Please use this identifier to cite or link to this item: https://hdl.handle.net/10321/1749
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dc.contributor.advisorBisetty, Krishna-
dc.contributor.advisorSingh, Parvesh-
dc.contributor.authorMpanza, Thabani Eugeneen_US
dc.date.accessioned2016-11-18T07:53:54Z-
dc.date.available2016-11-18T07:53:54Z-
dc.date.issued2016-
dc.identifier.other663052-
dc.identifier.urihttp://hdl.handle.net/10321/1749-
dc.descriptionSubmitted in fulfillment of the requirements for the Degree of Master of Applied Science in Chemistry, Durban University of Technology, Durban, South Africa, 2016.en_US
dc.description.abstractThis study involves the development of a sensitive electrochemical biosensor for the determination of capsaicin extracted from chilli pepper fruit, based on a novel signal amplification strategy. The study therefore, seeks to provide a sensitive electro-analytical technique to be used for the determination of capsaicin in food and spicy products. Electrochemical measurements using cyclic voltammetry (CV) and differential pulse voltammetry (DPV) modes were utilized in order to understand the redox mechanism of capsaicin and to test the performance of the developed biosensor supported with computational techniques. In this work two different enzymes, Phenylalanine ammonia lyase (PAL) and Glucose oxidase (GOx) were used for electrode modifications respectively. For this purpose three different types of working electrodes namely: glassy carbon electrode (GCE), platinum electrode (Pt-E) and gold electrode (Au-E) were used and their performances were compared. For the first time, the three electrodes were modified with PAL and GOx enzymes on multiwalled carbon nanotubes used in this study and characterized by attenuated total reflectance infrared spectroscopy, transmittance electron microscopy and thermo-gravimetric analysis supported by computational methods. The comparison of the results obtained from the bare and modified platinum electrodes revealed the sensitivity of the developed biosensor with modified electrode having high sensitivity of 0.1863 µg.L-1 and electron transfer rate constant (ks) of 3.02 s-1. To understand the redox mechanism completely, adsorption and ligand-enzyme docking simulations were carried out. Docking studies revealed that capsaicin formed hydrogen bonds with Glutamates (GLU355, GLU541, GLU586), Arginine (ARG) and other amino acids of the hydrophobic channel of the binding sites which facilitated the redox reaction for detection of capsaicin. These results confirm that the PAL enzyme facilitated the electron transfer from the capsaicin ligand, hence improving the biosensing response. Our results suggest potential applications of this methodology for the determination of capsaicin in the food industry.en_US
dc.format.extent160 pen_US
dc.language.isoenen_US
dc.subject.lcshCarbon nanotubesen_US
dc.subject.lcshElectrochemical sensorsen_US
dc.subject.lcshBiosensorsen_US
dc.subject.lcshCapsicum annuumen_US
dc.subject.lcshPeppersen_US
dc.titleDetermination of capsaicin using carbon nanotube based electrochemical biosensorsen_US
dc.typeThesisen_US
dc.description.levelMen_US
dc.identifier.doihttps://doi.org/10.51415/10321/1749-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextWith Fulltext-
item.grantfulltextopen-
item.openairetypeThesis-
item.languageiso639-1en-
Appears in Collections:Theses and dissertations (Applied Sciences)
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