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Nanoparticles in Inhaled Drug Delivery

A special issue of International Journal of Molecular Sciences (ISSN 1422-0067). This special issue belongs to the section "Materials Science".

Deadline for manuscript submissions: 20 July 2025 | Viewed by 3528

Special Issue Editor


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Guest Editor
Pharmacy Discipline, School of Clinical Sciences, Faculty of Health, Queensland University of Technology, Brisbane, QLD 4001, Australia
Interests: inhaled drug delivery; nanotechnology; natural/synthetic polymeric nanoparticles; lung delivery of anticancer drugs; nanoparticulate lung drug delivery against lower respiratory tract infections
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Special Issue Information

Dear Colleagues,

Drug delivery directly into the lungs is an efficient method to achieve both local and systemic effects for therapeutic agents. The advantages of pulmonary drug delivery include superior efficacy, low toxicity, and sustained and rapid onset of action, which other drug administration routes (except injections) cannot achieve. The large epithelial surface area, extremely thin absorptive alveolar epithelial membrane, and good blood supply are notable factors that make the lung an ideal drug delivery route for the treatment of both local and systemic disorders. Delivery of drugs into the lungs ensures low systemic side-effects compared with oral or intravenous administration and no first-pass metabolism, which is a common problem for orally administered drugs.

The use of nanoparticulate drugs has been found to resolve various challenges in drug delivery, especially to cancer cells. This includes a preferential accumulation of the nanoparticles into the cancer cells, extending the half-lives of drugs in the circulation and reducing unwanted adverse effects in non-target organs. Nanoparticulate delivery of many anticancer drugs has been reported with significant success. Inhaled nanoparticles of various antibacterial drugs prepared using a variety of natural and synthetic polymers have been investigated for lung infections. Nanoparticles of the polymer–drug conjugate, polymer-encapsulated drug, solid lipid nanoparticles, and drug-loaded liposomes are very commonly used nanomedicines targeted for lung delivery. Respiratory tract infections, especially lower respiratory tract infections (LRTIs), are a leading cause of death and morbidity globally. There is an urgent need to develop effective new antibiotic delivery approaches in respiratory tract infections that allow accurate targeting of pathogens with enhanced bacterial killing, especially resistant bacteria without off-target adverse effects.

The Special Issue of the International Journal of Molecular Sciences entitled “Nanoparticles in Inhaled Drug Delivery” focuses on the studies of inhaled nanoparticulate drugs for the management of various diseases.

In this Special Issue, original research articles and critical reviews are welcome. 

Dr. Nazrul Islam
Guest Editor

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Keywords

  • inhaled nanoparticles
  • inhaled antibacterial formulations and delivery
  • inhaled anticancer drugs
  • polymeric drug nanoparticles for lung delivery
  • controlled release of inhalable antibacterial/anticancer drugs and their toxicity

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Published Papers (1 paper)

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Research

23 pages, 6496 KiB  
Article
Cytotoxic and Bactericidal Effects of Inhalable Ciprofloxacin-Loaded Poly(2-ethyl-2-oxazoline) Nanoparticles with Traces of Zinc Oxide
by Mohammad Zaidur Rahman Sabuj, Flavia Huygens, Kirsten M. Spann, Abdullah A. Tarique, Tim R. Dargaville, Geoffrey Will, Md Abdul Wahab and Nazrul Islam
Int. J. Mol. Sci. 2023, 24(5), 4532; https://doi.org/10.3390/ijms24054532 - 25 Feb 2023
Cited by 8 | Viewed by 2810
Abstract
The bactericidal effects of inhalable ciprofloxacin (CIP) loaded-poly(2-ethyl-2-oxazoline) (PEtOx) nanoparticles (NPs) with traces of zinc oxide (ZnO) were investigated against clinical strains of the respiratory pathogens Staphylococcus aureus and Pseudomonas aeruginosa. CIP-loaded PEtOx NPs retained their bactericidal activity within the formulations compared to [...] Read more.
The bactericidal effects of inhalable ciprofloxacin (CIP) loaded-poly(2-ethyl-2-oxazoline) (PEtOx) nanoparticles (NPs) with traces of zinc oxide (ZnO) were investigated against clinical strains of the respiratory pathogens Staphylococcus aureus and Pseudomonas aeruginosa. CIP-loaded PEtOx NPs retained their bactericidal activity within the formulations compared to free CIP drugs against these two pathogens, and bactericidal effects were enhanced with the inclusion of ZnO. PEtOx polymer and ZnO NPs did not show bactericidal activity alone or in combination against these pathogens. The formulations were tested to determine the cytotoxic and proinflammatory effects on airway epithelial cells derived from healthy donors (NHBE), donors with chronic obstructive pulmonary disease (COPD, DHBE), and a cell line derived from adults with cystic fibrosis (CFBE41o-) and macrophages from healthy adult controls (HCs), and those with either COPD or CF. NHBE cells demonstrated maximum cell viability (66%) against CIP-loaded PEtOx NPs with the half maximal inhibitory concentration (IC50) value of 50.7 mg/mL. CIP-loaded PEtOx NPs were more toxic to epithelial cells from donors with respiratory diseases than NHBEs, with respective IC50 values of 0.103 mg/mL for DHBEs and 0.514 mg/mL for CFBE41o- cells. However, high concentrations of CIP-loaded PEtOx NPs were toxic to macrophages, with respective IC50 values of 0.002 mg/mL for HC macrophages and 0.021 mg/mL for CF-like macrophages. PEtOx NPs, ZnO NPs, and ZnO-PEtOx NPs with no drug were not cytotoxic to any cells investigated. The in vitro digestibility of PEtOx and its NPs was investigated in simulated lung fluid (SLF) (pH 7.4). The analysed samples were characterized using Fourier transform infrared spectroscopy (ATR-FTIR), scanning electron microscopy (SEM), and UV–Vis spectroscopy. Digestion of PEtOx NPs commenced one week following incubation and was completely digested after four weeks; however, the original PEtOx was not digested after six weeks of incubation. The outcome of this study revealed that PEtOx polymer could be considered an efficient drug delivery carrier in respiratory linings, and CIP-loaded PEtOx NPs with traces of ZnO could be a promising addition to inhalable treatments against resistant bacteria with reduced toxicity. Full article
(This article belongs to the Special Issue Nanoparticles in Inhaled Drug Delivery)
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