Cited by 137Inhalation and Respiratory Drug DeliveryRNA Interference and Gene DeliveryNanoparticle-Based Drug Delivery

Nanodelivery in airway diseases: Challenges and therapeutic applications

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Roy, Indrajit, Vij, Neeraj·2010·Nanomedicine: Nanotechnology, Biology and Medicine

Abstract

This review describes the challenges and therapeutic applications of nanodelivery systems for treatment of airway diseases. Therapeutic applications of nanodelivery in airway diseases involve targeted delivery of DNA, short interfering RNA, drugs, or peptides to hematopoietic progenitor cells and pulmonary epithelium to control chronic pathophysiology of obstructive and conformational disorders. The major challenges to nanodelivery involve physiologic barriers such as mucus and alveolar fluid. It is necessary for the nanoparticles to be biodegradable and capable of providing sustained drug delivery to the selected cell type. Once inside the cell, the nanoparticle should be capable of escaping the endocytic degradation machinery. In addition, for effective gene delivery, nuclear entry and chromosomal integration are critical. The strategies to overcome these pathophysiologic barriers are discussed as an attempt to synchronize the efforts of pulmonary biologists, chemists, and clinicians to develop novel nanodelivery therapeutics for airway diseases.From the clinical editor Therapeutic applications of nano-delivery in airway diseases involve targeted delivery of DNA, siRNA, drugs or peptides to hematopoietic progenitor cells and pulmonary epithelium. These nano-particles must be biodegradable, capable of providing sustained drug delivery to specific cells, and should escape the endocytic degradation machinery. For effective gene-delivery they should also provide nuclear entry and chromosomal integration.

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Crossref · 10.1016/j.nano.2009.07.001

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  • Formulations that cannot penetrate mucous layers and biofilms have low pulmonary bioavailability due to rapid enzymatic deactivation, sequestration and elimination by coughing.

    “However, formulations that cannot penetrate mucous layers and biofilms have low pulmonary bioavailability due to rapid enzymatic deactivation, sequestration and elimination by coughing 22,29 .”

    From Nanotechnology approaches for global infectious diseases (2021) · cites this paper as [29]

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References 82 · Cited by 137

Research works printed but not linked: 1

  1. [26]Azarmi S Roa WH Löbenberg R Targeted delivery of nanoparticles for the treatment of lung diseases Adv Drug Deliv Rev 2008 60 863 875 18308418

Authors
Roy, I., & Vij, N.
Affiliations
  • University at Buffalo, State University of New York (US)
  • Johns Hopkins University (US)
Corresponding author
Vij, Neeraj
Venue
Nanomedicine: Nanotechnology, Biology and Medicine
Publisher
Elsevier BV
Published
2010-04
Volume
6
Issue
2
Pages
237-244
ISSN
1549-9634 (ISSN-L)
OpenAlex
W2107766412
Cited by
137
References
82
Citations by year
2026: 6 · 2025: 4 · 2024: 7 · 2023: 10 · 2022: 5 · 2021: 16 · 2020: 7 · 2019: 9 · 2018: 2 · 2017: 4 · 2016: 11 · 2015: 6 · 2014: 8 · 2013: 10 · 2012: 13
FWCI
1.58
Type
journal article
Language
en
Open access
Locations
  • Nanomedicine Nanotechnology Biology and Medicine (publishedVersion)
  • PubMed (publishedVersion)
  • Europe PMC (PubMed Central) (acceptedVersion)
  • PubMed Central (acceptedVersion)
Funders
  • U.S. Public Health Service (RHL-096931)
  • National Heart, Lung, and Blood Institute (R03HL096931)
  • National Center for Research Resources (UL1RR025005, UL-RR-025005)
Topics
  • Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Inhalation and Respiratory Drug Delivery
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA Interference and Gene Delivery
  • Physical Sciences › Materials Science › Biomaterials › Nanoparticle-Based Drug Delivery
Keywords
nanodelivery, airway disease, pulmonary drug delivery, mucus barrier, alveolar fluid, gene delivery, siRNA delivery, hematopoietic progenitor cells, lung epithelium, biodegradable nanoparticles, sustained drug release, nuclear entry, chromosomal integration
MeSH terms
Administration, Inhalation, Drug Carriers, Humans, Lung Diseases, Genetic Therapy, Nanostructures

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