Evidence map›Paper›PMID 21028937›Full record

ReviewMolecular membrane biology2010

Receptor-targeted nanocarriers for therapeutic delivery to cancer.

Bo Yu, Heng Chiat Tai, Weiming Xue, L James Lee, Robert J Lee

Abstract readReview
In one paragraph

Review in Molecular membrane biology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 133 papers.

0numbers the graph read from it
0cells of the map it votes in
133citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

133 citing papers in PubMed.

  1. Article
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  14. Innovative nanoparticle strategies for treating oral cancers.Medical oncology (Northwood, London, England) · 2025
    Review
  15. Recent Update on siRNA Therapeutics.International journal of molecular sciences · 2025
    Review
  16. Article
  17. Article
  18. Article
  19. Review
  20. Review

73 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Bo YuDepartment of Chemical and Biomolecular Engineering, College of Pharmacy, The Ohio State University, Columbus, Ohio 43210, USA.
Heng Chiat Tai
Weiming Xue
L James Lee
Robert J Lee

Funding

University of Iowa Clinical and Translational Science Program (TL1)UL1RR025755 · NCRR · OHIO STATE UNIVERSITY · PI JACKSON, REBECCA D · 2008 to 2011
$26.3M
Targeted Lipopolyplexes for Oligonucleotide Delivery to AMLR01CA135243 · NCI · OHIO STATE UNIVERSITY · PI LEE, ROBERT J · 2008 to 2012
$2.3M
Targeted Liposomal Doxorubicin Delivery to LeukemiaR01CA095673 · NCI · OHIO STATE UNIVERSITY · PI LEE, ROBERT J. · 2003 to 2007
$1.5M
Novel Micro/nanofluidic Electroporation Devices for DNA&Oligonucleotide DeliveryR21EB008247 · NIBIB · OHIO STATE UNIVERSITY · PI LEE, LY JAMES · 2007 to 2008
$383k
Microfluidic Synthesis of Nanoparticles for Oligonucleotide DeliveryR21CA131832 · NCI · OHIO STATE UNIVERSITY · PI LEE, ROBERT J · 2008 to 2009
$349k
NCI NIH HHS R01 CA095673NCI NIH HHS R01 CA135243NCI NIH HHS R21 CA131832NCRR NIH HHS UL1 RR025755NIBIB NIH HHS R21 EB008247NIBIB NIH HHS R21EB008247
6 · The paper itself

Abstract

Efficient and site-specific delivery of therapeutic drugs is a critical challenge in clinical treatment of cancer. Nano-sized carriers such as liposomes, micelles, and polymeric nanoparticles have been investigated for improving bioavailability and pharmacokinetic properties of therapeutics via various mechanisms, for example, the enhanced permeability and retention (EPR) effect. Further improvement can potentially be achieved by conjugation of targeting ligands onto nanocarriers to achieve selective delivery to the tumour cell or the tumour vasculature. Indeed, receptor-targeted nanocarrier delivery has been shown to improve therapeutic responses both in vitro and in vivo. A variety of ligands have been investigated including folate, transferrin, antibodies, peptides and aptamers. Multiple functionalities can be incorporated into the design of nanoparticles, e.g., to enable imaging and triggered intracellular drug release. In this review, we mainly focus on recent advances on the development of targeted nanocarriers and will introduce novel concepts such as multi-targeting and multi-functional nanoparticles.

Indexed as

Antineoplastic AgentsDrug Delivery SystemsHumansLipidsLiposomesMicellesNanoconjugatesNanomedicineNeoplasmsPolymersAntineoplastic AgentsLipidsLiposomesMicellesNanoconjugatesPolymers

Identifiers

PMID21028937
PMCPMC3789246

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.