New old challenges in tuberculosis: Potentially effective nanotechnologies in drug delivery

被引:190
作者
Sosnik, Alejandro [1 ,2 ]
Carcaboso, Angel M. [1 ]
Glisoni, Romina J. [1 ,2 ]
Moretton, Marcela A. [1 ,2 ]
Chiappetta, Diego A. [1 ,2 ]
机构
[1] Univ Buenos Aires, Fac Pharm & Biochem, Dept Pharmaceut Technol, Grp Biomat & Nanotechnol Improved Med BIONIMED, RA-1113 Buenos Aires, DF, Argentina
[2] Univ Buenos Aires, Natl Sci Res Council CONICET, RA-1113 Buenos Aires, DF, Argentina
关键词
Tuberculosis; Pharmaceutical nanotechnology; Polymeric and non-polymeric nanoparticles; Polymeric micelles and liposomes; Complexation; Local delivery to the lung; Targeting to alveolar macrophages; BLOCK-COPOLYMER MICELLES; RAT ALVEOLAR MACROPHAGES; AVIUM COMPLEX INFECTION; MYCOBACTERIUM-TUBERCULOSIS; ANTITUBERCULOSIS DRUGS; CYCLODEXTRIN COMPLEXES; MANNOSYLATED LIPOSOMES; POLYMERIC MICELLES; BETA-CYCLODEXTRIN; STEALTH LIPOSOMES;
D O I
10.1016/j.addr.2009.11.023
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Tuberculosis (TB) is the second most deadly infectious disease. Despite potentially curative pharmacotherapies being available for over 50 years, the length of the treatment and the pill burden can hamper patient lifestyle. Thus, low compliance and adherence to administration schedules remain the main reasons for therapeutic failure and contribute to the development of multi-drug-resistant (MDR) strains. Pediatric patients constitute a high risk population. Most of the first-line drugs are not commercially available in pediatric form. The design of novel antibiotics attempts to overcome drug resistance, to shorten the treatment course and to reduce drug interactions with antiretroviral therapies. On the other hand, the existing anti-TB drugs are still effective. Overcoming technological drawbacks of these therapeutic agents as well as improving the effectiveness of the drug by targeting the infection reservoirs remains the central aims of Pharmaceutical Technology. In this framework, nanotechnologies appear as one of the most promising approaches for the development of more effective and compliant medicines. The present review thoroughly overviews the state-of-the-art in the development of nano-based drug delivery systems for encapsulation and release of anti-TB drugs and discusses the challenges that are faced in the development of a more effective, compliant and also affordable TB pharmacotherapy. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:547 / 559
页数:13
相关论文
共 129 条
[81]   One-step preparation of rifampicin/poly(lactic-co-glycolic acid) nanoparticle-containing mannitol microspheres using a four-fluid nozzle spray drier for inhalation therapy of tuberculosis [J].
Ohashi, Katsuya ;
Kabasawa, Takahiro ;
Ozeki, Tetsuya ;
Okada, Hiroaki .
JOURNAL OF CONTROLLED RELEASE, 2009, 135 (01) :19-24
[82]  
Onyebujoh P, 2005, B WORLD HEALTH ORGAN, V83, P857
[83]   Opsonization, biodistribution, and pharmacokinetics of polymeric nanoparticles [J].
Owens, DE ;
Peppas, NA .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2006, 307 (01) :93-102
[84]   Oral solid lipid nanoparticle-based antitubercular chemotherapy [J].
Pandey, R ;
Sharma, S ;
Khuller, GK .
TUBERCULOSIS, 2005, 85 (5-6) :415-420
[85]   Antitubercular inhaled therapy: opportunities, progress and challenges [J].
Pandey, R ;
Khuller, GK .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2005, 55 (04) :430-435
[86]   Subcutaneous nanoparticle-based antitubercular chemotherapy in an experimental model [J].
Pandey, R ;
Khuller, GK .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2004, 54 (01) :266-268
[87]   Nanoparticle encapsulated antitubercular drugs as a potential oral drug delivery system against murine tuberculosis [J].
Pandey, R ;
Zahoor, A ;
Sharma, S ;
Khuller, GK .
TUBERCULOSIS, 2003, 83 (06) :373-378
[88]   Poly (DL-lactide-co-glycolide) nanoparticle-based inhalable sustained drug delivery system for experimental tuberculosis [J].
Pandey, R ;
Sharma, A ;
Zahoor, A ;
Sharma, S ;
Khuller, GK ;
Prasad, B .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2003, 52 (06) :981-986
[89]   Oral nanoparticle-based antituberculosis drug delivery to the brain in an experimental model [J].
Pandey, Rajesh ;
Khuller, G. K. .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2006, 57 (06) :1146-1152
[90]   Preparation of a clofazimine nanosuspension for intravenous use and evaluation of its therapeutic efficacy in murine Mycobacterium avium infection [J].
Peters, K ;
Leitzke, S ;
Diederichs, JE ;
Borner, K ;
Hahn, H ;
Müller, RH ;
Ehlers, S .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2000, 45 (01) :77-83