Evidence map›Paper›PMID 33521418›Full record

ReviewACS omega2021

Extracellular Nanovesicles: From Intercellular Messengers to Efficient Drug Delivery Systems.

Sachin Kumar Deshmukh, Mohammad Aslam Khan, Seema Singh, Ajay Pratap Singh

Open access · goldAbstract readReview
In one paragraph

Review in ACS omega, 2021. 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
1.5field-weighted citation impact, top 17% 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

12 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
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  9. MicroRNAs in T Cell-Immunotherapy.International journal of molecular sciences · 2022
    Review
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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

4 authors at 1 institution in 1 country.

Sachin Kumar DeshmukhCancer Biology Program, Mitchell Cancer Institute, University of South Alabama, Mobile, Alabama 36604, United States.
Mohammad Aslam KhanCancer Biology Program, Mitchell Cancer Institute, University of South Alabama, Mobile, Alabama 36604, United States.
Seema SinghCancer Biology Program, Mitchell Cancer Institute, University of South Alabama, Mobile, Alabama 36604, United States.
Ajay Pratap SinghCancer Biology Program, Mitchell Cancer Institute, University of South Alabama, Mobile, Alabama 36604, United States.
USA Mitchell Cancer Institute · US

Funding

Impact of social factors on breast cancer biology in African-American womenR01CA231925 · NCI · UNIVERSITY OF SOUTH ALABAMA · PI SINGH, SEEMA · 2019 to 2023
$3.0M
Molecular causes and mechanistic underpinning of breast cancer racial disparityR01CA204801 · NCI · UNIVERSITY OF SOUTH ALABAMA · PI SINGH, SEEMA · 2016 to 2020
$1.7M
A novel molecular cross-talk driving pancreatic cancer progressionR01CA224306 · NCI · UNIVERSITY OF SOUTH ALABAMA · PI SINGH, AJAY PRATAP · 2018 to 2022
$1.7M
Molecular determinant of racial disparity in prostate cancerU01CA185490 · NCI · UNIVERSITY OF SOUTH ALABAMA · PI SINGH, AJAY PRATAP · 2014 to 2018
$1.7M
NCI NIH HHS R01 CA204801NCI NIH HHS R01 CA224306NCI NIH HHS R01 CA231925NCI NIH HHS U01 CA185490
6 · The paper itself

Abstract

Nanosized extracellular vesicles (nEV) are released by all the eukaryotic cells into the extracellular spaces. They serve as crucial mediators of intercellular communication, and their presence has been detected in a variety of body fluids. nEV carry nucleic acids, lipids, proteins, and metabolites from the donor cells and transfer them to the recipient cells in the vicinity or distant locations to cause changes in their biological phenotypes. This very property of nEV makes them a suitable carrier of the drugs for therapeutic applications. The use of nEV as a drug delivery system offers several advantages over synthetic nanoparticles, including biocompatibility, natural targeting ability, and long-term safety. Further, nEV can be isolated from various biological sources, quickly loaded with the drug of choice, and modified to further enhance their utility as targeted drug delivery vehicles. Here we review these aspects of nEV and discuss the parameters that should be kept in mind while choosing the nEV source, drug loading method, and surface modification strategies. We also discuss the challenges associated with the nEV-based drug delivery platforms that must be overcome before realizing their full potential in clinical applications.

Identifiers

PMID33521418
PMCPMC7841770
OpenAlexW3120073884

What OpenQuestion holds

Textmetadata
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.