Cited by 106Nanoparticle-Based Drug DeliveryLipid Membrane Structure and BehaviorExtracellular vesicles in disease

Clinically approved liposomal nanomedicines: lessons learned from the biomolecular corona

Caracciolo, Giulio·2018·Nanoscale

Abstract

The biomolecular corona that forms around liposomes in vivo does confer on them a selective targeting ability.

Integrity signals

Registry

Crossref · 10.1039/c7nr07450f

Cites

61 of 61 references verified0 citation errors · 0 not checkable

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  • The targeting capability of PCSN could be partly linked with some serum proteins recruited at the surface of PCSN.

    “Considering that apolipoproteins on nanoparticle play an important role in association with cellular uptake to target cells32–34, targeting capability of PCSN partly could be linked with some serum proteins recruited at the surface of PCSN.”

Cites

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Research works printed but not linked: 2

  1. Gabizon, 1994, Cancer Res., 54, 987
  2. Findlaya, 2018, Environ. Sci.: Nano, 5, 64

Cited by

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Authors
Caracciolo, G.
Affiliations
Sapienza University of Rome (IT)
Corresponding author
Caracciolo, Giulio
Venue
Nanoscale
Published
2018
Volume
10
Issue
9
Pages
4167-4172
ISSN
  • 2040-3364 (ISSN-L)
  • 2040-3372
OpenAlex
W2787356256
Cited by
106
References
61
Citations by year
2026: 6 · 2025: 7 · 2024: 11 · 2023: 8 · 2022: 14 · 2021: 15 · 2020: 15 · 2019: 20 · 2018: 10
FWCI
4.49
Type
journal article
Language
en
Open access
closed
Locations
  • Nanoscale (publishedVersion)
  • PubMed (publishedVersion)
  • IRIS Research product catalog (Sapienza University of Rome) (submittedVersion)
Topics
  • Physical Sciences › Materials Science › Biomaterials › Nanoparticle-Based Drug Delivery
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Lipid Membrane Structure and Behavior
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Extracellular vesicles in disease
Keywords
liposomes, biomolecular corona, PEGylation, targeted drug delivery, liposome design, off-target interactions, personalized nanomedicine, tumor targeting, plasma proteins, liposome physicochemical properties
MeSH terms
Protein Corona, Humans, Liposomes, Polyethylene Glycols, Drug Delivery Systems, Nanomedicine

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