Evidence map›Paper›PMID 29484558›Full record

ReviewThe AAPS journal2018

Targeting Inflammatory Vasculature by Extracellular Vesicles.

Sihan Wang, Xinyue Dong, Jin Gao, Zhenjia Wang

Open access · greenAbstract readReview
In one paragraph

Review in The AAPS journal, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

17 citing papers in PubMed, 25 citations in OpenAlex.

  1. Review
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  8. COVID-19 inflammation and implications in drug delivery.Journal of controlled release : official journal of the Controlled Release Society · 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.

Sihan WangDepartment of Pharmaceutical Sciences, College of Pharmacy, Washington State University, Spokane, WA, 99202, USA.
Xinyue DongDepartment of Pharmaceutical Sciences, College of Pharmacy, Washington State University, Spokane, WA, 99202, USA.
Jin GaoDepartment of Pharmaceutical Sciences, College of Pharmacy, Washington State University, Spokane, WA, 99202, USA.
Zhenjia WangDepartment of Pharmaceutical Sciences, College of Pharmacy, Washington State University, Spokane, WA, 99202, USA. zhenjia.wang@wsu.edu.
Washington State University Spokane · US

Funding

Neutrophil-mediated Drug DeliveryR01GM116823 · NIGMS · WASHINGTON STATE UNIVERSITY · PI WANG, ZHENJIA · 2016 to 2020
$1.8M
NIGMS NIH HHS R01 GM116823
6 · The paper itself

Abstract

Extracellular vesicles (EVs) are cell membrane-derived compartments that regulate physiology and pathology in the body. Naturally secreted EVs have been well studied in their biogenesis and have been exploited in targeted drug delivery. Due to the limitations on production of EVs, nitrogen cavitation has been utilized to efficiently generate EV-like drug delivery systems used in treating inflammatory disorders. In this short review, we will discuss the production and purification of EVs, and we will summarize what technologies are needed to improve their production for translation. We describe the drug-loading processes in EVs and their applications as drug delivery systems for inflammatory therapies, focusing on a new type of EVs made from neutrophil membrane using nitrogen cavitation.

Indexed as

AnimalsAnti-Inflammatory AgentsCell MembraneDrug Delivery SystemsEndothelium, VascularExtracellular VesiclesHumansInflammationNeutrophilsNitrogenAnti-Inflammatory AgentsNitrogendrug deliveryextracellular vesiclesinflamed endotheliumneutrophils

Identifiers

PMID29484558
PMCPMC6288379
OpenAlexW2791450810

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.