Evidence map›Paper›PMID 23395689›Full record

ArticleJournal of controlled release : official journal of the Controlled Release Society2013

Manganese-loaded lipid-micellar theranostics for simultaneous drug and gene delivery to lungs.

M Howell, J Mallela, C Wang, S Ravi, S Dixit, U Garapati, S Mohapatra

Abstract read
In one paragraph

Article in Journal of controlled release : official journal of the Controlled Release Society, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing 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

23 citing papers in PubMed.

  1. Disulfide-Crosslinked mPEG-PLA-(LA)Molecules (Basel, Switzerland) · 2026
    Article
  2. Review
  3. Review
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  5. Review
  6. Review
  7. Review
  8. Review
  9. Article
  10. Review
  11. Recent Advances in Nanomicelles Delivery Systems.Nanomaterials (Basel, Switzerland) · 2020
    Review
  12. Review
  13. Review
  14. Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Near-infrared light activated delivery platform for cancer therapy.Advances in colloid and interface science · 2015
    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

7 authors.

M HowellMolecular Medicine Department, Morsani College of Medicine, University of South Florida, Box MDC7, 12901 Bruce B Downs, Tampa, FL 33612, United States.
J Mallela
C Wang
S Ravi
S Dixit
U Garapati
S Mohapatra

Funding

An Integrated Nano-Cell Delivery Platform of Theranostics for Lung CancersR01CA152005 · NCI · UNIVERSITY OF SOUTH FLORIDA · PI MOHAPATRA, SHYAM S, MOHAPATRA, SUBHRA · 2010 to 2014
$1.4M
Targeting of Curcumin-genistein nanocomplexes for Treatment of Prostate CancerR41CA139785 · NCI · TRANSGENEX NANOBIOTECH, INC. · PI MOHAPATRA, SUBHRA · 2009 to 2009
$159k
NCI NIH HHS 1R41CA139785NCI NIH HHS 5R01CA152005NCI NIH HHS R01 CA152005NCI NIH HHS R41 CA139785
6 · The paper itself

Abstract

Gadolinium (Gd) contrast agents are predominantly used for T(1) MR imaging. However, the high toxicity of Gd(3+) and potential side effects including nephrogenic systemic fibrosis have led to the search for alternative T(1) contrast agents. Since manganese (Mn) has paramagnetic properties with five unpaired electrons that permit high spin number, long electronic relaxation times, and labile water exchange, we evaluated Mn as a T(1) magnetic resonance imaging (MRI) contrast agent for lung imaging. Here we report on the design and synthesis of multifunctional lipid-micellar nanoparticles (LMNs) containing Mn oxide (M-LMNs) for MRI that can also be used for DNA and drug delivery. Oleic acid-coated MnO nanoparticles were encapsulated in micelles composed of polyethylene glycol (PEG-2000), phosphatidylethanolamine (PE), DC-cholesterol, and dioleoyl-phosphatidylethanolamine (DOPE). The particles are taken up in vitro by human embryonic kidney (HEK293), Lewis lung carcinoma (LLC1), and A549 cells and are devoid of cytotoxicity. When administered to mice intranasally, they preferentially accumulate in the lungs. In vitro phantom and ex vivo lung MRI results confirmed that M-LMNs are able to enhance T(1) MRI contrast. M-LMNs loaded with plasmid DNA and/or doxorubicin are efficiently taken up by HEK293 cells in vitro and by target cells in vivo. Taken together, these results demonstrate that M-LMNs are capable of simultaneously providing MRI contrast and DNA and/or drug delivery to target cells in the lung and therefore may prove useful as a lung theranostic, especially for lung cancers.

Indexed as

AnimalsCell Line, TumorDNADoxorubicinDrug Delivery SystemsGene Transfer TechniquesHEK293 CellsHumansManganese CompoundsMetal NanoparticlesMiceMice, Inbred C57BLMicellesOleic AcidOxidesTissue DistributionDNADoxorubicinManganese Compoundsmanganese oxideMicellesOleic AcidOxides

Identifiers

PMID23395689
PMCPMC3783961

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Registered trials

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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.