Abstract
Nowadays, lungs are the most common organs affected by diseases due to climate
change, tobacco smoking, pollution and genetic factors. Conventional pharmacotherapy
(oral medication or injection) is poorly selective; this causes toxicity problems
and numerous systemic side effects. Furthermore, although pulmonary administration is
an interesting drug administration route for treating lung diseases, inhalation therapy is
complex mainly due to the lung defense mechanisms leading to rapid drug elimination.
Pulmonary drug delivery using nanocarriers appears to be the best therapeutic strategy to
overcome these issues. In fact, these nanosystems can reduce both drug therapeutic dose
and side effects, improving patient compliance, avoiding alveolar macrophage clearance,
protecting the drug from degradation processes, and providing a controlled and targeted
drug release. Therefore, this review aims to analyze the scientific literature regarding the
use of nanocarriers to treat the main lung diseases (cancer, asthma, infections). In particular,
attention was devoted to liposomes and polymer- and lipid-based nanoparticles, being
the topic of most published articles in the last decade.
Keywords:
Pulmonary Drug Delivery, Lung, Liposomes, Polymeric Nanoparticles, Lipid Nanoparticles, Lung Diseases
[1]
Ball, M.; Hossain, M.; Padalia, D. Anatomy, Airway; StatPearls, 2022.
[21]
Kirby, C.J.; Gregoriadis, G. Encyclopaedia of Controlled Drug Delivery; Mathiowitz, E., Ed.; Wiley: New York, 1999, pp. 461-492.
[49]
Müller, R.H. "Zeta potential and particle charge in laboratory practice"; Wissenschaftliche Verlagsgesellschaft mbH, Stuttgart, 1996.
[77]
Ausborn, M.; Nuhn, P.; Schreier, H. Stabilization of liposomes by freeze–thaw and lyophilization techniques: Problems and opportunities. Eur. J. Pharm. Biopharm., 1992, 38, 133-139.
[80]
Strauss, G. Freezing and thawing of liposomes suspensions. In: Liposome Technology, Preparation of Liposomes; Gregoriadis, G., Ed.; CRC Press, 1984; 1, pp. 197-219.
[84]
Abdelwahed, W. Lyophilization of solid lipid nanoparticles for brain targeting. Int. J. Pharm. Pharm. Sci., 2015, 7(10), 381-385.
[121]
Nair, S.S.; Pharande, R.R.; Bannalikar, A.S.; Mukne, A.P. In vitro anti-mycobacterial activity of acetone extract of Glycyrrhiza glabra. J. Pharm. Pharmacogn. Res., 2015, 3(4), 80-86.
[138]
Liparulo, A.; Esposito, R.; Santonocito, D.; Muñoz-ramírez, A.; Spaziano, G.; Bruno, F.; Xiao, J.; Puglia, C.; Filosa, R.; Berrino, L.; D'agostino, B. Formulation and characterization of solid lipid nanoparticles loading rf22-c, a potent and selective 5-LO inhibitor, in a monocrotaline-induced model of pulmonary hypertension. Front. Pharmacol., 2020, 11, 83.