Evidence map›Paper›PMID 37379254›Full record

ArticleACS biomaterials science & engineering2023

Thiol-Michael Addition Microparticles: Their Synthesis, Characterization, and Uptake by Macrophages.

Emerson L Grey, Jazalle McClendon, Joshita Suresh, Scott Alper, William J Janssen, Stephanie J Bryant

Abstract read
In one paragraph

Article in ACS biomaterials science & engineering, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

6 authors.

Emerson L GreyDepartment of Chemical and Biological Engineering, University of Colorado, 3415 Colorado Ave., Boulder, Colorado 80309-0596, United States.
Jazalle McClendonDivision of Pulmonary, Critical Care, and Sleep Medicine, Department of Medicine, National Jewish Health, 1400 Jackson St., Denver, Colorado 80206, United States.
Joshita SureshDepartment of Chemical and Biological Engineering, University of Colorado, 3415 Colorado Ave., Boulder, Colorado 80309-0596, United States.
Scott AlperDepartment of Immunology and Genomic Medicine, Center for Genes, Environment and Health, National Jewish Health, 1400 Jackson St., Denver, Colorado 80206, United States.
William J JanssenDivision of Pulmonary, Critical Care, and Sleep Medicine, Department of Medicine, National Jewish Health, 1400 Jackson St., Denver, Colorado 80206, United States.
Stephanie J BryantDepartment of Chemical and Biological Engineering, University of Colorado, 3415 Colorado Ave., Boulder, Colorado 80309-0596, United States.ORCID 0000-0003-1907-5216

Funding

Temporal regulation of pulmonary inflammation by MyD88 alternative pre-mRNA splicingR01HL148335 · NHLBI · NATIONAL JEWISH HEALTH · PI ALPER, SCOTT · 2019 to 2022
$2.3M
The Role of C-Flip in Mediating Pro-Survival Macrophages in the Foreign Body ResponseR21EB029261 · NIBIB · UNIVERSITY OF COLORADO · PI BRYANT, STEPHANIE J, JANSSEN, WILLIAM · 2020 to 2021
$447k
NHLBI NIH HHS R01 HL148335NIBIB NIH HHS R21 EB029261
6 · The paper itself

Abstract

Polymeric microparticles are promising biomaterial platforms for targeting macrophages in the treatment of disease. This study investigates microparticles formed by a thiol-Michael addition step-growth polymerization reaction with tunable physiochemical properties and their uptake by macrophages. The hexafunctional thiol monomer dipentaerythritol hexa-3-mercaptopropionate (DPHMP) and tetrafunctional acrylate monomer di(trimethylolpropane) tetraacrylate (DTPTA) were reacted in a stepwise dispersion polymerization, achieving tunable monodisperse particles over a size range (1-10 μm) relevant for targeting macrophages. An off-stoichiometry thiol-acrylate reaction afforded facile secondary chemical functionalization to create particles with different chemical moieties. Uptake of the microparticles by RAW 264.7 macrophages was highly dependent on treatment time, particle size, and particle chemistry with amide, carboxyl, and thiol terminal chemistries. The amide-terminated particles were non-inflammatory, while the carboxyl- and thiol-terminated particles induced pro-inflammatory cytokine production in conjunction with particle phagocytosis. Finally, a lung-specific application was explored through time-dependent uptake of amide-terminated particles by human alveolar macrophages

Indexed as

MacrophagesSulfhydryl CompoundsAcrylatesAmidesAnimalsHumansMiceAcrylatesacrylic acidAmidesSulfhydryl Compoundshuman alveolar macrophagelungmicroparticlesphagocytosisRAW 264.7 macrophagesthiol-Michael addition

Identifiers

PMID37379254
PMCPMC10619202

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Registered trials

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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.