Cited by 89Nanoparticle-Based Drug DeliveryRNA Interference and Gene DeliveryInhalation and Respiratory Drug Delivery

Enhanced localization of liposomes with prolonged blood circulation time in infected lung tissue

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Bakker-Woudenberg, Irma A.J.M., Lokerse, August F., ten Kate, Marian T., Storm, Gert·1992·Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease

Abstract

In an experimental model of unilateral pneumonia caused by Klebsiella pneumoniae in rats we investigated whether intravenous administration of liposomes with prolonged blood circulation time resulted in significant localization of liposomes in infected lung tissue. Liposomes (100 nm) composed of hydrogenated phosphatidylinositol:hydrogenated phosphatidylcholine:cholesterol (molar ratio, 1:10:5) radiolabeled with gallium-67-deferoxamine showed relatively long blood circulation time. The degree of localization of these long circulating liposomes in the infected left lung was significantly higher compared to that of localization of 110 nm egg phosphatidylglycerol:egg phosphatidylcholine:cholesterol (molar ratio, 1:10:5) liposomes which exhibited relatively short blood circulation time. At 16 h after administration of the long circulating liposomes (when 10% of the injected dose was still present in the bloodstream) localization of liposomes in the infected left lung was increased up to 10-fold compared to the left lung of uninfected rats, and appeared to be highly correlated with the intensity of the infection. In the uninfected right lung the localization of long circulating liposomes was not increased. The degree of localization of liposomes in the infected tissue is dependent on the residence time of liposomes in the blood compartment. The extent of localization of long circulating liposomes in infected tissue appeared to be dependent on the liposomal dose administered.

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  • The degree of targeting is directly correlated with the severity of infection.

    “some studies show that the degree of targeting is directly correlated with the severity of infection 51,52 .”

    From Nanotechnology approaches for global infectious diseases (2021) · cites this paper as [52]

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References 16 · Cited by 89

Research works printed but not linked: 3

  1. 6 Juliano, R.L. (1989) in Drug carrier systems (Roerdink, F.H.D. and Kroon, A.M., eds.), pp. 249–279, John Wiley and Sons. Chichester.
  2. 8 Gabizon, A. and Papahadjopoulos, D. (1988) Proc. Natl. Acad. Sci. USA 85, 6949–6953.
  3. 19 Maruyama, K., Kennel, S.J. and Huang. L. (1990) Proc. Natl. Acad. Sci. USA 87, 5744–5748.

Authors
Bakker-Woudenberg, I. A. J. M., Lokerse, A. F., ten Kate, M. T., & Storm, G.
Affiliations
  • Erasmus University Rotterdam (NL)
  • Utrecht University (NL)
Venue
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
Publisher
Elsevier BV
Published
1992-04
Volume
1138
Issue
4
Pages
318-326
ISSN
0925-4439 (ISSN-L)
OpenAlex
W2160025282
Cited by
89
References
16
Citations by year
2025: 1 · 2024: 2 · 2023: 2 · 2021: 1 · 2020: 2 · 2019: 2 · 2017: 2 · 2016: 1 · 2014: 2 · 2013: 3 · 2012: 1
FWCI
8.47
Type
journal article
Language
en
Open access
Locations
  • Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease (publishedVersion)
  • PubMed (publishedVersion)
  • RePub (Erasmus University Rotterdam) (submittedVersion, other-oa)
Topics
  • Physical Sciences › Materials Science › Biomaterials › Nanoparticle-Based Drug Delivery
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA Interference and Gene Delivery
  • Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Inhalation and Respiratory Drug Delivery
Keywords
liposomes, blood circulation time, pulmonary infection, pneumonia, Klebsiella pneumoniae, phosphatidylinositol, phosphatidylglycerol, radiolabeled liposomes, pulmonary drug delivery
MeSH terms
Animals, Disease Models, Animal, Female, Klebsiella Infections, Klebsiella pneumoniae, Liposomes, Lung, Pneumonia, Rats, Inbred Strains, Specific Pathogen-Free Organisms, Tissue Distribution, Rats

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