Nanoparticle agglomerates of fluticasone propionate in combination with albuterol sulfate as dry powder aerosols

被引:34
作者
El-Gendy, Nashwa [1 ,3 ]
Pornputtapitak, Warangkana [1 ]
Berkland, Cory [1 ,2 ]
机构
[1] Univ Kansas, Dept Pharmaceut Chem, Lawrence, KS 66047 USA
[2] Univ Kansas, Dept Chem & Petr Engn, Lawrence, KS 66047 USA
[3] Beni Suef Univ, Fac Pharm, Dept Pharmaceut & Ind Pharm, Bani Suwayf, Egypt
基金
美国国家科学基金会;
关键词
Fluticasone; Albuterol; Combination therapy; Dry powder; Aerosols; SALBUTAMOL SULFATE; SALMETEROL XINAFOATE; SINGLE INHALER; PARTICLES; FORMULATION; INHALATION; BUDESONIDE; PERFORMANCE; STABILITY; THERAPY;
D O I
10.1016/j.ejps.2011.09.014
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Particle engineering strategies remain at the forefront of aerosol research for localized treatment of lung diseases and represent an alternative for systemic drug therapy. With the hastily growing popularity and complexity of inhalation therapy, there is a rising demand for tailor-made inhalable drug particles capable of affording the most proficient delivery to the lungs and the most advantageous therapeutic outcomes. To address this formulation demand, nanoparticle agglomeration was used to develop aerosols of the asthma therapeutics, fluticasone or albuterol. In addition, a combination aerosol was formed by drying agglomerates of fluticasone nanoparticles in the presence of albuterol in solution. Powders of the single drug nanoparticle agglomerates or of the combined therapeutics possessed desirable aerodynamic properties for inhalation. Powders were efficiently aerosolized (similar to 75% deposition determined by cascade impaction) with high fine particle fraction and rapid dissolution. Nanoparticle agglomeration offers a unique approach to obtain high performance aerosols from combinations of asthma therapeutics. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:522 / 533
页数:12
相关论文
共 50 条
[31]   Formulation strategy and use of excipients in pulmonary drug delivery [J].
Pilcer, Gabrielle ;
Amighi, Karim .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2010, 392 (1-2) :1-19
[32]   Nifedipine nanoparticle agglomeration as a dry powder aerosol formulation strategy [J].
Plumley, Carl ;
Gorman, Eric M. ;
El-Gendy, Nashwa ;
Bybee, Connor R. ;
Munson, Eric J. ;
Berkland, Cory .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2009, 369 (1-2) :136-143
[33]   The influence of lung deposition on clinical response [J].
Pritchard, JN .
JOURNAL OF AEROSOL MEDICINE-DEPOSITION CLEARANCE AND EFFECTS IN THE LUNG, 2001, 14 :S19-S26
[34]  
RAJESWARI S, 2006, VIROL J, V3, P32
[35]   Investigations on the humidity-induced transformations of salbutamol sulphate particles coated with L-leucine [J].
Raula, Janne ;
Thielmann, Frank ;
Kansikas, Jarno ;
Hietala, Sami ;
Annala, Minna ;
Seppala, Jukka ;
Lahde, Anna ;
Kauppinen, Esko I. .
PHARMACEUTICAL RESEARCH, 2008, 25 (10) :2250-2261
[36]   Optimisation of powders for pulmonary delivery using supercritical fluid technology [J].
Rehman, M ;
Shekunov, BY ;
York, P ;
Lechuga-Ballesteros, D ;
Miller, DP ;
Tan, T ;
Colthorpe, P .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2004, 22 (01) :1-17
[37]   Meta-analysis:: Effect of long-acting β-agonists on severe asthma exacerbations and asthma-related deaths [J].
Salpeter, Shelley R. ;
Buckley, Nicholas S. ;
Ormiston, Thomas M. ;
Salpeter, Edwin E. .
ANNALS OF INTERNAL MEDICINE, 2006, 144 (12) :904-912
[38]   Biodegradable nanoparticle flocculates for dry powder aerosol formulation [J].
Shi, Lianjun ;
Plumley, Carl J. ;
Berkland, Cory .
LANGMUIR, 2007, 23 (22) :10897-10901
[39]   Cospray-Dried Unfractionated Heparin With L-Leucine as a Dry Powder Inhaler Mucolytic for Cystic Fibrosis Therapy [J].
Shur, Jagdeep ;
Nevell, Thomas G. ;
Ewen, Richard J. ;
Price, Robert ;
Smith, Andrew ;
Barbu, Eugen ;
Conway, Joy H. ;
Carroll, Mary P. ;
Shute, Janis K. ;
Smith, James R. .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2008, 97 (11) :4857-4868
[40]   In vitro characterization of jet-milled and in-situ-micronized fluticasone-17-propionate [J].
Steckel, H ;
Rasenack, N ;
Villax, P ;
Müller, BW .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2003, 258 (1-2) :65-75