Inhaled Formulation Design for the Treatment of Lung Infections

被引:7
作者
Garcia-Contreras, Lucila [1 ]
Yadav, Khushwant S. [1 ]
机构
[1] Univ Oklahoma, Hlth Sci Ctr, Coll Pharm, Dept Pharmaceut Sci, Oklahoma City, OK 73126 USA
关键词
Tuberculosis; dry powder inhalers; antibiotics; pneumonia; INVASIVE FUNGAL-INFECTIONS; CYSTIC-FIBROSIS PATIENTS; LARGE POROUS PARTICLES; VENTILATOR-ASSOCIATED PNEUMONIA; RESPIRABLE PLGA MICROSPHERES; TARGET ALVEOLAR MACROPHAGES; CHRONIC BRONCHIAL INFECTION; GRAM-NEGATIVE BACTERIA; DRUG-DELIVERY SYSTEM; SPRAY-DRYING METHOD;
D O I
10.2174/1381612821666150820110305
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Lung infections may be bacterial, viral or fungal and they are typically treated with oral or parenteral antibiotics. Inhaled dry powder formulations offer unique opportunities for treating lung infections with enhanced effectiveness and stability. Since drug delivery to the lungs requires chronic and repeated administration of larger amounts of therapeutics, dry powder formulations are attractive alternatives to deliver drugs directly to the lungs as they are not limited by solubility issues and they are regarded as being more stable than liquid dosage forms. This state-of-the-art review presents the use of inhaled formulations for tuberculosis as a main focus, but also for other diseases such as bronchiectasis, chronic obstructive pulmonary disease (COPD), pneumonia and respiratory infections occurring as complications during lung transplants. Opportunities for the use of inhaled therapies and other respiratory diseases or as prevention or antidotes against warfare agents are offered. Typical and novel inhaled formulations that have been used as well as preclinical and clinical studies and evaluation of these inhaled therapies are discussed for each disease state. Lastly, the use of inhaled therapies as an alternative to end the emergence of drug resistant strains is discussed along with the risks of increasing these resistant strains if the inhaled therapy is not designed based on dosing regimens established by well-planned pharmacokinetic and pharmacodynamic studies.
引用
收藏
页码:3875 / 3901
页数:27
相关论文
共 229 条
[1]   CLINICAL PHARMACOKINETICS OF RIFAMPICIN [J].
ACOCELLA, G .
CLINICAL PHARMACOKINETICS, 1978, 3 (02) :108-127
[2]   Determination of the bioavailability of gentamicin to the lungs following inhalation from two jet nebulizers [J].
Al-Amoud, AI ;
Clark, BJ ;
Assi, KA ;
Chrystyn, H .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 2005, 59 (05) :542-545
[3]   Association of Inhalation Toxicologists (AIT) Working Party Recommendation for Standard Delivered Dose Calculation and Expression in Non-Clinical Aerosol Inhalation Toxicology Studies with Pharmaceuticals [J].
Alexander, David J. ;
Collins, Christopher J. ;
Coombs, Derek W. ;
Gilkison, Ian S. ;
Hardy, Colin J. ;
Healey, Graham ;
Karantabias, George ;
Johnson, Neil ;
Karlsson, Anna ;
Kilgour, Joanne D. ;
McDonald, Paddy .
INHALATION TOXICOLOGY, 2008, 20 (13) :1179-1189
[4]   Community acquired bacterial pneumonia [J].
Anevlavis, Stavros ;
Bouros, Demosthenes .
EXPERT OPINION ON PHARMACOTHERAPY, 2010, 11 (03) :361-374
[6]  
[Anonymous], 2008, Tuberculosis (Edinb), V88, P162, DOI 10.1016/S1472-9792(08)70027-1
[7]  
[Anonymous], 2008, Tuberculosis (Edinb), V88, P87, DOI 10.1016/S1472-9792(08)70003-9
[8]  
[Anonymous], 2008, Tuberculosis (Edinb), V88, P100, DOI 10.1016/S1472-9792(08)70007-6
[9]  
[Anonymous], 2008, Tuberculosis (Edinb), V88, P96, DOI 10.1016/S1472-9792(08)70006-4
[10]  
[Anonymous], 2008, Tuberculosis (Edinb), V88, P127, DOI 10.1016/S1472-9792(08)70016-7