dc.contributor.author |
Kalombo, Lonji
|
|
dc.contributor.author |
Lemmer, Yolandy
|
|
dc.contributor.author |
Semete-Makokotlela, Boitumelo
|
|
dc.contributor.author |
Ramalapa, Bathabile
|
|
dc.contributor.author |
Nkuna, Patric
|
|
dc.contributor.author |
Booysen, Laetitia L.L.I.J.
|
|
dc.contributor.author |
Naidoo, Saloshnee
|
|
dc.contributor.author |
Hayeshi, Rose
|
|
dc.contributor.author |
Verschoor, J.A. (Jan Adrianus), 1953-
|
|
dc.contributor.author |
Swai, Hulda S.
|
|
dc.date.accessioned |
2020-09-09T15:15:53Z |
|
dc.date.available |
2020-09-09T15:15:53Z |
|
dc.date.issued |
2019-08 |
|
dc.description.abstract |
Aiming to improve the treatment outcomes of current daily tuberculosis (TB) chemotherapy
over several months, we investigated whether nanoencapsulation of existing drugs would allow
decreasing the treatment frequency to weekly, thereby ultimately improving patient compliance.
Nanoencapsulation of three first-line anti-TB drugs was achieved by a unique, scalable spray-drying
technology forming free-flowing powders in the nanometer range with encapsulation efficiencies of
82, 75, and 62% respectively for rifampicin, pyrazinamide, and isoniazid. In a pre-clinical study on TB
infected mice, we demonstrate that the encapsulated drugs, administered once weekly for nine weeks,
showed comparable efficacy to daily treatment with free drugs over the same experimental period.
Both treatment approaches had equivalent outcomes for resolution of inflammation associated with
the infection of lungs and spleens. These results demonstrate how scalable technology could be used
to manufacture nanoencapsulated drugs. The formulations may be used to reduce the oral dose
frequency from daily to once weekly in order to treat uncomplicated TB. |
en_ZA |
dc.description.department |
Biochemistry |
en_ZA |
dc.description.department |
Genetics |
en_ZA |
dc.description.department |
Microbiology and Plant Pathology |
en_ZA |
dc.description.librarian |
pm2020 |
en_ZA |
dc.description.sponsorship |
The South African Department of Science and Technology and the South African Council for Scientific and Industrial Research (CSIR). |
en_ZA |
dc.description.uri |
http://www.mdpi.com/journal/nanomaterials |
en_ZA |
dc.identifier.citation |
Kalombo, L., Lemmer, Y., Semete-Makokotlela, B. et al. 2019,'Spray-dried, nanoencapsulated, multi-drug anti-tuberculosis therapy aimed at once weekly administration for the duration of treatment', Nanomaterials, vol. 9, no. 8, art. 1167, pp. 1-14. |
en_ZA |
dc.identifier.issn |
2079-4991 (online) |
|
dc.identifier.other |
10.3390/nano9081167 |
|
dc.identifier.uri |
http://hdl.handle.net/2263/76130 |
|
dc.language.iso |
en |
en_ZA |
dc.publisher |
MDPI Open Access Journals |
en_ZA |
dc.rights |
© 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access
article distributed under the terms and conditions of the Creative Commons Attribution
(CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
en_ZA |
dc.subject |
Nanomedicine |
en_ZA |
dc.subject |
Spray-drying technology |
en_ZA |
dc.subject |
Efficacy |
en_ZA |
dc.subject |
Dose frequency |
en_ZA |
dc.subject |
Tuberculosis (TB) |
en_ZA |
dc.subject |
Chemotherapy |
en_ZA |
dc.title |
Spray-dried, nanoencapsulated, multi-drug anti-tuberculosis therapy aimed at once weekly administration for the duration of treatment |
en_ZA |
dc.type |
Article |
en_ZA |