Review paper
Improving the efficacy of inhaled drugs in cystic fibrosis: Challenges and emerging drug delivery strategies
Abstract
Cystic fibrosis (CF) is the most common autosomal recessive disease in Caucasians associated with early death. Although the faulty gene is expressed in epithelia throughout the body, lung disease is still responsible for most of the morbidity and mortality of CF patients. As a local delivery route, pulmonary administration represents an ideal way to treat respiratory infections, excessive inflammation and other manifestations typical of CF lung...
Paper Details
Title
Improving the efficacy of inhaled drugs in cystic fibrosis: Challenges and emerging drug delivery strategies
Published Date
Aug 1, 2014
Volume
75
Pages
92 - 111
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