Evidence map›Paper›PMID 25382209›Full record

ArticleCurrent drug targets2015

Proteomic Profiling of a Biomimetic Drug Delivery Platform.

Claudia Corbo, Alessandro Parodi, Michael Evangelopoulos, David A Engler, Rise K Matsunami, Anthony C Engler, Roberto Molinaro, Shilpa Scaria, Francesco Salvatore, Ennio Tasciotti

Abstract read
In one paragraph

Article in Current drug targets, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
3.1field-weighted citation impact, top 9% 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

25 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
  2. Nanoparticle-Based Interventions for Liver Transplantation.International journal of molecular sciences · 2023
    Review
  3. Review
  4. Article
  5. Review
  6. Review
  7. Research Progress on Cell Membrane-Coated Biomimetic Delivery Systems.Frontiers in bioengineering and biotechnology · 2021
    Review
  8. Article
  9. Review
  10. Article
  11. Review
  12. Review
  13. Review
  14. Trends towards Biomimicry in Theranostics.Nanomaterials (Basel, Switzerland) · 2018
    Review
  15. Inflammation and Cancer: In Medio Stat Nano.Current medicinal chemistry · 2018
    Review
  16. Review
  17. Article
  18. Article
  19. Article
  20. 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

10 authors at 4 institutions in 2 countries.

Claudia Corbo
Alessandro Parodi
Michael Evangelopoulos
David A Engler
Rise K Matsunami
Anthony C Engler
Roberto Molinaro
Shilpa Scaria
Francesco Salvatore
Ennio TasciottiDepartment of Nanomedicine, The Houston Methodist Research Institute, Houston, 6670 Bertner Avenue, Houston Texas 77030, USA. etasciotti@HoustonMethodist.org.
Houston Methodist · USIstituti di Ricovero e Cura a Carattere Scientifico · ITSDN Istituto di Ricerca Diagnostica e Nucleare · ITUniversity of Padua · IT

Funding

TRANS-NETWORK PROJECTSU54CA143837 · NCI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI FERRARI, MAURO · 2009 to 2014
$10.8M
Leukocyte Membrane Cloaked Carriers to Target and Overcome Tumor VasculatureR21CA173579 · NCI · METHODIST HOSPITAL RESEARCH INSTITUTE · PI TASCIOTTI, ENNIO · 2013 to 2014
$371k
NCI NIH HHS 5U54CA143837NCI NIH HHS R21 CA173579NCI NIH HHS U54 CA143837
6 · The paper itself

Abstract

Current delivery platforms are typically designed for prolonged circulation that favors superior accumulation of the payload in the targeted tissue. The design of efficient surface modifications determines both a longer circulation time and targeting abilities of particles. The optimization of synthesis protocols to efficiently combine targeting molecules and elements that allow for an increased circulation time can be challenging and almost impossible when several functional elements are needed. On the other hand, in the last decade, the development of bioinspired technologies was proposed as a new approach with which to increase particle safety, biocompatibility and targeting, while maintaining the synthesis protocols simple and reproducible. Recently, we developed a new drug delivery system inspired by the biology of immune cells called leukolike vector (LLV) and formed by a nanoporous silicon core and a shell derived from the leucocyte cell membrane. The goal of this study is to investigate the protein content of the LLV. Here we report the proteomic profiling of the LLV and demonstrate that our approach can be used to modify the surface of synthetic particles with more than 150 leukocyte membrane associated proteins that determine particle safety, circulation time and targeting abilities towards inflamed endothelium.

Indexed as

Drug Delivery SystemsNanoparticlesAnimalsBiomimeticsCell LineCell MembraneLeukocytesMicePorosityProteinsProteomicsSiliconProteinsSilicon

Identifiers

PMID25382209
PMCPMC4426090
OpenAlexW1989766521

What OpenQuestion holds

Textmetadata
LicenceTDM
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.