Bioengineeiring of therapeutic aerosols

被引:88
作者
Edwards, DA [1 ]
Dunbar, C
机构
[1] Harvard Univ, Div Engn & Appl Sci, Cambridge, MA 02138 USA
[2] Alkermes Inc, Cambridge, MA 02139 USA
关键词
inhalation; drug delivery; lung deposition; insulin;
D O I
10.1146/annurev.bioeng.4.100101.132311
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The new field of therapeutic aerosol bioengineering (TAB), driven primarily by the medical need for inhaled insulin, is now expanding to address medical needs ranging from respiratory to systemic diseases, including asthma, growth deficiency, and pain. Bioengineering of therapeutic aerosols involves a level of aerosol particle design absent in traditional therapeutic aerosols, which are created by conventionally spraying a liquid solution or suspension of drug or milling and mixing a dry drug form into respirable particles. Bioengineered particles may be created in liquid form from devices specially designed to create an unusually fine size distribution, possibly with special purity properties, or solid particles that possess a mixture of drug and excipient, with designed shape, size, porosity, and drug release characteristics. Such aerosols have enabled several high-visibility clinical programs of inhaled insulin, as well as earlier-stage programs involving inhaled morphine, growth hormone, beta-interferon, alpha-1-antitrypsin, and several asthma drugs. The design of these aerosols, limited by partial knowledge of the lungs' physiological environment, and driven largely at this stage by market forces, relies on a mixture of new and old science, pharmaceutical science intuition, and a degree of biological-impact empiricism that speaks to the importance of an increased level of academic involvement.
引用
收藏
页码:93 / 107
页数:15
相关论文
共 75 条
[1]  
ADJEI A, 2000, INHALATION DELIVERY
[2]  
[Anonymous], PHARM TECH
[3]  
[Anonymous], 1996, RESP DRUG DELIVERY
[4]  
Ansel H. C., 1999, PHARM DOSAGE FORMS D, DOI DOI 10.1016/j.ijpharm.2006.03.010
[5]   Current issues for establishing inhaled corticosteroids as the antiinflammatory agents of choice in asthma [J].
Barnes, PJ .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1998, 101 (04) :S427-S433
[6]   BETA-ADRENOCEPTORS ON SMOOTH-MUSCLE, NERVES AND INFLAMMATORY CELLS [J].
BARNES, PJ .
LIFE SCIENCES, 1993, 52 (26) :2101-2109
[7]   Large porous particles for sustained protection from carbachol-induced bronchoconstriction in guinea pigs [J].
Ben-Jebria, A ;
Chen, DH ;
Eskew, ML ;
Vanbever, R ;
Langer, R ;
Edwards, DA .
PHARMACEUTICAL RESEARCH, 1999, 16 (04) :555-561
[8]   Receptor-mediated targeting of spray-dried lipid particles coformulated with immunoglobulin and loaded with a prototype vaccine [J].
Bot, AI ;
Smith, DJ ;
Bot, S ;
Dellamary, L ;
Tarara, TE ;
Harders, S ;
Phillips, W ;
Weers, JG ;
Woods, CM .
PHARMACEUTICAL RESEARCH, 2001, 18 (07) :971-979
[9]   Novel lipid-based hollow-porous microparticles as a platform for immunoglobulin delivery to the respiratory tract [J].
Bot, AI ;
Tarara, TE ;
Smith, DJ ;
Bot, SR ;
Woods, CM ;
Weers, JG .
PHARMACEUTICAL RESEARCH, 2000, 17 (03) :275-283
[10]   LUNG MACROPHAGES - HOW MANY KINDS ARE THERE - WHAT DO THEY DO [J].
BRAIN, JD .
AMERICAN REVIEW OF RESPIRATORY DISEASE, 1988, 137 (03) :507-509