Evidence map›Paper›PMID 31932600›Full record

ArticleScientific reports2020

Biomimetic cellular vectors for enhancing drug delivery to the lungs.

Michael Evangelopoulos, Iman K Yazdi, Stefania Acciardo, Roberto Palomba, Federica Giordano, Anna Pasto, Manuela Sushnitha, Jonathan O Martinez, Nupur Basu, Armando Torres and 3 more

Abstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Review
  6. Review
  7. Article
  8. Review
  9. Cells-Based Drug Delivery for Cancer Applications.Nanoscale research letters · 2021
    Review
  10. Engineering MacrophagesFrontiers in oncology · 2021
    Review
  11. Recent Advances in Macrophage-Mediated Drug Delivery Systems.International journal of nanomedicine · 2021
    Review
  12. Review
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

13 authors.

Michael EvangelopoulosCenter for Biomimetic Medicine, Houston Methodist Research Institute, Houston, TX, USA.ORCID http://orcid.org/0000-0002-5300-4289
Iman K YazdiCenter for Biomimetic Medicine, Houston Methodist Research Institute, Houston, TX, USA.ORCID http://orcid.org/0000-0002-0020-6960
Stefania AcciardoCenter for Biomimetic Medicine, Houston Methodist Research Institute, Houston, TX, USA.
Roberto PalombaCenter for Biomimetic Medicine, Houston Methodist Research Institute, Houston, TX, USA.
Federica GiordanoCenter for Biomimetic Medicine, Houston Methodist Research Institute, Houston, TX, USA.
Anna PastoCenter for Biomimetic Medicine, Houston Methodist Research Institute, Houston, TX, USA.
Manuela SushnithaCenter for Biomimetic Medicine, Houston Methodist Research Institute, Houston, TX, USA.
Jonathan O MartinezCenter for Biomimetic Medicine, Houston Methodist Research Institute, Houston, TX, USA.ORCID http://orcid.org/0000-0002-0517-366X
Nupur BasuCenter for Biomimetic Medicine, Houston Methodist Research Institute, Houston, TX, USA.
Armando TorresCenter for Biomimetic Medicine, Houston Methodist Research Institute, Houston, TX, USA.
Sarah HmaidanCenter for Biomimetic Medicine, Houston Methodist Research Institute, Houston, TX, USA.
Alessandro ParodiCenter for Biomimetic Medicine, Houston Methodist Research Institute, Houston, TX, USA. aparodi.sechenovuniversity@gmail.com.
Ennio TasciottiCenter for Biomimetic Medicine, Houston Methodist Research Institute, Houston, TX, USA. etasciotti@houstonmethodist.org.ORCID http://orcid.org/0000-0003-1187-3205

Funding

Biomimetic nanovesicles to overcome multiple physiological barriers for primary and metastatic triple negative breast cancer therapyR56CA213859 · NCI · METHODIST HOSPITAL RESEARCH INSTITUTE · PI CHANG, JENNY C-N · 2017 to 2017
$300k
NCI NIH HHS R56 CA213859
6 · The paper itself

Abstract

Despite recent advances in drug delivery, the targeted treatment of unhealthy cells or tissues continues to remain a priority. In cancer (much like other pathologies), delivery vectors are designed to exploit physical and biological features of unhealthy tissues that are not always homogenous across the disease. In some cases, shifting the target from unhealthy tissues to the whole organ can represent an advantage. Specifically, the natural organ-specific retention of nanotherapeutics following intravenous administration as seen in the lung, liver, and spleen can be strategically exploited to enhance drug delivery. Herein, we outline the development of a cell-based delivery system using macrophages as a delivery vehicle. When loaded with a chemotherapeutic payload (i.e., doxorubicin), these cellular vectors (CELVEC) were shown to provide continued release within the lung. This study provides proof-of-concept evidence of an alternative class of biomimetic delivery vectors that capitalize on cell size to provide therapeutic advantages for pulmonary treatments.

Indexed as

BiomimeticsDrug Delivery SystemsAnimalsAntibiotics, AntineoplasticDoxorubicinDrug CarriersDrug LiberationLiposomesLungMacrophagesMaleMiceMice, NudeTissue DistributionAntibiotics, AntineoplasticDoxorubicinDrug CarriersLiposomes

Identifiers

PMID31932600
PMCPMC6957529

What OpenQuestion holds

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LicenceCC BY
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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.