Continuously producible aztreonam-loaded inhalable lipid nanoparticles for cystic fibrosis-associated Pseudomonas aeruginosa infections – Development and in-vitro characterization

Author:

Chauhan Gautam,Shaik Abdul A.,Sawant Shruti S.,Diwan Rimpy,Mokashi Meghana,Goyal Mimansa,Shukla Snehal K.,Kunda Nitesh K.,Gupta Vivek

Publisher

Elsevier BV

Reference109 articles.

1. Warnock L, Gates A. Airway clearance techniques compared to no airway clearance techniques for cystic fibrosis. Cochrane Database Syst. Rev. [Internet]. 2023;(4). [cited 2023 Oct 1], Available from: https://doi.org/10.1002/14651858.CD001401.pub4/full.

2. Cystic fibrosis: pathophysiology of lung disease;Bergeron;Semin. Respir. Crit. Care Med.,2019

3. chapter-7-cystic-fibrosis.pdf [Internet]. [cited 2019 Oct 14]. Available from: https://www.thoracic.org/patients/patient-resources/breathing-in-america/resources/chapter-7-cystic-fibrosis.pdf.

4. Positive and negative impacts of elexacaftor/tezacaftor/ivacaftor: healthcare providers’ observations across US centers;Bathgate;Pediatr. Pulmonol.,2023

5. CFTR modulators for the treatment of cystic fibrosis;Pettit;Pharm. Ther.,2014

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