This thesis was focused on monitoring the viability of eukaryotic and prokaryotic cells after exposure of termites-isolated chemicals. Recently, evidence of antibacterial and antifungal properties of these defense substances has grown, and they can find a wide range of uses not only in the pharmaceutical industry. In this work, three defensive substances from termites were studied: nerolidol, nitropentadecene and methylanthranilate. Their antibacterial effects, minimal inhibitory concentrations and minimal bactericidal concentrations against Escherichia coli STBL3 strain were monitored. Further, their cytotoxic effects on eukaryotic non-tumor (HEK293FT) and tumor cells (MCF7) as well as their effect on plasmid DNA were studied. Antibiotic ampicillin and cytostatic cisplatin were used as control substances for antibacterial and cytotoxic effects, respectively. In the case of the action of nerolidol, nitropentadecene and methylanthranilate on the STBL3 strain, antibacterial activity was not demonstrated. Cytotoxic effects were observed nerolidol and nitropentadecene. None of the examined substances modified the plasmid DNA.

Thesis (MSc. (Microbiology)) -- University of Limpopo, 2017 / This study was aimed at isolating and evaluating the antibacterial, antioxidant and cytotoxic effects of active compounds from selected medicinal plant species. The biological activities and cytotoxic effects of Commelina africana, Dombeya rotundifolia, Elephantorrhiza elephantina and Schkuhria pinnata were investigated based on their traditional uses. The plants were extracted with different solvents of varying polarities. Methanol was the best extractant with the highest yield. The presence of different phytoconstituents was screened using standard methods; this revealed the presence of terpenoids, flavonoids, tannins, and saponins. Meanwhile, the phytochemicals were screened on TLC, where different colours observed indicated the presence of different compounds. The total phenolic, tannin and flavonoid content were estimated using spectrophotometric methods. D. rotundifolia had the highest amounts of phenol, tannin and flavonoid content, while S. pinnata had the least. The antibacterial and antioxidant screening employed both qualitative and quantitative assays. Although not separated, this study demonstrated the antioxidant potential of D. rotundifolia extracts developed in BEA and CEF. D. rotundifolia also demonstrated the highest free radical scavenging and reducing power antioxidant potential. These activities could be attributed to the high phenolic, tannin and flavonoid content observed. All the selected plants had antibacterial potential against E. coli and P. aeruginosa. Only S. pinnata extracts were active against E. faecalis and S. aureus. The MIC values of the plants and ampicillin ranged from 0.02 to 2.50 mg/mL and 0.02 to 0.08 mg/mL, respectively. The plants were combined to determine any interaction effects in exhibiting antibacterial activity. Among all the possible combinations, combinations with S. pinnata had improved antibacterial activity. The effects of D. rotundifolia and S. pinnata extracts on the inhibition of the production of reactive oxygen species on LPS-induced RAW 264.7 macrophages was determined using the DCFHD-A assay. Both plants demonstrated anti-inflammatory potential by inhibiting the production of ROS in a dose-dependent manner. Cell viability assays revealed that S. pinnata had cytotoxic effects on African green monkey kidney (Vero) cells with the lowest LC50 (25 µg/mL). Bioassay guided fractionation and nuclear magnetic resonance spectroscopy of dichloromethane extracts of S. pinnata on column chromatography afforded isolation and characterisation of three sesquiterpene lactones. These were identified as 6-(2, 3- xxvi dihydroangeloylory)-6α-hydroxyinuviscolide, heliangolide and eucannabiolide. All three compounds had antibacterial, anti-inflammatory and cytotoxic effects. The compounds may serve as leads for synthesis of less toxic therapeutic antibacterial and anti-inflammatory drugs in the pharmaceutical industry. / National Research Foundation (NRF)

This study aims at the development of materials for biodegradable fiducial markers for X-ray based medical imaging and their anchorage in soft tissue. Towards this goal a degradable polymer matrix of poly(L-lactide-co-ε-caprolactone) (P[LAcoCL]) was combined with barium sulfate (BaSO₄) and hydroxyapatite (HAp) as radio-opaque fillers. Low pressure plasma treatment was applied to the composite materials to improve cell adhesion and subsequent tissue integration. In particular, the effects of oxygen and ammonia plasmas were evaluated and compared using X-ray photoelectron spectroscopy, atomic force microscopy and dynamic water contact angle measurements as well as in vitro studies using the murine fibroblast cell line L929. To exclude the cytotoxic effects of degradation products of P[LAcoCL] and released BaSO₄ or HAp cytotoxicity assays with the degradation products of the composite materials were conducted. The results obtained by this broad range of analytical techniques suggest the application of composites of P[LAcoCL] with BaSO₄ and HAp as promising material systems for innovative fiducial markers for soft tissue in X-ray based medical imaging.