Evidence map›Paper›PMID 23957812›Full record

ArticleMolecular pharmaceutics2013

LHRH-targeted nanogels as a delivery system for cisplatin to ovarian cancer.

Natalia V Nukolova, Hardeep S Oberoi, Yi Zhao, Vladimir P Chekhonin, Alexander V Kabanov, Tatiana K Bronich

Abstract read
In one paragraph

Article in Molecular pharmaceutics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.6field-weighted citation impact, top 8% 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

22 citing papers in PubMed, 61 citations in OpenAlex.

  1. Review
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  14. Synthesis and Evaluation ofContrast media & molecular imaging · 2019
    Article
  15. Article
  16. Review
  17. Article
  18. LHRH-Targeted Drug Delivery Systems for Cancer Therapy.Mini reviews in medicinal chemistry · 2017
    Review
  19. Nanogels: An overview of properties, biomedical applications and obstacles to clinical translation.Journal of controlled release : official journal of the Controlled Release Society · 2016
    Review
  20. Article
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

6 authors at 4 institutions in 2 countries.

Natalia V NukolovaDepartment of Chemistry, Lomonosov Moscow State University , Leninskie Gory, Moscow, 119992, Russia.
Hardeep S Oberoi
Yi Zhao
Vladimir P Chekhonin
Alexander V Kabanov
Tatiana K Bronich
Nebraska Medical Center · USFederal Medical Research Centre for Psychiatry and Narcology · RULomonosov Moscow State University · RUUniversity of Nebraska Medical Center · US

Funding

Project 9 - Renal Drug Targeting for the Treatment of Lupus NephritisP20GM103480 · NIGMS · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI BRONICH, TATIANA K · 2012 to 2017
$13.3M
TARGETED NANOCARRIER FOR SIRNA DELIVERY TO TUMOR VASCULATUREP20RR021937 · NCRR · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI KABANOV, ALEXANDER V · 2008 to 2011
$8.6M
Cross-linked Polymer Micelles in Cancer TherapyR01CA116590 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI BRONICH, TATIANA K · 2006 to 2010
$1.3M
NCI NIH HHS CA116590NCI NIH HHS R01 CA116590NCRR NIH HHS P20 RR021937NIGMS NIH HHS P20 GM103480NIGMS NIH HHS P20GM103480
6 · The paper itself

Abstract

Targeted drug delivery using multifunctional polymeric nanocarriers is a modern approach for cancer therapy. Our purpose was to prepare targeted nanogels for selective delivery of chemotherapeutic agent cisplatin to luteinizing hormone-releasing hormone (LHRH) receptor overexpressing tumor in vivo. Building blocks of such delivery systems consisted of innovative soft block copolymer nanogels with ionic cores serving as a reservoir for cisplatin (loading 35%) and a synthetic analogue of LHRH conjugated to the nanogels via poly(ethylene glycol) spacer. Covalent attachment of (D-Lys6)-LHRH to nanogels was shown to be possible without loss in either the ligand binding affinity or the nanogel drug incorporation ability. LHRH-nanogel accumulation was specific to the LHRH-receptor positive A2780 ovarian cancer cells and not toward LHRH-receptor negative SKOV-3 cells. The LHRH-nanogel cisplatin formulation was more effective and less toxic than equimolar doses of free cisplatin or untargeted nanogels in the treatment of receptor-positive ovarian cancer xenografts in mice. Collectively, the study indicates that LHRH mediated nanogel-cisplatin delivery is a promising formulation strategy for therapy of tumors that express the LHRH receptor.

Indexed as

AnimalsAntineoplastic AgentsCell Line, TumorCisplatinDrug Delivery SystemsFemaleFlow CytometryHumansMice, NudeMicroscopy, ConfocalNanogelsNanoparticlesOvarian NeoplasmsPolyethylene GlycolsPolyethyleneimineAntineoplastic AgentsCisplatinNanogelspolyethylene glycol polyethyleneimine nanogelPolyethylene GlycolsPolyethyleneimine

Identifiers

PMID23957812
PMCPMC3809768
OpenAlexW2070912023

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.