Detection Of Levofloxacin Research Articles

A cost-effective method for the sensitive detection of levofloxacin using a 3D composite electrode composed of nail polish, graphite and aluminium oxide.

The potential impact on human health and the environment has spurred significant interest in detecting and quantifying pharmaceutical compounds across various matrices, from environmental to biological samples. Here, we present an electrochemical approach for determining levofloxacin in drug, synthetic urine, water, and breast milk samples. An affordable sensor was constructed using 3D printing and composite material based on nail polish, graphite, and aluminum oxide. The conductive composite material was characterized spectroscopically, electrochemically, and by imaging techniques. Subsequently, an electrochemical method based on square wave voltammetry was optimized and applied. The method exhibited good sensitivity (5.11 ± 0.0912 μA L μmol-1 cm-2) and enhanced stability (RSD = 7.2%), with electrochemical responses correlating with the concentration of levofloxacin in the samples tested, yielding recovery values in the range of 98 to 111%. The developed method demonstrated a robust linear working range from 2 to 100 μmol L-1 and a nanomolar detection limit of 128 nmol L-1, rendering it suitable for quantitative analysis. The sensor also shows promise as a platform for the sensitive detection of pharmaceutical compounds, contributing to greater safety and sustainability in these domains.

Target self-calibration ratiometric fluorescent sensor based on facile-synthesized europium metal-organic framework for multi-color visual detection of levofloxacin

Target self-calibration ratiometric fluorescent sensor based on facile-synthesized europium metal-organic framework for multi-color visual detection of levofloxacin

Alkaline metal tungstate anchored on functionalized-MWCNT: A co-active electrocatalyst for the detection of levofloxacin

The widespread usage of levofloxacin (LVF) intake is executed for several urinary and respiratory systems infections in human. But, its over intake leads to severe damage to humans and the environment by its exposure. Hence the detection of LVF is concerned and we herein developed an electrocatalyst, strontium tungsten oxide nanospheres and later decorated onto the functionalized multiwall carbon nanotubes (SrWO4/f-MWCNT) to perform effective electrochemical recognition of LVF in aquatic and biological samples. Binary metal oxide with carbon composite SrWO4/f-MWCNT was developed due to its specific features as nanostructures. Various methods of investigation have been examined to identify the physiochemical characteristics like X-ray diffraction, Raman spectroscopy, Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, and morphological characteristics including field emission scanning electron microscopy, and transmission electron microscopy. The synthesized SrWO4/f-MWCNT sample crystalline size was around 32.9 nm. The SrWO4/f-MWCNT modified glassy carbon electrode (GCE) has been subjected to electrochemical investigation with a wide linear range of 0.049 μM–574.73 μM with good sensitivity 2.86 μA μM−1 cm2, the limit of detection at 14.9 nM for LVF sensing. Furthermore, the designed LVF detection exhibited excellent anti-interference, stability, reproducibility, and repeatability. The as-developed sensor's electrochemical outcomes indicate the superior performance inherent in the developed composite.

Morphology-transforming AuNPs-based fluorescent probe for ultra-low sensitive detection of levofloxacin in urine samples at pH 7.0 through excimer formation

Fluorescent metal nanoparticles (MNPs) have garnered considerable interest in the realm of healthcare applications. Within this domain, we present a novel fluorescent sensor: Pamoic acid (PA) functionalized excitation-dependent gold nanoparticles (PA@AuNPs), designed to ascertain levofloxacin (LF) concentrations in human urine samples under pH 7.0 conditions. The synthesis of PA@AuNPs was achieved via a chemical reduction method employing PA as both a reducing and stabilizing agent. Validation of the successful synthesis of PA@AuNPs was conducted utilizing a suite of analytical techniques including X-ray diffraction (XRD), ultraviolet–visible absorption spectroscopy (UV–Vis), Fourier transform infrared spectroscopy (FTIR), Raman spectroscopy, and X-ray photoelectron spectroscopy (XPS). Microscopic examination via field emission scanning electron microscopy (FESEM) and high-resolution transmission electron microscopy (HRTEM) elucidated the spherical morphology of PA@AuNPs, with an average diameter ranging from 10 to 15 nm. Furthermore, atomic force microscopy (AFM) revealed an average surface roughness of 20.72 nm for PA@AuNPs. Thermal analysis results divulge that PA@AuNPs are highly stable up to 370 °C. The PA@AuNPs have shown more than 10-fold higher selectivity for LF in comparison with other commercially available antibiotics. The fluorescence emission intensity of PA@AuNPs (quantum yield (ΦF) 3.36 %) has shown enhanced redshift (436 → 497 nm; ∼61 nm) (λex 353 nm) upon the sequential addition of LF (0 → 100 µM) and achieved a lower detection limit (LoD = 36 nM; LoQ = 121 nM; Ka = 1.0457 × 104 M−1) with increased ΦF 18.96 %. This radiative process and fluorescence enhancement were confirmed by time-correlated single photon counting (TCSPC) measurement (4.89 → 5.36 ns). Interestingly, upon sensing LF, PA@AuNPs changed their morphology from spherical to octahedron and displayed an excimer formation through intermolecular π-π stacking. Furthermore, the stability of the complex, PA@AuNPs•LF which formed through coordination, by restoring the fluorescence intensity of PA@AuNPs•LF (turn on) in the presence of ethylenediamine tetraacetic acid (EDTA) (turn off) is demonstrated. The formation of the PA@AuNPs•LF complex was further confirmed by XRD analysis and FTIR spectroscopy. The HRTEM and FESEM validate that PA@AuNPs•LF have octahedral morphology with an average size of 20–30 nm, and the obtained moiré fringes in TEM images are due to the overlap of LF on the surface of PA@AuNPs. The AFM analysis divulges that PA@AuNPs•LF had a larger surface roughness (Sa = 26.91 nm). The experimentally attained zeta potential of PA@AuNPs (–12.6 mV) was further decreased (–17.6 mV) in the presence of LF, which confirms the interaction between PA@AuNPs and LF. The cell viability (82 %) in L929 Fibroblast cells augmented the biological applications of PA@AuNPs. The practicability of the fluorescent sensor probe was demonstrated in human urine samples with recovery ranges from 97.56 to 104.38 %.

Nano-cerium zinc molybdate embedded with activated graphene for detection of levofloxacin in polluted water resources

Antibiotics have widespread applications in personal care, animal muscle growth, and aquaculture, yet their pervasive use gives rise to substantial risks for human health and the ecosystem. Consequently, the imperative lies in developing accurate and highly sensitive detection techniques for analyzing levofloxacin (LFX). This research focuses on the hydrothermal synthesis of unique three-dimensional cubical-like ternary cerium-doped zinc molybdate (Ce@ZnMoO4) nanostructures. Ultrasonic methods were used to integrate Ce@ZnMoO4 with activated graphene (AGr) for LFX detection. X-ray diffraction, Raman spectroscopy, and field emission scanning electron microscopy were used to carefully analyze the resultant Ce@ZnMoO4/AGr composite's physical characteristics. The covalent integration of cubic-like Ce@ZnMoO4 with AGr produced a four-fold increase in sensor response compared to a Ce@ZnMoO4-modified electrode and displayed remarkable electrocatalytic activity. Due to its unique electronic and catalytic properties, Ce@ZnMoO4 synergistically interacts with the AGr layers. This synergy enhances conductivity, facilitating efficient electron transfer during electrochemical processes. Additionally, the composite offers a high surface area and numerous active sites, enabling more significant interaction between the electrode and the target analyte, LFX, thereby enhancing sensor response. The sensor demonstrated outstanding lower limits of detection (0.0031 µM), good sensitivity (0.3327 µA/µM cm-2), and a quantification limit (0.0375 µM) under optimal conditions. Along with high specificity and outstanding storage stability, a broad linear range spanning from 0.025 to 845 µM was also found. The effectiveness of the sensor is further confirmed by the successful detection of LFX in aquatic samples.

β-Cyclodextrin/carbon dots-grafted cellulose nanofibrils hydrogel for enhanced adsorption and fluorescence detection of levofloxacin

In this study, a novel hydrogel, β-cyclodextrin/carbon dots-grafted cellulose nanofibrils hydrogel (βCCH), was fabricated for removal and fluorescence determination of levofloxacin (LEV). A comprehensive analysis was performed to characterize its physicochemical properties. Batch adsorption experiments were conducted, revealing that βCCH reached a maximum adsorption capacity of 1376.9 mg/g, consistent with both Langmuir and pseudo-second-order models, suggesting that the adsorption process of LEV on βCCH was primarily driven by chemical adsorption. The removal efficiency of βCCH was 99.2 % under the fixed conditions (pH: 6, initial concentration: 20 mg/L, contact time: 300 min, temperature: 25 °C). The removal efficiency of βCCH for LEV still achieved 97.3 % after five adsorption-desorption cycles. By using βCCH as a fluorescent probe for LEV, a fast and sensitive method was established with linear ranges of 1–120 mg/L and 0.2–1.0 μg/L and a limit of detection (LOD) as low as 0.09 μg/L. The viability of βCCH was estimated based on the economic analysis of the synthesis process and the removal of LEV, demonstrating that βCCH was more cost-effective than commercial activated carbon. This study provides a novel approach for preparing a promising antibiotic detection and adsorption material with the advantages of stability, and cost-effectiveness.

Design of Potentiometric Sensor Based on Molecularly-imprinted Polymer for Direct Detection of Levofloxacin in Plasma for Point-of-Care Applications

Design of Potentiometric Sensor Based on Molecularly-imprinted Polymer for Direct Detection of Levofloxacin in Plasma for Point-of-Care Applications

An R-type hexagonal ferrite nanoparticles-based electrochemical sensor for Levofloxacin detection in pharmaceutical and clinical specimens

The usage of Levofloxacin (LEV) has increased in recent years for the treatment of bacterial infections in both human and veterinary fields. In this context, there has been a significant demand for the development of a highly sensitive and cost-effective approach to LEV quantification. In this study, R-type hexagonal ferrite nanoparticles (SrSn2Fe4O11-NPs) were prepared by an auto-ignition methodology and various analytical techniques were used for the materiaĺs characterization, including X-ray diffraction (XRD), Field emission scanning electron microscopy (FE-SEM), X-ray photoelectron spectroscopy (XPS), Brunauer Emmett and Teller (BET) analysis, dynamic light scattering (DLS), and vibrating sample magnetometer (VSM) analysis. The characterization confirmed that the prepared material has a crystalline structure single-phase with a crystalline size of 35.02 nm. The R-type hexagonal ferrite nanoparticles were immobilized on a glassy carbon electrode (GCE) by a simple drop-casting approach to developing an efficient electrochemical sensor (SrSn2Fe4O11-NPs/GCE) for sensitive and selective LEV detection through an extended concentration range (0.06 × 10−6 to 170 × 10−6 M) and a low detection limit of (41.5nM). The developed sensor was applied successfully to quantitatively determine LEV in clinical samples and pharmaceutical preparations with excellent recoveries from 95.2 to 102.5 %.

Ultra-sensitive electrochemical detection of levofloxacin using a binder-free copper and graphene composite

Given the levels of pollution in the aquatic environment and the development of antimicrobial resistance, it is essential to develop sensors, with sensitivity, selectivity, stability, and cost-effectiveness, for the determination of antibiotics. The present article highlights the fabrication of an ultra-sensitive graphene and copper sensor, Gr/Cu, supported on glassy carbon (GCE/Gr/Cu) for the electroanalysis of levofloxacin through a cost-effective electrodeposition method. The sequential electrodeposition of graphene and Cu was optimised to give GCE/Gr/Cu, with the Cu particles well dispersed on the graphene sheets. The composite exhibited very good conducting properties as evidenced from electrochemical impedance studies. Using cyclic voltammetry, an impressive sensitivity of 19.7 μA μM−1 cm−2 was achieved with a detection limit of 11.86 nM, providing a promising electrocatalytic material for the determination of this antibiotic. Moreover, good selectivity was observed in the presence of various ions typically found in water and other drug molecules, while very good stability exceeding a 21-day period was achieved, and recovery values between 97.7 and 103.8 % were obtained in tap water.

Ratiometric Fluorescence Detection of Levofloxacin Based on a Cube-like Zn(II)-Eu(III) Nanocluster: Functionalized Sodium Alginate Film for the Detection in Serum and Medicine.

A cube-like Zn(II)-Eu(III) nanocluster 1 (molecular sizes: 1.8 × 2.0 × 2.0 nm) was constructed by the use of a new long-chain Schiff base ligand. It shows a ratiometric fluorescence response to levofloxacin (LFX) with high sensitivity and selectivity, which can be expressed as I615nm/I550nm = A*[LFX]2 + B*[LFX] + C. It is used to quantitatively detect the LFX concentrations in fetal calf serum (FCS) and tablets sold in pharmacy. Filter paper strips bearing 1 can be used to qualitatively detect LFX by a color change to red under a UV lamp. 1 and its hybrid with sodium alginate (SA), 1@SA, display potential applications in the qualitative detection of LFX in FCS and the medicine. The limit of detection of 1 to LFX is as low as 2.1 × 10-2 nM.

A novel molecularly imprinted electrochemical sensor from poly (3, 4-ethylenedioxythiophene)/chitosan for selective and sensitive detection of levofloxacin

The improper usage of levofloxacin (LEV) endangers both environmental safety and human public health. Therefore, trace analysis and detection of LEV have extraordinary significance. In this paper, a novel molecularly imprinted polymer (MIP) electrochemical sensor was developed for the specific determination of LEV by electrochemical polymerization of o-phenylenediamine (o-PD) using poly(3,4-ethylenedioxythiophene)/chitosan (PEDOT/CS) with a porous structure and rich functional groups as a carrier and LEV as a template molecule. The morphology, structure and properties of the modified materials were analyzed and studied. The result showed that the electron transfer rate and the electroactive strength of the electrode surface are greatly improved by the interconnection of PEDOT and CS. Meanwhile, PEDOT/CS was assembled by imprinting with o-PD through non-covalent bonding, which offered more specific recognition sites and a larger surface area for the detection of LEV and effectively attracted LEV through intermolecular association. Under the optimized conditions, MIP/PEDOT/CS/GCE showed good detection performance for LEV in a wide linear range of 0.0019– 1000 μM, with a limit of detection (LOD, S/N = 3) of 0.4 nM. Furthermore, the sensor has good stability and selectivity, and exhibits excellent capabilities in the microanalysis of various real samples.

Activity augmentation of a functionalized 2D conjugated polymer matrix with iron vanadate nano-bulbs for real-time detection of levofloxacin

This work presents a pioneering approach to the electrochemical detection of levofloxacin (LVO) in human blood samples using FVO/CN, which enhances the sensitivity and selectivity of the sensor towards the detection of LVO.

Mesoporous silica imprinted nanocomposites for selective adsorption and detection of levofloxacin

The proper treatment of antibiotics has become a formidable challenge in environmental remediation. In this work, a mesoporous molecularly imprinted polymer (mMIP) was successfully fabricated on SiO2 by the sol gel process and used to selectively adsorb and detect antibiotic levofloxacin (LEVO). The adsorption characteristics of LEVO-mMIP were explored in diverse respects (e.g., kinetics, isotherms, and selectivity). The mMIP exhibited higher LEVO adsorption capacity (115 mg/g), higher specific selectivity, and faster kinetics (10 min). The prepared mMIP also exhibited enhanced reusability/durability (n = 8 cycles). The LEVO-mMIP was thus used as dispersive solid phase extraction material for the extraction of LEVO from actual samples (e.g., tap/river water and pharmaceutical formulations) with the aid of high performance liquid chromatography (LOD of 0.07 ng/mL and good recoveries of 90.76–108.17% (RSD of 2.55–5.09%)). As such, the potential utility of mMIP is validated for the adsorption and detection of LEVO in environmental matrices.

Improved electrochemical detection of levofloxacin in diverse aquatic samples using 3D flower-like Co@CaPO4 nanospheres

The misuse of antibiotics has become a concerning environmental issue, posing a significant threat to public health. Levofloxacin (LFX), a fluoroquinolone antibiotic, is particularly worrisome due to its detrimental impact on human health and the ecosystem. Therefore, the selective and accurate identification of LFX is of utmost importance. In this study, we have developed an electrochemical sensor based on cobalt-doped calcium phosphate (Co@CaHPO) for the sensitive and selective detection of LFX in various water samples. Under optimized conditions, the Co@CaHPO-modified glassy carbon electrode (GCE) exhibited exceptional electrochemical activity, low charge transfer resistance, and a fast electron transfer rate, outperforming the unmodified GCE. The proposed Co@CaHPO-modified GCE demonstrated remarkable electrochemical characteristics, including a wide linear range (0.3–460 μM) and a lower detection limit (0.151 μM) with high sensitivity (0.676 μAμM−1 cm2). This detection approach may enable the direct detection of LFX in the pharmaceutical environment. Furthermore, the resulting sensor exhibited good selectivity, excellent cyclic and storage stability, reproducibility, and repeatability. The practical application of this LFX sensor can be extended to various water samples, yielding reliable and satisfactory results.

Micromeria biflora mediated gold and silver nanoparticles for colourimetric detection of antibiotics and dyes degradation

The study reports on synthesis of aqueous extract mediated gold and silver nanoparticles of M. biflora (MBAuNPs and MBAgNPs) via hydrated chloroauric acid and silver nitrate salts. The nanoparticles (NPs) were produced in 1:15 (MBAuNPs) and 1:6 (MBAgNPs) ratios under sunlight displaying localized surface plasmon resonance (LSPR) peaks at 541 and 431 nm, respectively. The sizes characterized by transmission electron, scanning electron, and atomic force microscopic (SEM, TEM, AFM) techniques were respectively 26.73 nm and 53.81 nm. The subject NPs demonstrated application in the degradation of methylene blue, Congo red, Rhodamine B, methyl orange, ortho-nitrophenol, and para-nitrophenol ranging from 65 to 86 %. For detection of levofloxacin, amoxicillin, and azithromycin antibiotics, the MBAuNPs and MBAgNPs exhibited efficiency in real water and biological (blood plasma and urine) samples. Conclusively, the MBAuNPs and MBAgNPs applications for dyes degradation and antibiotics detection was found as simple and cost-effective analytical method.

3,3′,5,5′-Tetramethylbenzidine assisted construction of a label-free colorimetric and ratiometric fluorescent dual-channel sensor for the detection of levofloxacin

A colorimetric and ratiometric fluorescent dual-channel sensor was constructed for levofloxacin (LVFX) detection only using 3,3′,5,5′-tetramethylbenzidine (TMB). LVFX was found to be a light-activatable oxidase mimic, which can generate free radicals and oxidize colorless TMB to blue product (oxTMB) upon irradiation at 365 nm, providing a visible color signal. Interestingly, increasing LVFX concentration causes more TMB to be oxidized, leading to a reduction in the fluorescence intensity of TMB at 410 nm and a rise in the fluorescence intensity of LVFX at 511 nm under excitation at 350 nm. The detection limits of the colorimetric and ratiometric fluorescent sensor for LVFX were 0.26 μM and 0.23 μM, respectively. Moreover, a smartphone-based dual-channel portable device was constructed to integrate the photocatalytic oxidation reaction and the colorimetric and fluorescent detection of LVFX. Successfully detecting LVFX in milk and egg white samples in 5 min suggests the device has great potential in on-site assays.

Electrochemical chiral sensor for levofloxacin detection base on Cu/Fe-BTC amplification.

The key to developing sensors for chiral drug determination is to exclude interference from enantiomers. In this study, metal-organic frameworks (MOFs) and molecularly imprinted polymer (MIP) were introduced to prepare a chiral sensor for levofloxacin detection. The MIP was electropolymerised on the surface of the Cu/Fe-benzene-1,3,5-tricarboxylate MOF (Cu/Fe-BTC)-modified Au electrode using levofloxacin as a template molecule. After eluting the levofloxacin, a chiral sensor with recognition sites for levofloxacin was obtained. With this site as a switch, a novel method for detecting levofloxacin was established. Because of the enhanced recognition effect, the sensor can effectively exclude the enantiomeric interference of d-ofloxacin. Moreover, Cu/Fe-BTC can effectively amplify the current response signal and improve the sensitivity of thesensor. The linear range of the sensor was 5 to 4000 × 10-11mol L-1, and the detection limit was 2.07 × 10-11mol L-1. Whenapplied to detecting levofloxacin in actual samples, the sensor showed a 92.7-109.8% recovery.

A novel electrochemical sensing platform based on double-active-center polyimide covalent organic frameworks for sensitive analysis of levofloxacin.

The development of a simple and sensitive electrochemical sensing platform for levofloxacin (LVF) analysis is of great significance to human health. In this work, a covalent organic framework (TP-COF) was in situ grown on the surface of Sn-MoC nanospheres with nanoflower-like morphology through a one-pot method to obtain the TP-COF@Sn-MoC composite. The prepared composite was used to modify a glassy carbon electrode (GCE) to realize the sensitive detection of levofloxacin. TP-COF was formed by polycondensation of 2,4,6-tris(4-aminophenyl)-1,3,5-triazine (TAPT) and pyromellitic dianhydride (PMDA), in which C = O and C = N groups served as double active centers forthe recognition and electrocatalytic oxidation of the target molecule. Meanwhile, the introduction of Sn-MoC improved the conductivity of the electrode. The TP-COF@Sn-MoC composite produced a strong synergistic effect and showed a high electrocatalytic ability toward levofloxacin oxidation. The linear range of LVF was 0.6-1000μM and the limit of detection (LOD) was 0.029μM (S/N = 3). In addition, the sensor has been successfully applied for the analysis of LVF in human urine and blood serum samples with acceptable recovery rates, demonstrating that the sensor was promising in practical applications.

Lamellar α-Zirconium Phosphate Nanoparticles Supported on N-Doped Graphene Nanosheets as Electrocatalysts for the Detection of Levofloxacin

Lamellar α-Zirconium Phosphate Nanoparticles Supported on N-Doped Graphene Nanosheets as Electrocatalysts for the Detection of Levofloxacin

Fast, Selective and Sensitive Fluorescence Detection of Levofloxacin, Fe3+ and Cu2+ Ions in 100% Aqueous Solution Via Their Reciprocal Recognition.

The fluorescence detection of ions and pharmaceutical effluents by using organic chemosensors is a valuable surrogate to the currently existing expensive analytical methods. In this regard, the design of multi-functional chemosensors to recognize desirable guests is of utmost importance. In this study, we first show that levofloxacin (LVO) is able to use as a fluorescent chemosensor for the detection of biologically important Cu2+ (turn-off) and Fe3+ (turn-on) ions via independent signal outputs in 100% aqueous buffer solutions. Next, using the reciprocal recognition of LVO and Fe3+ provides a unique emission pattern for the detection of LVO. This approach exhibited a high specificity to LVO among various pharmaceutical samples, namely acetaminophen (AC), azithromycin (AZ), gemifloxacin (GEM) and ciprofloxacin (CIP) and also showed great anti-interference property in urine. The attractive features of this sensing system are availability, easy-to-use, high sensitivity (limit of detection = 18 nM for Cu2+, 22 nM for Fe3+ and 0.12 nM for LVO), rapid response (5 s) with an excellent selectivity.