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New delivery systems-liposomes for pulmonary delivery of antibacterial drugs

Version 3 2024-03-12, 15:21
Version 2 2024-02-12, 09:42
chapter
posted on 2024-03-12, 15:21 authored by A. M. Elhissi, S. R. Dennison, Waqar AhmedWaqar Ahmed, K. M. Taylor, D. A. Phoenix

Liposomes are established drug carriers for inhalation owing to their biocompatibility, biodegradability, and ability to entrap drugs and prolong their therapeutic effects in the respiratory tract following inhalation. Amongst inhalation devices, nebulizers have been the most successful because they can deliver relatively large volumes of liposomes to the deep lung. Pulmonary delivery of liposome-entrapped antibacterial drugs is particularly promising because liposomes may reduce the minimum inhibitory concentration of the entrapped antibiotic compared to drug aerosolized using single-phase aqueous solutions. Arikace® is a novel liposomal amikacin formulation for inhalation using a Pari e-Flow vibrating-mesh nebulizer. This formulation has demonstrated marked success at fighting against pulmonary infections with Pseudomonas aeruginosa in patients with cystic fibrosis. Vibrating-mesh nebulizers have provided advantages for pulmonary delivery of liposomes owing to their ability to deliver the liposome-entrapped drug to the peripheral airways without markedly damaging the physical integrity of the vesicles. This chapter provides an up-to-date appraisal of liposomes in the field of pulmonary drug delivery with a main focus on liposome inhalation for the treatment of bacterial infections in the lung. © 2015 Wiley-VCH Verlag Gmbh & Co. KGaA. All rights reserved.

History

School affiliated with

  • School of Mathematics and Physics (Research Outputs)

Publication Title

Novel antimicrobial agents and strategies

Pages/Article Number

387-406

Publisher

Wiley Blackwell

ISBN

9783527676132

Date Submitted

2017-07-06

Date Accepted

2017-07-06

Date of First Publication

2017-07-06

Date of Final Publication

2017-07-06

ePrints ID

27124

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    University of Lincoln (Research Outputs)

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