Concentrations Of Norfloxacin Research Articles

Insight into efficient photocatalytic degradation of norfloxacin over a simple, economical biochar-based magnetic photocatalyst under solar illumination: a statistical and experimental approach.

The transformation of residual agricultural solid waste into an efficient value-added carbon product has been an ongoing strategy for solid waste management and a sustainable economy. Meanwhile, the upsurgence of antibiotic contamination in water bodies due to their inadvertent use poses a serious threat to human health and leads to antimicrobial resistance. Hence, to neutralize two evils in one stroke simultaneously, a simple, easy, and cost-effective pea shell-based magnetic photocatalyst (PSMC) has been synthesized and characterized by XRD (X-ray diffraction), VSM (vibrating sample magnetometer), XPS (X-ray photoelectron spectroscopy), TGA (thermogravimetric analysis), and FTIR (Fourier-transform infrared) spectroscopy techniques. Batch experimental studies revealed that PSMC efficiently eliminates norfloxacin (91.3%) within 180min from wastewater and mineralizes it into innocuous products at optimum parameters of norfloxacin concentration of 20mg/L, catalyst dosage of 15mg, and pH 3.5. Additionally, statistical parameters for the photodegradation of NX obtained from ANOVA by applying the Box-Behnken design are in close agreement with batch experiment parameters. PSMC has surplus advantages of facile recovery for recycling up to seven consecutive cycles by an external magnet and efficacy in natural solar light, making it cost-effective and economical. Radical scavenging studies revealed that O2•- and OH• were the potent reactive species in the photocatalytic degradation process.

Efficient degradation of norfloxacin by synergistic activation of PMS with a three-dimensional electrocatalytic system based on Cu-MOF

In this work, Cu-based metal-organic framework material (Cu-MOF) was combined with an electric field to construct a three-dimensional electrocatalytic synergistic activation of peroxymonosulfate sulfate (PMS) system (3D/Cu-MOF/EC/PMS) for the degradation of norfloxacin (NOR). The results show that the synergistic degradation efficiency of the Cu-MOF material with the electric field is enhanced by nearly 64 % relative to the degradation efficiency of the two alone. The quenching experimental and EPR characterization indicates that ROS plays an important role in the degradation process, with O2– playing a dominant role. Finally, the degradation pathway of NOR was explored by DFT study and LC-MS tests, and the toxicity evaluation software (TEST) and CCK-8 cytotoxicity experimental studies demonstrated that the sewage after the degradation of NOR by this system would have little or no effect on human liver cells (L02). This study not only shows that the 3D/Cu-MOF/EC/PMS system can treat the water containing higher concentrations of NOR into a state that is not harmful to the human body but also provides a new idea for the improvement of catalysts that do not have obvious catalytic degradation effects.

Lithium-doped ZrO2 nanoparticles for SERS-based norfloxacin drug detection

Surface-enhanced Raman scattering (SERS) spectroscopy is a highly specific and ultrasensitive analytical technique; thus, it is an ideal candidate for therapeutic drug monitoring. However, SERS measurements of drugs in a sample are inevitably affected by the environment. In this study, we synthesized ZrO2 nanoparticles (NPs) doped with the first group of elements (Li, Na, and K) in the main block and evaluated their SERS performance. The results showed that Li-ion doping could significantly enhance the SERS effect, and the degree of enhancement depended on the type and concentration of the doped ions. Compared with the highly stable ZrO2, Li ion-doped ZrO2 (Li-ZrO2) exhibited a significant increase in SERS activity. In particular, 1 % Li-ZrO2 NPs exhibited excellent SERS enhancement with an enhancement factor (EF) of 2.60 × 104, which was attributed to the decreased band gap and improved the charge transfer (CT) process after Li ion doping. The adsorption capacity of the Li-ZrO2 NPs for norfloxacin (NOR) molecules was gradually saturated with time. In addition, both acidic and alkaline conditions were unfavorable for NOR detection by the substrate. The SERS intensity exhibited a linear relationship within the NOR concentration range of 10−3–10–6 mol/L, and approximately 97.51 % of the active ingredients were detected, with a competitive detection limit of 10−6 mol/L. Furthermore, NOR detection is cost-effective and time-efficient, and the results of our study can aid in the research process and support practical applications. The proposed study provides a guidance for improving the SERS activity of semiconductors for sensing.

Integrated bio-electrochemical approach to Norfloxacin (NFX) degradation: Efficacy, degradation mechanisms, and toxicological insights

Norfloxacin (NFX), a widely used fluoroquinolone antibiotic, poses significant environmental concerns due to its persistence in ecosystems and its potential to foster antibiotic resistance. This study explores the degradation of NFX using a bio-electrochemical system (BES) facilitated by Bacillus subtilis isolated from animal waste sludge. Experimental parameters were optimized to maximize removal efficiency, with the optimal conditions determined as an NFX concentration of 200 mg/L, pH 7, and an applied potential of 1.2 V. The degradation pathway was elucidated through the identification of intermediate products, ultimately leading to the complete mineralization of NFX. To assess the environmental impact of BES-treated water, a series of eco-toxicity assays were conducted. Microbial diversity analysis revealed that soil exposed to BES-treated water maintained a balanced microbial community, contrasting with the disruptions observed in soils exposed to untreated NFX-contaminated water. Phytotoxicity tests, earthworm toxicity assay, and Artemia hatchability & lethality assays further confirmed the reduced toxicity of the BES-treated water. These findings highlight the efficacy of BES in the degradation of NFX, demonstrating its potential as a sustainable strategy for the remediation of antibiotic-contaminated environments and the mitigation of associated ecological risks.

Eco-friendly tea waste magnetite nanoparticles for enhanced adsorptive removal of norfloxacin and paroxetine from water

Traces of pharmaceuticals have been detected in water cycle raising concerns regarding the potential risks to human health and aquatic environment. Accordingly, removal of such compounds from water samples is a major concern. Herein, a facile and green NaOH modified tea waste magnetite nanoparticles have been fabricated for the adsorptive removal of a commonly used antibiotic (norfloxacin) and antidepressant (paroxetine) from water samples. The synthesized nanoparticles were characterized using TEM, FT-IR, DLS and VSM. Factors affecting the adsorption efficiency have been investigated with respect to pH (5, 7 and 9), adsorbent amount (0.125, 0.25 and 0.5 g), initial drug concentration (25, 50 and 100 µg/mL) and contact time (0.5, 1 and 2 h). The adsorption isotherms have been calculated. A percentage removal of 98 % and 99 % were obtained for simultaneous removal of 50 µg/mL norfloxacin and paroxetine, respectively in 2 h. Monitoring norfloxacin and paroxetine concentrations was performed through a validated HPLC-DAD method. The reusability of the nanoparticles has been studied for 3 adsorption–desorption cycles. No significant loss in adsorption efficiency was observed offering a sustainable water treatment. This study would offer a facile, green and economic protocol for the removal of complex organic compounds from water resources.

Bi2MoO6/MWCNTs-COOH/GCE electrochemical probe for ultrasensitively and selectively detecting antibiotic norfloxacin

Antibiotics have emerged as a class of contaminants of concern globally, raising widespread worry and unease, primarily because of their inappropriately use and endless migration in food chains. Electrochemical ultrasensitive and selective determination of norfloxacin (NOR) using bismuth-based bimetallic salt bismuth molybdate (Bi2MoO6) and carboxylated multi-walled carbon nanotube (MWCNTs-COOH) hybrid electrode as sensing platforms is presented hereby. The electrocatalytic ability of the electrodes was verified to be enhanced by the synergy effect of both Bi2MoO6 and MWCNTs-COOH using cyclic voltammetry and electrochemical impedance spectroscopy. Linear scan voltammetry was applied to detect NOR. The oxidation peak current was linearly correlated with NOR concentration of 0.03–10 μM and the low limit detection of the optimized method was 6.7 nM (S/N = 3). In addition, it was verified that Bi2MoO6/MWCNTs-COOH/GCE probe had good stability, reproducibility, repeatability and selectivity. The spiked recovery method for NOR in milk and lake water samples showed recoveries of 94.8 – 96.9% and 90.2 – 98.3%, respectively, which can be used to determine NOR in real samples with high sensitivity. The preparation of Bi2MoO6/MWCNTs-COOH/GCE provides a new prototype for probing NOR detection at nanomolar concentration and safeguarding antibiotic contamination in environmental and food chains.

Design of a novel direct Z-scheme BiOIO3/Bi2WO6 heterojunction for enhanced photocatalytic degradation of norfloxacin under visible light

The unique electronic structure, appropriate bandgap energy, and excellent electron transfer capability make bismuth-based semiconductors hotspots in the field of photocatalysis. Novel BiOIO3/Bi2WO6 Z-scheme heterojunctions were fabricated via in-situ hydrothermal synthesis. The BIOBIW-3 heterojunctions (BiOIO3:Bi2WO6=0.25:0.8, mole ratio) exhibited excellent photocatalytic activity for norfloxacin (NOR), with a degradation efficiency of 90.41 % after 90 min of photoreaction and a reaction kinetic constant of 0.02132 min−1, which was 5.02 and 9.35 times higher than that of BIO and BIW, respectively. The superior photocatalytic performance can be attributed to the intimate interface between BiOIO3 and Bi2WO6, as well as the staggered energy band structure that facilitates the formation of a Z-type heterojunction. This not only widens the range of visible light absorption but also enhances the separation and transfer of photogenerated carriers while maintaining a high capacity for redox reactions. The dominant active species in the degradation process were photogenerated holes (h+) and superoxide (∙O2−) radicals, and an in-depth exploration of the possible mechanism was conducted. Furthermore, the effects of various parameters, including solution pH, catalyst dosage, and NOR concentration on the photocatalytic degradation of NOR were also investigated. The prepared BiOIO3/Bi2WO6 heterojunctions exhibited remarkable photocatalytic performance and chemical stability, presenting a novel research direction for employing layered bismuth-based materials in the degradation of fluoroquinolone antibiotic wastewater.

Precursor effect on the hydrothermal synthesis of pure ZnO nanostructures and enhanced photocatalytic performance for norfloxacin degradation

The indiscriminate production and use of antibiotics have caused an environmental imbalance. Therefore, advanced oxidative processes such as photocatalysis have been proposed to eliminate the presence of such emerging pollutants. On the other hand, the use of photocatalytic processes requires the development of highly efficient photocatalysts. This paper introduces photocatalysts based on ZnO nanostructures with different morphologies and grown by low-temperature hydrothermal synthesis. The choice of zinc precursor resulted in significant variations in both the morphology and size of the ZnO particles. Morphologies, such as, dumbbell-like structures, nanogranules, and ellipsoidal particles were obtained by altering the zinc precursor in a slightly alkaline medium, and parameters such as photocatalyst dosage, initial concentration of antibiotic Norfloxacin (NOR), and pH in photocatalysis were thoroughly investigated. The reactive species responsible for NOR degradation were photogenerated holes, superoxide radicals, and hydroxyl radicals, with the latter showing a greater contribution. Degradation pathways are also proposed, and intermediate products were identified by LC-MS. Thirteen degradation products, of which six were reported for the first time, were detected. Among the synthesized morphologies, nanogranules exhibited superior photocatalytic activity, achieving 100% NOR degradation after 70 min under UV-C light and excellent reusability after three cycles (97%). The results surpass those from previous studies, since the simple and efficient photocatalysts employed led to shorter degradation times.

Norfloxacin affects inorganic nitrogen compound transformation in tailwater containing Corbicula fluminea

The Asian clam, Corbicula fluminea, commonly used in engineered wetlands receiving tailwater, affects nitrogen compound transformation in water. This study investigates how a commonly observed antibiotic in tailwater, norfloxacin, impact nitrogen compound transformation in tailwater containing C. fluminea. The clam was exposed to artificial tailwater with norfloxacin (0, 0.2, 20, and 2000 μg/L) for 15 days. Water properties, C. fluminea ecotoxicity responses, microorganism composition and nitrification- or denitrification-related enzyme activities were measured. Results revealed norfloxacin-induced increases and reductions in tailwater NH4+ and NO2− concentrations, respectively, along with antioxidant system inhibition, organ histopathological damage and disruption of water filtering and digestion system. Microorganism composition, especially biodiversity indices, varied with medium (clam organs and exposure water) and norfloxacin concentrations. Norfloxacin reduced NO2− content by lowering the ratio between microbial nitrifying enzyme (decreased hydroxylamine oxidoreductase and nitrite oxidoreductase activity) and denitrifying enzyme (increased nitrate reductase and nitrite reductase activity) in tailwater. Elevated NH4+ content resulted from upregulated ammonification and inhibited nitrification of microorganisms in tailwater, as well as increased ammonia emission from C. fluminea due to organ damage and metabolic disruption of the digestion system. Overall, this study offers insights into using benthic organisms to treat tailwater with antibiotic residues, especially regarding nitrogen treatment.

Conserved Evolutionary Trajectory Can Be Perturbed to Prevent Resistance Evolution under Norfloxacin Pressure by Forcing Mycobacterium smegmatis on Alternate Evolutionary Paths.

Antibiotic resistance is a pressing health issue, with the emergence of resistance in bacteria outcompeting the discovery of novel drug candidates. While many studies have used Adaptive Laboratory Evolution (ALE) to understand the determinants of resistance, the influence of the drug dosing profile on the evolutionary trajectory remains understudied. In this study, we employed ALE on Mycobacterium smegmatis exposed to various concentrations of Norfloxacin using both cyclic constant and stepwise increasing drug dosages to examine their impact on the resistance mechanisms selected. Mutations in an efflux pump regulator, LfrR, were found in all of the evolved populations irrespective of the drug profile and population bottleneck, indicating a conserved efflux-based resistance mechanism. This mutation appeared early in the evolutionary trajectory, providing low-level resistance when present alone, with a further increase in resistance resulting from successive accumulation of other mutations. Notably, drug target mutations, similar to those observed in clinical isolates, were only seen above a threshold of greater than 4× the minimum inhibitory concentration (MIC). A combination of three mutations in the genes, lfrR, MSMEG_1959, and MSMEG_5045, was conserved across multiple lineages, leading to high-level resistance and preceding the appearance of drug target mutations. Interestingly, in populations evolved from parental strains lacking the lfrA efflux pump, the primary target of the lfrR regulator, no lfrR gene mutations are selected. Furthermore, evolutional trajectories originating from the ΔlfrA strain displayed early arrest in some lineages and the absence of target gene mutations in those that evolved, albeit delayed. Thus, blocking or inhibiting the expression of efflux pumps can arrest or delay the fixation of drug target mutations, potentially limiting the maximum attainable resistance levels.

S-scheme BiOBr/Bi2WO6 with oxygen vacancies for synergistic photodegradation and hydrogen generation: Mechanisms insight and DFT calculations

An S-type heterojunction photocatalyst Bi2WO6/BiOBr (BWO/BiOBr) with an interlaced band structure and abundant oxygen vacancies (Ov) was synthesized using a hydrothermal method and high-temperature calcination. The surface was modified with carbon quantum dots (CQDs) to create a 0D/2D/2D structure. The resulting photocatalyst exhibited superior performance, with a degradation rate for Norfloxacin (NOR) antibiotics surpassing Bi2WO6 with oxygen vacancies (BWO-Ov) and BiOBr by 6.55 and 3.96 times, respectively. Notably, it achieved a high hydrogen generation rate of 459.49 μmol·g−1·h−1 under visible light. The enhanced carrier transfer and solar absorption were attributed to the synergistic effect of CQDs and S-type heterojunctions. The face-to-face 2D/2D structure provided abundant reaction sites. The influence of initial NOR concentration and photocatalyst dosage on photocatalytic activity was investigated in our study. Incorporating CQDs improved solar absorption, as confirmed by NOR degradation under various wavelengths. Electron spin resonance (ESR) analysis indicated the generation of reactive oxygen species. Density functional theory (DFT) calculations and characterization explored charge transfer mechanisms and degradation pathways. These findings contribute to the design of efficient S-type heterogeneous photocatalysts for sustainable energy and environmental applications.

Enhanced norfloxacin removal from sludge by dielectric barrier discharge plasma synthesis with Fe3O4/g-C3N4

The excess sludge adsorbed with antibiotics poses a huge threat to the ecological environment and human health, and the removal of antibiotics from sludge was focused on. The dielectric barrier discharge (DBD) coupled with Fe3O4/g-C3N4 to degrade norfloxacin (NOR) in excess sludge of wastewater treatment plant was studied, where Fe3O4/g-C3N4 was prepared through high-temperature calcination. At an input voltage of 90 V and at a current of 0.5 A, NOR concentration of 100 mg/kg total suspended solids (TSS), Fe3O4/g-C3N4 dosing of 100 mg/g TSS, and pH 6.94, the NOR degradation efficiency was 89.2 %, the energy yield was 1.98 mg/kWh, and the synergy factor of DBD with Fe3O4/g-C3N4 was 1.85. In this system, •OH, •O2−, h+, H2O2 and O3 played an important role in the degradation of NOR in sludge, and Fe3O4/g-C3N4 induced Fenton-like reactions using H2O2 generated by DBD and facilitated photocatalytic reactions with ultraviolet and visible light. There was a positive correlation between the NOR degradation efficiency and the sludge disintegration, and the sludge disintegration process released NOR from the solid phase to the liquid phase. Three possible degradation pathways and the toxicity evaluation of the intermediates were proposed based on the results of DFT and HPLC-MS. Additionally, the DBD/Fe3O4/g-C3N4 system improved the sludge disintegration and dewatering performance effectively.

Effects of two typical quinolone antibiotics in the marine environment on Skeletonema costatum

This study investigated the effects of levofloxacin (LEV) and norfloxacin (NOR) on Skeletonema costatum, focusing on cell growth, chlorophyll a (Chla) content, maximal quantum yield of PSII (Fv/Fm), protein content, enzyme activities of superoxide dismutase (SOD), glutathione reductase (GR), and glutathione peroxidase (GSH-PX), and the membrane lipid peroxidation product malondialdehyde (MDA) content were conducted to analyze the responses of S. costatum under LEV and NOR exposure. Cell growth, Chla content, Fv/Fm, protein content, enzyme activities, and MDA content were assessed to elucidate physiological changes. Both LEV and NOR inhibited S. costatum growth, except for 10 mg/L NOR, which promoted growth. Algal cells exhibited higher sensitivity to LEV, with 96h-IC50 values of 14.770 mg/L for LEV and 44.250 mg/L for NOR. Low NOR concentration (10 mg/L) increased Chla content, while high antibiotic concentrations (>20 mg/L for LEV, >100 mg/L for NOR) decreased Chla content and Fv/Fm, indicating an impact on photosynthesis. Elevated LEV and NOR levels reduced protein and MDA content but increased GR, SOD, and GSH activities, indicating induced oxidative stress. The study provides a comprehensive analysis of LEV and NOR effects on marine microalgae growth and underlying physiological mechanisms, shedding light on potential ecological risks posed by antibiotics in marine ecosystems.

Inhibition of norfloxacin on fermentative hydrogen production: Performance evaluation and metagenomic analysis

Toxic chemicals can inhibit the dark fermentation process for renewable biohydrogen production. Norfloxacin (NOR), a typical antibiotic, is present in various feedstocks of dark fermentation, which has excellent antibacterial properties. It is hypothesized that NOR could cause adverse effects on fermentative hydrogen production, while current understanding of this subject is scare. This study investigated the potential inhibitory effect of NOR on dark hydrogen fermentation, and explored the underlying mechanisms from the perspectives of bacterial community structure and functional gene abundance. The results showed that NOR significantly reduced the hydrogen-producing capacity upon exposure to concentrations exceeding 10 mg/L. The hydrogen yield decreased from 1.56 to 0.27 H2/mol-glucose at NOR concentrations of 50 mg/L. NOR also prolonged the hydrogen-producing lag period. Bacterial community analysis revealed that NOR reduced the abundance of high-yielding H2-generating bacteria, such as Clostridium sp., while increasing the abundance of H2-consuming bacteria (e.g. Enterococcus sp.). Metagenomic analysis further indicated that crucial genes involved in glycolysis (e.g. HK, tal-pgi, pfk and PK) and hydrogen formation (e.g. por and E1.12.7.2) were remarkably downregulated under NOR exposure, essentially causing the inhibition of hydrogen production. This study contributes to a better understanding of how antibiotics inhibit dark hydrogen fermentation and provides a theoretical basis for reducing potential inhibitory effects.

Effects of two pharmaceuticals: Doxycycline and norfloxacin on plant and animal organisms living in the freshwater

The main reason for the appearance of pharmaceutical compounds in the aquatic environment is their regular excretion by humans and animals in an unchanged form or slightly metabolized. Pharmaceuticals limit the habitable living environment for aquatic organisms, because they can be toxic not only to bacteria but also to non-target organisms. Plants of the Lemnoideae subfamily and crustaceans Daphniindae family are widely used as bioindicators in freshwater environmental risk assessments. This study aimed to use biotests (Lemna test and Daphtoxkit) to determine the effect of two pharmaceuticals: antibiotic – Doxycycline (DOX) and semi-synthetic chemotherapeutic drug – Norfloxacin (NOR) on plants Lemna minor and crustaceans Daphnia magna. Standard Lemna test was extended to include pharmaceutical effects on plant chlorophyll content (LCC) and fluorescence (Fo, Fm, and Fv/Fm), and the confirmation of drug toxicity was the biotest Daphtoxkit assessing the immobilization (IM) of organisms. Studies have shown that DOX was more toxic than NOR on tested aquatic organisms: plants and crustaceans. The lowest observed effect concentration (EC20) of DOX and NOR reduced by 20 % LCC and Iy of L. minor was 2.14 and 8.11 mg × L−1, respectively. The LCC was an early and sensitive indicator of the phytotoxic effects of DOX in L. minor before morphological changes were observed. Confirmation of drug toxicity was the Daphtoxkit. The EC20 (180. min) of DOX and NOR, IM of daphnia by 20 % was 117.18 and 215.42 mg × L−1, respectively. In conclusion, DOX and NOR in aquatic environments may have significant implications for tested organisms and their ecosystems.

Fluorescence turn off-on continuous response of dual lanthanide metal organic frameworks for selective detecting fluoroquinolone antibiotics

Eu3+ and Tb3+ as central ions and 1,4-phthalic acid (H2BDC) as ligand, a dual lanthanide metal-organic framework, Eu-Tb(BDC), was synthesized by co-precipitation method. The products performed stable crystal structure and adjustable fluorescence color. Eu0.15Tb2.85 (BDC) 3.0 was selected as an optimized probe to detect norfloxacin (NFX) in urine, and the fluorescence color was found to transfer from bright yellow to dark cyan and then to strong green with increasing NFX concentration. Mechanism analysis revealed that NFX with low concentration (10−6-10−3 M) stimulated light competition with BDC ligand due to internal filtration effect (IFE), resulting in the gradual fluorescence shutdown of Eu3+and Tb3+. While further increasing concentration of NFX to 10−3-10−2 M, the antibiotic molecules coordinated with lanthanide ions and transitioned their role from competitor to assistant. Where the energy transfer due to antenna effect overwhelmed IFE, the exciting light energy were retransferred to Eu3+ or Tb3+, and the probe's fluorescence restored. Generally, the Eu-Tb(BDC) probe performed fluorescence turn off-on response to norfloxacin with continuous concentration changing. Additionally, when detecting other fluoroquinolone antibiotics, the fluorescence of Eu0.15Tb2.85(BDC)3.0 changed from bright yellow to bright blue and eventually to dark red, which was attributed to the different coordination degrees of various antibiotic molecule with Tb3+ and Eu3+. It can be used to distinguish norfloxacin from other fluoroquinolone antibiotics.

Magnetic catalysts of MnFe2O4-AC activated peroxydisulfate for high-efficient treatment of norfloxacin wastewater

Norfloxacin (NOR) wastewater with a significant corrosive effect on human tissues requires deep treatment before discharge. Peroxydisulfate (PDS) activation with catalysts is an effective advanced method for wastewater treatment, and the key to its success lies in the design, synthesis, and preparation of efficient, stable, and easily prepared catalysts. In this study, magnetic catalysts of MnFe2O4-AC were synthesized through the hydrothermal method as the basic material activated PDS. The crystal structures were characterized using various techniques, including SEM-EDS, XRD, FT-IR, and XPS. The high magnetic properties of the prepared catalysts made them easily recoverable after wastewater treatment. In addition, the study investigated the effects of operating conditions on the treatment of NOR wastewater within the Electrochemistry/MnFe2O4-AC/PDS (EC/MnFe2O4-AC/PDS) system. Under the optimal conditions of current intensity of 0.15 A, catalyst dosage of 0.100 g/L, PDS concentration of 10 mmol/L, and NOR concentration of 5 mg/L, the removal rate of NOR was 97.33 %. The increased specific surface area of MnFe2O4-AC catalysts, when compared to MnFe2O4 catalysts, benefited the activation of PDS. MnFe2O4-AC catalysts showed a good stability in activating PDS for NOR wastewater treatment without causing secondary pollution in repeated use experiments. Finally, the NOR degradation was attributed to both the generation of free radicals (SO4•- and ‧OH radicals) and non-radical processes (electrode oxidation).

Electrophoretic Mobility Assay to Separate Supercoiled, Catenated, and Knotted DNA Molecules.

Two-dimensional (2D) agarose gel electrophoresis is the method of choice to analyze DNA topology. The possibility to use E. coli strains with different genetic backgrounds in combination with nicking enzymes and different concentrations of norfloxacin improves the resolution of 2D gels to study the electrophoretic behavior of three different families of DNA topoisomers: supercoiled DNA molecules, post-replicative catenanes, and knotted DNA molecules. Here, we describe the materials and procedures required to optimize their separation by 2D gels. Understanding the differences in their electrophoretic behavior can help explain some important physical characteristics of these different types of DNA topoisomers. Key features • Preparative method to enrich DNA samples of supercoiled, catenated, and knotted families of topoisomers, later analyzed by 2D gels (or other techniques, e.g., microscopy). • 2D gels facilitate the separation of the topoisomers of any given circular DNA molecule. • Separation of DNA molecules with the same molecular masses but different shapes can be optimized by modifying the conditions of 2D gels. • Evaluating the roles of electric field and agarose concentration on the electrophoretic mobility of DNA topoisomers sheds light on their physical characteristics.

Simultaneous photoactivation of a fluoroquinolone antibiotic and nitric oxide with fluorescence reporting.

The achievement of smart pharmaceuticals whose bioactivity can be spatiotemporally controlled by light stimuli is known as photopharmacology, an emerging area aimed at improving the therapeutic outcome and minimizing side effects. This is especially attractive for antibiotics, for which the inevitable development of multidrug resistance and the dwindling of new clinically approved drugs represent the main drawbacks. Here, we show that nitrosation of the fluoroquinolone norfloxacin (NF), a broad-spectrum antibiotic, leads to the nitrosated bioconjugate NF-NO, which is inactive at the typical minimum inhibitory concentration of NF. Irradiation of NF-NO with visible blue light triggers the simultaneous release of NF and nitric oxide (NO). The photouncaging process is accompanied by the revival of the typical fluorescence emission of NF, quenched in NF-NO, which acts as an optical reporter. This permits the real-time monitoring of the photouncaging process, even within bacteria cells where antibacterial activity is switched on exclusively upon light irradiation. The mechanism of photorelease seems to occur through a two-step hopping electron transfer mediated by the lowest triplet state of NF-NO and the phosphate buffer ions or aminoacids such as tyrosine. Considering the well-known role of NO as an "unconventional" antibacterial, the NF-NO conjugate may represent a potential bimodal antibacterial weapon activatable on demand with high spatio-temporal control.

Sensitive visual detection of norfloxacin in water by smartphone assisted colorimetric method based on peroxidase-like active cobalt-doped Fe3O4 nanozyme

Norfloxacin is widely used owing to its strong bactericidal effect on Gram-negative bacteria. However, the residual norfloxacin in the environment can be biomagnified via food chain and may damage the human liver and delay the bone development of minors. Present work described a reliable and sensitive smartphone colorimetric sensing system based on cobalt-doped Fe3O4 magnetic nanoparticles (Co-Fe3O4 MNPs) for the visual detection of norfloxacin. Compared with Fe3O4, Co-Fe3O4 MNPs earned more remarkably peroxidase-like activity and TMB (colorless) was rapidly oxidized to oxTMB (blue) with the presence of H2O2. Interestingly, the addition of low concentration of norfloxacin can accelerate the color reaction process of TMB, and blue deepening of the solution can be observed with the naked eye. However, after adding high concentration of norfloxacin, the activity of nanozyme was inhibited, resulting in the gradual fading of the solution. Based on this principle, a colorimetric sensor integrated with smartphone RGB mode was established. The visual sensor exhibited good linearity for norfloxacin monitoring in the range of 0.13-2.51 µmol/L and 17.5-100 µmol/L. The limit of visual detection was 0.08 µmol/L. In the actual water sample analysis, the spiked recoveries of norfloxacin were over the range of 95.7%-104.7 %. These results demonstrated that the visual sensor was a convenient and fast method for the efficient and accurate detection of norfloxacin in water, which may have broad application prospect.