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Please use this identifier to cite or link to this item:
http://hdl.handle.net/10204/6396
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| Title: | Potential of improving the treatment of tuberculosis through nanomedicine |
| Authors: | Semete, B Kalombo, L Katata, L Chelule, P Booysen, L Lemmer, Y Naidoo, S Ramalapa, B Hayeshi, R Swai, HS |
| Keywords: | Drug release Nanomedicine PLGA nanoparticles Tuberculosis |
| Issue Date: | Mar-2012 |
| Publisher: | Taylor & Francis |
| Citation: | Semete, B, Kalombo, L, Katata, L, Chelule, P, Booysen, L, Lemmer, Y, Naidoo S, Ramalapa, B, Hayeshi, R and Swai, HS. 2012. Potential of improving the treatment of tuberculosis through nanomedicine. Molecular Crystals and Liquid Crystals, Vol 556(1), pp 317-330 |
| Series/Report no.: | Workflow;8759 |
| Abstract: | Current treatment of tuberculosis is inadequate due to lengthy treatment course and drug-related toxicity. To address these setbacks, we developed a nanotechnology drug delivery system that can be administered in a single dose that maintains an active level of drug for at least a week. Polymeric poly(lactic-co-glycolic acid) nanoparticles of 200–300 nm were synthesized, with a drug encapsulation efficiency of 50–65% for isoniazid and rifampicin. The particles were taken up in vitro and in vivo and a slow release profile was observed in mice over 5 days. This study illustrates the feasibility of a sustained release system for tuberculosis treatment. |
| Description: | Copyright: 2012 Taylor & Francis. This is the pre print version of the work. The definitive version is published in the journal of Molecular Crystals and Liquid Crystals, Vol 556(1), pp 317-330. |
| URI: | http://www.tandfonline.com/doi/abs/10.1080/15421406.2012.635531 http://hdl.handle.net/10204/6396 |
| ISSN: | 1542-1406 |
| Appears in Collections: | Nanotechnology General science, engineering & technology
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