Investigating the effect of peptide-functionalized gold nanoparticles on colon cancer cells
- Authors: Ramagoma, Rolivhuwa Bishop
- Date: 2023-12
- Subjects: Colon (Anatomy) -- Cancer -- Research , Colon (Anatomy) -- Cancer -- Treatment , Nanoparticles
- Language: English
- Type: Master's theses , text
- Identifier: http://hdl.handle.net/10948/62564 , vital:72824
- Description: Colon cancer like any other cancer is a condition in which cells grow uncontrollably and may even spread to other regions of the body through metastasis. Colon cancer was ranked the second leading cause of cancer related deaths worldwide in 2018. Research to advance treatment of cancer keeps advancing daily, However, a big challenge is drug-induced side effects due to toxicity against normal body cells. Therefore, the development of controlled release technologies in conjunction with targeted drug delivery may provide a more efficient and less dangerous approach to overcome the limits of traditional chemotherapy. Including the creation of nanoscale delivery vehicles capable of directing the release of chemotherapeutic drugs into cancer cells only. This study aims to investigate p14 peptide that would specifically target colorectal cancer cells and not normal body cells to develop a targeted drug delivery system using gold nanoparticles. This study serves as a pilot study of the primary aim. To achieve this, the effect of the peptide p14 and peptide functionalized gold nanoparticles (p14-AuNP) on colon cancer cells (HT-29) and normal epithelial cells (KMST-6) was determined. Firstly, gold nanoparticles were chemically synthesised and then functionalized with p14 peptide through Polyethylene glycol. Then assessment of their effect through in vitro cytotoxicity assay (MTT) and gene expression analysis (RT-qPCR) was conducted. Nanoparticles’ synthesis and functionalization was performed and confirmed: In vitro cytotoxicity through MTT assay was successfully conducted and p14-AuNP showed toxicity against colon cancer cells and lesser toxicity towards normal cells as compared to 5-Flourouracil (commercially approved drug for colon cancer treatment). Gene expression analysis revealed that apoptosis was induced in both cell lines by p14-AuNP either through upregulation of caspase 3, 7 and/or BCL2. A cell survival gene, AKT1, also had significant effect on this. CDC42 was downregulated which indicates that cell proliferation was inhibited. , Thesis (MSc) -- Faculty of Science, School of Biomolecular & Chemical Sciences, 2023
- Full Text:
- Date Issued: 2023-12
Synthesis and characterization of molybdenum dichalcogenides nanoparticles via solution-processed technique for photovoltaic applications
- Authors: Shelter, Chikukwa Evernice
- Date: 2021-02
- Subjects: Nanoparticles , Colloids
- Language: English
- Type: Master's theses , text
- Identifier: http://hdl.handle.net/10353/20653 , vital:46417
- Description: Energy generated from non-renewable energy sources has a drawback of prompted outflow of ozone harming substances. These drawbacks of the non-renewable energy have quickened innovative work of renewable power sources, since they have an advantage of the provision of a better, preserved, decent environment that is free from natural contamination and commotion. Photovoltaic devices are prevalent in improving the green energy utilization and defeating the natural concerns yielded from the current most overwhelming energy sources. Herein, the synthesis, characterization, and application of Molybdenum chalcogenide nanoparticles (NP) as alternative sources in the absorber layer of quantum dot solar sensitized cells (QDSSCs) is discussed. The MoS2 NPs were synthesized from the aliphatic and aromatic dithiocarbamate (DTC) ligands and complexes as precursors. The successful synthesis of the DTC ligands and MoDTC complexes was confirmed through characterization with a variety of techniques including 1H and 13C-NMR, Raman Spectroscopy, Fourier Transform Infrared Spectroscopy (FTIR), Ultraviolet-visible spectroscopy (UV-VIS), Thermogravimetric analysis (TGA) and Derivative thermogravimetric (DTG) analysis. The synthesized MoDTC complexes (precursors) were further used in the synthesis of MoS2 nanoparticles. A bottom -up colloidal approach was employed for the synthesis of the MoX2 NPs. The successful synthesis of the NP was confirmed as the results from the diffractive peaks obtained from XRD which were positive and agreed in comparison with the standard. The diffractive peaks were shown in the planes (100), (002), (100) and (105) for MoS2 nanoparticles; (002), (100), (103) and (110) for MoSe2 and (0002), (0004), (103) as well as (0006) for the MoTe2 nanoparticles. The MoSe2 nanoparticles showed the least size of the nanoparticles followed by MoTe2 and lastly MoS2. These results agreed with the results obtained using SEM analysis. For the optical properties of the nanoparticles, UV-VIS and PL were used, the shift of the peaks from the red shift (600 nm) to the blue shift 270-5 nm and 287-9 nm (UV-VIS) confirmed that the nanoparticles were quantum confined. The application of the MoX2 NPs in QDSSCs was done with MoSe2 showing the greatest PCE of 7.86 percent followed by MoTe2 6.93 percent and lastly MoS2 with a PCE of 6.05 percent and 5.47 percent. , Thesis (MSc) (Chemistry) -- University of Fort Hare, 2021
- Full Text:
- Date Issued: 2021-02
Copper dithiocarbamate complexes and copper sulfide nanoparticles : Synthesis, characterization and antifungal studies
- Authors: Botha, Nandipha Loveness https://orcid.org/0000-0001-8353-3512
- Date: 2015-01
- Subjects: Copper sulfide , Complex compounds , Nanoparticles
- Language: English
- Type: Master's theses , text
- Identifier: http://hdl.handle.net/10353/24283 , vital:62598
- Description: Six dithiocarbamate ligands were synthesized from anisidine, aniline, ethyl aniline, butyl amine, morpholine and piperidine and used to synthesize homoleptic copper(II) dithiocarbamate complexes. The ligands and their corresponding complexes were characterized by conductivity measurement, FTIR and UV-Vis spectroscopy. The ligands were further characterized using NMR spectroscopy. The electronic spectra of the complexes showed that the coordination geometries around the Cu2+ ion is four coordinate square planar. FTIR spectroscopic studies indicated that the dithiocarbamate ligands are bidentately coordinated to the copper ion through the sulfur atoms with the C-S stretching frequencies changing from two peaks in the ligands to single sharp peaks in the corresponding metal complexes. The complexes were used as single source precursors to synthesize copper sulfide nanoparticles. All the six complexes were thermolysed at 180 oC to prepare copper sulfide nanoparticles and three of them were further thermolysed at 120 oC to study the effects of temperature on size and shape of the nanoparticles. All the nanoparticles were characterized with UV-Vis, PL, XRD, TEM, SEM and EDX. The optical properties of the as-prepared CuS nanoparticles showed that they are quantum confined with absorption band edges that are blue shifted compared to bulk CuS and all the as-prepared CuS nanoparticles showed narrow emission curves. The XRD diffraction patterns were indexed to the hexagonal covellite CuS crystalline phase with estimated particle sizes of 15.8-23.24 nm. These sizes are significantly different from the values, 3.02-98.94 nm obtained from TEM studies. The TEM images also showed nanoparticles with varied shapes with some agglomerations. SEM micrographs showed that the morphologies of the nanoparticles are mostly smooth surfaces and EDX spectra analyses confirmed the formation of the nanoparticles. Thermolysis of three of the complexes at 120 oC confirmed that temperature do affect the optical and structural properties of the CuS nanoparticles. Only three complexes soluble in DMSO were screened for their antimicrobial activity. Three complexes C1, C4 and C5 were screened against four fungi organisms, namely: Candida rugosa, Candida neoformans, Candida albicans and Trychophyton mucoides. All the compounds were promising as shown by the minimum inhibitory concentrations determined. C5 was the most active compound against all the organisms. They were also screened against four bacteria organisms and they were all active but not as they were against fungi organisms. , Thesis (MSc) -- Faculty of Science and Agriculture, 2015
- Full Text:
- Date Issued: 2015-01