scholarly journals Prevalence and fate of antibiotics and its derivatives in sewage treatment in Durban and the receiving environment

2019 ◽  
Author(s):  
◽  
Adekunle Christopher Faleye

Antibiotics are released to the environment either directly in an unchanged form or partially metabolized. The discharge is usually through untreated waste or through wastewater treatment effluents. The stable antibiotics in reduced amounts persist through the wastewater treatment processes and end up in receiving waters, where they may impact crops through irrigation or affect drinking water intakes. Antibiotics in the waste and sludge fractions may similarly impact crops and arable land through their use as fertilizers. Conventional wastewater treatment plants are not designed for the removal of antibiotics but may to a varying extent reduce their concentrations. Their quantitative occurrence within the water matrices depends on the frequency and quantities of use for therapeutic purposes or as growth promoters in animal production. Additional inputs may emanate from individual waste discharges. Antibiotics present in sub-inhibitory concentrations may predicate for resistance among the resident bacteria in the water matrix, biofilms or in humans and animals. In South Africa antibiotics are extensively used both in human therapy and in animal husbandry without clearly followed regulations and are sometimes readily available. The available studies have focused on the presence of antibiotic resistant bacteria in wastewater influent and effluent but there is a paucity of information relating to these antibiotics as emerging contaminants in South Africa wastewater. In this thesis a rapid and sensitive analytical methodology was initially assessed and applied, based on the use of HPLC/diode array UV detector for six antibiotics (ethionamide (ETI), metronidazole (MET), trimethoprim (TRI), ciprofloxacin (CIP), sulfisoxazole (SUF) and albendazole (ALB). Validation of the method was performed by screening assessment in selected wastewater treatment plants (WWTPs) with the aim of determining the sensitivity of the equipment (Shimadzu 2020), assess the limit of detection, optimize the extraction procedure (solid phase extraction) and screen for the most prevalent antibiotics. The percentage recovery for the optimized method using wastewater sample was above 65 % for all antibiotics of interest. The limit of detection, which ranges from 0.03 to 0.48 mg L-1, enables the determination of a range of concentration of antibiotics in polluted sample such as the wastewater influent sample. Furthermore in this thesis, a more advanced, online solid phase extraction – high performance liquid chromatography mass spectrometry (SPE-HPLC-MS) method, was applied to measure the concentration of these and an additional seven antibiotics, norfloxacin (NOR), ofloxacin (OFL), clindamycin (CLI), sulfamethoxazole (SUL), erythromycin (ERY), clarithromycin (CLA), azithromycin (AZI) and roxithromycin (ROX) in ng L-1 concentrations. The quantity and occurrence of the selected antibiotics was assessed in untreated wastewater in four wastewater treatment plants in Durban, KwaZulu-Natal (KZN), at different treatment stages and in the effluent and recipient surface water environment. In the influent the additive concentration of the antibiotics associated to the separated sediment fraction through centrifugation and in the supernatant of samples collected were accounted for and analyzed. The limit of detection (LOD) and the limit of quantification (LOQ), ranged from 0.07 – 0.33 ng L-1 and 0.23 – 1.09 ng L-1, respectively for the 13 assessed antibiotics and the percentage recovery were in the range of 51 to 111 %. The percentage of antibiotics recovered from the sediment (centrifuged) samples, which would have been lost to filtration if not analyzed in parallel, were in the range of 2.6% – 97% (n = 32), while the frequency of detection in the influent samples for the sampling period ranges from 62.5 – 100 % (n = 32). All the studied antibiotics were detected in the influent of each WWTP and the concentration was in the rage of 1.3 ng L-1 (AZI) – 81748 ng L-1 (CIP). The antibiotics with the highest concentrations (median) detected in the receiving water (downstream) for each of the four WWTPs in KZN, were TRI (217 ng L-1), SUL (239 ng L-1), CIP (708 ng L-1) and ALB (325 ng L-1) respectively. The overall percentage removal efficiency for the four WWTPs ranged from 21 % - 100 %. The most effective treatment steps were assessed with the focus on activated sludge filter and trickling filter. Within these, it was actually the sedimentation treatment stages (secondary clarifier), after these steps that played the most vital role in the reduction of antibiotics where > 70 % of the antibiotics was removed. Finally, the impact of post chlorination was analyzed for the effluent of the WWTPs. The presence of transformation product as a result of post chlorination was examined in a parallel study using a controlled experiment and full scale analysis. The efficiency of chlorine in the reduction of antibiotics was more of transformation of antibiotics than degradation. The oxidative ability of chlorine enhances its reaction with antibiotics thereby transforming the antibiotics. The percentage reduction of antibiotics in relation to chlorination was >85 % (pilot experiment) and ranged between 14 % - 97 % in the field experiments. Likewise, UV was effective in the degradation of antibiotics, with longer exposure time producing higher degradation. Future research should focus on determining the toxicological impact of these transformation products. The concentration of the antibiotics in the downstream samples were generally low when compared to their influent concentrations.

2017 ◽  
Vol 10 (1) ◽  
pp. 47-53 ◽  
Author(s):  
Pavlína Landová ◽  
Milada Vávrová

Abstract An effective and practical method for the determination of macrolide antibiotics azithromycin, clarithromycin, erythromycin and roxithromycin in wastewater samples has been developed. The analytical method combines solid phase extraction followed by a chromatographic separation by hydrophilic interaction liquid chromatography (HILIC) coupled with an ion trap mass spectrometer utilizing the electrospray ionization technique. Detection of positively charged ions was performed in full scan mode from 500 to 900 m/z. The method detection limits and method quantification limits obtained were in the range of 2.03-7.59 ng L-1 and 6.08-23.84 ng L-1, respectively. Recoveries of solid phase extraction were obtained using SupelTM-Select HLB cartridges ranging from 85.76 % to 92.54 %. All target antibiotics were detected in 100 % of the collected raw influent samples with concentrations varying from 15 ng L-1 to 1849 ng L-1. Azithromycin, clarithromycin and erythromycin were also detected in 100 % of the treated water samples and roxithromycin was present in 96 % of the samples. The highest determined concentration in the treated water samples was 1404 ng L-1 of azithromycin. Based on the determined macrolide concentrations, removal efficiencies of individual wastewater treatment plants were calculated to range from 13 % to 100 %.


2011 ◽  
Vol 89 (4) ◽  
pp. 517-523 ◽  
Author(s):  
Ke-Jing Huang ◽  
Cong-Hui Han ◽  
Ying-Ying Wu ◽  
Chao-Qun Han ◽  
De-Jun Niu ◽  
...  

A simple and efficient solid-phase extraction – spectrofluorimetric method has been developed to determine glutathione (GSH). Fluorescent probe N-(4,4-difluoro-5,7-dimethyl-4-bora-3a,4a-diaza-s-indacene-3-yl)methyl)iodoacetamide (BODIPY Fl-C1-IA) was used as the derivatization reagent. The procedure was based on a BODIPY Fl-C1-IA selective reaction with GSH to form the highly fluorescent product BODIPY Fl-C1-IA–GSH, using a solid-phase extraction column and spectrofluorimetric determination. The variables affecting analytical performance were studied and optimized. The calibration graph using the preconcentration system for GSH was linear over the range of 1–200 nmol/L with a limit of detection of 0.05 nmol/L (signal-to-noise ratio = 3). The relative standard deviation for six replicate determinations of GSH at the 100 nmol/L concentration level was 3.9%. The method was applied to water samples and average recoveries between 87.5% and 111.5% were obtained for spiked samples.


Molecules ◽  
2021 ◽  
Vol 26 (20) ◽  
pp. 6163
Author(s):  
Aree Choodum ◽  
Nareumon Lamthornkit ◽  
Chanita Boonkanon ◽  
Tarawee Taweekarn ◽  
Kharittha Phatthanawiwat ◽  
...  

Benzo(a)pyrene (BaP) has been recognized as a marker for the detection of carcinogenic polycyclic aromatic hydrocarbons. In this work, a novel monolithic solid-phase extraction (SPE) sorbent based on graphene oxide nanoparticles (GO) in starch-based cryogel composite (GO-Cry) was successfully prepared for BaP analysis. Rice flour and tapioca starch (gel precursors) were gelatinized in limewater (cross-linker) under alkaline conditions before addition of GO (filler) that can increase the ability to extract BaP up to 2.6-fold. BaP analysis had a linear range of 10 to 1000 µgL−1 with good linearity (R2 = 0.9971) and high sensitivity (4.1 ± 0.1 a.u./(µgL−1)). The limit of detection and limit of quantification were 4.21 ± 0.06 and 14.04 ± 0.19 µgL−1, respectively, with excellent precision (0.17 to 2.45%RSD). The accuracy in terms of recovery from spiked samples was in the range of 84 to 110% with no significant difference to a C18 cartridge. GO-Cry can be reproducibly prepared with 2.8%RSD from 4 lots and can be reused at least 10 times, which not only helps reduce the analysis costs (~0.41USD per analysis), but also reduces the resultant waste to the environment.


2019 ◽  
Vol 6 (1) ◽  
pp. 15-20 ◽  
Author(s):  
Ivo Safarik ◽  
Jitka Prochazkova ◽  
Eva Baldikova ◽  
Kristyna Pospiskova

Magnetically responsive materials have found many important applications in analytical chemistry. In this short review the basic information about Magnetic solid phase extraction and Magnetic textile solid phase extraction is given. These analytical techniques enable to preconcentrate target biologically active compounds or pollutants from water samples. Both procedures enable to lower the limit of detection using conventional analytical procedures.


2013 ◽  
Vol 2013 ◽  
pp. 1-6 ◽  
Author(s):  
Nahid Pourreza ◽  
Saadat Rastegarzadeh ◽  
Ali Reza Kiasat ◽  
Hossein Yahyavi

A new solid phase extraction procedure was developed for preconcentration of iron(II) using silica gel-polyethylene glycol (silica-PEG) as an adsorbent. The method is based on retention of iron(II) as 2,2′ bipyridine complex on silica-PEG. The retained complex is eluted by 1.0 mol L−1of sulfuric acid-acetone mixture (1:2) and its absorbance is measured at 518 nm, spectrophotometrically. The effects of different parameters such as pH, concentration of the reagent, eluting reagent, sample volume, amount of adsorbent, and interfering ions were investigated. The calibration graph was linear in the range of 1–60 ng mL−1of iron(II). The limit of detection based on3Sbwas 0.57 ng mL−1and relative standard deviations (R.S.D) for ten replicate measurements of 12 and 42 ng mL−1of iron(II) were 2.4 and 1.7%, respectively. The method was applied to the determination of of iron(II) in water, multivitamin tablet, and spinach samples.


2013 ◽  
Vol 2013 ◽  
pp. 1-6 ◽  
Author(s):  
Paras P. Vekariya ◽  
Hitendra S. Joshi

Simple and rapid reverse phase high-performance liquid chromatography (RP-HPLC) method was developed and validated using solid phase extraction (SPE) technique for the determination of Azilsartan Medoxomil Potassium (AMP) in human plasma; detection was carried out by photo diode array detector. Chromatographic separation of the analyte AMP was achieved within 7.5 min by Waters symmetry C18 (4.6 × 250 mm, 5 µm) column, mobile phase was 25 mM ammonium acetate buffer (pH 5.5): acetonitrile 55 : 45 v/v, flow rate was 1.0 mL/min, and the detection was carried out at 254 nm. Calibration curve was linear (r2 > 0.9985) in the range of 1.0–9.0 µg/mL, limit of detection (LOD) and limit of quantitation (LOQ) were 0.150 µg/mL and 0.400 µg/mL, respectively, and intra- and interday deviations were between 1.53–8.41% and 1.78–4.59%, respectively. The overall mean recovery of AMP was 92.35%. No any endogenous constituents were found to interfere at retention time of the analyte. This new RP-HPLC method was successfully validated and may be applied to conduct bioavailability and bioequivalence studies of AMP.


2019 ◽  
Vol 7 (2) ◽  
pp. 245-253 ◽  
Author(s):  
Wan Norfazilah Wan Ismail ◽  
Dzul Iskandar Muhammad Fauzi ◽  
Nurlin Abu Samah

A rapid solid phase extraction (SPE) combined with gas chromatography equipped with mass spectrometry (GC-MS) method was developed and validated for the determination of acenaphthylene, acenaphthene and naphthalene in wastewater sample collected from petroleum industry’s drainage. Important SPE parameters, namely absorbent amount, sample volume, type of elution solvent and its volume were optimized. The optimum parameters obtained are: 200 mg silica nano-powder, 2.0 mL sample volume and 2.0 mL n-hexane as elution solvent. The method showed good linearity in the range of 0.1-10.0 mg/L with satisfactory limit of detection (≤1.0 mg/L) and limit of quantitation (≤3.2 mg/L) under the optimized conditions. Good relative recoveries (94.7-99.9%) and intra- and inter-day precisions (≤2.8%, n=3) for acenaphthene, acenaphthylene and naphthalene were obtained. Toxicity study has revealed that it is a non-toxic absorbent and safe to be used for the removal of organic pollutants in water which is advantageous for routine wastewater analysis.


2013 ◽  
pp. 101-109 ◽  
Author(s):  
Igor Jajic ◽  
Sasa Krstovic ◽  
Biljana Perisic ◽  
Sandra Jaksic ◽  
Vojislava Bursic ◽  
...  

A total of 45 samples of wheat from three different locations in Vojvodina were analyzed for the presence of zearalenone. Analytical methods based on clean-up by solid-phase extraction (SPE) columns and detection by liquid chromatography were used after validation. Limit of detection for ZEA in wheat was 18.6 ?g/kg and the limit of quantification was 56.5 ?g/kg. Recovery values ranged between 86% and 97%. The occurrence of ZEA in wheat was rather high with 53.3% of positive samples with the average value of 330 ?g/kg. Incidences were found from 68 ?g/kg to 1079 ?g/kg. Contamination levels were above the established maximum limit for unprocessed cereals, other than maize, in as many as seventeen samples. These results were compared to the results of investigation of deoxynivalenol and fumonisin content, established in our previous work on the same samples. The results obtained were also compared to those of the neighboring countries where the relevant data existed and to the data of previous studies in our country.


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