Mechanisms of the effectiveness of lipid nanoparticle formulations loaded with anti-tubercular drugs combinations toward overcoming drug bioavailability in tuberculosis
Author:
Affiliation:
1. Centre for Biodesign & Diagnostics (CBD), Translational Health Science & Technology Institute (THSTI), Faridabad, India;
2. Department of Pharmaceutics, National Institute of Pharmaceutical Education & Research (NIPER), Guwahati, India
Funder
Science and Engineering Research Board
Publisher
Informa UK Limited
Subject
Pharmaceutical Science
Link
https://www.tandfonline.com/doi/pdf/10.1080/1061186X.2019.1613409
Reference65 articles.
1. Encapsulation of Rifampicin in a solid lipid nanoparticulate system to limit its degradation and interaction with Isoniazid at acidic pH
2. World Health Organization. Global tuberculosis control: a short update to the 2009 report. 2009.
3. The Reason for an Increase in Decomposition of Rifampicin in the Presence of Isoniazid under Acid Conditions
4. Impaired bioavailability of rifampicin in presence of isoniazid from fixed dose combination (FDC) formulation
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