Adsorption Of Antibiotics Research Articles

Current Progress on Antibiotic Resistance Genes Removal by Composting in Sewage Sludge: Influencing Factors and Possible Mechanisms

Antibiotic resistance genes (ARGs) present in sewage sludge pose significant environmental and public health challenges. Composting has emerged as a promising method to mitigate these risks by reducing ARGs. This review paper evaluated the current progress in the removal of ARGs through composting, incorporating a bibliometric analysis of 228 publications from January 2010 to January 2024. This review highlights the increasing scholarly interest in this field, with a notable rise in publications since 2010. Key mechanisms identified include the denaturation of proteins and DNA at high temperatures, the adsorption of antibiotics and heavy metals by additives like biochar, and shifts in microbial communities, all contributing to the reduction of ARGs during composting. Despite these findings, challenges remain in achieving consistent ARG removal rates, addressing the potential for ARG regrowth, and understanding horizontal gene transfer post-composting. This review suggests further research into optimizing composting conditions and integrating additional treatment methods to enhance ARG removal and minimize associated risks.

Analyzing and optimizing the adsorption of metronidazole antibiotic on nano-scale pumice mine waste based RSM-CCD technique in water

Analyzing and optimizing the adsorption of metronidazole antibiotic on nano-scale pumice mine waste based RSM-CCD technique in water

Green room-temperature fabrication of phosphotungstic acid functionalized MOF-808 for efficient removal of cationic antibiotics

ZrⅣ-based metal–organic frameworks (MOFs)–featuring exceptional water stability, large surface area, and structural tunability–hold promise for efficient antibiotics adsorption from water. However, their inherent positive charge in neutral environments and the harsh conditions required for their synthesis hinder their effective removal of cationic antibiotics. To address this challenge, a green one-pot synthesis approach was proposed to fabricate phosphotungstic acid-functionalized MOF-808 (termed as PTA@MOF-808) at room temperature for elevated antibiotic adsorption. This approach not only leverages the strong electronegativity of PTA to improve electrostatic interactions and π-π stacking but also finely tailors the pore size of MOF-808, resulting in enhanced adsorption capacity of PTA@MOF-808. The influence of PTA loading, solution pH, and absorbent dosage on the performance of PTA@MOF-808 were studied in detail. Adsorption experiments demonstrated that PTA@MOF-808 outperformed unmodified MOF-808 in removing various positively charged antibiotics, with 5 % PTA@MOF-808 exhibiting maximum adsorption capacities of 548.1 mg g−1 and 482.9 mg g−1, for DOX and TCHC, respectively. The adsorption process followed the Langmuir isothermal model and the pseudo-second-order kinetic equation. Furthermore, the composite PTA@MOF-808 displayed excellent reusability after multiple adsorption–desorption cycles. These findings highlight the potential of PTA@MOF-808 as a promising absorbent for removing specific antibiotics from water, with significant implications for wastewater treatment.

In-situ growth of Fe-MOF on magnetic materials by self-template method to enhance practicality and removal of tetracycline antibiotics from aqueous solution

In this work, core–shell structured Fe3O4@PCN-333 (Fe) composite was constructed using a self-template method, in which Fe3O4 microspheres not only serve as magnetic centers but also provide Fe (III) for the preparation of PCN-333 (Fe). PCN-333 (Fe) uniformly grew as a shell on the surfaces of the microspheres, and the shell thickness was approximately 38 nm. The composite exhibited high adsorption performance, with maximum adsorption capacities of 471.7, 303.3 and 314.5 mg/g for chlortetracycline, tetracycline and oxytetracycline, respectively. The adsorption of tetracycline antibiotics (TCs) was based on the Langmuir and pseudo-second-order model, and external diffusion and pore diffusion were the rate-limiting steps in adsorption. The strong adsorption capacity was attributed to the mechanism of π–π interaction, coordination bonds, electrostatic interaction, hydrogen bonding, and van der Waals force. Fe3O4@PCN-333 (Fe) composite displayed good stability in the aqueous solution, strong TCs adsorption capacity, high selectivity, anti-interference performance for adsorbing TCs, fast recovery with external magnetic field, reusability, thus effectively reducing the cost for removing water pollutants. These features make the composite a potential material for removing TCs in the environment.

Efficient adsorption of antibiotics using MXene nanosheet delaminated by Taylor vortex flow

MXenes are emerging as a promising class of two-dimensional (2D) adsorbents suitable for various environmental applications. The present study explores the use of Ti3C2Tx MXene nanosheet, delaminated by Taylor vortex flow (TVF), namely d-MXene-CT, as an efficient adsorbent for fluoroquinolones (FQs). The TVF induced in the gap between two coaxial cylinders of the Couette-Taylor reactor enhances the delamination process, yielding larger and thinner MXene nanosheets with a specific surface area 12 fold higher than that of nanosheets delaminated by turbulent eddy flow (TEF), namely d-MXene-MT in a conventional mixing tank (MT) reactor. As a result, the d-MXene-CT exhibited superior adsorption performance, with removal capacity for ciprofloxacin (CIP) of 349 mg/g and for levofloxacin (LEV) of 290.51 mg/g, representing 40 ∼ 60 % improvement over d-MXene-MT (249 mg/g for CIP and 180.22 mg/g for LEV). The adsorption process follows the pseudo-second-order kinetics model and fits the Langmuir isotherm, indicating the involvement of a monolayer chemisorption mechanism. Further investigation revealed that the removal of CIP and LEV was mainly driven by electrostatic attraction between oxygen functionality of MXene and protonated nitrogen group of FQs. The study highlights the potential of d-MXene-CT as a promising adsorbent for treating (FQs) from contaminant water.

Polyacrylonitrile nanofibrous mat modified with cysteamine and ionic liquid as a recyclable and efficient adsorbent for selective removal of sulfonamides and Cu(II) from aqueous solution: Roles of multi-function adsorption

The combined contamination of heavy metals and antibiotics is a prevalent occurrence, yet the distinct chemical characteristics of these substances pose a significant obstacle to their simultaneous elimination. In this work, novel polyacrylonitrile nanofibrous mat (NFsM) modified with cysteamine and ionic liquid (IL@Cys@PAN NFsM) was developed using a cascade thiol-ene click reaction. The IL@Cys@PAN NFsM exhibits a rich array of functional groups and demonstrates strong binding affinity, fast mass transfer, and exceptional selectivity for sulfonamides (SAs) and Cu(II). The maximum adsorption capacities for SAs and Cu(II) in single-component systems were 122.3 and 97.4 mg/g respectively, according to the Langmuir isotherm model. The time dependent adsorption capacities followed a pseudo-second-order kinetic model, demonstrating a chemisorption-dominant process for each analyte. In binary pollutant systems, the co-occurrence of SAs and Cu(II) in water produced a competitive effect; however, the decrease in adsorption capacity was minimal. Through experimental analysis, FTIR characterization and density functional theory (DFT) studies, reasonable interactions of hydrogen-bond, electrostatic interactions, π-π stacking for SAs, and chelation effect for Cu(II) were proposed. Additionally, the reusability and recyclability of IL@Cys@PAN NFsM enhance its practicality for real-world applications. This paper presents the first systematic study on the simultaneous adsorption of heavy metals and antibiotics using NFsM, offering a novel perspective on the design of custom adsorbents capable of efficiently removing multiple contaminants with diverse characteristics while balancing eco-friendliness, excellent adsorption performance, and impressive recyclability for wastewater remediation.

Harnessing the power of ternary nanocomposites: Iron oxide, multiwalled carbon nanotubes, and bentonite for superior ciprofloxacin adsorption

Water contamination from antibiotics can have detrimental effects on one’s health. Consequently, treating the polluted water is required to fix this issue. Fe3O4-multiwalled Carbon Nanotubes (MWCNTs)-Bentonite nanocomposite has been successfully prepared using a customized co-precipitation process. The synthesized nanocomposite was used as an adsorbent to extract the ciprofloxacin from aqueous solutions. The synthesized nanocomposite was examined using several characterization methods. Scanning electron microscopy demonstrates that the Fe3O4 nanoparticles and bentonite are well-decorated on MWCNTs. The nanocomposite exhibits a high BET surface area of 221.577 m2/g and a pore volume of 0.411 cm3/g. According to the analysis, the average pore diameter was found to be 3.717 nm. Additionally, the adsorption model agreed with the Jovanovic model, which had a 137.35 mg/g adsorption capacity, with a χ2 of 2.161, and a good nonlinear R2 value of 0.999. Moreover, adsorbent was found to be highly stable even after 4 cycles. The ΔS and ΔH values were found to be positive, which suggested an endothermic process. The synthesized nanocomposite proved to be a viable option for water treatment applications, and there is no literature available on CIP antibiotic adsorption using Fe3O4-MWCNT-Bentonite nanocomposite.

Evaluating the antibiotic adsorption ability of diatomite minerals: the role of treatment agents

Evaluating the antibiotic adsorption ability of diatomite minerals: the role of treatment agents

Carbon Dots Derived from Waste Fish Scale for Enhanced Removal of Levofloxacin Drug: Parametric Optimization, Isotherm and Kinetic Studies

The public health and environmental protection have been facing a great challenge for efficient antibiotics' adsorption from aqueous solution. In this work, a carbon dots nanoparticle from biomass (fish scale) was synthesized and employed for antibiotic adsorption. The synthesized fish scale carbon dots (FCD) were characterized by means of the X-ray diffraction (XRD), Scanning Electron Microscopy (SEM) and Fourier transform infrared (FTIR) analyses. Experiments on adsorption were performed to examine the capability of the synthesized adsorbent for adsorption of Levofloxacin. The optimum conditions were ascertained through the use of Response Surface Methodology (RSM) design to increase the effectiveness of levofloxacin removal, and there was 96.03% removal efficiency of 60 minutes contact time, 10 mg/L levofloxacin concentration and FCD dosage of 0.2 g/L. Also, the adsorption experiments indicated that at the lowest concentration of 10 mg/L, at time 45 min and 0.15 mg dosage the adsorption rate was high. For the kinetics data, the pseudo-second order model best fit the data. Furthermore, the Redlich-Peterson model fit isothermal data the best.

Preparation and characterization of biochar from four different solid wastes and its ampicillin adsorption performance.

The integration of biochar (BC) production from organic waste with ampicillin (AMP), an emerging pollutant, adsorption is a novel and promising treatment approach. In this study, peanut shells, coffee grounds, digestates, and oyster shells were used for BC production. Among these, the use of anaerobic digestate from food waste fermentation to produce extracts for antibiotic adsorption is relatively unexplored. The pyrolysis temperature was determined using thermogravimetric analysis (TGA) and the materials were characterized with BET, SEM, FTIR, and XRD. The TGA results indicate that PSB, CRB, and DSB underwent pyrolysis involving cellulose, hemicellulose, and lignin, whereas OSB underwent crystal formation. Characterization revealed that DSB has more functional groups, a superior mesoporous structure, appropriate O/C ratio, and trace amounts of calcite crystals, which are favorable for AMP adsorption. Adsorption experiments demonstrate that all four materials adhere to the Freundlich and Langmuir isotherm and Elovich kinetic models, indicating predominant physical adsorption, with some chemical adsorption also present. Thermodynamic studies demonstrate that BC is spontaneous during adsorption and is a heat-absorbing reaction. DSB exhibits the strongest AMP adsorption. A 53.81mgg-1 adsorbance was obtained at a dosage of 150mg, pH = 2, and 60°C. This study introduces innovative approaches for managing waste types and provides data to support the selection of suitable solid wastes for the preparation of BC with excellent adsorption properties. Furthermore, it lays the groundwork for future studies aimed at enhancing the AMP treatment efficacy.

Advanced biopolymer-based Ti/Si-terephthalate hybrid materials for sustainable and efficient adsorption of the tetracycline antibiotic

This study involves the synthesis of an organic-inorganic hybrid material consisting of Ti/Si-terephthalate (Ti-TPA-Si) in a 1:1:1 ratio using sol-gel method and its reaction with cellulose and chitosan (Ti-TPA-Si-C and Ti-TPA-Si-CS). Characterization techniques such as XRD, FTIR, SEM, EDS, XPS, BET, TGA, and DTA were used. The incorporation of biopolymers (cellulose and chitosan) into the Ti/Si-terephthalate structure improved the morphology and textural properties of the hybrid materials, leading to increased adsorption capacity and sustainability. Adsorption experiments reveal that Ti-TPA-Si, Ti-TPA-Si-C, and Ti-TPA-Si-CS hybrid materials exhibit a high affinity towards tetracycline, achieving remarkable adsorption efficiencies of 88.27, 89.60, and 88.98 %, respectively. Isotherm studies indicate that the adsorption process follows both Langmuir (R2 = 0.971, 0.990, and 0.994) and Dubinin-Radushkevich (R2 = 0.922, 0.965, and 0.949) isotherm models. According to the Langmuir model, the maximum adsorption capacity (qm) of Ti-TPA-Si, Ti-TPA-Si-C, and Ti-TPA-Si-CS adsorbents was found to be 24.10, 33.56, and 26.59 mg/g, respectively. Kinetic studies indicate that the adsorption process follows both pseudo-second-order (R2 = 0.998, 0.984, and 0.989) and intra-particle diffusion (R2 = 0.995, 0.994, and 0.988) models. Thermodynamic studies reveal that adsorption processes are spontaneous and endothermic in nature. Reusability studies demonstrate their potential for repeated use without significant loss in performance.

Facile Fabrication of Zeolitic Imidazolate Framework-8@Regenerated Cellulose Nanofibrous Membranes for Effective Adsorption of Tetracycline Hydrochloride.

The excessive utilization of antimicrobials in humans and animals has resulted in considerable environmental contamination, necessitating the development of high-performance antibiotic adsorption media. A significant challenge is the development of composite nanofibrous materials that are both beneficial and easy to fabricate, with the aim of improving adsorption capacity. Herein, a new kind of zeolitic imidazolate framework-8 (ZIF-8)-modified regenerated cellulose nanofibrous membrane (ZIF-8@RC NFM) was designed and fabricated by combining electrospinning and in situ surface modification technologies. Benefiting from its favorable surface wettability, enhanced tensile strength, interconnected porous structure, and relatively large specific surface area, the resulting ZIF-8@RC NFMs exhibit a relatively high adsorption capacity for tetracycline hydrochloride (TCH) of 105 mg g-1 within 3 h. Moreover, a Langmuir isotherm model and a pseudo-second-order model have been demonstrated to be more appropriate for the description of the TCH adsorption process of ZIF-8@RC-3 NFMs. Additionally, this composite fibrous material could keep a relatively stable adsorption capability under various ionic strengths. The successful fabrication of the novel ZIF-8@RC NFMs may shed light on the further development of wastewater adsorption treatment materials.

Effect of pH on hydroxyapatite coatings obtained by spray pyrolysis and their use as matrices for antibiotic adsorption by spin coating and release properties.

Calcium phosphate materials, particularly hydroxyapatite (HA), are extensively used in biomedical applications because of their prominence as primary inorganic constituents of human hard tissues. This study investigates the synthesis of HA coatings via spray pyrolysis using various precursors, including HA derived from bovine bone. The effects of pH on the formation and properties of HA coatings were systematically examined. Samples exposed to acidic conditions or left without pH adjustment led to the formation of HA, contrasting with the outcomes observed through dissolution methods. Different characterization techniques, such as scanning electron microscopy (SEM), transmission electron microscopy (TEM), and X-ray diffraction (XRD), were employed to evaluate the quality and crystallinity of the coatings. Among the samples, those exhibiting superior crystallinity and nanostructured features, including bovine HA, were selected for further surface functionalization with the antibiotic enrofloxacin using spin coating. As expected, the antibiotic loading on each material's surface depended on the amount of HA deposited on the substrate. However, the desorption results indicated that, in all cases, desorption persisted beyond 38 h, implying that HA-loaded matrices could be effective systems for controlled and prolonged drug release, which could be useful in dental or orthopedic implants for inhibiting the growth of bacterial biofilms.

A pharmacokinetic framework describing antibiotic adsorption to cardiopulmonary bypass devices.

Cardiopulmonary bypass (CPB) can alter pharmacokinetic (PK) parameters and the drug may adsorb to the CPB device, altering exposure. Cefazolin is a beta-lactam antibiotic used for antimicrobial prophylaxis during cardiac surgery supported by CPB. Adsorption of cefazolin could result in therapeutic failure. An exvivo study was undertaken using CPB devices primed and then dosed with cefazolin and samples were obtained over 1 hour of recirculation. Twelve experimental runs were conducted using different CPB device sizes (neonate, infant, child, and adult), device coatings (Xcoating™, Rheoparin®, PH.I.S.I.O), and priming solutions. The time course of saturable binding, using Bmax (binding capacity), Kd (dissociation constant), and T2off (half-time of dissociation), described cefazolin adsorption. Bmax estimates for the device sizes were neonate 40.0 mg (95% CI 24.3, 67.4), infant 48.6 mg (95% CI 5.97, 80.2), child 77.8 mg (95% CI 54.9, 103), and adult 196 mg (95% CI 191, 199). The Xcoating™ Kd estimate was 139 mg/L (95% CI 27.0, 283) and the T2off estimate was 98.4 min (95% CI 66.8, 129). The Rheoparin® and PH.I.S.I.O coatings had similar binding parameters with Kd and T2off estimates of 0.169 mg/L (95% CI 0.01, 1.99) and 4.94 min (95% CI 0.17, 59.4). The Bmax was small (< 10%) relative to a typical total patient dose during cardiac surgery supported by CPB. A dose adjustment for cefazolin based solely on drug adsorption is not required. This framework could be extended to other PK studies involving CPB.

Design of High-Performance Molecular Imprinted Magnetic Nanoparticles-Loaded Hydrogels for Adsorption and Photodegradation of Antibiotics from Wastewater.

A hydrogel formulation of 2-hydroxy ethyl methacrylate (HEMA) containing covalently linked magnetite nanoparticles was developed to actively facilitate the selective removal and photocatalytic degradation of antibiotics. To this purpose, the hybrid materials were molecularly imprinted with Lomefloxacin (Lome) or Ciprofloxacin (Cipro), achieving a selectivity of 60% and 45%, respectively, starting from a solution of XX concentration. After the adsorption, the embedded magnetite was used with the double function of (i) magnetically removing the material from water and (ii) triggering photo-Fenton (PF) reactions assisted by UVA light and H2O2 to oxidize the captured antibiotic. The success of the material design was confirmed by a comprehensive characterization of the system from chemical-physical and morphological perspectives. Adsorption and degradation tests demonstrated the material's ability to efficiently degrade Lome until its complete disappearance from the electrospray ionization (ESI) mass spectra. Regeneration tests showed the possibility of reusing the material for up to three cycles. Ecotoxicological tests using algae Rapidocelis subcapitata, crustaceans Daphnia magna, and bacteria Vibrio fischeri were performed to evaluate the ecosafety of our synthesized materials.

Selective adsorption of antibiotics from human urine using biochar modified by dimethyl sulfoxide, deep eutectic solvent, and ionic liquid

Antibiotics present in human urine pose significant challenges for the use of urine-based fertilizers in agriculture. This study introduces a novel two-stage approach utilizing distinct biochar types to mitigate this concern. Initially, a modified biochar selectively adsorbed azithromycin (AZ), ciprofloxacin (CPX), sulfamethoxazole (SMX), trimethoprim (TMP), and tetracycline (TC) from human urine. Subsequently, a separate pristine biochar was employed to capture nutrients. Biochar, derived from sewage sludge and pyrolyzed at 550 and 700 °C, was modified using dimethyl sulfoxide, deep eutectic solvent, and ionic liquid to enhance antibiotic removal in the first stage. The modifications introduced hydrophilic functional groups (-OH/-COOH), which favor antibiotic adsorption. Adsorption kinetics followed the pseudo-second-order model, with the Langmuir isotherm model best describing the adsorption data. The maximum adsorption capacities for AZ, CPX, SMX, TMP, and TC after the modification were 196.08, 263.16, 81.30, 370.37, and 833.33 μg/g, respectively. Pristine biochar exhibited a superior ammonia adsorption capacity compared to the modified biochar. Hydrogen bonding, electrostatic attraction, and chemisorption drove antibiotic adsorption on the modified biochar. Regeneration efficiency declined due to solvent accumulation and potential byproduct formation on the biochar surface (<30% removal capacity after three cycles). This study presents innovative biochar modification strategies for selective antibiotic adsorption, laying the groundwork for environmentally friendly urine-based fertilizers in agriculture.

A review on utilization potential of functionalized biochar for the removal of antibiotics from water

Globally, water resources are facing serious threat owing to the increasing concentration of various emerging contaminants. Indiscriminately discarded and/or excreted antibiotics and their residues are one such emerging contaminants. Since long-term persistence of these residues in environment is responsible for developing antimicrobial (antibacterial) resistance in the organisms, their removal from water / wastewater is essential. Hence, scientists are attempting to evolve novel methods to encounter antibiotics and their residues in water. One such method is the adsorption of antibiotics onto a suitable matrix thereby reducing their concentration in water. Biochar has been proven to act as a suitable adsorbent for various contaminants; however, their removal efficiency remains a concern. Therefore, functionalization of biochar using various physical and chemical modifications, was developed as a technique that can help in efficient removal of antibiotics. Functionalization has been seen to improve the physical and chemical properties of biochar; such as, pore volume, pore diameter, surface morphology, surface functional groups, polarity, porosity etc. In this review, functionalized biochars have been explored to understand their efficacy and mechanism for the removal of antibiotics and their residues. The discussion includes biochar functionalization methods, impact of property modifications on the removal of antibiotic residues, and their removal mechanism. In addition, cost-effectiveness, economy of the adsorption process, and its environmental effects have also been dealt with.

Preparation and application of cattail residue-based magnetic cellulose composites for tetracycline antibiotics adsorption

Tetracycline antibiotics (TCs) are widely present in wastewater and surface water due to their extensive use. Removal of TCs from water is urgent. In this study, magnetic cellulose (MC) composites were prepared from cattail residues to adsorb oxytetracycline hydrochloride (OTC·HCl), chlortetracycline hydrochloride (CTC·HCl), and tetracycline hydrochloride (TC·HCl) from water. The influence of Fe3O4 content on the antibiotics removal was studied. The synthesized MC composites were characterized using FTIR, XPS, zeta potential, SEM, and XRD. Adsorption mechanisms and characteristics were explored using classic isotherm models (Langmuir, Freundlich, Temkin, and Dubinin-Radushkevich models) and common kinetic models (pseudo-first-order, pseudo-second-order, Elovich and Intraparticle diffusion models). Optimum adsorption capacity was achieved by MC2–1 (mass ratio of cellulose to Fe3O4 was 2:1), with a larger specific surface area (18.24 m2 g−1) and mesoporous structure. The adsorption processes were well described by the pseudo-second-order and Langmuir models. MC2–1 demonstrated maximum adsorption capacities of CTC·HCl (194.29 mg g−1), OTC·HCl (168.25 mg g−1), and TC·HCl (41.10 mg g−1). The results of models fitting and characterizations of the MC composites before and after the adsorption processes revealed that the main adsorption mechanisms were pore filling, hydrogen bonding, electrostatic interactions, and metal complexation. This study proposes a practical approach for utilizing wetland plant residues as an effective adsorbent for tetracycline antibiotics removal.

Unveiling the adsorption mechanisms of macrolides by mesoporous carbons through molecular dynamics simulation and multilinear regression modelling

Mesoporous carbon materials (MCs) are known for their high specific surface area and porous structure, rendering them promising candidates for efficient antibiotic adsorption. However, the influence of antibiotic properties and the porous structure of MCs on adsorption remains unclear. This study investigated the adsorption behaviors of ten macrolides (MLs) onto four MCs with porous structures, aiming to understanding the key factors governing their adsorption. The results revealed that the adsorption rate constant (k2) and adsorption constant of Freundlich isotherm (KF) were influenced by the McGowan molar volume of MLs. Molecular dynamics simulations uncovered that a distance of approximately 4 Å between adsorbed MLs from the material surface, suggesting hydrophobic interactions play a crucial role. Moreover, ML diffusion was more favorable on the surface of 10 nm pore compared to 2 nm pores, highlighting the impact of pore size on diffusion. Additionally, the diffusion coefficient of MLs was mainly determined by logKow, emphasizing the significance of hydrophobic interactions in diffusion. Multilinear regression modelling further supports hydrophobic interactions as the main adsorption mechanism for MLs. Overall, this study provides valuable insights into the complex adsorption mechanisms of MLs on MCs, informing the development of more effective antibiotic removal strategies.

Continuous flow column adsorption and desorption for the study of interaction of fluoroquinolone antibiotic ofloxacin hydrochloride with ZnO and CuO nanometal oxides in aqueous solution: (Continuous column adsorption desorption)

Broad-spectrum antibiotic, major veterinary medicines, due to large consumption and inappropriate disposal contribute a major part in generation of pharmaceutical pollutants in aquatic environment. The study investigates the interaction of nanometal oxides for adsorption and desorption of Fluoroquinolone antibiotic, ofloxacin hydrochloride from aqueous solution using vertical and sequential bed adsorption columns: designing parameters of adsorption column determined using bed depth service time model. To optimize the continuous flow column adsorption, varying initial drug concentration and flow rates have been studied using ZnO and CuO nanoparticles at pH 4, already determined for optimized batch studies. To access the characteristic behaviour of breakthrough curves, Thomas model and Yoon-Nelson models have been studied, which were in good agreement with experimental data. Sequential bed column shows slightly better results than vertical bed column as the sequential bed is simple and economical, the solution flows in continuous manner under gravity without any mechanical devices and come into contact with fresh adsorbent bed having same amount as that in vertical bed. Therefore sequential bed column can consider in small scale industries for pharmaceutical wastewater treatment. Column desorption experiments have also been carried out by using HCl/NaOH as desorbing agent for the regeneration of drug loaded adsorbent column.