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Inhaled nano- and microparticles for drug delivery
- Source :
- Global Cardiology Science & Practice
- Publication Year :
- 2014
-
Abstract
- The 21st century has seen a paradigm shift to inhaled therapy, for both systemic and local drug delivery, due to the lung's favourable properties of a large surface area and high permeability. Pulmonary drug delivery possesses many advantages, including non-invasive route of administration, low metabolic activity, control environment for systemic absorption and avoids first bypass metabolism. However, because the lung is one of the major ports of entry, it has multiple clearance mechanisms, which prevent foreign particles from entering the body. Although these clearance mechanisms maintain the sterility of the lung, clearance mechanisms can also act as barriers to the therapeutic effectiveness of inhaled drugs. This effectiveness is also influenced by the deposition site and delivered dose. Particulate-based drug delivery systems have emerged as an innovative and promising alternative to conventional inhaled drugs to circumvent pulmonary clearance mechanisms and provide enhanced therapeutic efficiency and controlled drug release. The principle of multiple pulmonary clearance mechanisms is reviewed, including mucociliary, alveolar macrophages, absorptive, and metabolic degradation. This review also discusses the current approaches and formulations developed to achieve optimal pulmonary drug delivery systems.
- Subjects :
- liposomes
Liposome
Lung
business.industry
micelles
pulmonary delivery
Systemic absorption
Review Article
Pharmacology
pulmonary clearance mechanisms
Bioavailability
Route of administration
particulate-based drug delivery system
solid lipid nanoparticles
medicine.anatomical_structure
Targeted drug delivery
Drug delivery
Solid lipid nanoparticle
medicine
business
bioavailability
polymeric micro/nanoparticles
Subjects
Details
- ISSN :
- 23057823
- Volume :
- 2015
- Database :
- OpenAIRE
- Journal :
- Global cardiology sciencepractice
- Accession number :
- edsair.doi.dedup.....35e663b680920f369ae9f70bf6ef8e81