Evidence map›Paper›PMID 36590645›Full record

ArticleAdvanced therapeutics2022

Functionalized core-shell nanogel scavenger for immune modulation therapy in sepsis.

Xiaotian Ji, Xiguang Yang, Changying Shi, Dandan Guo, Xiaojing Wang, Jennifer M Messina, Qinghe Meng, Norifumi Urao, Robert Cooney, Juntao Luo

Open access · greenAbstract read
In one paragraph

Article in Advanced therapeutics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.5field-weighted citation impact, top 39% 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

6 citing papers in PubMed, 9 citations in OpenAlex.

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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

10 authors at 1 institution in 1 country.

Xiaotian JiDepartment of Pharmacology, State University of New York Upstate Medical University, Syracuse, NY 13210, United States.
Xiguang YangDepartment of Pharmacology, State University of New York Upstate Medical University, Syracuse, NY 13210, United States.
Changying ShiDepartment of Pharmacology, State University of New York Upstate Medical University, Syracuse, NY 13210, United States.
Dandan GuoDepartment of Pharmacology, State University of New York Upstate Medical University, Syracuse, NY 13210, United States.
Xiaojing WangDepartment of Pharmacology, State University of New York Upstate Medical University, Syracuse, NY 13210, United States.
Jennifer M MessinaDepartment of Pharmacology, State University of New York Upstate Medical University, Syracuse, NY 13210, United States.
Qinghe MengDepartment of Surgery, State University of New York Upstate Medical University, Syracuse, NY 13210, United States.
Norifumi UraoDepartment of Pharmacology, State University of New York Upstate Medical University, Syracuse, NY 13210, United States.
Robert CooneyDepartment of Pharmacology, State University of New York Upstate Medical University, Syracuse, NY 13210, United States.
Juntao LuoDepartment of Pharmacology, State University of New York Upstate Medical University, Syracuse, NY 13210, United States.
SUNY Upstate Medical University · US

Funding

Novel Anti-HCMV StrategiesR01HL139824 · NHLBI · UPSTATE MEDICAL UNIVERSITY · PI CHAN, GARY CHING TAO · 2018 to 2021
$3.0M
An innovative hemoperfusion nanotrap for sepsis treatment.R01GM130941 · NIGMS · UPSTATE MEDICAL UNIVERSITY · PI LUO, JUNTAO · 2018 to 2021
$1.5M
NHLBI NIH HHS R01 HL139824NIGMS NIH HHS R01 GM130941
6 · The paper itself

Abstract

Sepsis is a complex, life-threatening hyperinflammatory syndrome associated with organ failure and high mortality due to lack of effective treatment options. Here we report a core-shell hydrogel nanoparticle with the core functionalized with telodendrimer (TD) nanotrap (NT) to control hyperinflammation in sepsis. The combination of multi-valent charged and hydrophobic moieties in TD enables effective binding with biomolecules in NT. The higher crosslinking in the shell structure of nanogel excludes the abundant large serum proteins and allows for size-selectivity in scavenging the medium-sized septic molecules (10-30 kDa), e.g., lipopolysaccharides (LPS, a potent endotoxin in sepsis), thus reducing cytokine production. At the same time, the core-shell TD NT nanogel captures the over-flowing proinflammatory cytokines effectively both

Indexed as

core-shell nanogelcytokine adsorptionendotoxin removalimmune modulationsepsis treatmentsize-exclusivetelodendrimer nanotrap

Identifiers

PMID36590645
PMCPMC9797201
OpenAlexW4288084524

What OpenQuestion holds

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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.