated with water pollution and negative impacts on local ecosystems and communities. There is a need for testing technologies to detect the presence of pesticide residues in water sources, especially in developing countries where access to standard laboratory methods is cost prohibitive. Herein, we outline the development of a facile electrochemical sensor for amperometric determination of organophosphorus pesticides in environmental water samples. A three-electrode system was fabricated via UV laser-inscribing on a polyimide film. The working electrode was functionalized with copper nanoparticles with affinity toward organophosphate compounds. The sensor showed a limit of detection (LOD) of 3.42 ± 1.69 µM for glyphosate, 7.28 ± 1.20 µM for glufosinate, and 17.78 ± 7.68 µM for aminomethylphosphonic acid (AMPA). Sensitivity was highest for glyphosate (145.52 ± 36.73 nA⋅µM-1⋅cm-2) followed by glufosinate (56.98 ± 10.87 nA⋅µM-1⋅cm-2), and AMPA (30.92 ± 8.51 nA⋅µM-1⋅cm-2). The response of the sensor is not significantly affected by the presence of several ions and organic molecules commonly present in natural water samples. The developed sensor shows promising potential for facilitating environmental monitoring of organophosphorus pesticide residues, which is a current need in several parts of the world.

Recent Trends and Advances of Co3O4 Nanoparticles in Environmental Remediation of Bacteria in Wastewater.

Antibiotic resistance is a formidable global threat. Wastewater is a contributing factor to the prevalence of antibiotic-resistant bacteria and genes in the environment. There is increased interest evident from research trends in exploring nanoparticles for the remediation of antibiotic-resistant bacteria. Cobalt oxide (Co3O4) nanoparticles have various technological, biomedical, and environmental applications. Beyond the environmental remediation applications of degradation or adsorption of dyes and organic pollutants, there is emerging research interest in the environmental remediation potential of Co3O4 nanoparticles and its nanocomposites on antibiotic-resistant and/or pathogenic bacteria. This review focuses on the recent trends and advances in remediation using Co3O4 nanoparticles and its nanocomposites on antibiotic-resistant or pathogenic bacteria from wastewater. Additionally, challenges and future directions that need to be addressed are discussed.

Highly sensitive plasmonic metal nanoparticle-based sensors for the detection of organophosphorus pesticides.

Plasmonic nanoparticles offer attractive benefits for the detection of environmental contaminants due to their high extinction coefficients and unique optical properties. Excess use of OP pesticides has been found to have adverse effects on human health and the environment. Here, we demonstrate the use of plasmonic silver (Ag), gold (Au) and bimetallic silver-gold (Ag-Au) nanoparticles (NPs) to detect and distinguish between organophosphorus (OP) pesticides. The NPs were found to detect the thion pesticides: ethion, parathion, malathion, and fenthion) in real time. In each case, the interaction of the pesticides with the plasmonic NPs were found to result in wavelength shifts of the localized surface plasmon resonance (LSPR) accompanied by color changes. The wavelength shifts were characteristic of the pesticide structure and concentration. The interaction between the sensors and the pesticide was a result of the soft metal surface binding to the soft sulfur atom of the pesticide. Similarly, oxon pesticides showed no effect on the LSPR of the NPs. The three plasmonic NPs showed limits of detections (LOD) in ppm range for all pesticides under real-time analysis. The LOD of Ag NPs with ethion, fenthion, malathion, and parathion were 9 ppm, 11 ppm, 18 ppm, and 44 ppm, respectively. The LOD of Au NPs with ethion, fenthion, malathion, parathion were 58 ppm, 53 ppm, 139 ppm, and 3203 ppm, respectively. Ag-Au NPs with ethion, fenthion, malathion, and parathion showed LOD values of 228 ppm, 231 ppm, 1189 ppm, and 1835 ppm, respectively. The ability of the plasmonic NPs to detect the selected pesticides in natural environments was tested under simulated natural conditions in the presence of dissolved organic matter (DOM). Steep gradients in the sedimentation plots revealed that the time dependent interaction of each OP pesticide with the NP surface was accompanied by a considerable change in the LSPR indicative of colloidal destabilization over time. All pesticides showed nearly the same trend in their sedimentation with the plasmonic NPs. The stability of the nanoparticles in the colloidal medium was described by classical DLVO theory, which showed that the net interaction was attractive.

Rapid prototyping of a novel and flexible paper based oxygen sensing patch via additive inkjet printing process.

A novel and flexible oxygen sensing patch was successfully developed for wearable, industrial, food packaging, pharmaceutical and biomedical applications using a cost-efficient and rapid prototypable additive inkjet print manufacturing process. An oxygen sensitive ink was formulated by dissolving ruthenium dye and ethyl cellulose polymer in ethanol in a 1 : 1 : 98 (w/w/w) ratio. The patch was fabricated by depositing the oxygen sensitive ink on a flexible parchment paper substrate using an inkjet printing process. A maximum absorbance from 430 nm to 480 nm and a fluorescence of 600 nm was observed for the oxygen sensitive ink. The capability of the oxygen sensitive patch was investigated by measuring the fluorescence quenching lifetime of the printed dye for varying oxygen concentration levels. A fluorescence lifetime decay (τ) from ≈4 µs to ≈1.9 µs was calculated for the printed oxygen sensor patch, for oxygen concentrations varying from ≈5 mg L-1 to ≈25 mg L-1. A sensitivity of 0.11 µs mg L-1 and a correlation coefficient of 0.9315 was measured for the printed patches. The results demonstrated the feasibility of employing an inkjet printing process for the rapid prototyping of flexible and moisture resistant oxygen sensitive patches which facilitates a non-invasive method for monitoring oxygen and its concentration levels.

Synthesis of a novel hexaazatriphenylene derivative for the selective detection of copper ions in aqueous solution.

A hexaazatriphenylene (HAT) derivative, naphtho[2,3-h]naphtho[2',3':7,8]quinoxalino[2,3-a]naphtho[2',3':7,8]quinoxalino[2,3-c]phenazine-5,10,15,20,25,30-hexaone (NQH) was synthesized, characterized, and found to have novel properties in being selective toward the detection of copper (Cu2+) ions. The capability of NQH to be employed as a colorimetric, chemo-fluorescence and electrochemical sensor for the detection of Cu2+ was demonstrated by performing UV-Vis absorbance, fluorescence intensity, and cyclic voltammetry (CV) measurements. The interaction between NQH and Cu2+ was initially observed with an obvious color change from yellow to brown upon the addition of Cu2+ ions to NQH. The interaction was also confirmed by UV-Vis absorbance, fluorescence intensity, and mass spectroscopy (MS/MS) measurements. UV absorbance, fluorescence and CV of NQH toward Cu2+ showed good linearity with a detection limit of 3.32 µM, 2.20 µM and 0.78 µM, respectively, which are lower than the toxicity levels of copper in drinking water (20-30 µM) set by the U.S. Environmental Protection Agency (EPA) and World Health Organization (WHO). A 1 : 2 stoichiometry complexation between NQH and Cu2+ was confirmed by Job's plot and MS/MS. In addition, the selectivity and sensitivity of the NQH compound towards Cu2+ ions were further confirmed by performing CV on a screen printed flexible and planar electrochemical sensor.

A highly sensitive printed humidity sensor based on a functionalized MWCNT/HEC composite for flexible electronics application.

A novel functionalized multi-walled carbon nanotube (FMWCNT)/hydroxyethyl cellulose (HEC) composite-based humidity sensor was successfully developed for humidity monitoring applications. FMWCNTs were synthesized by covalently functionalizing multi-walled carbon nanotubes (MWCNTs) in a mixture of sulfuric and nitric acid to enhance their hydrophilicity. The FMWCNTs were characterized using transmission electron microscopy, Raman spectroscopy, Fourier transform infrared spectroscopy and dispersion analysis to verify the presence of functional hydroxyl and carboxyl groups. A FMWCNT/HEC (1 : 6 w/w) composite ink was formulated using the solution blending technique with 2.5 wt% FMWCNTs. A multi-layered humidity sensor was fabricated using additive print manufacturing processes on a flexible polyethylene terephthalate (PET) substrate. Screen printing and gravure printing processes were used to deposit the bottom silver (Ag) electrode and FWMCNT/HEC sensing layers, respectively. The capability of the fabricated humidity sensor was investigated by measuring its resistive response towards relative humidity (RH) varying from 20% RH to 80% RH. As the RH was increased from 20% RH to 80% RH in steps of 10% RH at 25 °C, it was observed that the resistance of the printed sensor increased linearly. The printed sensor demonstrated resistance changes as high as ≈290% at 80% RH, when compared to its base resistance at 20% RH. A sensitivity and a response time of 0.048/%RH and ≈20 s were obtained for the printed sensor, respectively. The results thus demonstrated the feasibility of employing additive print manufacturing processes to develop a highly sensitive sensor for humidity monitoring applications.

Effect of Iron Oxide Nanoparticles and Amoxicillin on Bacterial Growth in the Presence of Dissolved Organic Carbon.

The impact of emerging contaminants in the presence of active pharmaceutical pollutants plays an important role in the persistence and activity of environmental bacteria. This manuscript focuses on the impact of amoxicillin functionalized iron oxide nanoparticles on bacterial growth, in the presence of dissolved organic carbon (humic acid). The impact of these emerging contaminants individually and collectively on the growth profiles of model gram positive and negative bacteria was tracked for 24 h. Results indicate exposure to subinhibitory concentrations of amoxicillin bound iron oxide nanoparticles, in the presence of humic acid, increase bacterial growth in Pseudomonas aeruginosa and Staphylococcus aureus. Accelerated bacterial growth was associated with an increase in iron ions, which have been shown to influence upregulation of cellular metabolism. Though iron oxide nanoparticles are often regarded as benign, this work demonstrates the distinguishable impact of amoxicillin bound iron oxide nanoparticles in the presence of dissolved organic carbon. The results indicate differential impacts of combined contaminants on bacterial growth, having potential implications for environmental and human health.

Mutagenic Effects of Iron Oxide Nanoparticles on Biological Cells.

In recent years, there has been an increased interest in the design and use of iron oxide materials with nanoscale dimensions for magnetic, catalytic, biomedical, and electronic applications. The increased manufacture and use of iron oxide nanoparticles (IONPs) in consumer products as well as industrial processes is expected to lead to the unintentional release of IONPs into the environment. The impact of IONPs on the environment and on biological species is not well understood but remains a concern due to the increased chemical reactivity of nanoparticles relative to their bulk counterparts. This review article describes the impact of IONPs on cellular genetic components. The mutagenic impact of IONPs may damage an organism's ability to develop or reproduce. To date, there has been experimental evidence of IONPs having mutagenic interactions on human cell lines including lymphoblastoids, fibroblasts, microvascular endothelial cells, bone marrow cells, lung epithelial cells, alveolar type II like epithelial cells, bronchial fibroblasts, skin epithelial cells, hepatocytes, cerebral endothelial cells, fibrosarcoma cells, breast carcinoma cells, lung carcinoma cells, and cervix carcinoma cells. Other cell lines including the Chinese hamster ovary cells, mouse fibroblast cells, murine fibroblast cells, Mytilus galloprovincialis sperm cells, mice lung cells, murine alveolar macrophages, mice hepatic and renal tissue cells, and vero cells have also shown mutagenic effects upon exposure to IONPs. We further show the influence of IONPs on microorganisms in the presence and absence of dissolved organic carbon. The results shed light on the OPEN ACCESS Int. J. Mol. Sci. 2015, 16 23483 transformations IONPs undergo in the environment and the nature of the potential mutagenic impact on biological cells.

Size-dependent antimicrobial effects of novel palladium nanoparticles.

Investigating the interactions between nanoscale materials and microorganisms is crucial to provide a comprehensive, proactive understanding of nanomaterial toxicity and explore the potential for novel applications. It is well known that nanomaterial behavior is governed by the size and composition of the particles, though the effects of small differences in size toward biological cells have not been well investigated. Palladium nanoparticles (Pd NPs) have gained significant interest as catalysts for important carbon-carbon and carbon-heteroatom reactions and are increasingly used in the chemical industry, however, few other applications of Pd NPs have been investigated. In the present study, we examined the antimicrobial capacity of Pd NPs, which provides both an indication of their usefulness as target antimicrobial compounds, as well as their potency as potential environmental pollutants. We synthesized Pd NPs of three different well-constrained sizes, 2.0 ± 0.1 nm, 2.5 ± 0.2 nm and 3.1 ± 0.2 nm. We examined the inhibitory effects of the Pd NPs and Pd(2+) ions toward gram negative Escherichia coli (E. coli) and gram positive Staphylococcus aureus (S. aureus) bacterial cultures throughout a 24 hour period. Inhibitory growth effects of six concentrations of Pd NPs and Pd(2+) ions (2.5 × 10(-4), 10(-5), 10(-6), 10(-7), 10(-8), and 10(-9) M) were examined. Our results indicate that Pd NPs are generally much more inhibitory toward S. aureus than toward E. coli, though all sizes are toxic at ≥ 10(-5) M to both organisms. We observed a significant difference in size-dependence of antimicrobial activity, which differed based on the microorganism tested. Our work shows that Pd NPs are highly antimicrobial, and that fine-scale (<1 nm) differences in size can alter antimicrobial activity.

Effects of surface activation on the structural and catalytic properties of ruthenium nanoparticles supported on mesoporous silica.

Using colloid-based methods to prepare supported catalytic metallic nanoparticles (NPs) often faces the challenge of removing the stabilizer used during synthesis and activating the catalyst without modifying the particles or the support. We explored three surface activation protocols (thermal oxidation at 150 °C, thermal reduction at 350 °C, and argon-protected calcination at 650 °C) to activate ruthenium NPs supported on mesoporous silica (MSU-F), and assessed their effects on the structural and catalytic properties of the catalysts, and their activity by the aqueous phase hydrogenation of pyruvic acid. The NPs were synthesized by polyol reduction using poly-N-vinyl-2-pyrrolidone (PVP) as a stabilizer, and supported on MSU-F by sonication-assisted deposition. The NPs maintained their original morphology on the support during activation. Ar-protected calcination was the most efficient of the three for completely removing PVP from particle surfaces, and provided the highest degree of particle crystallinity and a metal dispersion comparable to commercial Ru/SiO2. Its catalytic performance was significantly higher than the other two protocols, although all three thermally activated catalysts achieved higher activity than the commercial catalyst at the same Ru loading. Post-reaction analysis also showed that the supported catalyst activated at 650 °C retained its morphology during the reaction, which is an important requirement for recyclability.

Nanoparticles functionalized with ampicillin destroy multiple-antibiotic-resistant isolates of Pseudomonas aeruginosa and Enterobacter aerogenes and methicillin-resistant Staphylococcus aureus.

We show here that silver nanoparticles (AgNP) were intrinsically antibacterial, whereas gold nanoparticles (AuNP) were antimicrobial only when ampicillin was bound to their surfaces. Both AuNP and AgNP functionalized with ampicillin were effective broad-spectrum bactericides against Gram-negative and Gram-positive bacteria. Most importantly, when AuNP and AgNP were functionalized with ampicillin they became potent bactericidal agents with unique properties that subverted antibiotic resistance mechanisms of multiple-drug-resistant bacteria.

Dual fluorescence and electrochemical detection of the organophosphorus pesticides--ethion, malathion and fenthion.

Organophosphorus (OP) based pesticides are known powerful inhibitors of cholinesterases, thus the toxicity of this class of compounds causes serious environmental and human health concerns. We report that benzodipyrido[3,2-a:2',3'-c]phenazine (BDPPZ) and 3,6-dimethylbenzodipyrido-[3,2-a:2',3'-c]phenazine (DM-BDPPZ) provide independent fluorescent and electrochemical signal transductions in the presence of the organophosphorus (OP) pesticides; fenthion, malathion and ethion. The presence of the methyl groups at the 3 and 6 positions in DM-BDPPZ was found to significantly influence the sensor performance. The difference in the fluorescence and electrochemical signals produced by the interaction of the sensor compound with each of the OP pesticides provides a means for differentiating between the three pesticides. Detection limits of 10(-8)M, 10(-9) and 10(-12)M were obtained for fenthion, malathion and ethion, respectively. Due to the high sensitivity and ability to minimize false positives these new sensors will be useful for potential integration for future environmental use.

In situ immobilization of palladium nanoparticles in microfluidic reactors and assessment of their catalytic activity.

We report on the synthesis and characterization of catalytic palladium nanoparticles (Pd NPs) and their immobilization in microfluidic reactors fabricated from polydimethylsiloxane (PDMS). The Pd NPs were stabilized with D-biotin or 3-aminopropyltrimethoxysilane (APTMS) to promote immobilization inside the microfluidic reactors. The NPs were homogeneous with narrow size distributions between 2 and 4 nm, and were characterized by transmission electron microscopy (TEM), selected-area electron diffraction (SAED), and x-ray diffraction (XRD). Biotinylated Pd NPs were immobilized on APTMS-modified PDMS and glass surfaces through the formation of covalent amide bonds between activated biotin and surface amino groups. By contrast, APTMS-stabilized Pd NPs were immobilized directly onto PDMS and glass surfaces rich in hydroxyl groups. Fourier transform infrared spectroscopy (FT-IR) and x-ray photoelectron spectroscopy (XPS) results showed successful attachment of both types of Pd NPs on glass and PDMS surfaces. Both types of Pd NPs were then immobilized in situ in sealed PDMS microfluidic reactors after similar surface modification. The effectiveness of immobilization in the microfluidic reactors was evaluated by hydrogenation of 6-bromo-1-hexene at room temperature and one atmosphere of hydrogen pressure. An average first-run conversion of 85% and selectivity of 100% were achieved in approximately 18 min of reaction time. Control experiments showed that no hydrogenation occurred in the absence of the nanocatalysts. This system has the potential to provide a reliable tool for efficient and high throughput evaluation of catalytic NPs, along with assessment of intrinsic kinetics.

Fluorescent chemosensors for toxic organophosphorus pesticides: a review.

Many organophosphorus (OP) based compounds are highly toxic and powerful inhibitors of cholinesterases that generate serious environmental and human health concerns. Organothiophosphates with a thiophosphoryl (P=S) functional group constitute a broad class of these widely used pesticides. They are related to the more reactive phosphoryl (P=O) organophosphates, which include very lethal nerve agents and chemical warfare agents, such as, VX, Soman and Sarin. Unfortunately, widespread and frequent commercial use of OP-based compounds in agricultural lands has resulted in their presence as residues in crops, livestock, and poultry products and also led to their migration into aquifers. Thus, the design of new sensors with improved analyte selectivity and sensitivity is of paramount importance in this area. Herein, we review recent advances in the development of fluorescent chemosensors for toxic OP pesticides and related compounds. We also discuss challenges and progress towards the design of future chemosensors with dual modes for signal transduction.

Controlling the reactivity of chlorinated ethylenes with flavin mononucleotide hydroquinone.

Reduction rate constants of the chlorinated ethylenes cis-1,2-dichloroethylene (cis-DCE), trichloroethylene (TCE), and tetrachloroethylene (PCE) reacted with flavin mononucleotide hydroquinone (FMNH2) under anoxic conditions were investigated. FMNH2 was produced in methanol solvent by the photoreduction of FMN. In aqueous solution, FMN was not fully reduced to FMNH2 but instead yielded the semiquinone radical FMNH*. However, when FMN was anchored to nanocrystalline TiO2, band gap irradiation resulted in electron transfer from the TiO2 conduction band to FMN, thus yielding FMNH2. The FMNH2 generated in aqueous solution on the TiO2 surface was a stronger reductant toward chlorinated ethylenes, relative to FMNH2 in solution. Furthermore, by combining the reactivity of the TiO2 conduction band electrons [TiO2(e-(CB)] with FMNH2, reduction rate constants for the chlorinated ethylenes increased by 2 orders of magnitude relative to FMNH2 alone. The results show how biological molecules such as FMNH2 could have significant effects toward the remediation of organic pollutants.