Faculty of Applied Sciences
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Item Experimental and theoretical study of molecular interactions between 2-vinyl pyridine and acidic pharmaceuticals used as multi-template molecules in molecularly imprinted polymer(Elsevier, 2016) Madikizela, Lawrence Mzukisi; Mdluli, Phumlani Selby; Chimuka, LukeMolecular interactions between functional monomer and template molecules are regarded as the driving force for the success of a molecularly imprinted polymer. In this study, a multi-template molecularly imprinted poly-mer (MIP) for ibuprofen, naproxen and diclofenac was synthesized in an oil bath set at 70 °C for 24 hours. 2-vinyl pyridine, ethylene glycol dimethacrylate, toluene and 1,1’-azobis-(cyclohexanecarbonitrile) were used as func-tional monomer, cross-linker, porogen and radical initiator, respectively. A non-imprinted polymer (NIP) was synthesized using a similar approach with the omission of templates. Monomer-template interactions were ex-amined using Molecular Dynamics and Fourier Transform Infrared Spectroscopy (FTIR). Both molecular dynam-ics and FT-IR results indicated the formation of the hydrogen bond between the templates and 2-vinyl pyridine. Molecular dynamics further revealed the identity of the hydrogen atoms in the templates involved in interactions with nitrogen atom on the functional monomer in the presence of toluene molecules. Surface area obtained for the MIP using Brunauer, Emmett and Teller method was 282 m2/g, whereas 232 m2/g was obtained for the NIP. This indicated that MIP has more binding sites compared to the NIP. Furthermore, batch adsorption and se-lectivity experiments were carried out in the presence of gemfibrozil as the competitor. When such experiments were carried out in toluene, the adsorption capacities (mg/g) obtained for naproxen, ibuprofen, diclofenac and gemfibrozil were 14.4, 11.0, 14.0 and 7.5, respectively. These results show that the MIP was more selective to the compounds that were used as template molecules.Item Determination of Triclosan and Ketoprofen in river water and wastewater by solid phase extraction and high performance liquid chromatography(SACI, 2014-09-17) Madikizela, Lawrence Mzukisi; Muthwa, Sindisiwe Fortunate; Chimuka, LukeThis paper describes a simple, sensitive and rapid method for the determination of triclosan and ketoprofen in wastewater influent, effluent and river water. The method involves solid phase extraction (SPE) of target compounds using Oasis HLB sorbent. Several extraction parameters such as sample pH, sample volume, SPE cartridge and SPE elution solvent were optimized. The pH of the collected samples was adjusted to 5.5, and then 100 mL of the sample was loaded into an Oasis HLB cartridge. Methanol was used to elute the retained compounds. The eluted compounds were analyzed using reversed-phase high performance liquid chromatography with photo diode array detection (HPLC-PDA). The method was validated by spiking ultra-pure water and wastewater with different concentrations of both compounds ranging from 5 µg L–1 to 1000 µg L–1. Recoveries were in the range of 73 % to 104 %, and % RSD ranged from8%to15%.The method gave good detection limits of 0.01 and 0.08 µg L–1 for triclosan and ketoprofen, respectively. Traces of both compounds were detected in all wastewater (influent and efflu-ent) samples at a range of 1.2 to 9.0 µg L–1 and in some river water samples.Item Optimisation of HPLC-based methods for the separation and detection of herbicide glyphosate and its major metabolite in water(2010) Madikizela, Lawrence Mzukisi; Moodley, Kandasamy Govindsamy; Chetty, Deenadayalan KistenWater storage dams play an important part in the collection and purification of water destined for human consumption. However, the nutrient rich silt in these dams promotes rapid growth of aquatic plants which tend to block out light and air. Glyphosate is universally used as the effective non-selective herbicide for the control of aquatic plants in rivers and dams. Invariably there is residual glyphosate present in water after spraying of dams and rivers with glyphosate herbicide. The amount of residual glyphosate is difficult to determine on account of high solubility of glyphosate in water. Thus a method of sample preparation and a sensitive HPLC method for the detection of trace amounts of glyphosate and its major metabolite aminomethylphosphonic acid (AMPA) in water is required. A crucial step in sample preparation is pre-column derivitization of glyphosate with 9-fluorenylmethyl chloroformate (FMOC-Cl). For sample pretreatment, water samples were derivatized with FMOC-Cl at pH 9, extracted with ethyl acetate and sample clean-up was carried out by passing a sample through the SPE cartridge. For SPE, recovery studies were done to choose a suitable cartridge for glyphosate and AMPA analysis. The following cartridges were compared, namely, C18, Oasis HLB and Oasis MAX SPE cartridges. Best recoveries (101% for glyphosate and 90% for AMPA) were obtained using 500 mg of C18 solid-phase extraction cartridge. The eluent from SPE cartridge was injected into HPLC column. Three types of separation columns (namely; C18 column, silica based amino column and polymeric amino column) were compared for the separation of glyphosate and AMPA. The best separation of glyphosate and AMPA in water samples was achieved using a polymeric amino column and a mobile phase at pH 10 which contained a mixture of acetonitrile and 0.05 M phosphate buffer (pH 10) 55:45, (v/v) respectively. The method was validated by spiking tap water , deionized water and river water at a level of 100 μg/l. Recoveries were in the range of 77% -111% for both analytes. The method was also used in determining the levels of glyphosate and AMPA in environmental samples. This method gave detection limits of 3.2 μg/l and 0.23 μg/l for glyphosate and AMPA respectively. The limits of quantification obtained for this method were 10.5 μg/l and 3.2 μg/l for glyphosate and AMPA respectively.