dc.contributor.author |
Lemmer, Yolandy
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dc.contributor.author |
Semete, B
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dc.contributor.author |
Kalombo, Lonji
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dc.contributor.author |
Ramalapa, B
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dc.contributor.author |
Jones, AT
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dc.contributor.author |
Swai, HS
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dc.contributor.author |
Verschoor, JA
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dc.date.accessioned |
2010-09-02T08:21:27Z |
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dc.date.available |
2010-09-02T08:21:27Z |
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dc.date.issued |
2010-09-01 |
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dc.identifier.citation |
Lemmer, Y, Semete, B, Kalombo, L et al. 2010. Lipid containing nanodrug delivery system for the treatment of Tuberculosis. CSIR 3rd Biennial Conference 2010. Science Real and Relevant. CSIR International Convention Centre, Pretoria, South Africa, 30 August – 01 September 2010, pp 1 |
en |
dc.identifier.uri |
http://hdl.handle.net/10204/4286
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|
dc.description |
CSIR 3rd Biennial Conference 2010. Science Real and Relevant. CSIR International Convention Centre, Pretoria, South Africa, 30 August – 01 September 2010 |
en |
dc.description.abstract |
Challenges in treatment of Tuberculosis (TB) include non-specific localisation of the drugs which results in too low concentrations of the drugs reaching the target site of infection, thus leading to reduced effectiveness. To improve the current inadequate therapeutic management of TB, a polymeric nanodrug delivery system, for anti-TB drugs was developed by a double emulsion evaporation technique. The system could enable entry, targeting, sustained release for longer periods and uptake of the antibiotics in the cells, hence reducing the dose frequency and simultaneously improve patient compliance. The cell wall envelope of Mycobacterium tuberculosis (M.tb) contains unique high molecular weight lipids. Of these, the most abundant are mycolic acids (MA), an extended family of long 2-alkyl 3-hydroxyl fatty acids, typically 70-90 carbon atoms in length, with peculiar physical and biological properties. MA have further been shown to have a similarity in the structural properties with cholesterol1. MA were explored as the targeting agent to infected macrophages containing abundance of cholesterol. |
en |
dc.language.iso |
en |
en |
dc.publisher |
CSIR |
en |
dc.subject |
Lipids |
en |
dc.subject |
Nanodrugs |
en |
dc.subject |
Tuberculosis |
en |
dc.subject |
CSIR Conference 2010 |
en |
dc.subject |
Mycobacterium tuberculosis |
en |
dc.title |
Lipid containing nanodrug delivery system for the treatment of Tuberculosis |
en |
dc.type |
Conference Presentation |
en |
dc.identifier.apacitation |
Lemmer, Y., Semete, B., Kalombo, L., Ramalapa, B., Jones, A., Swai, H., & Verschoor, J. (2010). Lipid containing nanodrug delivery system for the treatment of Tuberculosis. CSIR. http://hdl.handle.net/10204/4286 |
en_ZA |
dc.identifier.chicagocitation |
Lemmer, Yolandy, B Semete, Lonji Kalombo, B Ramalapa, AT Jones, HS Swai, and JA Verschoor. "Lipid containing nanodrug delivery system for the treatment of Tuberculosis." (2010): http://hdl.handle.net/10204/4286 |
en_ZA |
dc.identifier.vancouvercitation |
Lemmer Y, Semete B, Kalombo L, Ramalapa B, Jones A, Swai H, et al, Lipid containing nanodrug delivery system for the treatment of Tuberculosis; CSIR; 2010. http://hdl.handle.net/10204/4286 . |
en_ZA |
dc.identifier.ris |
TY - Conference Presentation
AU - Lemmer, Yolandy
AU - Semete, B
AU - Kalombo, Lonji
AU - Ramalapa, B
AU - Jones, AT
AU - Swai, HS
AU - Verschoor, JA
AB - Challenges in treatment of Tuberculosis (TB) include non-specific localisation of the drugs which results in too low concentrations of the drugs reaching the target site of infection, thus leading to reduced effectiveness. To improve the current inadequate therapeutic management of TB, a polymeric nanodrug delivery system, for anti-TB drugs was developed by a double emulsion evaporation technique. The system could enable entry, targeting, sustained release for longer periods and uptake of the antibiotics in the cells, hence reducing the dose frequency and simultaneously improve patient compliance. The cell wall envelope of Mycobacterium tuberculosis (M.tb) contains unique high molecular weight lipids. Of these, the most abundant are mycolic acids (MA), an extended family of long 2-alkyl 3-hydroxyl fatty acids, typically 70-90 carbon atoms in length, with peculiar physical and biological properties. MA have further been shown to have a similarity in the structural properties with cholesterol1. MA were explored as the targeting agent to infected macrophages containing abundance of cholesterol.
DA - 2010-09-01
DB - ResearchSpace
DP - CSIR
KW - Lipids
KW - Nanodrugs
KW - Tuberculosis
KW - CSIR Conference 2010
KW - Mycobacterium tuberculosis
LK - https://researchspace.csir.co.za
PY - 2010
T1 - Lipid containing nanodrug delivery system for the treatment of Tuberculosis
TI - Lipid containing nanodrug delivery system for the treatment of Tuberculosis
UR - http://hdl.handle.net/10204/4286
ER -
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en_ZA |