Environmental Water Samples Research Articles

Magnetite/MXene (Fe3O4/Ti3C2) Nanocomposite as a Novel Adsorbent for Environmental Remediation of Malachite Green Dye.

In this work, a novel adsorbent called magnetite/MXene (Fe3O4/Ti3C2) nanocomposite was prepared, characterized, and applied for the removal of organic dye, malachite green dye (MG), from both real water and model solutions. Numerous techniques were used to characterize the prepared Fe3O4/Ti3C2 nanocomposite: XRD, SEM, TEM, FTIR, and surface area analysis. The outcomes showed that the Al layer had been selectively etched, that the MAX phase (Ti3AlC2) had been transformed into layered Ti3C2 MXene, that the cubic Fe3O4 phase had been prepared, and that the prepared Fe3O4 NPs had been evenly distributed on the MXene surface. Also, SEM pictures showed the successful etching of the MAX phase and the formation of the ultrathin multi-layered MXene, which the Fe3O4 NPs covered upon forming the Fe3O4/Ti3C2 nanocomposite at the surface and inside the ultrathin multi-layered MXene. The effect of different operational parameters affecting the removal process was explored and optimized. The MG dye was removed mostly within 60 min, with a 4.68 mg/g removal capacity using 5 mg of the Fe3O4/Ti3C2 nanocomposite. The removal was examined from both kinetic and thermodynamic perspectives, and the findings demonstrated the spontaneity of the removal process as well as the applicability of fractal-like pseudo-first-order and fractal-like pseudo-second-order kinetics when compared to other kinetics models. The Fe3O4/Ti3C2 nanocomposite was used to remove MG dye from real spiked environmental water samples, and the results revealed the successful remediation of the real samples from the organic dye by the Fe3O4/Ti3C2 nanocomposite. Accordingly, Fe3O4/Ti3C2 nanocomposite could be considered a potential adsorbent for the environmental remediation of polluted water.

Combined fabrication of zeolitic imidazolate framework-8 and lanthanide towards coordination polymers: A dual-signal fluorescent probe for sensing Cu2+ based on synergistic effect of aggregation-induced emission and antenna effect

Copper ion (Cu2+) detection remains an important task for monitoring water quality because of its specific toxicity. Herein, a new dual-signal fluorescent probe was developed by combining zeolitic imidazolate framework-8 (ZIF-8) and lanthanide for the detection of Cu2+ for the first time. The lanthanide coordination polymer (guanosine monophosphate and Eu3+, GMP/Eu) was initially incorporated into ZIF-8 to yield ZIF-8/GMP/Eu nanomaterials with extremely weak single emission fluorescence at 618 nm. It was found that the resulted nanomaterials could display a dual emission fluorescence at 515 nm and 618 nm after the introduction of tetracycline (TC) due to the synergistic effect of aggregation-induced emission effect (AIE, TC induced by ZIF-8) and antenna effect (AE, between TC and GMP/Eu). Interestingly, in the presence of Cu2+, the AIE of TC was destroyed because of the interaction of Cu2+ with ZIF-8 and TC. The AE between TC and GMP/Eu disappeared due to the formation of complex between TC and Cu2+. A dual-signal fluorescent probe of ZIF-8/GMP/Eu/TC was thereby established for sensing Cu2+ in the range of 0.5–100 μM. Such a dual-signal response strategy that intelligently utilized the “ON”/“OFF” of AIE and AE can not only eliminate the background interference, but also ensure the improved selectivity of Cu2+ sensing. Subsequently, the dual-signal fluorimetric strategy was applied for the detection of Cu2+ in environmental water samples, indicating the potential feasibility of applications for water quality monitoring.

A group-targeting biosensor for sensitive and rapid detection of quinolones in water samples

BackgroundQuinolones (QNs) widely exist in the environment due to their wide range of applications and poor metabolic properties, resulting in the generation and spread of resistance genes, posing a potential threat to human health. Traditional analytical methods cannot detect all broad ranges of QNs simultaneously. The development of facile, efficient and reliable method for quantification and assessment of the total QNs is a long-lasting challenge. ResultsWe hereby provide a simple, sensitive and instantaneous group-targeting biosensor for the detection of total QNs in environmental water samples. The biosensor is based on a group-specific antibodies with high affinity against QNs. Fluorescent labeled antibodies bound to the coated antigen modified on the surface of the transducer, and excited by the evanescent waves. The detected fluorescent signal is inversely proportional to the QNs concentration. This biosensor exhibited excellent performance with detection limits lower than 0.15 μg L−1 for all five QNs variants, and even lower than 0.075 μg L−1 for ciprofloxacin (CIP) and ofloxacin (OFL). Environmental water samples can be detected after simple pretreatment, and all detection steps can be completed in 10 min. The transducer has a high regenerative capacity and shows no significant signal degradation after two hundred detection cycles. The recoveries of QNs in a variety of wastewater range from 105 to 119%, confirming its application potential in the measurement of total QNs in reality. SignificanceThe biosensor can realize rapid and sensitive detection of total QNs in water samples by simple pretreatment, which overcomes the disadvantage of the traditional methods that require complex pretreatment and time-consuming, and pave the groundwork for expansive development centered around this technology.

A naked-eye colorimetric assay for highly sensitive detection of CL-20 explosive

2,4,6,8,10,12-hexanitro-2,4,6,8,10,12-hexaazaisowurtzitane (CL-20) stands as the most energetically condensed explosive ever found, and poses a great security threat to humans. Here we report a naked-eye colorimetric assay for highly sensitive detection of CL-20. Through effective cascading of the hydrolysis process of CL-20 with nitrite-involved Griess reaction to yield a pink-colored azo product, the visual quantification of CL-20 is realized by taking advantage of corresponding colorimetric signals. Under optimal experimental conditions, the present colorimetric assay is successfully used for highly selective determination of CL-20 in deionized water and environmental water samples with a nanomolar sensitivity. The resulting limit of detection is much lower than conventional methods. Moreover, benefiting from the distinct color change of the detection solution, direct naked-eye semi-quantitative analysis of CL-20 is achieved with a threshold concentration of 1 μM. Such simple, cost-effective, selective, and highly sensitive visual colorimetric assay will have valuable applications in public safety, environmental monitoring, and other related fields.

DNA extraction using FTA Elute cards for detection and enumeration of fecal indicator bacteria in the Chao Phraya River, Thailand

Utilizing molecular methods for monitoring and determining water quality in developing countries can be problematic. Effective extraction and storage of DNA from environmental samples is especially difficult due to lack of access to sufficient laboratory facilities for molecular work. Use of a commercial product for the extraction of DNA, as well as its application in determining the microbial quality of surface waters, was evaluated and compared. Surface water samples collected from the Chao Phraya River in Thailand were processed to enumerate Escherichia coli. Quantification was done through culture methods (Colilert Quanti-tray) and quantitative real-time PCR (SYBR green and Taqman assays). Processing of surface water samples and culture enumeration of E. coli was done in Thailand, while DNA extraction and enumeration using real-time PCR was done in Korea. E. coli MPN counts were mean log 2.89/100ml. Quantitative real-time PCR assays counts ranged from 2.38 to 3.59 mean log CFU/100 ml. Taqman PCR assays had no significant difference in mean log counts compared to conventional culture methods. However mean log counts of SYBR green PCR assays were significantly higher than counts obtained by culture methods and Taqman PCR assays (P<0.05). Results demonstrated FTA Elute cards can be employed for the extraction of microbial DNA from surface waters and have potential use in detection of fecal indicator bacteria from environmental water samples.

Dual-response fluorescent probe for simultaneously detecting HOCl and Zn2+ in environmental water samples and evaluating the oxidative stress in the zebrafishes induced by pollutants via fluorescence imaging

Both of hypochlorous acid (HOCl) and Zn2+ ions play important roles in fundamental biological processes. They not only simultaneously exist in the biological organisms, but also coexist in the environment. Thus, developing a novel method for simultaneous detection of HOCl and Zn2+ is very necessary. Herein, the nitrogen- and sulfur-codoped carbon dots (N,S-CDs) were synthesized through a simple and rapid microwave method, it emits dual-emission fluorescence centered at 452 nm and 685 nm, which has specific recognition to HOCl and Zn2+, respectively, and they do not interfere with each other. A dual-emission and dual-response fluorescent probe was thus developed for the simultaneous detection of HOCl and Zn2+ in the environment and fluorescence imaging in the zebrafishes. The limits of detection for HOCl and Zn2+ are 27.0 nM and 13.0 nM, respectively. It has been successfully applied for the simultaneous determination of HOCl and Zn2+ in real water samples. The sensing mechanisms of the N,S-CDs to HOCl and Zn2+ were also discussed in detail. Moreover, the fluorescent probe not only can be used to real-time dynamic monitoring of HOCl and Zn2+ in the zebrafishes, but also can be applied to evaluate the oxidative stress in the zebrafishes induced by pollutions via fluorescence imaging. This work provided a new strategy for developing multifunctional fluorescent probes, and a potential application prospect for environmental monitoring and evaluating the health risks of environmental pollutants to organisms.

Coumarin Linked Cyanine Dye for the Selective Detection of Cyanide Ion in Environmental Water Sample.

A benzoxazole-coumarin-based probe BOC, was synthesized and validated for its anion sensing ability and found to be effective in recognizing cyanide ions. Upon addition of cyanide, a spontaneous color change was observed that was visible to the naked eye. The sensitization process takes place with nucleophilic addition, and the cyanide ion added to the probe disrupts the intra molecular charge transfer transition (ICT) between the donor and acceptor units, causing the pink colored probe to become yellow. Ultraviolet and fluorescence methods were applied to measure the detection limits of probes with added cyanide ions, which were found to be 3.47 µM and 2.48 nM. The stoichiometry of the probe with the cyanide ion was determined by the Job's method, NMR titration, and mass spectrometry and was found to be in a 1:1 ratio. The results obtained from the visual and UV-visible spectral studies are justified by theoretical calculations. The cyanide-loaded probe induced visual changes, which enabled the development of a test strip for field application, and the prepared strip can be used to detect the ppm level of cyanide in water samples. The developed probe, BOC, can be used to detect cyanide ions in various water samples.

Analysis and remediation of phthalates in aquatic matrices: current perspectives.

Phthalic acid esters (PAEs) are high production volume chemicals used extensively as plasticizers, to increase the flexibility of the main polymer. They are reported to leach into their surroundings from plastic products and are now a ubiquitous environmental contaminant. Phthalate levels have been determined in several environmental matrices, especially in water. These levels serve as an indicator of plasticizer abuse and plastic pollution, and also serve as a route of exposure to different species including humans. Reports published on effects of different PAEs on experimental models demonstrate their carcinogenic, teratogenic, reproductive, and endocrine disruptive effects. Therefore, regular monitoring and remediation of environmental water samples is essential to ascertain their hazard quotient and daily exposure levels. This review summarises the extraction and detection techniques available for phthalate analysis in water samples such as chromatography, biosensors, immunoassays, and spectroscopy. Current remediation strategies for phthalate removal such as adsorption, advanced oxidation, and microbial degradation have also been highlighted.

A Convenient Strategy for the Voltammetric Direct Determination of Ce(III) in Environmental Waters Using a Multi-Walled Carbon Nanotubes Modified Screen-Printed Carbon Electrode.

A simple and fast stripping voltammetric procedure for trace determination of Ce(III) in environmental water samples has been developed. The procedure of cerium determination in the presence of Alizarin S and acetate buffer was employed as the initial method. The adsorption material, multi-walled carbon nanotubes, was used as a screen-printed electrode modifier ensuring efficient accumulation of the Ce(III)-Alizarin S complex. The calibration graph for Ce(III) for an accumulation time of 60 s was linear in the range from 1 × 10-8 to 7 × 10-7 mol L-1 with the linear correlation coefficient r = 0.997. The detection limit was estimated from three times the standard deviation of low Ce(III) concentration and an accumulation time of 60 s was about 3.5 × 10-9 mol L-1. The proposed method was successfully applied to Ce(III) determination at trace levels in environmental water samples, such as river, lake and rain water with recoveries ranged from 93% to 98%.

A highly sensitive electrochemical sensing probe incorporating classical Berthelot's reaction and glassy carbon electrode for measuring ultra-trace levels of ammonia/ NH4+ in water

In quantifying NH3 and/or NH4+ ions, the wavelength-based spectrochemical methods involving formation of colored products of the Berthelot’s or Nessler reactions might be challenging due to auto-self absorbance, spectral overlap, and background scattering noise. Thus, the current study reports a renewable glassy carbon electrode (GCE) sensing probe combined with Berthelot’s reaction (indophenol formation) and adsorptive square - wave-anodic stripping voltammetry (Ads SWSV) at pH = 10 for detection of NH3 and/or NH4+ in water. The redox characteristics and the high surface coverage of the oxidation product of indophenol on the sensing platform suggested its use for NH3 and/or NH4+ detection. The electrochemical sensing probe for NH4+ displayed good linear relationship between 5.56 nM and 55.6 μM of NH4+ with limits of detection (LOD) and quantitation (LOQ) of 4.83 × 10-9 and 1.47 × 10-8 M, and sensing probe sensitivity of 1.27μA/μM−1 cm−2,respectively. The probe was applied for measuring NH3/NH4+in fresh and seawater samples, and the results were validated using standard ion chromatography (IC) and micro spectrophotometry assays. The assembled probe was also tolerably selective against interfering of other contaminants in a comparable potential window. Additionally, the probe has exceptional selectivity, long-term stability, and repeatability, and has good capacity to detect NH3 and/or NH4+ ions with high accuracy (recovery range = 97.14 ± 4.12–102.9 ± 4.7) in environmental water samples. The calculated Student texp and Fexp values (n = 5) were less than the tabulated ttab (2.78) and Ftab (6.39) at 95 % probability (P = 0.05, n = 5). The study offer high reliability towards NH3 and/or NH4+ detection in complex environments.

Enhanced long-term stability of stained microplastics with carbon nitride fluorescent polymer for tracking

Fluorescent labeling and imaging is a useful tool to track the temporal and spatial distribution of microplastics (MPs) with size and shape features. However, the limited fluorescently labeled MPs spheres, photo-bleaching and leaching of organic small molecular dyes hamper the tracking of MPs in the environment. In this work, phenyl-modified carbon nitride (PMCN) fluorescent polymer was prepared and applied for the staining of eight different types of MPs. The interface interaction mechanism between PMCN fluorescent polymer and MPs was investigated by the desorption experiments. The long-time photo-stability of the stained MPs against ultraviolet (UV) light irradiation, freeze-thaw cycles, various environmental factors and real environmental water samples was evaluated. The MPs stained with PMCN fluorescent polymer showed more robust stability than the common dye (Nile red) against the damage when exposure to UV light for 72 h, treatment with freeze-thaw cycles for 60 days, exposure to strong acid, strong alkali, high salinity, freshwater (river and lake) or seawater for 60 days. Results indicate PMCN fluorescent polymer is promising as a convenient, efficient and universal fluorescent tracer for visually tracking the migration and distribution of MPs in environmental water system.

Exploring the potential applications of amphiphilic carbon dots based nanocomposite hydrogel in liquid chromatographic separations

BackgroundDue to their excellent stability, low toxicity, flexible modification and adjustable functionality, carbon dots (CDs) have a promising application prospect in the field of chromatographic stationary phases. Hydrogels are new functional polymer materials with three-dimensional network structure that have excellent hydrophilicity, high porosity and unique mechanical properties, which are also good candidate materials for liquid chromatography. Nevertheless, a review of the literature reveals that CDs based nanocomposite hydrogels have not yet been reported as HPLC stationary phases. ResultsIn this work, amphiphilic CDs with multiple functional groups and polyacrylic acid hydrogel were grafted to the surface of silica gel by an in-situ polymerization method, and a CDs/polyacrylic acid nanocomposite hydrogel stationary phase (CDs/hydrogel@SiO2) was prepared. CDs act as the macroscopic cross-linking agents to form a cross-linked network with polyacrylic acid chains through physical cross-linking by hydrogen bonding and chemical cross-linking by amidation and esterification reactions, which not only improve the swelling property of the hydrogel but also increase its stability. Additionally, the introduction of CDs with multifunctional groups modulates the hydrophilic-hydrophobic balance of the hydrogel that also imparts good hydrophobicity to the composite hydrogel. Through the study of retention mechanism and influencing factors, it is certificate that the CDs/hydrogel@SiO2 has mixed-mode chromatographic performance. Furthermore, the CDs/hydrogel@SiO2 column shows great potential for the determination of organic contaminants in environmental water samples. SignificanceThis work confirms the potential application of CDs/hydrogel composite for the separation of various samples and provides the possibility of developing CDs based nanocomposite hydrogel in the field of liquid chromatography. Introducing CDs into hydrogel can open up a new way for nanocomposite hydrogels to be used in HPLC, which expands the advance of hydrogel and CDs in separation field.

Synthesis and Application of 3-[3-Phenylpyrazylazo]-2,7-Naphthalendiol for Improved Palladium Determination in Environmental Samples and Enhanced ZnO Nanoparticle Performance

In this study, a spectrophotometric method for the determination of low levels of palladium (II) was developed by forming a complex with the new reagent 3-(3-phenyl pyrazyl azo)-2,7-naphthalendiol (3PPAN). The complex showed maximum absorption at 612 nm with a maximum molar absorptivity of 4.911?104 L/mol/cm, and a linear correlation was established between absorbance and concentration. The accuracy and repeatability of the method were evaluated and found to be precise (RSD 1.22%) and accurate (relative error 0.157%). The method?s selectivity was also tested by evaluating the effect of various ions. The stability constant of the complex was determined to be 2.759?107 L/mol. The method was successfully applied to the determination of Pd (II) ions in environmental samples of water and soil. In addition, the new ligand (3PPAN) was used to improve the properties of nano ZnO through a ligand exchange reaction on nanoparticles.. KEYWORDS :Azo, Palladium, Spectrophotometric, ZnO nanoparticles.

Development of a multiplex droplet digital PCR assay for simultaneous detection and quantification of Escherichia coli, E. marmotae, and E. ruysiae in water samples

Escherichia coli are widely used by water quality managers as Fecal Indicator Bacteria, but current quantification methods do not differentiate them from benign, environmental Escherichia species such as E. marmotae (formerly named cryptic clade V) or E. ruysiae (cryptic clades III and IV). Reliable and specific techniques for their identification are required to avoid confounding microbial water quality assessments. To address this, a multiplex droplet digital PCR (ddPCR) assay targeting lipB (E. coli and E. ruysiae) and bglC (E. marmotae) was designed. The ddPCR performance was assessed using in silico analysis; genomic DNA from 40 local, international, and reference strains of target and non-target coliforms; and spiked water samples in a range relevant to water quality managers (1 to 1000 cells/100 mL). Results were compared to an analogous quantitative PCR (qPCR) and the Colilert method. Both PCR assays showed excellent sensitivity with a limit of detection of 0.05 pg/μL and 0.005 pg/μl for ddPCR and qPCR respectively, and of quantification of 0.5 pg/μL of genomic DNA. The ddPCR allowed differentiation and quantification of three Escherichia species per run by amplitude multiplexing and showed a high concordance with concentrations measured by Colilert once proportional bias was accounted for. In silico specificity testing underlined the possibility to further detect and distinguish Escherichia cryptic clade VI. Finally, the applicability of the ddPCR was successfully tested on environmental water samples where E. marmotae and E. ruysiae potentially confound E. coli counts based on the Most Probable Number method, highlighting the utility of this novel ddPCR as an efficient and rapid discriminatory test to improve water quality assessments.

Construction of a Miniaturized Electrochemical Sensor for Voltammetric Detection of 17β-Estradiol Using a g-C3N4-Decorated Gold Nanoparticles Electrode

Background: 17β-estradiol (E2) is a steroid hormone that has the potential to disrupt the endocrine system, leading to adverse effects on both humans and ecosystems, even when present in low concentrations. The quantitative determination of E2 is of great practical significance. Hypothesis: Electrochemical methods offer several advantages, including low cost, ease of operation, and potential for miniaturization, which makes them suitable for on-field detection applications. Methods: This research developed a miniaturized electrochemical sensor utilizing graphitic carbon nitride (g-C3N4) assembled on an AuNPs/ITO film electrode for sensitive voltammetric detection of a steroid hormone, E2. Results: Compared with AuNPs/ITO electrodes, the g-C3N4/AuNPs/ITO exhibits higher sensitivity for voltammetric detection of E2. Under optimal conditions, the differential pulse voltammetric response on the g-C3N4/AuNPs/ITO electrode was proportional to E2 concentration in the 25 ~ 600 μmol/L range, with a detection limit of 6.5 μmol/L. Conclusion: The proposed g-C3N4/AuNPs/ITO electrode exhibited a wide linear range, good selectivity, and practical applicability for determining E2 in environmental water samples with acceptable recovery.

Multi-responsive fluorescent covalent organic framework based on phenanthro[9,10-d]imidazole moiety for relayed detection of Cu2+/Al3+ followed by PO43− and its applications

Designation and application of the luminescent COFs remains a tough challenge and imperative task because of their limited building block structure, the unavailable raw material, the tedious modification process, or the onefold sensing function. Herein, a fluorinated fluorescent covalent organic framework containing a phenanthro[9,10-d]imidazole moiety [TFPB-PI(F)–COF] had been successfully designed for Cu2+ and Al3+ detection relayed by PO43−. TFPB-PI(F)–COF serves as a highly sensing platform with the superior selectivity toward Cu2+ and Al3+ based on the coordination interaction and the chelation enhancement quenching (CHEQ) effect, and the detection limits are 2.3 and 4.2 nmol L−1, respectively. Subsequently, accompanied with the gradual introduction of PO43−, TFPB-PI(F)–COF@M (Cu2+ and Al3+) complex is wrecked due to electrostatic attraction with the detection limit of 10 nmol L−1, led to the fluorescent recovery of TFPB-PI(F)–COF. Furthermore, the reversible fluorescent performance by the mode of “on–off–on” is perfect. Besides, the established relayed method can be successfully employed for the analysis of Cu2+ and Al3+ in environmental water samples with recoveries of 96.00–104.63 % and RSD <4.62 %. Moreover, the fluorescent images for the visual detection of Cu2+ is also fabricated in living HeLa cells, which provides a modest contribution and an effective platform to the biological analysis.

Generic qPCR assays for quality control in environmental DNA research

AbstractEnvironmental DNA (eDNA) has been widely used for species surveillance. However, the lack of adequate quality control in many eDNA research projects and applications can lead to false‐negative results, greatly affecting biosecurity surveillance and conservation efforts. Exogenous DNA is routinely added to eDNA samples and used as a positive control, typically after DNA extraction. However, this type of positive control is only able to identify false negatives due to errors at the amplification stage. Therefore, errors in upstream processes, such as sample collection will not be identified by an exogenous control. We designed two independent sets of generic quality control qPCR assays (QCqPCR) targeting abundant endogenous DNA that is obtained during sample collection. Our QCqPCR assays target the chloroplast 16S and 23S ribosomal RNA sequences. In silico analyses indicated these regions were highly conserved among plants, algae and bacteria commonly found in freshwater, marine, or terrestrial environments. These QCqPCR assays were purposely mismatched against the human genome to avoid false positives resulting from human DNA contamination. Both assays remained highly efficient and sensitive under annealing temperatures between 58 and 62°C, allowing them to be multiplexed with most qPCR analyses. We validated our assays by multiplexing with a species‐specific Murray cod (Maccullochella peelii) assay on field‐collected environmental water samples. Potential false‐negative reactions can be identified by the failed or suppressed QCqPCR assay and the negative species‐specific assay. We recommend incorporating either one of the QCqPCR assays in qPCR‐based eDNA analysis to identify potential false negatives and improve the reliability of eDNA surveys.

Characterization of two bacteriophages specific to Acinetobacter baumannii and their effects on catheters biofilm.

Multidrug-resistant strains of Acinetobacter baumannii cause major nosocomial infections. Bacteriophages that are specific to the bacterial species and destroy bacteria can be effectively used for treatment. In this study, we characterized lytic bacteriophages specific to A. baumannii strains. We isolated lytic bacteriophages from environmental water samples and then investigated their morphology, host range, growth characteristics, stability, genome analysis, and biofilm destruction on the catheter surface. Our results showed that the efficacy of the phages varied between 32% and 78%, tested on 78 isolates of A. baumannii; 80 phages were isolated, and two lytic bacteriophages, vB_AbaP_HB01 (henceforth called C2 phage) and vB_AbaM_HB02 (henceforth called K3 phage), were selected for characterization. Electron microscopy scans revealed that the C2 and K3 phages were members of the Podoviridae and Myoviridae families, respectively. Whole-genome sequencing revealed that the sequence of the C2 phage is available in the NCBI database (accession number: OP917929.1), and it was found sequence identity with Acinetobacter phage AB1 18%, the K3 phage DNA sequence is closely related to Acinetobacter phage vB_AbaM_phiAbaA1 (94% similarity). The cocktail of C2 and K3 phages demonstrated a promising decrease in the bacterial cell counts of the biofilm after 4 h. Under a scanning electron microscope, the cocktail treatment destructed the biofilm on the catheter. We propose that the phage cocktail could be a strong alternative to antibiotics to control the A. baumannii biofilm in catheter infections.

A Fluorescence Biosensor Based on Carbon Quantum Dots Prepared from Pomegranate Peel and T-Hg2+-T Mismatch for Hg2+ Detection.

Mercury ions (Hg2+) can cause damage to human health, and thus, the study of the detection of Hg2+ is extraordinarily important in daily life. This work reported a fluorescence biosensor for the detection of Hg2+. The key point of this strategy was that the fluorescence of carbon quantum dots made from pomegranate peel (P-CQDs) was quenched by hemin, and restored after G-quadruplex binding with hemin. The presence of Hg2+ caused thymine (T)-rich DNA fragments to form T-Hg2+-T mismatches, and this change allowed the release of G-quadruplex. G-quadruplex could change the fluorescence of hemin/P-CQDs. P-CQDs exhibited excellent properties through characterization analysis, such as transmission electron microscope, X-ray photoelectron spectroscopy and Fourier transform infrared. This proposed fluorescence detection strategy established the linear ranges of Hg2+ from 1 nM to 50 nM. In conclusion, this simple biosensor had the advantages of strong sensitivity, high selectivity, and low cost for Hg2+ detection in environmental water samples.

High enrichment and measurement of heterocyclic aromatic hydrocarbons from environmental waters with magnetic resorcinol-formaldehyde nanocomposites coupled with high performance liquid chromatography

Heterocyclic aromatic hydrocarbons are concerned pollutants with carcinogenic toxicity, which exist universally in various environmental matrices and have great harm to environmental and human health. In present work, magnetic resorcinol-formaldehyde composites (Fe3O4@SiO2@R–F) were fabricated via aldol condensation reaction under alkaline condition. The prepared magnetic materials were examined and analyzed with Fourier transform infrared spectroscopy and other related instruments. The Fe3O4@SiO2@R–F composites were utilized to develop an efficient magnetic solid phase extraction (MSPE) method for extracting six heteropolyclic aromatic hydrocarbons from environmental water samples including carbazole (CB), 7-methylquinoline (7-MQL), 9-methylcarbazole (9-MCB), dibenzothiophene (DBT), 4-methyldibenzothiophene (4-MDBT), and 4,6-dimethyldibenzothiophene (4,6-DMDBT). The analytes were analyzed by high performance liquid chromatography-ultraviolet variable wavelength detector (HPLC-VWD). The main factors affecting MSPE were optimized. With the optimal parameters, 9-MCB and 4-MDBT have good linearity over the concentration range of 0.1–300 μg L−1, and 7-MQL, CB, DBT and 4,6-DMDBT have good linearity over the concentration range of 0.5–300 μg L−1. The limits of detection were over the concentration range of 0.012–0.031 μg L−1. This method was successfully employed to measure real waters, and the spiked recoveries ranged from 89.4% to 99.9%. The results confirmed that the developed method was reliable, robust and could be employed as a usefully alternate way for analyzing such pollutants in waters.