Pulmonary drug delivery systems for tuberculosis treatment

被引:132
作者
Dinh-Duy Pham [1 ,2 ,3 ]
Fattal, Elias [1 ]
Tsapis, Nicolas [1 ]
机构
[1] Univ Paris Sud, Inst Galien Paris Sud, LabEx LERMIT, CNRS UMR 8612, F-92296 Chatenay Malabry, France
[2] Univ Med & Pharm, Fac Pharm, Dept Pharmaceut, Ho Chi Minh City, Vietnam
[3] Ton Duc Thang Univ, Fac Sci Appl, Div Pharmacotechnol & Biopharm, Ho Chi Minh City, Vietnam
关键词
Tuberculosis; Lung delivery; Dry powders; Liposomes; Nanoparticles; LARGE POROUS PARTICLES; ENCAPSULATED ANTITUBERCULAR DRUGS; RESPIRABLE PLGA MICROSPHERES; DRY POWDER FORMULATIONS; FIXED-DOSE COMBINATION; IN-VIVO EVALUATION; INHALABLE MICROPARTICLES; ALVEOLAR MACROPHAGES; MYCOBACTERIUM-BOVIS; INTERFERON-GAMMA;
D O I
10.1016/j.ijpharm.2014.12.009
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Tuberculosis (TB) remains a major global health problem as it is the second leading cause of death from an infectious disease worldwide, after the human immunodeficiency virus (HIV). Conventional treatments fail either because of poor patient compliance to the drug regimen or due to the emergence of multidrug-resistant tuberculosis. The aim of this review is to give an update on the information available on tuberculosis, its pathogenesis and current antitubercular chemotherapies. Direct lung delivery of anti-TB drugs using pulmonary delivery systems is then reviewed since it appears as an interesting strategy to improve first and second line drugs. A particular focus is place on research performed on inhalable dry powder formulations of antitubercular drugs to target alveolar macrophages where the bacteria develop. Numerous studies show that anti-TB drugs can be incorporated into liposomes, microparticles or nanoparticles which can be delivered as dry powders to the deep lungs for instantaneous, targeted and/or controlled release. Treatments of infected animals show a significant reduction of the number of viable bacteria as well as a decrease in tissue damage. These new formulations appear as interesting alternatives to deliver directly drugs to the lungs and favor efficient TB treatment. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:517 / 529
页数:13
相关论文
共 117 条
[1]   Lectin-functionalized liposomes for pulmonary drug delivery:: effect of nebulization on stability and bioadhesion [J].
Abu-Dahab, R ;
Schäfer, UF ;
Lehr, CM .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2001, 14 (01) :37-46
[2]   Comparative bioavailability of rifampicin, isoniazid and pyrazinamide from a four drug fixed dose combination with separate formulations at the same dose levels [J].
Agrawal, S ;
Singh, I ;
Kaur, KJ ;
Bhade, SR ;
Kaul, CL ;
Panchagnula, R .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2004, 276 (1-2) :41-49
[3]   Pulmonary delivery of inhalable nanoparticles: dry powder inhalers [J].
Al-Hallak, M. H. D. Kamal ;
Sarfraz, Muhammad Khan ;
Azarmi, Shirzad ;
Roa, Wilson H. ;
Finlay, Warren H. ;
Lobenberg, Raimar .
THERAPEUTIC DELIVERY, 2011, 2 (10) :1313-1324
[4]   Nanotechnology and pulmonary delivery to overcome resistance in infectious diseases [J].
Andrade, Fernando ;
Rafael, Diana ;
Videira, Mafalda ;
Ferreira, Domingos ;
Sosnik, Alejandro ;
Sarmento, Bruno .
ADVANCED DRUG DELIVERY REVIEWS, 2013, 65 (13-14) :1816-1827
[5]  
[Anonymous], 2003, AM J RESP CRIT CARE, V167, P603
[6]  
[Anonymous], 2006, MALAYSIAN J PHARM SC
[7]  
[Anonymous], 2012, Lippincott's Illustrated Reviews: Pharmacology, V5th
[8]  
[Anonymous], 2013, CORE CURRICULUM TUBE, V6th
[9]  
[Anonymous], GLOB TUB REP 2013
[10]   Epidemiology of selected mycobacteria that infect humans and other animals [J].
Ashford, DA ;
Whitney, E ;
Raghunathan, P ;
Cosivi, O .
REVUE SCIENTIFIQUE ET TECHNIQUE-OFFICE INTERNATIONAL DES EPIZOOTIES, 2001, 20 (01) :325-337