Affiliations 

  • 1 Discipline of Pharmacy, Graduate School of Health, University of Technology Sydney, Ultimo NSW 2007, Australia; Priority Research Centre for Healthy Lungs, Hunter Medical Research Institute (HMRI) & School of Biomedical Sciences and Pharmacy, The University of Newcastle, Callaghan, NSW 2308, Australia. Electronic address: Kamal.Dua@uts.edu.au
  • 2 Department of Pharmacy, Birla Institute of Technology and Science (BITS), Pilani, 333031, India
  • 3 Priority Research Centre for Healthy Lungs, Hunter Medical Research Institute (HMRI) & School of Biomedical Sciences and Pharmacy, The University of Newcastle, Callaghan, NSW 2308, Australia
  • 4 Department of Pharmacy, Birla Institute of Technology and Science (BITS), Pilani, 333031, India. Electronic address: gautam.singhvi@pilani.bits-pilani.ac.in
  • 5 School of Health Sciences, College of Health and Medicine, University of Tasmania, Launceston, Australia
  • 6 Department of Life Sciences, School of Pharmacy, International Medical University, Bukit Jalil, Kuala Lumpur 57000, Malaysia
  • 7 School of Pharmaceutical Sciences, Lovely faculty of Applied Medical Sciences, Lovely Professional University, Phagwara, Punjab 144441, India
  • 8 Department of Pharmacy, Faculty of Pharmaceutical Sciences, University of São Paulo, São Paulo, Brazil
  • 9 School of Pharmaceutical Sciences, Jaipur National University, Jagatpura, 302017, Jaipur, India
  • 10 Discipline of Pharmacy, Graduate School of Health, University of Technology Sydney, Ultimo NSW 2007, Australia; Priority Research Centre for Healthy Lungs, Hunter Medical Research Institute (HMRI) & School of Biomedical Sciences and Pharmacy, The University of Newcastle, Callaghan, NSW 2308, Australia
Biomed Pharmacother, 2018 Nov;107:1218-1229.
PMID: 30257336 DOI: 10.1016/j.biopha.2018.08.101

Abstract

Tuberculosis (caused by Mycobacterium tuberculosis, Mtb) treatment involves multiple drug regimens for a prolonged period. However, the therapeutic benefit is often limited by poor patient compliance, subsequently leading to treatment failure and development of antibiotic resistance. Notably, oxidative stress is a crucial underlying factor that adversely influences the various treatment regimens in tuberculosis. Little information is available with advanced drug delivery systems that could be effectively utilized, in particular, for targeting the oxidative stress in tuberculosis. Thus, this presents an opportunity to review the utility of various available, controlled-release drug delivery systems (e.g., microspheres, liposomes, niosomes, solid lipid nanoparticles, dendrimers) that could be beneficial in tuberculosis treatments. This will help the biological and formulation scientists to pave a new path in formulating a treatment regimen for multi-drug resistant Mtb.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.