Tuberculosis chemotherapy: current drug delivery approaches

<p>Abstract</p> <p>Tuberculosis is a leading killer of young adults worldwide and the global scourge of multi-drug resistant tuberculosis is reaching epidemic proportions. It is endemic in most developing countries and resurgent in developed and developing countries with high rates...

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Main Authors: Danckwerts Michael, Pillay Viness, du Toit Lisa
Format: Article
Language:English
Published: BMC 2006-09-01
Series:Respiratory Research
Online Access:http://respiratory-research.com/content/7/1/118
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spelling doaj-cada13354ee141128f8f2878158db3932020-11-24T22:24:00ZengBMCRespiratory Research1465-99212006-09-017111810.1186/1465-9921-7-118Tuberculosis chemotherapy: current drug delivery approachesDanckwerts MichaelPillay Vinessdu Toit Lisa<p>Abstract</p> <p>Tuberculosis is a leading killer of young adults worldwide and the global scourge of multi-drug resistant tuberculosis is reaching epidemic proportions. It is endemic in most developing countries and resurgent in developed and developing countries with high rates of human immunodeficiency virus infection. This article reviews the current situation in terms of drug delivery approaches for tuberculosis chemotherapy. A number of novel implant-, microparticulate-, and various other carrier-based drug delivery systems incorporating the principal anti-tuberculosis agents have been fabricated that either target the site of tuberculosis infection or reduce the dosing frequency with the aim of improving patient outcomes. These developments in drug delivery represent attractive options with significant merit, however, there is a requisite to manufacture an oral system, which directly addresses issues of unacceptable rifampicin bioavailability in fixed-dose combinations. This is fostered by the need to deliver medications to patients more efficiently and with fewer side effects, especially in developing countries. The fabrication of a polymeric once-daily oral multiparticulate fixed-dose combination of the principal anti-tuberculosis drugs, which attains segregated delivery of rifampicin and isoniazid for improved rifampicin bioavailability, could be a step in the right direction in addressing issues of treatment failure due to patient non-compliance.</p> http://respiratory-research.com/content/7/1/118
collection DOAJ
language English
format Article
sources DOAJ
author Danckwerts Michael
Pillay Viness
du Toit Lisa
spellingShingle Danckwerts Michael
Pillay Viness
du Toit Lisa
Tuberculosis chemotherapy: current drug delivery approaches
Respiratory Research
author_facet Danckwerts Michael
Pillay Viness
du Toit Lisa
author_sort Danckwerts Michael
title Tuberculosis chemotherapy: current drug delivery approaches
title_short Tuberculosis chemotherapy: current drug delivery approaches
title_full Tuberculosis chemotherapy: current drug delivery approaches
title_fullStr Tuberculosis chemotherapy: current drug delivery approaches
title_full_unstemmed Tuberculosis chemotherapy: current drug delivery approaches
title_sort tuberculosis chemotherapy: current drug delivery approaches
publisher BMC
series Respiratory Research
issn 1465-9921
publishDate 2006-09-01
description <p>Abstract</p> <p>Tuberculosis is a leading killer of young adults worldwide and the global scourge of multi-drug resistant tuberculosis is reaching epidemic proportions. It is endemic in most developing countries and resurgent in developed and developing countries with high rates of human immunodeficiency virus infection. This article reviews the current situation in terms of drug delivery approaches for tuberculosis chemotherapy. A number of novel implant-, microparticulate-, and various other carrier-based drug delivery systems incorporating the principal anti-tuberculosis agents have been fabricated that either target the site of tuberculosis infection or reduce the dosing frequency with the aim of improving patient outcomes. These developments in drug delivery represent attractive options with significant merit, however, there is a requisite to manufacture an oral system, which directly addresses issues of unacceptable rifampicin bioavailability in fixed-dose combinations. This is fostered by the need to deliver medications to patients more efficiently and with fewer side effects, especially in developing countries. The fabrication of a polymeric once-daily oral multiparticulate fixed-dose combination of the principal anti-tuberculosis drugs, which attains segregated delivery of rifampicin and isoniazid for improved rifampicin bioavailability, could be a step in the right direction in addressing issues of treatment failure due to patient non-compliance.</p>
url http://respiratory-research.com/content/7/1/118
work_keys_str_mv AT danckwertsmichael tuberculosischemotherapycurrentdrugdeliveryapproaches
AT pillayviness tuberculosischemotherapycurrentdrugdeliveryapproaches
AT dutoitlisa tuberculosischemotherapycurrentdrugdeliveryapproaches
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