Evidence map›Paper›PMID 29180866›Full record

ArticleInternational journal of nanomedicine2017

Biotransport kinetics and intratumoral biodistribution of malonodiserinolamide-derivatized [60]fullerene in a murine model of breast adenocarcinoma.

Norman A Lapin, Leoncio A Vergara, Yuri Mackeyev, Jared M Newton, Sean A Dilliard, Lon J Wilson, Steven A Curley, Rita E Serda

Abstract read
In one paragraph

Article in International journal of nanomedicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Review
  2. ACS biomaterials science & engineering · 2022
    Article
  3. Article
  4. Article
  5. Evaluation of the Biodistribution of Serinolamide-Derivatized CNanomaterials (Basel, Switzerland) · 2020
    Article
  6. A Novel Nanoconjugate of Landomycin A with CCellular and molecular bioengineering · 2019
    Article
  7. Development of photoactive Sweet-CNanomedicine (London, England) · 2018
    Article
  8. 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.

Norman A LapinMichael E DeBakey Department of Surgery, Baylor College of Medicine.
Leoncio A VergaraMichael E DeBakey Department of Surgery, Baylor College of Medicine.
Yuri MackeyevDepartment of Chemistry, Rice University.
Jared M NewtonMichael E DeBakey Department of Surgery, Baylor College of Medicine.
Sean A DilliardDepartment of Chemical and Biomolecular Engineering, Rice University, Houston, TX.
Lon J WilsonDepartment of Chemistry, Rice University.
Steven A CurleyMichael E DeBakey Department of Surgery, Baylor College of Medicine.
Rita E SerdaMichael E DeBakey Department of Surgery, Baylor College of Medicine.

Funding

Training Program in Translational Biology and Molecular MedicineT32GM088129 · NIGMS · BAYLOR COLLEGE OF MEDICINE · PI ROONEY, CLIONA M., VAN DEN VEYVER, IGNATIA B · 2010 to 2019
$3.0M
NIGMS NIH HHS T32 GM088129
6 · The paper itself

Abstract

[60]Fullerene is a highly versatile nanoparticle (NP) platform for drug delivery to sites of pathology owing to its small size and both ease and versatility of chemical functionalization, facilitating multisite drug conjugation, drug targeting, and modulation of its physicochemical properties. The prominent and well-characterized role of the enhanced permeation and retention (EPR) effect in facilitating NP delivery to tumors motivated us to explore vascular transport kinetics of a water-soluble [60]fullerene derivatives using intravital microscopy in an immune competent murine model of breast adenocarcinoma. Herein, we present a novel local and global image analysis of vascular transport kinetics at the level of individual tumor blood vessels on the micron scale and across whole images, respectively. Similar to larger nanomaterials, [60]fullerenes displayed rapid extravasation from tumor vasculature, distinct from that in normal microvasculature. Temporal heterogeneity in fullerene delivery to tumors was observed, demonstrating the issue of nonuniform delivery beyond spatial dimensions. Trends in local region analysis of fullerene biokinetics by fluorescence quantification were in agreement with global image analysis. Further analysis of intratumoral vascular clearance rates suggested a possible enhanced penetration and retention effect of the fullerene compared to a 70 kDa vascular tracer. Overall, this study demonstrates the feasibility of tracking and quantifying the delivery kinetics and intratumoral biodistribution of fullerene-based drug delivery platforms, consistent with the EPR effect on short timescales and passive transport to tumors.

Indexed as

AdenocarcinomaAnimalsDrug Delivery SystemsDynamic Light ScatteringFemaleFluorescenceFullerenesIntravital MicroscopyKineticsMammary Neoplasms, ExperimentalMice, Inbred BALB CMicroscopy, Electron, ScanningMolecular ImagingNanoparticlesSolubilityTissue DistributionFullerenesWaterbreast cancerdrug deliveryenhanced permeation and retentionfullereneintravital microscopy

Identifiers

PMID29180866
PMCPMC5695510

What OpenQuestion holds

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LicenceCC BY-NC
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.