Efficacy of exopolysaccharide in dye-laden wastewater treatment: A comprehensive review.

The discharge of dye-laden wastewater into the water streams causes severe water and soil pollution, which poses a global threat to aquatic ecosystems and humans. A diverse array of microorganisms such as bacteria, fungi, and algae produce exopolysaccharides (EPS) of different compositions and exhibit great bioflocculation potency to sustainably eradicate dyes from water bodies. Nanomodified chemical composites of EPS enable their recyclability during dye-laden wastewater treatment. Nevertheless, the selection of potent EPS-producing strains and physiological parameters of microbial growth and the remediation process could influence the removal efficiency of EPS. This review will intrinsically discuss the fundamental importance of EPS from diverse microbial origins and their nanomodified chemical composites, the mechanisms in EPS-mediated bioremediation of dyes, and the parametric influences on EPS-mediated dye removal through sorption/bioflocculation. This review will pave the way for designing and adopting futuristic green and sustainable EPS-based bioremediation strategies for dye-laden wastewater in situ and ex situ.

Explicating the recognition phenomenon of hazardous nitro-aromatic compound from contaminated environmental and cellular matrices by rationally designed pyridine-functionalized molecular probes.

In the quest of recognizing hazardous nitro-aromatic compounds in water, two pyridine-functionalized Schiff-base chemosensors, DMP ((E)-N-(3,4-dimethoxybenzylidene)(pyridin-2-yl)methanamine)) and MP (4-((E)-((pyridin-2-yl)methylimino)methyl)-2-ethoxyphenol) have been synthesized to detect mutagenic 2,4,6-Trinitrophenol (TNP) in soil, water as well as cellular matrices by producing turn-off emission responses as a combined consequence of PET and RET processes. Several experimental analyses including ESI-MS, FT-IR, photoluminescence, 1H NMR titration, and the theoretical calculations ascertained the formation and sensing efficacies of the chemosensors. The analytical substantiations revealed that structural variation of the chemosensors played a significant role in improving the sensing efficiency, which would certainly be worthwhile in developing small molecular TNP sensors. The present work depicted that the electron density within the MP framework was more than that of DMP due to the intentional incorporation of -OEt and -OH groups. As a result, MP represented a strong interaction mode towards the electron-deficient TNP with a detection limit of 39 µM.

Recent Progress in Fluorescent Probes for Real-Time Monitoring of Glioblastoma.

Treating glioblastoma (GBM) by resecting to a large extent can prolong a patient's survival by controlling the tumor cells, but excessive resection may produce postoperative complications by perturbing the brain structures. Therefore, various imaging procedures have been employed to successfully diagnose and resect with utmost caution and to protect vital structural or functional features. Fluorescence tagging is generally used as an intraoperative imaging technique in glioma cells in collaboration with other surgical tools such as MRI and navigation methods. However, the existing fluorescent probes may have several limitations, including poor selectivity, less photostability, false signals, and intraoperative re-administration when used in clinical and preclinical studies for glioma surgery. The involvement of smart fluorogenic materials, specifically fluorescent dyes, and biomarker-amended cell-penetrable fluorescent probes have noteworthy advantages for precise glioma imaging. This review outlines the contemporary advancements of fluorescent probes for imaging glioma cells along with their challenges and visions, with the anticipation to develop next-generation smart glioblastoma detection modalities.

Knoevenagel condensation triggered synthesis of dual-channel oxene based chemosensor: Discriminative spectrophotometric recognition of F-, CN- and HSO4- with breast cancer cell imaging, real sample analysis and molecular keypad lock applications.

A novel oxene based unusual sensory receptor (HyMa) has been synthesized via.Knoevenagel condensation triggered carbon-heteroatom (oxygen) intramolecular bond formation reaction at room temperature for discriminative detection of multi-analytes like HSO4-, CN- & F- by spectro-photometric alterations with profound selectivity with the detection limit of 38 ppb, 18 ppb & 94 ppb respectively. Examination of the sensing mechanism was exhaustively investigated through several spectroscopic means like 1H NMR, FT-IR, absorption and fluorescence spectra etc. In addition, quantum mechanical calculations like DFT and Loewdin spin population analyses also validated the rationality of the host-guest interaction. Apart from these, the reversible spectroscopic responses of HyMa towards F- and Al3+ can imitate several complex logic functions that in turn help in preparing molecular keypad lock. This molecular keypad lock has the potential to protect the confidential information at the molecular scale. Additionally, the MTT assay of HyMa showed low cytotoxicity and membrane permeability indicating its attractive capability for bio-imaging towards triple negative breast cancer. HyMa-coated test strips could also be employed towards on-site detection of these deadly contaminants via "Dip Stick" approach without help of any instrumentation. In addition, HyMa has also been exploited for quantitative determination of HSO4- from various real water samples. In a nutshell, detection of lethal contaminants like CN-, F- & HSO4- at ppb level with in vitro live cell imaging has been explored with proper photophysical characterisation and theoretical calculations with real field applications.

Solvothermal Synthesis of High-Performance d10-MOFs with Hydrogel Membranes @ "Turn-On" Monitoring of Formaldehyde in Solution and Vapor Phase.

Herein, two luminescent porous networks (CMERI-1 & CMERI-2) have been reported for the efficient detection of formaldehyde (FA) from aqueous medium. Judicious solvent screening using a high-throughput solvothermal procedure leads to two completely different metal-organic framework (MOFs) with different architectures. It is perceived that the framework CMERI-1 shows better sensitivity with a very short response time (1 min) in the realm of FA detection due to the facile imine (-N═CH-) formation, which is restricted in the case of CMERI-2. The fluorescence "turn-on" behavior is ascribed due to the inhibition of photoinduced electron transfer (PET) (from amine subunit to secondary building unit) process. The detection limits of CMERI-1 & CMERI-2 toward FA in aqueous medium were found to be 0.62 µM (0.019 ppm) and 1.39 µM (0.041 ppm), respectively, that lie far below the intracellular concentration of formaldehyde (100-400 µM). In addition, MOF-based hydrogel membrane was fabricated, which shows vapor-phase detection of FA, which is hitherto unexplored in this realm. Moreover, the response mechanisms of MOFs are supported by density functional theory (DFT) and Fukui indices analysis. The high stability of the porous frameworks along with its interesting sensing features such as fast recognition phenomenon, appreciable detection limit, etc. instigated us to explore its real-world applicability in various food sample and water analyses. In view of the modular design principle of our polymeric probe, the proposed approach could open a new horizon to construct powerful sensing materials for the ultrafast detection of other industrial pollutants in the domain of supramolecular and analytical chemistry.

Coumarin functionalized molecular scaffolds for the effectual detection of hazardous fluoride and cyanide.

Fluoride and cyanide contamination in drinking water imposes detrimental impacts on human health above their permissible limits. Hence, the quantitative detection of these colourless water-soluble toxins has attracted attention. Even though a plethora of chemosensors have been reported so far for the detection of fluoride and cyanide from various matrices, still their applicability is limited to a few examples. Nevertheless, recent advances in the syntheses of coumarin derivatives have shown significant impact on fluoride and cyanide detection. Therefore, this present review provides a brief overview of the application of coumarin-coupled molecular scaffolds towards the detection of perilous fluoride and cyanide along with their sensing mechanisms in order to develop more innovative, simple, sensitive, real-time responsive and cost-effective coumarin-based supramolecular chemosensors to promote next generation approaches towards the ultra-trace quantitative detection of these toxic anions.

Discerning Detection of Mutagenic Biopollutant TNP from Water and Soil Samples with Transition Metal-Containing Luminescence Metal-Organic Frameworks.

Two luminescent MOFs, Mn@MOF and Cd@MOF, have been reported herein, which are capable of selectively detecting 2,4,6-trinitrophenol (TNP), one of the potent organic water pollutants in the class of mutagenic explosive nitroaromatic compounds (epNACs). It is perceived that the d10-based Cd(II)-constituting MOF shows a better response in the realm of TNP-like nitroaromatic sensing in comparison to the d5-based Mn@MOF which may possess lower electron density over the conjugated building blocks. The sensing competences of these chemosensors have been explored by means of various spectroscopic experimentations, and it is observed that for both d5 and d10-containing MOFs, the initial fluorescence intensity is significantly quenched in response to an aqueous solution of TNP. However, Cd@MOF is more selective and sensitive toward TNP over several other epNACs than Mn@MOF. The high chemical stability of the MOF samples, as well as its amusing sensing efficiency of Cd@MOF, further instigated to investigate the sensing ability in various environmental specimens like soil and water culled from several zones of West Bengal, India.

Tandem Detection of Sub-Nano Molar Level CN- and Hg2+ in Aqueous Medium by a Suitable Molecular Sensor: A Viable Solution for Detection of CN- and Development of the RGB-Based Sensory Device.

An inimitable urea-based multichannel chemosensor, DTPH [1,5-bis-(2,6-dichloro-4-(trifluoromethyl)phenyl)carbonohydrazide], was examined to be highly proficient to recognize CN- based on the H-bonding interaction between sensor -NH moiety and CN- in aqueous medium with explicit selectivity. In the absorption spectral titration of DTPH, a new peak at higher wavelength was emerged in titrimetric analytical studies of CN- with the zero-order reaction kinetics affirming the substantial sensor-analyte interaction. The isothermal titration calorimetry (ITC) experiment further affirmed that the sensing process was highly spontaneous with the Gibbs free energy of -26 × 104 cal/mol. The binding approach between DTPH and CN- was also validated by more than a few experimental studies by means of several spectroscopic tools along with the theoretical calculations. A very low detection limit of the chemosensor toward CN- (0.15 ppm) further instigated to design an RGB-based sensory device based on the colorimetric upshots of the chemosensor in order to develop a distinct perception regarding the presence of innocuous or precarious level of the CN- in a contaminated solution. Moreover, the reversibility of the sensor in the presence of CN- and Hg2+ originated a logic gate mimic ensemble. Additionally, the real-field along with the in vitro CN- detection efficiency of the photostable DTPH was also accomplished by using various biological specimens.

A simple urea-based multianalyte and multichannel chemosensor for the selective detection of F-, Hg2+ and Cu2+ in solution and cells and the extraction of Hg2+ and Cu2+ from real water sources: a logic gate mimic ensemble.

Herein, a hydrazine-based chromogenic, fluorogenic and electrochemical chemosensor BCC [1,5-bis(4-cyanophenyl) carbonohydrazide] was premeditated and synthesized through a simple one-step synthetic procedure for the selective detection of toxic anions, such as F-, in a DMSO-ACN medium and cations, such as Hg2+ and Cu2+, in a MeOH-water medium. The detection limit for F- was reckoned to be 0.5 ppm, and for Hg2+ and Cu2+, it was 0.8 ppm and 50 nM, respectively. The chemosensor exhibited a distinct change in colour from colourless to dark blue in the presence of F-, and upon the addition of Hg2+ and Cu2+, the BCC turned from colourless to light blue and purple accordingly. Moreover, turn-on fluorescence response transpired by the attenuation of PET signified the selective sensing of analytes with a zero-order rate constant. Sophisticated analytical experiments, such as ESI-MS, UV-Vis, photoluminescence, cyclic voltammetry, FTIR, and 1H-NMR, along with the theoretical calculations corroborated the probable sensing pathways. The reversible colorimetric response of BCC towards F- and H+ can be advantageous in the design of electronic circuits derived from Boolean algebra. The complexation ability of the sensor with toxic Hg2+- and Cu2+-like ions made it an efficient material to remove these metal ions from real water sources polluted with these toxic elemental ions. Furthermore, the in vitro studies were accomplished using the Bauhinia acuminate pollen cell to check the cell penetrability of the sensor molecule.

Hydrazine functionalized probes for chromogenic and fluorescent ratiometric sensing of pH and F-: experimental and DFT studies.

Two novel hydrazine based sensors, BPPIH (N1,N3-bis(perfluorophenyl)isophthalohydrazide) and BPBIH (N1',N3'-bis(perfluorobenzylidene)isophthalohydrazide), are presented here. BPPIH is found to be a highly sensitive pH sensor in the pH range 5.0 to 10.0 in a DMSO-water solvent mixture with a pKa value of 9.22. Interesting optical responses have been observed for BPPIH in the above mentioned pH range. BPBIH on the other hand turns out to be a less effective pH sensor in the above mentioned pH range. The increase in fluorescence intensity at a lower pH for BPPIH was explained by using density functional theory. The ability of BPPIH to monitor the pH changes inside cancer cells is a useful application of the sensor as a functional material. In addition fluoride (F-) selectivity studies of these two chemosensors have been performed and show that between them, BPBIH shows greater selectivity towards F-. The interaction energy calculated from the DFT-D3 supports the experimental findings. The pH sensor (BPPIH) can be further interfaced with suitable circuitry interfaced with desired programming for ease of access and enhancement of practical applications.