https://vital.seals.ac.za/vital/access/manager/Index ${session.getAttribute("locale")} 5 Formulation and process optimisation of ethionamide 250 MGtablets using quality by design principles https://vital.seals.ac.za/vital/access/manager/Repository/vital:20497 Wed 12 May 2021 23:45:03 SAST ]]> The medicinal chemistry of Cyclo (D-PHE-4I-PRO) and Cyclo (L-PHE-4I-PRO) https://vital.seals.ac.za/vital/access/manager/Repository/vital:10152 Wed 12 May 2021 22:25:34 SAST ]]> The medicinal chemistry of cyclo(Phe-4CI-Pro) and Cyclo(D-Phe-4CI-Pro) https://vital.seals.ac.za/vital/access/manager/Repository/vital:10157 Wed 12 May 2021 19:28:44 SAST ]]> Application of a quality by design approach to optimise an existing product https://vital.seals.ac.za/vital/access/manager/Repository/vital:32341 Wed 12 May 2021 19:18:31 SAST ]]> Solid-phase extraction based sample preparation for the determination of drug and organic pollutant residue https://vital.seals.ac.za/vital/access/manager/Repository/vital:4406 0.9990) was attained for most analytes. The limits of detection and quantification ranged from 0.03 - 0.84 μg/ml and 0.81 - 1.89 μg/ml respectively for analytes in biological samples. LODs and LOQs for analytes in food and environmental samples ranged from 0.02 to 0.39 and 0.25 to 1.30 ng/g respectively.]]> Wed 12 May 2021 17:31:55 SAST ]]> Isolation, structural characterisation and evaluation of cytotoxic activity of natural products from selected South African marine red algae https://vital.seals.ac.za/vital/access/manager/Repository/vital:3862 Wed 12 May 2021 16:47:29 SAST ]]> The medicinal chemistry of cyclo(D-Phe-2Cl-Pro) and cyclo(Phe-4F-Pro) https://vital.seals.ac.za/vital/access/manager/Repository/vital:21223 Thu 13 May 2021 13:55:44 SAST ]]> An investigation into the introduction of process analytical technology, using near infrared analysis, to selected pharmaceutical processes https://vital.seals.ac.za/vital/access/manager/Repository/vital:10153 Thu 13 May 2021 07:09:28 SAST ]]> The medicinal chemistry of the isomers of the cyclic dipeptide: cyclo(Trp-Pro) https://vital.seals.ac.za/vital/access/manager/Repository/vital:11023 Thu 13 May 2021 07:07:36 SAST ]]> The medicinal chemistry of cyclo (Ser-Ser) and cyclo (Ser-Tyr) https://vital.seals.ac.za/vital/access/manager/Repository/vital:10155 Thu 13 May 2021 05:05:04 SAST ]]> Optimisation of a legacy product with a history of tablet friability failures utilising quality by design https://vital.seals.ac.za/vital/access/manager/Repository/vital:33938 Thu 13 May 2021 01:39:13 SAST ]]> Synthesis of chromium carbene scaffolds for use in medicinal chemistry https://vital.seals.ac.za/vital/access/manager/Repository/vital:4456 Thu 13 May 2021 00:57:32 SAST ]]> Formulation of methyldopa 250 mg tablets by direct compression using a quality by design approach https://vital.seals.ac.za/vital/access/manager/Repository/vital:59929 Thu 08 Dec 2022 11:38:02 SAST ]]> Synthesis of L-menthyl glyoxylate, an important intermediate in the manufacture of ARVS, using flow chemistry technology https://vital.seals.ac.za/vital/access/manager/Repository/vital:27018 Fri 15 Mar 2024 12:32:30 SAST ]]> New synergic biomaterials for anti-cancer therapy https://vital.seals.ac.za/vital/access/manager/Repository/vital:37087 1, antagonism, respectively. Most combination treatments showed to have an antagonistic effect except for cisplatin:BC-7 (1:3, 1:1, 2:1, 3:1) and cisplatin:A. afra (1:3, 1:2, 1:1, 3:1) combinations that showed synergism. The 1:2 ratio of cisplatin:BC-7 and the 2:1 ratio of cisplatin:A. afra were additive. CI values were also calculated at inhibition of 10, 25 and 75% of HeLa cell growth, for each combination mixture. Antagonistic effects were frequently observed at lower effect levels such as at 10 and 25% inhibition of growth. However, this was not seen for the cisplatin:BC-7 combinations as all the ratios indicated synergism. Some of these ratios, such as the 1:3 and 1:2, even led to a greater degree of synergism being obtained, with noticeable antagonistic effects seen at 50 and 75% inhibition of growth. The current finding is that BC-7 and A. afra could lower the dose of cisplatin in combination to achieve a similar anti-cancer efficacy compared to the higher cisplatin dose when used alone. The lower dosage in combination could result in reduced drug resistance as well as limit the toxicity on normal cells associated with cisplatin treatment. In conclusion, this study shows, for the first time, that A. nemorosa has the potential to induce apoptosis and also has some anti- and pro-inflammatory activity in HeLa cancer cells. This study also enhanced the knowledge of the mechanism of apoptosis induction of BC-7, in a more detailed manner, as well as investigated its inflammatory effects for the first time. Results obtained for A. afra correlated nicely to previously reported studies and confirmed that the methods used in this study, although different, leads to the same conclusions. Combination treatments also indicated, for the first time, that BC-7 and A. afra have the ability to function in a synergic manner with cisplatin and proves that, although extensive research may have been done on a plant or compound, more can be discovered. This new information can lead to identification of new compounds in the plants and the integration of signalling pathways that can be targeted for treatment of cancer.]]> Fri 15 Mar 2024 11:56:53 SAST ]]>