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Design of novel copper(II) based anti-inflammatory drugs for the elevation associated with Rheumatoid Arthritis

Includes bibliographical references.

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Bibliographic Details
Main Author: Mhlambiso, Zizile
Other Authors: Jackson, Graham Ellis
Format: Thesis
Language:English
Published: Department of Chemistry 2014
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access_status_str Open Access
author Mhlambiso, Zizile
author2 Jackson, Graham Ellis
author_browse Jackson, Graham Ellis
Mhlambiso, Zizile
author_facet Jackson, Graham Ellis
Mhlambiso, Zizile
author_sort Mhlambiso, Zizile
collection Thesis
description Includes bibliographical references.
format Thesis
id oai:open.uct.ac.za:11427/9280
institution University of Cape Town (South Africa)
language eng
last_indexed 2026-06-10T12:34:36.552Z
license_str Not specified — see source repository
provenance_str_mv Harvested via OAI-PMH from UCTD — University of Cape Town Open Access Repository
publishDate 2014
publishDateRange 2014
publishDateSort 2014
publisher Department of Chemistry
publisherStr Department of Chemistry
record_format dspace
source_str UCTD — University of Cape Town Open Access Repository
spelling oai:open.uct.ac.za:11427/9280 Design of novel copper(II) based anti-inflammatory drugs for the elevation associated with Rheumatoid Arthritis Mhlambiso, Zizile Jackson, Graham Ellis Chemistry Includes bibliographical references. It has been shown that copper complexes are able to alleviate inflammation associated with Rheumatoid Arthritis (RA). Serum copper levels are elevated in RA and it has been postulated that endogenous copper might have a protective function in chronic inflammatory conditions. In designing Cu(I1) anti-inflammatory drugs, one needs to know the stability constants of the ligand together with Cu(I1) and the competitive metal ions, Zn(I1) and Ca(I1) in blood plasma. For this purpose glass electrode potentiometry, infrared (lR) spectroscopy, nuclear magnetic resonance (NMR) spectroscopy, UV/Visible spectroscopy as well as blood plasma modelling were used to explore the coordination chemistry of a newly designed ligand, PCUL (Bis-(3- aminoethy-2-aminomethylpyridine )-oxahexacyclo-dodecane). PCUL protonation and formation constants with Cu(I1) and Zn(I1) were investigated by potentiometric analysis at 2SoC and 0.ISmol/dm3 Na + (CI) The potentiometric analysis showed that CU(I1) formed far more stable complexes at physiological pH with PCUL than the in vivo competitor Zn(I1). In this study the IR spectroscopic analysis was used to determine the Cu(I1)-PCUL complexation sequence. The IR spectra show that the central amines are coordinated to the metal ion first. The small frequency shift between pH 4.02 to 6.91 proves that the pyridyl nitrogen atoms are also coordinated to CU(I1). 2014-11-05T17:41:58Z 2014-11-05T17:41:58Z 2009 Master Thesis Masters MSc http://hdl.handle.net/11427/9280 eng application/pdf Department of Chemistry Faculty of Science University of Cape Town
spellingShingle Chemistry
Mhlambiso, Zizile
Design of novel copper(II) based anti-inflammatory drugs for the elevation associated with Rheumatoid Arthritis
thesis_degree_str Master's
title Design of novel copper(II) based anti-inflammatory drugs for the elevation associated with Rheumatoid Arthritis
title_full Design of novel copper(II) based anti-inflammatory drugs for the elevation associated with Rheumatoid Arthritis
title_fullStr Design of novel copper(II) based anti-inflammatory drugs for the elevation associated with Rheumatoid Arthritis
title_full_unstemmed Design of novel copper(II) based anti-inflammatory drugs for the elevation associated with Rheumatoid Arthritis
title_short Design of novel copper(II) based anti-inflammatory drugs for the elevation associated with Rheumatoid Arthritis
title_sort design of novel copper ii based anti inflammatory drugs for the elevation associated with rheumatoid arthritis
topic Chemistry
url http://hdl.handle.net/11427/9280
work_keys_str_mv AT mhlambisozizile designofnovelcopperiibasedantiinflammatorydrugsfortheelevationassociatedwithrheumatoidarthritis