Evidence map›Paper›PMID 28846728›Full record

ArticlePloS one2017

Carbon nanotubes exhibit fibrillar pharmacology in primates.

Simone Alidori, Daniel L J Thorek, Bradley J Beattie, David Ulmert, Bryan Aristega Almeida, Sebastien Monette, David A Scheinberg, Michael R McDevitt

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.0field-weighted citation impact, top 16% 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

11 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Review
  6. Membrane fusion and drug delivery with carbon nanotube porins.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  7. Article
  8. Nanoparticles in Targeted Alpha Therapy.Nanomaterials (Basel, Switzerland) · 2020
    Review
  9. Article
  10. Review
  11. 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

8 authors at 2 institutions in 1 country.

Simone AlidoriDepartment of Radiology, Memorial Sloan Kettering Cancer Center, New York, New York, United States of America.
Daniel L J ThorekDepartments of Radiology and Radiological Sciences, Johns Hopkins School of Medicine, Baltimore, Maryland, United States of America.
Bradley J BeattieDepartment of Medical Physics, Memorial Sloan Kettering Cancer Center, New York, New York, United States of America.
David UlmertDepartment of Radiology, Memorial Sloan Kettering Cancer Center, New York, New York, United States of America.
Bryan Aristega AlmeidaDepartment of Radiology, Memorial Sloan Kettering Cancer Center, New York, New York, United States of America.
Sebastien MonetteTri-Instituitional Laboratory of Comparative Pathology, Memorial Sloan Kettering Cancer Center, The Rockefeller University, Weill Cornell Medicine, New York, New York, United States of America.
David A ScheinbergMolecular Pharmacology Program, Memorial Sloan Kettering Cancer Center, New York, New York, United States of America.
Michael R McDevittDepartment of Radiology, Memorial Sloan Kettering Cancer Center, New York, New York, United States of America.ORCID http://orcid.org/0000-0002-8855-0917
Memorial Sloan Kettering Cancer Center · USJohns Hopkins University · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Elisa de Stanchina · 1985 to 2026
$347.4M
Weill Cornell/Rockefeller/Sloan-Kettering MST ProgramT32GM007739 · NIGMS · WEILL MEDICAL COLL OF CORNELL UNIV · PI HSU, KATHARINE C · 1985 to 2023
$51.1M
TREATMENT OF CANCER PATIENTS WITH THYMIC FACTORSP01CA033049 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI VAN DEN BRINK, MARCEL R M · 1985 to 2009
$19.8M
RECOMBINANT ANTICD33 ANTIBODY FOR AMLR01CA055349 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SCHEINBERG, DAVID A · 1991 to 2020
$6.8M
Memorial Sloan Kettering Small Animal Imaging ResearchR24CA083084 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI KOUTCHER, JASON ARTHUR · 1999 to 2006
$4.4M
Memorial Sloan Kettering Small Animal Imaging ResearchU24CA083084 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI KOUTCHER, JASON ARTHUR · 2007 to 2008
$1.5M
Improving therapy of glioblastoma multiforme by enhancing therapeutic drug deliveR01CA166078 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI MCDEVITT, MICHAEL R. · 2012 to 2015
$1.3M
Novel Nano-Constructs to Target and Destroy Tumor NeovasculatureR21CA128406 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI MCDEVITT, MICHAEL R. · 2007 to 2009
$562k
The Roles of Microglia and Macrophage Populations in the Glioma MicroenvironmentF31CA167863 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI BOWMAN, ROBERT LYLE · 2012 to 2015
$170k
NCI NIH HHS F31 CA167863NCI NIH HHS P01 CA033049NCI NIH HHS P30 CA008748NCI NIH HHS R01 CA055349NCI NIH HHS R01 CA166078NCI NIH HHS R21 CA128406NCI NIH HHS R24 CA083084NCI NIH HHS U24 CA083084NIGMS NIH HHS T32 GM007739
6 · The paper itself

Abstract

Nanomedicine rests at the nexus of medicine, bioengineering, and biology with great potential for improving health through innovation and development of new drugs and devices. Carbon nanotubes are an example of a fibrillar nanomaterial poised to translate into medical practice. The leading candidate material in this class is ammonium-functionalized carbon nanotubes (fCNT) that exhibits unexpected pharmacological behavior in vivo with important biotechnology applications. Here, we provide a multi-organ evaluation of the distribution, uptake and processing of fCNT in nonhuman primates using quantitative whole body positron emission tomography (PET), compartmental modeling of pharmacokinetic data, serum biomarkers and ex vivo pathology investigation. Kidney and liver are the two major organ systems that accumulate and excrete [86Y]fCNT in nonhuman primates and accumulation is cell specific as described by compartmental modeling analyses of the quantitative PET data. A serial two-compartment model explains renal processing of tracer-labeled fCNT; hepatic data fits a parallel two-compartment model. These modeling data also reveal significant elimination of the injected activity (>99.8%) from the primate within 3 days (t1/2 = 11.9 hours). These favorable results in nonhuman primates provide important insight to the fate of fCNT in vivo and pave the way to further engineering design considerations for sophisticated nanomedicines to aid late stage development and clinical use in man.

Indexed as

Nanotubes, CarbonAnimalsBiocompatible MaterialsBiomarkersKidneyLiverMiceMice, Inbred BALB CPharmacokineticsPositron-Emission TomographyPrimatesTissue DistributionYttrium RadioisotopesBiocompatible MaterialsBiomarkersNanotubes, CarbonYttrium Radioisotopes

Identifiers

PMID28846728
PMCPMC5573305
OpenAlexW2748775185

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.