Fluorescence “turn on” probe for bromide ion using nanoconjugates of glutathione-capped CdTe@ ZnS quantum dots with nickel tetraamino-phthalocyanine
- Adegoke, Oluwasesan, Nyokong, Tebello
- Authors: Adegoke, Oluwasesan , Nyokong, Tebello
- Date: 2013
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/190479 , vital:44998 , xlink:href="https://doi.org/10.1016/j.jphotochem.2013.05.013"
- Description: In this paper, three differently sized glutathione (GSH)-capped CdTe@ZnS quantum dots (QDs) have been successfully conjugated to nickel tetraamino-phthalocyanine (NiTAPc) to form different QDs-NiTAPc nanocomplexes. Several techniques such as TEM, FT-IR, time-resolved fluorescence measurement and electronic spectroscopy were employed to characterize the nanocomplex. Bromide ion was chosen as a model anion to test the efficacy of the nanoprobe. The fluorescence of the nanoconjugate was “turned off” upon binding but was progressively “turned on” upon interaction with varying concentrations of bromide ion. Experimental results showed that the quantum size effect of nanocrystal QD determined the overall sensitivity and selectivity of the nanoprobe and followed the order QD563-NiTAPc > QD605-NiTAPc > QD621-NiTAPc. The mechanism of reaction is proposed.
- Full Text:
- Date Issued: 2013
- Authors: Adegoke, Oluwasesan , Nyokong, Tebello
- Date: 2013
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/190479 , vital:44998 , xlink:href="https://doi.org/10.1016/j.jphotochem.2013.05.013"
- Description: In this paper, three differently sized glutathione (GSH)-capped CdTe@ZnS quantum dots (QDs) have been successfully conjugated to nickel tetraamino-phthalocyanine (NiTAPc) to form different QDs-NiTAPc nanocomplexes. Several techniques such as TEM, FT-IR, time-resolved fluorescence measurement and electronic spectroscopy were employed to characterize the nanocomplex. Bromide ion was chosen as a model anion to test the efficacy of the nanoprobe. The fluorescence of the nanoconjugate was “turned off” upon binding but was progressively “turned on” upon interaction with varying concentrations of bromide ion. Experimental results showed that the quantum size effect of nanocrystal QD determined the overall sensitivity and selectivity of the nanoprobe and followed the order QD563-NiTAPc > QD605-NiTAPc > QD621-NiTAPc. The mechanism of reaction is proposed.
- Full Text:
- Date Issued: 2013
Comparative phototransformation of environmental pollutants using metallophthalocyanines supported on electrospun polymer fibers
- Zugle, Ruphino, Nyokong, Tebello
- Authors: Zugle, Ruphino , Nyokong, Tebello
- Date: 2013
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/190509 , vital:45001 , xlink:href="https://doi.org/10.1002/app.38381"
- Description: The fluorescence and photoactivity of a series of Zn and Lu phthalocyanine complexes incorporated in various polymer fibers were investigated for the phototransformation of 4-chlorophenol, 4-nitrophenol, and methyl orange. The phthalocyanine complexes functionalized on polystyrene and polysulfone polymer fibers could be applied in the degradation of 4-chlorophenol, 4-nitrophenol, and methyl orange with 4-chlorophenol being much more susceptible to degradation while methyl orange was the least. Also polymer fibers of polystyrene were found to be reusable.
- Full Text:
- Date Issued: 2013
- Authors: Zugle, Ruphino , Nyokong, Tebello
- Date: 2013
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/190509 , vital:45001 , xlink:href="https://doi.org/10.1002/app.38381"
- Description: The fluorescence and photoactivity of a series of Zn and Lu phthalocyanine complexes incorporated in various polymer fibers were investigated for the phototransformation of 4-chlorophenol, 4-nitrophenol, and methyl orange. The phthalocyanine complexes functionalized on polystyrene and polysulfone polymer fibers could be applied in the degradation of 4-chlorophenol, 4-nitrophenol, and methyl orange with 4-chlorophenol being much more susceptible to degradation while methyl orange was the least. Also polymer fibers of polystyrene were found to be reusable.
- Full Text:
- Date Issued: 2013
Zinc (II) 2, 9, 16, 23-tetrakis [4-(N-methylpyridyloxy)]-phthalocyanine anchored on an electrospun polysulfone polymer fiber: Application for photosensitized conversion of methyl orange
- Zugle, Ruphino, Nyokong, Tebello
- Authors: Zugle, Ruphino , Nyokong, Tebello
- Date: 2013
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/232741 , vital:50020 , xlink:href="https://doi.org/10.1016/j.molcata.2012.10.001"
- Description: In this work, a comparative study of photodegradation of methyl orange, an azo dye, in homogeneous aqueous solution of a quarternized cationic zinc phthalocyanine and a heterogeneous catalytic system based on the same phthalocyanine anchored on polysulfone polymer fiber is presented. In both cases, conversion involved the azo bond of the dye with no detectable opening up of the aromatic benzene rings. The reaction kinetics in both cases were consistent with first order with the conversion occurring in the homogeneous system being faster than when the functionalized polymer fiber was used. The reaction products consisted of a coupling product as well as a series of oligopolymeric products.
- Full Text:
- Date Issued: 2013
- Authors: Zugle, Ruphino , Nyokong, Tebello
- Date: 2013
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/232741 , vital:50020 , xlink:href="https://doi.org/10.1016/j.molcata.2012.10.001"
- Description: In this work, a comparative study of photodegradation of methyl orange, an azo dye, in homogeneous aqueous solution of a quarternized cationic zinc phthalocyanine and a heterogeneous catalytic system based on the same phthalocyanine anchored on polysulfone polymer fiber is presented. In both cases, conversion involved the azo bond of the dye with no detectable opening up of the aromatic benzene rings. The reaction kinetics in both cases were consistent with first order with the conversion occurring in the homogeneous system being faster than when the functionalized polymer fiber was used. The reaction products consisted of a coupling product as well as a series of oligopolymeric products.
- Full Text:
- Date Issued: 2013
Surface patterning using scanning electrochemical microscopy to locally trigger a “click” chemistry reaction
- Quinton, Damien, Maringa, Audacity, Griveau, Sophie, Nyokong, Tebello, Bedioui, Fethi
- Authors: Quinton, Damien , Maringa, Audacity , Griveau, Sophie , Nyokong, Tebello , Bedioui, Fethi
- Language: English
- Type: Article
- Identifier: vital:7331 , http://hdl.handle.net/10962/d1020592
- Description: We report on the surface micropatterning of conductive surfaces via the electrochemical triggering of a click reaction, the copper(I) catalyzed azide–alkyne cycloaddition reaction (CuAAC) by SECM via a two-step approach: (i) functionalization on the entire surface with azido-aryl groups by using the diazonium approach followed by (ii) the covalent linkage of alkyne-bearing ferrocene by CuAAC within a local area by SECM. More precisely, the click reaction was triggered by Cu(I) catalyst generation for 30 min at the SECM tip positioned ≈ 10 μm above the azido-aryl modified surface. The dimension of the spot obtained under these conditions was ≈ 75 μm. The electrochemical imaging by SECM of the ultra thin area locally clicked with ferrocene moieties was made thanks to the electrocatalytic properties of the ferrocene modified surface towards ferrocyanide electrooxidation. This local clicking procedure opens the gate to further controlled functionalization of restricted small substrates. , Original publication is available at http://dx.doi.org/10.1016/j.elecom.2013.03.021
- Full Text: false
- Authors: Quinton, Damien , Maringa, Audacity , Griveau, Sophie , Nyokong, Tebello , Bedioui, Fethi
- Language: English
- Type: Article
- Identifier: vital:7331 , http://hdl.handle.net/10962/d1020592
- Description: We report on the surface micropatterning of conductive surfaces via the electrochemical triggering of a click reaction, the copper(I) catalyzed azide–alkyne cycloaddition reaction (CuAAC) by SECM via a two-step approach: (i) functionalization on the entire surface with azido-aryl groups by using the diazonium approach followed by (ii) the covalent linkage of alkyne-bearing ferrocene by CuAAC within a local area by SECM. More precisely, the click reaction was triggered by Cu(I) catalyst generation for 30 min at the SECM tip positioned ≈ 10 μm above the azido-aryl modified surface. The dimension of the spot obtained under these conditions was ≈ 75 μm. The electrochemical imaging by SECM of the ultra thin area locally clicked with ferrocene moieties was made thanks to the electrocatalytic properties of the ferrocene modified surface towards ferrocyanide electrooxidation. This local clicking procedure opens the gate to further controlled functionalization of restricted small substrates. , Original publication is available at http://dx.doi.org/10.1016/j.elecom.2013.03.021
- Full Text: false
Adsorption and separation of platinum and palladium by polyamine functionalized polystyrene-based beads and nanofibers
- Fayemi, Omolola E, Ogunlaja, Adeniyi S, Kempgens, Pierre F M, Antunes, Edith M, Torto, Nelson, Nyokong, Tebello, Tshentu, Zenixole R
- Authors: Fayemi, Omolola E , Ogunlaja, Adeniyi S , Kempgens, Pierre F M , Antunes, Edith M , Torto, Nelson , Nyokong, Tebello , Tshentu, Zenixole R
- Date: 2013
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/241694 , vital:50961 , xlink:href="https://doi.org/10.1016/j.mineng.2013.06.006"
- Description: Adsorption and separation of platinum and palladium chlorido species (PtCl62- and PdCl42-) on polystyrene beads as well as nanofibers functionalized with ammonium centres based on ethylenediamine (EDA), diethylenetriamine (DETA), triethylenetetramine (TETA) and tris-(2-aminoethyl)amine (TAEA) are described. The functionalized sorbent materials were characterized by microanalysis, SEM, XPS, BET and FTIR. The surface area of the functionalized fibers was in the range 69–241 m2/g while it was 73–107 m2/g for the beads. The adsorption and loading capacities of the sorption materials were investigated using both the batch and column studies at 1 M HCl concentration. The adsorption studies for both PtCl62- and PdCl42- on the different sorbent materials fit the Langmuir isotherm with R2 values >0.99. The highest loading capacity of Pt and Pd were 7.4 mg/g and 4.3 mg/g respectively for the nanofiber sorbent material based on ethylenediamine (EDA) while the beads with ethylenediamine (EDA) gave 1.0 mg/g and 0.2 mg/g for Pt and Pd respectively. Metals loaded on the sorbent materials were recovered by using 3% m/v thiourea solution as the eluting agent with quantitative desorption efficiency under the selected experimental conditions. Separation of platinum from palladium was partially achieved by selective stripping of PtCl62- with 0.5 M of NaClO4 in 1.0 M HCl while PdCl42- was eluted with 0.5 M thiourea in 1.0 M HCl. Separation of platinum from iridium and rhodium under 1 M HCl concentration was successful on triethylenetriamine (TETA)-functionalized Merrifield beads. This material (M-TETA) showed selectivity for platinum albeit the low loading capacity.
- Full Text:
- Date Issued: 2013
- Authors: Fayemi, Omolola E , Ogunlaja, Adeniyi S , Kempgens, Pierre F M , Antunes, Edith M , Torto, Nelson , Nyokong, Tebello , Tshentu, Zenixole R
- Date: 2013
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/241694 , vital:50961 , xlink:href="https://doi.org/10.1016/j.mineng.2013.06.006"
- Description: Adsorption and separation of platinum and palladium chlorido species (PtCl62- and PdCl42-) on polystyrene beads as well as nanofibers functionalized with ammonium centres based on ethylenediamine (EDA), diethylenetriamine (DETA), triethylenetetramine (TETA) and tris-(2-aminoethyl)amine (TAEA) are described. The functionalized sorbent materials were characterized by microanalysis, SEM, XPS, BET and FTIR. The surface area of the functionalized fibers was in the range 69–241 m2/g while it was 73–107 m2/g for the beads. The adsorption and loading capacities of the sorption materials were investigated using both the batch and column studies at 1 M HCl concentration. The adsorption studies for both PtCl62- and PdCl42- on the different sorbent materials fit the Langmuir isotherm with R2 values >0.99. The highest loading capacity of Pt and Pd were 7.4 mg/g and 4.3 mg/g respectively for the nanofiber sorbent material based on ethylenediamine (EDA) while the beads with ethylenediamine (EDA) gave 1.0 mg/g and 0.2 mg/g for Pt and Pd respectively. Metals loaded on the sorbent materials were recovered by using 3% m/v thiourea solution as the eluting agent with quantitative desorption efficiency under the selected experimental conditions. Separation of platinum from palladium was partially achieved by selective stripping of PtCl62- with 0.5 M of NaClO4 in 1.0 M HCl while PdCl42- was eluted with 0.5 M thiourea in 1.0 M HCl. Separation of platinum from iridium and rhodium under 1 M HCl concentration was successful on triethylenetriamine (TETA)-functionalized Merrifield beads. This material (M-TETA) showed selectivity for platinum albeit the low loading capacity.
- Full Text:
- Date Issued: 2013
Probing the sensitive and selective luminescent detection of peroxynitrite using thiol-capped CdTe and CdTe@ ZnS quantum dots
- Adegoke, Oluwasesan, Nyokong, Tebello
- Authors: Adegoke, Oluwasesan , Nyokong, Tebello
- Date: 2013
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/193757 , vital:45393 , xlink:href="https://doi.org/10.1016/j.jlumin.2012.08.002"
- Description: CdTe and CdTe@ZnS quantum dots (QDs) capped with 3-mercaptopropionic acid (MPA), thioglycolic acid (TGA), or glutathione (GSH) have been employed for the first time as luminescent probes for the sensitive and selective detection of peroxynitrite (ONOO−) in aqueous solution. The sensitivity of the proposed probe followed the order: MPA–TGA–CdTe@ZnS>GSH–TGA–CdTe@ZnS>MPA–CdTe QDs. The varying degree of quenching is elucidated based on the QD–thiolate bond of CdTe@ZnS being more sensitive to oxidation from ONOO− than CdTe. The selectivity of the probe in the presence of co-existing species followed the order: GSH–TGA–CdTe@ZnS>MPA–TGA–CdTe@ZnS>MPA–CdTe QDs. QDs capped with MPA showed less selectivity for ONOO− than GSH. The best limit of detection (LOD) of 12.6 nM was obtained for MPA–TGA–CdTe@ZnS QDs. Time-resolved fluorescence measurements indicated that the interaction between ONOO− and the QDs is static in nature.
- Full Text:
- Date Issued: 2013
- Authors: Adegoke, Oluwasesan , Nyokong, Tebello
- Date: 2013
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/193757 , vital:45393 , xlink:href="https://doi.org/10.1016/j.jlumin.2012.08.002"
- Description: CdTe and CdTe@ZnS quantum dots (QDs) capped with 3-mercaptopropionic acid (MPA), thioglycolic acid (TGA), or glutathione (GSH) have been employed for the first time as luminescent probes for the sensitive and selective detection of peroxynitrite (ONOO−) in aqueous solution. The sensitivity of the proposed probe followed the order: MPA–TGA–CdTe@ZnS>GSH–TGA–CdTe@ZnS>MPA–CdTe QDs. The varying degree of quenching is elucidated based on the QD–thiolate bond of CdTe@ZnS being more sensitive to oxidation from ONOO− than CdTe. The selectivity of the probe in the presence of co-existing species followed the order: GSH–TGA–CdTe@ZnS>MPA–TGA–CdTe@ZnS>MPA–CdTe QDs. QDs capped with MPA showed less selectivity for ONOO− than GSH. The best limit of detection (LOD) of 12.6 nM was obtained for MPA–TGA–CdTe@ZnS QDs. Time-resolved fluorescence measurements indicated that the interaction between ONOO− and the QDs is static in nature.
- Full Text:
- Date Issued: 2013
X-ray photoelectron spectroscopy analysis of the effect of alkyl-and arylthio substituents on manganese phthalocyanines for self-assembled monolayer formation on gold
- Coates, Megan, Nyokong, Tebello
- Authors: Coates, Megan , Nyokong, Tebello
- Date: 2013
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/190490 , vital:44999 , xlink:href="https://doi.org/10.1016/j.elecom.2013.03.019"
- Description: Self-assembled monolayers of an octa-substituted alkylthio and arylthio manganese phthalocyanines were formed on gold. X-ray photoelectron spectroscopy was used to analyse both of the phthalocyanine layers on gold. Approximately 60% of the sulphur groups in the aryl substituted-SAM surface were bound to gold through the cleavage of the C S bond, as opposed to only 37% for the alkyl substituted-SAM.
- Full Text:
- Date Issued: 2013
- Authors: Coates, Megan , Nyokong, Tebello
- Date: 2013
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/190490 , vital:44999 , xlink:href="https://doi.org/10.1016/j.elecom.2013.03.019"
- Description: Self-assembled monolayers of an octa-substituted alkylthio and arylthio manganese phthalocyanines were formed on gold. X-ray photoelectron spectroscopy was used to analyse both of the phthalocyanine layers on gold. Approximately 60% of the sulphur groups in the aryl substituted-SAM surface were bound to gold through the cleavage of the C S bond, as opposed to only 37% for the alkyl substituted-SAM.
- Full Text:
- Date Issued: 2013
The interaction of silver nanoparticles with low symmetry cysteinyl metallophthalocyanines and their antimicrobial effect
- Masilela, Nkosiphile, Nyokong, Tebello
- Authors: Masilela, Nkosiphile , Nyokong, Tebello
- Date: 2013
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/193735 , vital:45391 , xlink:href="https://doi.org/10.1016/j.jphotochem.2013.01.009"
- Description: This work reports on the synthesis of silver nanoparticles and their antimicrobial activity alone and in the presence of low symmetry phthalocyanines. The photochemical behaviour of various low symmetry phthalocyanines in the presence of AgNPs is investigated in DMF. A slight improvement in the photochemical behaviour and antimicrobial activity was achieved in the presence of AgNPs for all the complexes. The spherically shaped AgNPs gave the highest antimicrobial activity compared to the triangular and cubic structures. The (OH)2GeMCsPc complex gave the highest antimicrobial activity towards Staphylococcus aureas, both alone and in the presence of AgNPs under illumination with light.
- Full Text:
- Date Issued: 2013
- Authors: Masilela, Nkosiphile , Nyokong, Tebello
- Date: 2013
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/193735 , vital:45391 , xlink:href="https://doi.org/10.1016/j.jphotochem.2013.01.009"
- Description: This work reports on the synthesis of silver nanoparticles and their antimicrobial activity alone and in the presence of low symmetry phthalocyanines. The photochemical behaviour of various low symmetry phthalocyanines in the presence of AgNPs is investigated in DMF. A slight improvement in the photochemical behaviour and antimicrobial activity was achieved in the presence of AgNPs for all the complexes. The spherically shaped AgNPs gave the highest antimicrobial activity compared to the triangular and cubic structures. The (OH)2GeMCsPc complex gave the highest antimicrobial activity towards Staphylococcus aureas, both alone and in the presence of AgNPs under illumination with light.
- Full Text:
- Date Issued: 2013
Catalytic oxidation of thioanisole using oxovanadium (IV)‐functionalized electrospun polybenzimidazole nanofibers
- Walmsley, Ryan S, Hlangothi, Percy, Litwinski, Christian, Nyokong, Tebello, Torto, Nelson, Tshentu, Zenixole R
- Authors: Walmsley, Ryan S , Hlangothi, Percy , Litwinski, Christian , Nyokong, Tebello , Torto, Nelson , Tshentu, Zenixole R
- Date: 2013
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/242083 , vital:51000 , xlink:href="https://doi.org/10.1002/app.38067"
- Description: Polybenzimidazole fibers, with an average diameter of 262 nm, were produced by the process of electrospinning. These fibers were used as a solid support material for the immobilization of oxovanadium(IV) which was achieved via a reaction with vanadyl sulfate. The oxovanadium(IV)-functionalized nanofibers were used as heterogeneous catalysts for the oxidation of thioanisole under both batch and pseudo-continuous flow conditions with great success. Under batch conditions near quantitative oxidation of thioanisole was achieved in under 90 min, even after four successive catalytic reactions. Under continuous conditions, excellent conversion of thioanisole was maintained throughout the period studied at flow rates of up to 2 mLh−1. This study, therefore, proposes that electrospun polybenzimidazole nanofibers, with their small diameters, impressive chemical and thermal stability, as well as coordinating benzimidazole group, may be a desirable support material for immobilization of homogeneous catalysts.
- Full Text:
- Date Issued: 2013
- Authors: Walmsley, Ryan S , Hlangothi, Percy , Litwinski, Christian , Nyokong, Tebello , Torto, Nelson , Tshentu, Zenixole R
- Date: 2013
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/242083 , vital:51000 , xlink:href="https://doi.org/10.1002/app.38067"
- Description: Polybenzimidazole fibers, with an average diameter of 262 nm, were produced by the process of electrospinning. These fibers were used as a solid support material for the immobilization of oxovanadium(IV) which was achieved via a reaction with vanadyl sulfate. The oxovanadium(IV)-functionalized nanofibers were used as heterogeneous catalysts for the oxidation of thioanisole under both batch and pseudo-continuous flow conditions with great success. Under batch conditions near quantitative oxidation of thioanisole was achieved in under 90 min, even after four successive catalytic reactions. Under continuous conditions, excellent conversion of thioanisole was maintained throughout the period studied at flow rates of up to 2 mLh−1. This study, therefore, proposes that electrospun polybenzimidazole nanofibers, with their small diameters, impressive chemical and thermal stability, as well as coordinating benzimidazole group, may be a desirable support material for immobilization of homogeneous catalysts.
- Full Text:
- Date Issued: 2013
Characterization of glassy carbon electrodes modified with carbon nanotubes and iron phthalocyanine through grafting and click chemistry
- Coates, Megan, Nyokong, Tebello
- Authors: Coates, Megan , Nyokong, Tebello
- Date: 2013
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/193746 , vital:45392 , xlink:href="https://doi.org/10.1016/j.electacta.2012.12.112"
- Description: A glassy carbon electrode was modified by adsorption of single-walled carbon nanotubes, followed by electrochemical grafting of 4-azidobenzenediazonium salt, which was in turn reacted with ethynylpyridine through the Sharpless “click chemistry” reaction. Thereafter, iron phthalocyanine was attached to the electrode through axial ligation to the pyridine group. The modified electrode was characterised using X-ray photoelectron spectroscopy and scanning electrochemical microscopy, and well as electrochemistry. The electrocatalytic ability of the modified electrode was tested using hydrazine as a sample analyte, and showed a significant 10-fold improvement in the detection of hydrazine compared to the surface without nanotubes, and comparable stability. The linear range for this surface was over 1.0 × 10−5 to 1.0 × 10−4 mol dm−3, with a limit of detection of 1.10 ± 0.06 μmol dm−3 and sensitivity of 15.61 μA mM−1.
- Full Text:
- Date Issued: 2013
- Authors: Coates, Megan , Nyokong, Tebello
- Date: 2013
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/193746 , vital:45392 , xlink:href="https://doi.org/10.1016/j.electacta.2012.12.112"
- Description: A glassy carbon electrode was modified by adsorption of single-walled carbon nanotubes, followed by electrochemical grafting of 4-azidobenzenediazonium salt, which was in turn reacted with ethynylpyridine through the Sharpless “click chemistry” reaction. Thereafter, iron phthalocyanine was attached to the electrode through axial ligation to the pyridine group. The modified electrode was characterised using X-ray photoelectron spectroscopy and scanning electrochemical microscopy, and well as electrochemistry. The electrocatalytic ability of the modified electrode was tested using hydrazine as a sample analyte, and showed a significant 10-fold improvement in the detection of hydrazine compared to the surface without nanotubes, and comparable stability. The linear range for this surface was over 1.0 × 10−5 to 1.0 × 10−4 mol dm−3, with a limit of detection of 1.10 ± 0.06 μmol dm−3 and sensitivity of 15.61 μA mM−1.
- Full Text:
- Date Issued: 2013
Surface patterning using scanning electrochemical microscopy to locally trigger a “click” chemistry reaction
- Quinton, Damien, Maringa, Audacity, Griveau, Sophie, Nyokong, Tebello, Bedioui, Fethi
- Authors: Quinton, Damien , Maringa, Audacity , Griveau, Sophie , Nyokong, Tebello , Bedioui, Fethi
- Date: 2013
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/241805 , vital:50971 , xlink:href="https://doi.org/10.1016/j.elecom.2013.03.021"
- Description: We report on the surface micropatterning of conductive surfaces via the electrochemical triggering of a click reaction, the copper(I) catalyzed azide–alkyne cycloaddition reaction (CuAAC) by SECM via a two-step approach: (i) functionalization on the entire surface with azido-aryl groups by using the diazonium approach followed by (ii) the covalent linkage of alkyne-bearing ferrocene by CuAAC within a local area by SECM. More precisely, the click reaction was triggered by Cu(I) catalyst generation for 30 min at the SECM tip positioned ≈ 10 μm above the azido-aryl modified surface. The dimension of the spot obtained under these conditions was ≈ 75 μm. The electrochemical imaging by SECM of the ultra thin area locally clicked with ferrocene moieties was made thanks to the electrocatalytic properties of the ferrocene modified surface towards ferrocyanide electrooxidation. This local clicking procedure opens the gate to further controlled functionalization of restricted small substrates.
- Full Text:
- Date Issued: 2013
- Authors: Quinton, Damien , Maringa, Audacity , Griveau, Sophie , Nyokong, Tebello , Bedioui, Fethi
- Date: 2013
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/241805 , vital:50971 , xlink:href="https://doi.org/10.1016/j.elecom.2013.03.021"
- Description: We report on the surface micropatterning of conductive surfaces via the electrochemical triggering of a click reaction, the copper(I) catalyzed azide–alkyne cycloaddition reaction (CuAAC) by SECM via a two-step approach: (i) functionalization on the entire surface with azido-aryl groups by using the diazonium approach followed by (ii) the covalent linkage of alkyne-bearing ferrocene by CuAAC within a local area by SECM. More precisely, the click reaction was triggered by Cu(I) catalyst generation for 30 min at the SECM tip positioned ≈ 10 μm above the azido-aryl modified surface. The dimension of the spot obtained under these conditions was ≈ 75 μm. The electrochemical imaging by SECM of the ultra thin area locally clicked with ferrocene moieties was made thanks to the electrocatalytic properties of the ferrocene modified surface towards ferrocyanide electrooxidation. This local clicking procedure opens the gate to further controlled functionalization of restricted small substrates.
- Full Text:
- Date Issued: 2013
Overcrowding of false codling moth, Thaumatotibia leucotreta (Meyrick) leads to the isolation of five new Cryptophlebia leucotreta granulovirus (CrleGV-SA) isolates
- Opoku-Debrah, John K, Hill, Martin P, Knox, Caroline M, Moore, Sean D
- Authors: Opoku-Debrah, John K , Hill, Martin P , Knox, Caroline M , Moore, Sean D
- Date: 2013
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/419360 , vital:71637 , xlink:href="https://doi.org/10.1016/j.jip.2012.12.008"
- Description: False codling moth, Thaumatotibia leucotreta (Meyrick) is a serious pest of economic importance to the South African fruit industry. As part of sustainable efforts to control this pest, biological control options that involve the application of baculovirus-based biopesticides such as Cryptogran and Cryptex (both formulated with a South African isolate of Cryptophlebia leucotreta granulovirus, CrleGV-SA) are popularly used by farmers. In order to safeguard the integrity of these biopesticides as well as protect against any future development of resistance in the host, we conducted a study to bioprospect for additional CrleGV isolates as alternatives to existing ones. Using overcrowding as an induction method for latent infection, we recovered five new CrleGV isolates (CrleGV-SA Ado, CrleGV-SA Mbl, CrleGV-SA Cit, CrleGV-SA MixC and CrleGV-SA Nels). Single restriction endonuclease (REN) analysis of viral genomic DNA extracted from purified occlusion bodies showed that isolates differed in their DNA profiles. Partial sequencing of granulin and egt genes from the different isolates and multiple alignments of nucleotide sequences revealed the presence of single nucleotide polymorphisms (SNPs), some of which resulted in amino acid substitutions in the protein sequence. Based on these findings as well as comparisons with other documented CrleGV isolates, we propose two phylogenetic groups for CrleGV-SA isolates recovered in this study.
- Full Text:
- Date Issued: 2013
- Authors: Opoku-Debrah, John K , Hill, Martin P , Knox, Caroline M , Moore, Sean D
- Date: 2013
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/419360 , vital:71637 , xlink:href="https://doi.org/10.1016/j.jip.2012.12.008"
- Description: False codling moth, Thaumatotibia leucotreta (Meyrick) is a serious pest of economic importance to the South African fruit industry. As part of sustainable efforts to control this pest, biological control options that involve the application of baculovirus-based biopesticides such as Cryptogran and Cryptex (both formulated with a South African isolate of Cryptophlebia leucotreta granulovirus, CrleGV-SA) are popularly used by farmers. In order to safeguard the integrity of these biopesticides as well as protect against any future development of resistance in the host, we conducted a study to bioprospect for additional CrleGV isolates as alternatives to existing ones. Using overcrowding as an induction method for latent infection, we recovered five new CrleGV isolates (CrleGV-SA Ado, CrleGV-SA Mbl, CrleGV-SA Cit, CrleGV-SA MixC and CrleGV-SA Nels). Single restriction endonuclease (REN) analysis of viral genomic DNA extracted from purified occlusion bodies showed that isolates differed in their DNA profiles. Partial sequencing of granulin and egt genes from the different isolates and multiple alignments of nucleotide sequences revealed the presence of single nucleotide polymorphisms (SNPs), some of which resulted in amino acid substitutions in the protein sequence. Based on these findings as well as comparisons with other documented CrleGV isolates, we propose two phylogenetic groups for CrleGV-SA isolates recovered in this study.
- Full Text:
- Date Issued: 2013
Synthesis and nonlinear optical examination of 3 (4), 15 (16)-Bis-(4-tert-butyl-phenoxy)-10, 22-diaminohemiporphyrazinato chloroindium
- Britton, Jonathan, Antunes, Edith M, Nyokong, Tebello
- Authors: Britton, Jonathan , Antunes, Edith M , Nyokong, Tebello
- Date: 2013
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/241739 , vital:50965 , xlink:href="https://doi.org/10.1016/j.molstruc.2013.05.001"
- Description: 3(4),15(16)-Bis-(4-tert-butyl-phenoxy)-10,22-diaminohemiporphyrazinato chloroindium hemiporphyrazine was synthesized from 1,3,5-triaminobenzene and 4-tert-butyl-phenoxyisoindoline. The structure of the complex was confirmed using mass, nuclear magnetic resonance and infrared spectroscopies. The nonlinear parameters of the compound was also analyzed in dimethylformamide and found to be significantly greater than previously analyzed phthalocyanines.
- Full Text:
- Date Issued: 2013
- Authors: Britton, Jonathan , Antunes, Edith M , Nyokong, Tebello
- Date: 2013
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/241739 , vital:50965 , xlink:href="https://doi.org/10.1016/j.molstruc.2013.05.001"
- Description: 3(4),15(16)-Bis-(4-tert-butyl-phenoxy)-10,22-diaminohemiporphyrazinato chloroindium hemiporphyrazine was synthesized from 1,3,5-triaminobenzene and 4-tert-butyl-phenoxyisoindoline. The structure of the complex was confirmed using mass, nuclear magnetic resonance and infrared spectroscopies. The nonlinear parameters of the compound was also analyzed in dimethylformamide and found to be significantly greater than previously analyzed phthalocyanines.
- Full Text:
- Date Issued: 2013
Optical limiting analysis of phthalocyanines in polymer thin films
- Britton, Jonathan, Litwinski, Christian, Antunes, Edith M, Durmus, Mahmut, Chaukea, Vongani, Nyokong, Tebello
- Authors: Britton, Jonathan , Litwinski, Christian , Antunes, Edith M , Durmus, Mahmut , Chaukea, Vongani , Nyokong, Tebello
- Date: 2013
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/232488 , vital:49996 , xlink:href="https://doi.org/10.1080/10601325.2013.736269"
- Description: This paper reports on the effect of embedding twelve phthalocyanines containing In, Ga, Zn and Al as central metals in polymer thin films on their optical limiting abilities. This paper also examines the effect of forming a covalent link between zinc tetraamino phthalocyanine (10) and poly (methyl acrylic acid) (PMAA), and Zn (11) or OHAl (12) octacarboxy phthalocyanines with polyethylenimine (PEI). The average film thickness (for phthalocyanines mixed or linked to polymers) of each Pc/Polymer films on glass was 95 μm. The hyperpolarizability of the twelve phthalocyanines was found to be in the range of 10−26 to 10−24 esu.L. This is significantly higher than the hyperpolarizabilities of these phthalocyanines in solution, which ranged from 10−30 to 10−26 esu.L. Degradation studies seem to indicate that placing a phthalocyanine within a polymer thin film may protect it slightly from photo- and thermal degradation.
- Full Text:
- Date Issued: 2013
- Authors: Britton, Jonathan , Litwinski, Christian , Antunes, Edith M , Durmus, Mahmut , Chaukea, Vongani , Nyokong, Tebello
- Date: 2013
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/232488 , vital:49996 , xlink:href="https://doi.org/10.1080/10601325.2013.736269"
- Description: This paper reports on the effect of embedding twelve phthalocyanines containing In, Ga, Zn and Al as central metals in polymer thin films on their optical limiting abilities. This paper also examines the effect of forming a covalent link between zinc tetraamino phthalocyanine (10) and poly (methyl acrylic acid) (PMAA), and Zn (11) or OHAl (12) octacarboxy phthalocyanines with polyethylenimine (PEI). The average film thickness (for phthalocyanines mixed or linked to polymers) of each Pc/Polymer films on glass was 95 μm. The hyperpolarizability of the twelve phthalocyanines was found to be in the range of 10−26 to 10−24 esu.L. This is significantly higher than the hyperpolarizabilities of these phthalocyanines in solution, which ranged from 10−30 to 10−26 esu.L. Degradation studies seem to indicate that placing a phthalocyanine within a polymer thin film may protect it slightly from photo- and thermal degradation.
- Full Text:
- Date Issued: 2013
Poly methyl methacrylate films containing metallophthalocyanines in the presence of CdTe quantum dots
- Britton, Jonathan, Durmus, Mahmut, Chauke, Vongani, Nyokong, Tebello
- Authors: Britton, Jonathan , Durmus, Mahmut , Chauke, Vongani , Nyokong, Tebello
- Date: 2013
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/241629 , vital:50956 , xlink:href="https://doi.org/10.1016/j.molstruc.2013.09.017"
- Description: Non-linear optical (NLO) parameters were determined for phthalocyanine complexes containing In, Ga and Zn as central metals when embedded in poly (methyl methacrylate) polymer in the absence and presence of quantum dots (QDs) in an effort to create the most optimal optical limiting material. The QDs employed were CdTe–TGA (TGA = thioglylcolic acid). Triplet lifetimes generally increased as the value of the ratio of absorption cross sections of the excited state to that of the ground state (k) decreased on addition of CdTe–TGA to the phthalocyanines. The saturation energy density (Fsat) values were generally smaller in the films when compared to the solutions. Fsat, Ilim, Im[χ(3)]/α and γ all gave values which were of optimal range (i.e. the Im[χ(3)]/α and γ values were high enough to ensure adequate optical limiting but not too high to make the compounds behave like optical filters. Also, the Fsat and Ilim values were small enough to mean that the optical limiting process started at an intensity which was not too high) for complex 10 containing Zn central metal and tetrasubstituted with amino groups.
- Full Text:
- Date Issued: 2013
- Authors: Britton, Jonathan , Durmus, Mahmut , Chauke, Vongani , Nyokong, Tebello
- Date: 2013
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/241629 , vital:50956 , xlink:href="https://doi.org/10.1016/j.molstruc.2013.09.017"
- Description: Non-linear optical (NLO) parameters were determined for phthalocyanine complexes containing In, Ga and Zn as central metals when embedded in poly (methyl methacrylate) polymer in the absence and presence of quantum dots (QDs) in an effort to create the most optimal optical limiting material. The QDs employed were CdTe–TGA (TGA = thioglylcolic acid). Triplet lifetimes generally increased as the value of the ratio of absorption cross sections of the excited state to that of the ground state (k) decreased on addition of CdTe–TGA to the phthalocyanines. The saturation energy density (Fsat) values were generally smaller in the films when compared to the solutions. Fsat, Ilim, Im[χ(3)]/α and γ all gave values which were of optimal range (i.e. the Im[χ(3)]/α and γ values were high enough to ensure adequate optical limiting but not too high to make the compounds behave like optical filters. Also, the Fsat and Ilim values were small enough to mean that the optical limiting process started at an intensity which was not too high) for complex 10 containing Zn central metal and tetrasubstituted with amino groups.
- Full Text:
- Date Issued: 2013
Perceptions and use of public green space is influenced by its relative abundance in two small towns in South Africa
- Shackleton, Charlie M, Blair, Andrew
- Authors: Shackleton, Charlie M , Blair, Andrew
- Date: 2013
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/181026 , vital:43688 , xlink:href="https://doi.org/10.1016/j.landurbplan.2013.01.011"
- Description: The challenges in planning and maintaining urban public green spaces in poor towns of the developing world differ markedly from those of the developed world. This paper reports on residents’ perceptions, use and willingness to get involved in urban public green space (PGS) issues in two poor towns in South Africa which differed markedly in the amount of PGS. The disparities in PGS between the two towns were also replicated in different suburbs within the two towns. We hypothesised that levels of dissatisfaction would be highest in those suburbs and the town with the least PGS. The results indicated that the distance from residents’ homesteads to the nearest PGS was similar across towns and suburbs. Most residents felt that having accessible PGS was important, and the majority agreed that there was insufficient PGS in their respective town and suburb, and that the local municipality did not do enough in providing PGS or maintaining what there was. The level of dissatisfaction with the amount and condition of PGS was generally highest in the suburbs and town with the least PGS. Many felt that the municipality had insufficient commitment and funds to adequately maintain PGS, and consequently the willingness of residents to get involved through either a commitment of time or funds was high. The more affluent town and suburbs were willing to pay more than the poorer ones, and the poorer ones were willing to provide more time than the more affluent ones.
- Full Text:
- Date Issued: 2013
- Authors: Shackleton, Charlie M , Blair, Andrew
- Date: 2013
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/181026 , vital:43688 , xlink:href="https://doi.org/10.1016/j.landurbplan.2013.01.011"
- Description: The challenges in planning and maintaining urban public green spaces in poor towns of the developing world differ markedly from those of the developed world. This paper reports on residents’ perceptions, use and willingness to get involved in urban public green space (PGS) issues in two poor towns in South Africa which differed markedly in the amount of PGS. The disparities in PGS between the two towns were also replicated in different suburbs within the two towns. We hypothesised that levels of dissatisfaction would be highest in those suburbs and the town with the least PGS. The results indicated that the distance from residents’ homesteads to the nearest PGS was similar across towns and suburbs. Most residents felt that having accessible PGS was important, and the majority agreed that there was insufficient PGS in their respective town and suburb, and that the local municipality did not do enough in providing PGS or maintaining what there was. The level of dissatisfaction with the amount and condition of PGS was generally highest in the suburbs and town with the least PGS. Many felt that the municipality had insufficient commitment and funds to adequately maintain PGS, and consequently the willingness of residents to get involved through either a commitment of time or funds was high. The more affluent town and suburbs were willing to pay more than the poorer ones, and the poorer ones were willing to provide more time than the more affluent ones.
- Full Text:
- Date Issued: 2013
Current and potential carbon stocks of trees in urban parking lots in towns of the Eastern Cape, South Africa
- O'Donoghue, Alexandra, Shackleton, Charlie M
- Authors: O'Donoghue, Alexandra , Shackleton, Charlie M
- Date: 2013
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/181037 , vital:43689 , xlink:href="https://doi.org/10.1016/j.ufug.2013.07.001"
- Description: Greening of shopping centre parking lots is a potentially important strategy that can contribute to urban carbon mitigation efforts, improve aesthetics and the shopping experience of consumers, whilst adding to urban biodiversity. Twenty-eight shopping centre parking lots in six Eastern Cape urban centres, South Africa, were sampled to determine tree species composition, density and annual carbon sequestration potential. The best case parking lot found during the study was used as a benchmark to display the difference between current tree density and above-ground carbon stocks relative to the potential optimum. The highest tree density was 66 trees ha−1, whereas the average density across all sampled parking lots was less than half that (27.2 ± 22.6 trees ha−1). The average annual carbon sequestration potential per parking lot was 1390 ± 2503 kg ha−1. Planting density was positively related to annual sequestration rates, whilst parking lot age and the mean annual rainfall of the town had no influence. Mean tree species richness per parking lot was 2.3 ± 1.8 species, with a positive relationship to parking lot size, but not to mean annual rainfall of the site. The majority of trees (62.5%) in parking lots were alien species, although newer parking lots had significantly greater proportions of indigenous species. There was no difference in mean annual carbon sequestration rate per tree between indigenous and alien trees species. Low tree densities and small parking lot areas constrained the potential for earning carbon credits from trees in parking lots. Nonetheless, planners and designers need to be more aware of the potential contribution of trees towards urban sustainability.
- Full Text:
- Date Issued: 2013
- Authors: O'Donoghue, Alexandra , Shackleton, Charlie M
- Date: 2013
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/181037 , vital:43689 , xlink:href="https://doi.org/10.1016/j.ufug.2013.07.001"
- Description: Greening of shopping centre parking lots is a potentially important strategy that can contribute to urban carbon mitigation efforts, improve aesthetics and the shopping experience of consumers, whilst adding to urban biodiversity. Twenty-eight shopping centre parking lots in six Eastern Cape urban centres, South Africa, were sampled to determine tree species composition, density and annual carbon sequestration potential. The best case parking lot found during the study was used as a benchmark to display the difference between current tree density and above-ground carbon stocks relative to the potential optimum. The highest tree density was 66 trees ha−1, whereas the average density across all sampled parking lots was less than half that (27.2 ± 22.6 trees ha−1). The average annual carbon sequestration potential per parking lot was 1390 ± 2503 kg ha−1. Planting density was positively related to annual sequestration rates, whilst parking lot age and the mean annual rainfall of the town had no influence. Mean tree species richness per parking lot was 2.3 ± 1.8 species, with a positive relationship to parking lot size, but not to mean annual rainfall of the site. The majority of trees (62.5%) in parking lots were alien species, although newer parking lots had significantly greater proportions of indigenous species. There was no difference in mean annual carbon sequestration rate per tree between indigenous and alien trees species. Low tree densities and small parking lot areas constrained the potential for earning carbon credits from trees in parking lots. Nonetheless, planners and designers need to be more aware of the potential contribution of trees towards urban sustainability.
- Full Text:
- Date Issued: 2013
Electrochemical impedimetric immunosensor for the detection of measles-specific IgG antibodies after measles infections
- Mashazi, Philani N, Tetyana, Phumlani, Vilakazi, Sibulelo, Nyokong, Tebello
- Authors: Mashazi, Philani N , Tetyana, Phumlani , Vilakazi, Sibulelo , Nyokong, Tebello
- Language: English
- Type: Article
- Identifier: vital:7325 , http://hdl.handle.net/10962/d1020575
- Description: The detection of measles-specific primary antibodies (IgG) using electrochemical impedimetric immunosensors is reported. The optimum conditions for electrode saturation were reached after 40 min for 1 μg ml−1 antibody concentrations. Surface roughness using AFM increased with each immobilization or antigen-antibody reaction step clearly confirming the surface modification and recognition between antigen and antibody. The human serum (HS) and new-born calf serum (NCS) spiked with antigen-specific antibody were studied to mimic the real sample analysis. The HS and NCS sera containing antibodies due to measles exhibited correlation between the increasing antibody serum concentrations and the charge-transfer resistance (electrochemically measured). This work clearly showed the potential use of impedance as the preferred electrochemical method for detecting measles-antibodies in label-free manner. , Original publication is available at http://dx.doi.org/10.1016/j.bios.2013.04.028
- Full Text: false
- Authors: Mashazi, Philani N , Tetyana, Phumlani , Vilakazi, Sibulelo , Nyokong, Tebello
- Language: English
- Type: Article
- Identifier: vital:7325 , http://hdl.handle.net/10962/d1020575
- Description: The detection of measles-specific primary antibodies (IgG) using electrochemical impedimetric immunosensors is reported. The optimum conditions for electrode saturation were reached after 40 min for 1 μg ml−1 antibody concentrations. Surface roughness using AFM increased with each immobilization or antigen-antibody reaction step clearly confirming the surface modification and recognition between antigen and antibody. The human serum (HS) and new-born calf serum (NCS) spiked with antigen-specific antibody were studied to mimic the real sample analysis. The HS and NCS sera containing antibodies due to measles exhibited correlation between the increasing antibody serum concentrations and the charge-transfer resistance (electrochemically measured). This work clearly showed the potential use of impedance as the preferred electrochemical method for detecting measles-antibodies in label-free manner. , Original publication is available at http://dx.doi.org/10.1016/j.bios.2013.04.028
- Full Text: false
Electrochemical impedimetric immunosensor for the detection of measles-specific IgG antibodies after measles infections
- Mashazi, Philani N, Tetyana, Phumlani, Vilakazi, Sibulelo, Nyokong, Tebello
- Authors: Mashazi, Philani N , Tetyana, Phumlani , Vilakazi, Sibulelo , Nyokong, Tebello
- Date: 2013
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/241677 , vital:50960 , xlink:href="https://doi.org/10.1016/j.bios.2013.04.028"
- Description: The detection of measles-specific primary antibodies (IgG) using electrochemical impedimetric immunosensors is reported. The optimum conditions for electrode saturation were reached after 40 min for 1 μg ml−1 antibody concentrations. Surface roughness using AFM increased with each immobilization or antigen-antibody reaction step clearly confirming the surface modification and recognition between antigen and antibody. The human serum (HS) and new-born calf serum (NCS) spiked with antigen-specific antibody were studied to mimic the real sample analysis. The HS and NCS sera containing antibodies due to measles exhibited correlation between the increasing antibody serum concentrations and the charge-transfer resistance (electrochemically measured). This work clearly showed the potential use of impedance as the preferred electrochemical method for detecting measles-antibodies in label-free manner.
- Full Text:
- Date Issued: 2013
- Authors: Mashazi, Philani N , Tetyana, Phumlani , Vilakazi, Sibulelo , Nyokong, Tebello
- Date: 2013
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/241677 , vital:50960 , xlink:href="https://doi.org/10.1016/j.bios.2013.04.028"
- Description: The detection of measles-specific primary antibodies (IgG) using electrochemical impedimetric immunosensors is reported. The optimum conditions for electrode saturation were reached after 40 min for 1 μg ml−1 antibody concentrations. Surface roughness using AFM increased with each immobilization or antigen-antibody reaction step clearly confirming the surface modification and recognition between antigen and antibody. The human serum (HS) and new-born calf serum (NCS) spiked with antigen-specific antibody were studied to mimic the real sample analysis. The HS and NCS sera containing antibodies due to measles exhibited correlation between the increasing antibody serum concentrations and the charge-transfer resistance (electrochemically measured). This work clearly showed the potential use of impedance as the preferred electrochemical method for detecting measles-antibodies in label-free manner.
- Full Text:
- Date Issued: 2013
Design and evaluation of an electrochemical immunosensor for measles serodiagnosis using measles-specific Immunoglobulin G antibodies
- Mashazi, Philani N, Vilakazi, Sibulelo, Nyokong, Tebello
- Authors: Mashazi, Philani N , Vilakazi, Sibulelo , Nyokong, Tebello
- Date: 2013
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/241705 , vital:50962 , xlink:href="https://doi.org/10.1016/j.talanta.2013.06.036"
- Description: The design of electrochemical immunosensors for the detection of measles-specific antibodies is reported. The measles-antigen modified surface was used as an antibody capture surface. The detection of measles-specific IgG antibodies was accomplished using the voltammetric method and horse-radish peroxidase (HRP) labeled secondary antibody (anti-IgG) as a detecting antibody. The potential applications of the designed immunosensor were evaluated in buffer and serum solutions. The immunosensor exhibited good linearity at concentrations less than 100 ng mL−1 with R2=0.997 and the limit of detection of 6.60 ng mL−1 at 3σ. The potential application of the immunosensor was evaluated in the deliberately infected human and newborn calf serum samples with measles-IgG antibody mimicking real-life samples. The designed electrochemical immunosensor could differentiate between infected and un-infected serum samples as higher catalytic currents were obtained for infected serum samples.
- Full Text:
- Date Issued: 2013
- Authors: Mashazi, Philani N , Vilakazi, Sibulelo , Nyokong, Tebello
- Date: 2013
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/241705 , vital:50962 , xlink:href="https://doi.org/10.1016/j.talanta.2013.06.036"
- Description: The design of electrochemical immunosensors for the detection of measles-specific antibodies is reported. The measles-antigen modified surface was used as an antibody capture surface. The detection of measles-specific IgG antibodies was accomplished using the voltammetric method and horse-radish peroxidase (HRP) labeled secondary antibody (anti-IgG) as a detecting antibody. The potential applications of the designed immunosensor were evaluated in buffer and serum solutions. The immunosensor exhibited good linearity at concentrations less than 100 ng mL−1 with R2=0.997 and the limit of detection of 6.60 ng mL−1 at 3σ. The potential application of the immunosensor was evaluated in the deliberately infected human and newborn calf serum samples with measles-IgG antibody mimicking real-life samples. The designed electrochemical immunosensor could differentiate between infected and un-infected serum samples as higher catalytic currents were obtained for infected serum samples.
- Full Text:
- Date Issued: 2013