Evidence map›Paper›PMID 28745123›Full record

ArticleNanomedicine (London, England)2017

iRGD-functionalized PEGylated nanoparticles for enhanced colon tumor accumulation and targeted drug delivery.

Lijun Ma, Qiubing Chen, Panpan Ma, Moon Kwon Han, Zhigang Xu, Yuejun Kang, Bo Xiao, Didier Merlin

Open access · greenAbstract read
In one paragraph

Article in Nanomedicine (London, England), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.8field-weighted citation impact, top 17% of its field
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

16 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. An effective tumor-inhibiting siRNA delivery platform.Biochemical and biophysical research communications · 2026
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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

8 authors at 2 institutions in 2 countries.

Lijun MaInstitute for Clean Energy & Advanced Materials, Faculty of Materials & Energy, Southwest University, Chongqing 400715, PR China.
Qiubing ChenInstitute for Clean Energy & Advanced Materials, Faculty of Materials & Energy, Southwest University, Chongqing 400715, PR China.
Panpan MaInstitute for Clean Energy & Advanced Materials, Faculty of Materials & Energy, Southwest University, Chongqing 400715, PR China.
Moon Kwon HanInstitute for Biomedical Sciences, Center for Diagnostics & Therapeutics, Georgia State University, Atlanta, GA 30302, USA.
Zhigang XuInstitute for Clean Energy & Advanced Materials, Faculty of Materials & Energy, Southwest University, Chongqing 400715, PR China.
Yuejun KangInstitute for Clean Energy & Advanced Materials, Faculty of Materials & Energy, Southwest University, Chongqing 400715, PR China.
Bo XiaoInstitute for Clean Energy & Advanced Materials, Faculty of Materials & Energy, Southwest University, Chongqing 400715, PR China.
Didier MerlinInstitute for Biomedical Sciences, Center for Diagnostics & Therapeutics, Georgia State University, Atlanta, GA 30302, USA.
Southwest University · CNGeorgia State University · US

Funding

ROLE OF CD98 IN INTESTINAL PERMEABILITYR01DK071594 · NIDDK · GEORGIA STATE UNIVERSITY · PI MERLIN, DIDIER · 2006 to 2017
$3.3M
NIDDK NIH HHS R01 DK071594
6 · The paper itself

Abstract

aimTo enhance the tumor accumulation and targeted drug delivery for colon cancer therapy, iRGD peptide was introduced to the surface of PEGylated camptothecin-loaded nanoparticles (NPs).

methodsCellular uptake, targeting specificity, biodistribution and antitumor capacity were evaluated.

resultsThe functionalization of iRGD facilitated tumor accumulation and cellular uptake of NPs by Colon-26 cells. Furthermore, the resultant iRGD-PEG-NPs remarkably improved the therapeutic efficacy of camptothecin in vitro and in vivo by inducing a higher degree of tumor cell apoptosis compared with PEG-NPs.

conclusioniRGD-PEG-NP is a desired drug delivery system to facilitate the drug accumulation in orthotopic colon tumor tissues and further drug internalization by colon cancer cells.

Indexed as

AnimalsAntineoplastic AgentsApoptosisCamptothecinCell Line, TumorColonic NeoplasmsDrug CarriersDrug LiberationFemaleHumansMiceNanoparticlesOligopeptidesParticle SizePolyglycolic AcidSurface PropertiesAntineoplastic AgentsCamptothecinDrug CarriersN-end cysteine peptide tumor-homing peptideOligopeptidesPolyglycolic Acidactive targetingiRGD peptideorthotopic colon cancerPEGylated nanoparticletumor accumulation

Identifiers

PMID28745123
PMCPMC5551526
OpenAlexW2737081976

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.