Evidence map›Paper›PMID 36341688›Full record

ArticleBiomaterials science2022

Sustained release of drug-loaded nanoparticles from injectable hydrogels enables long-term control of macrophage phenotype.

Shreya S Soni, Arielle M D'Elia, Abdulrahman Alsasa, Sylvia Cho, Tina Tylek, Erin M O'Brien, Ricardo Whitaker, Kara L Spiller, Christopher B Rodell

Abstract read
In one paragraph

Article in Biomaterials science, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
–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

20 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  8. Dynamic Hydrogels in Breast Tumor Models.Gels (Basel, Switzerland) · 2025
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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

9 authors.

Shreya S SoniSchool of Biomedical Engineering, Science and Health Systems, Drexel University, Philadelphia, PA, USA. christopher.b.rodell@drexel.edu.ORCID http://orcid.org/0000-0002-8102-8413
Arielle M D'EliaSchool of Biomedical Engineering, Science and Health Systems, Drexel University, Philadelphia, PA, USA. christopher.b.rodell@drexel.edu.ORCID http://orcid.org/0000-0003-0013-1601
Abdulrahman AlsasaSchool of Biomedical Engineering, Science and Health Systems, Drexel University, Philadelphia, PA, USA. christopher.b.rodell@drexel.edu.
Sylvia ChoSchool of Biomedical Engineering, Science and Health Systems, Drexel University, Philadelphia, PA, USA. christopher.b.rodell@drexel.edu.
Tina TylekSchool of Biomedical Engineering, Science and Health Systems, Drexel University, Philadelphia, PA, USA. christopher.b.rodell@drexel.edu.ORCID http://orcid.org/0000-0003-1102-8431
Erin M O'BrienSchool of Biomedical Engineering, Science and Health Systems, Drexel University, Philadelphia, PA, USA. christopher.b.rodell@drexel.edu.
Ricardo WhitakerSchool of Biomedical Engineering, Science and Health Systems, Drexel University, Philadelphia, PA, USA. christopher.b.rodell@drexel.edu.
Kara L SpillerSchool of Biomedical Engineering, Science and Health Systems, Drexel University, Philadelphia, PA, USA. christopher.b.rodell@drexel.edu.ORCID http://orcid.org/0000-0001-7798-1490
Christopher B RodellSchool of Biomedical Engineering, Science and Health Systems, Drexel University, Philadelphia, PA, USA. christopher.b.rodell@drexel.edu.ORCID http://orcid.org/0000-0003-2168-0802

Funding

Understanding and Controlling Macrophage Behavior in AngiogenesisR01HL130037 · NHLBI · DREXEL UNIVERSITY · PI SPILLER, KARA LORRAINE · 2016 to 2024
$4.7M
Designing supramolecular delivery strategies to understand and exploit synergies in immunoregenerative medicineR35GM147184 · NIGMS · DREXEL UNIVERSITY · PI Christopher B Rodell · 2022 to 2026
$2.0M
NHLBI NIH HHS R01 HL130037NIGMS NIH HHS R35 GM147184
6 · The paper itself

Abstract

Injectable hydrogels may be pre-formed through dynamic crosslinks, allowing for injection and subsequent retention in the tissue by shear-thinning and self-healing processes, respectively. These properties enable the site-specific delivery of encapsulated therapeutics; yet, the sustained release of small-molecule drugs and their cell-targeted delivery remains challenging due to their rapid diffusive release and non-specific cellular biodistribution. Herein, we develop an injectable hydrogel system composed of a macrophage-targeted nanoparticle (cyclodextrin nanoparticles, CDNPs) crosslinked by adamantane-modified hyaluronic acid (Ad-HA). The polymer-nanoparticle hydrogel uniquely leverages cyclodextrin's interaction with small molecule drugs to create a spatially discrete drug reservoir and with adamantane to yield dynamic, injectable hydrogels. Through an innovative two-step drug screening approach and examination of 45 immunomodulatory drugs with subsequent in-depth transcriptional profiling of both murine and human macrophages, we identify celastrol as a potent inhibitor of pro-inflammatory (M1-like) behavior that furthermore promotes a reparatory (M2-like) phenotype. Celastrol encapsulation within the polymer-nanoparticle hydrogels permitted shear-thinning injection and sustained release of drug-laden nanoparticles that targeted macrophages to modulate cell behavior for greater than two weeks

Indexed as

CyclodextrinsHydrogelsAnimalsDelayed-Action PreparationsHumansMacrophagesMicePolymersTissue DistributionCyclodextrinsDelayed-Action PreparationsHydrogelsPolymers

Identifiers

PMID36341688
PMCPMC9724601

What OpenQuestion holds

Textmetadata
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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.