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Supramolecular derivatives of selected bioactive compounds : a physicochemical study

Includes abstract.

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Bibliographic Details
Main Author: Samsodien, Halima
Other Authors: Caira, Mino R
Format: Thesis
Language:English
Published: Department of Chemistry 2014
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access_status_str Open Access
author Samsodien, Halima
author2 Caira, Mino R
author_browse Caira, Mino R
Samsodien, Halima
author_facet Caira, Mino R
Samsodien, Halima
author_sort Samsodien, Halima
collection Thesis
description Includes abstract.
format Thesis
id oai:open.uct.ac.za:11427/6360
institution University of Cape Town (South Africa)
language eng
last_indexed 2026-06-10T12:33:19.547Z
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:11427/6360 Supramolecular derivatives of selected bioactive compounds : a physicochemical study Samsodien, Halima Caira, Mino R Bourne, Susan Chemistry Includes abstract. Includes bibliographical references (p. 270-271). The author’s objective was to prepare new solid phases of three bioactive compounds: the steroidal anticancer agent 2-methoxyestradiol [polymorphs and cyclodextrin (CD) inclusion complexes], its derivative 2-methoxyestradiol-bis-sulfamate (polymorphs), and the antiretroviral agent, nevirapine (co-crystals). The solubility and dissolution profiles of the three compounds and those of selected ‘supramolecularly-derived’ species were also assessed. Three distinct phases of 2-methoxyestradiol (2ME) were successfully isolated, the most stable form (a polymorph) by the recrystallisation method, an amorph by melt studies and a solvated form by recrystallisation. 2-methoxyestradiol-bis-sulfamate (2MES), in the form of a hemihydrate, remained unchanged when recrystallised from various solvents. Several CDs were used for possible 2-methoxyestradiol inclusion; these were α-, β -,γ-CD, and nine derivatised cyclodextrins. Co-precipitation and kneading techniques were employed in attempts to produce inclusion complexes. An inclusion complex of 2ME was isolated with each of the following: -CD, HPBCD, RAMEB, DIMEB and TRIMEB. Co-crystallisation of nevirapine was attempted using twelve potential co-formers with GRAS status. Two co-crystals, one with saccharin and one with rac-tartaric acid, were isolated by the co-precipitation method. Physicochemical characterisation techniques used to assess the thermal behaviour of the products included hot stage microscopy, differential scanning calorimetry and thermogravimetric analysis. UV spectrophotometry and elemental analysis were used for hostguest stoichiometric assay and purity determination respectively. X-ray powder diffraction and single crystal X-ray structure determination were used for structural analysis. 2014-08-13T14:29:52Z 2014-08-13T14:29:52Z 2010 Doctoral Thesis Doctoral PhD http://hdl.handle.net/11427/6360 eng application/pdf Department of Chemistry Faculty of Science University of Cape Town
spellingShingle Chemistry
Samsodien, Halima
Supramolecular derivatives of selected bioactive compounds : a physicochemical study
thesis_degree_str Doctoral
title Supramolecular derivatives of selected bioactive compounds : a physicochemical study
title_full Supramolecular derivatives of selected bioactive compounds : a physicochemical study
title_fullStr Supramolecular derivatives of selected bioactive compounds : a physicochemical study
title_full_unstemmed Supramolecular derivatives of selected bioactive compounds : a physicochemical study
title_short Supramolecular derivatives of selected bioactive compounds : a physicochemical study
title_sort supramolecular derivatives of selected bioactive compounds a physicochemical study
topic Chemistry
url http://hdl.handle.net/11427/6360
work_keys_str_mv AT samsodienhalima supramolecularderivativesofselectedbioactivecompoundsaphysicochemicalstudy