Evidence map›Paper›PMID 37693598›Full record

ArticlebioRxiv : the preprint server for biology2023

Versatile Tissue-Injectable Hydrogels with Extended Hydrolytic Release of Bioactive Protein Therapeutics.

Eric S Nealy, Steven J Reed, Steve M Adelmund, Barry A Badeau, Jared A Shadish, Emily J Girard, Fiona J Pakiam, Andrew J Mhyre, Jason P Price, Surojit Sarkar and 3 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 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

5 · Who and what money

Authors and funding

13 authors.

Eric S NealySeattle Children's Research Institute, Seattle WA.
Steven J ReedSeattle Children's Research Institute, Seattle WA.
Steve M AdelmundDepartment of Chemical Engineering, University of Washington, Seattle WA.
Barry A BadeauDepartment of Chemical Engineering, University of Washington, Seattle WA.
Jared A ShadishDepartment of Chemical Engineering, University of Washington, Seattle WA.
Emily J GirardSeattle Children's Research Institute, Seattle WA.
Fiona J PakiamFred Hutch Cancer Center, Seattle WA.
Andrew J MhyreSeattle Children's Research Institute, Seattle WA.
Jason P PriceSeattle Children's Research Institute, Seattle WA.
Surojit SarkarSeattle Children's Research Institute, Seattle WA.
Vandana KaliaSeattle Children's Research Institute, Seattle WA.
Cole A DeForestDepartment of Chemical Engineering, University of Washington, Seattle WA.
James M OlsonSeattle Children's Research Institute, Seattle WA.

Funding

Interdisciplinary Tranining in Cancer ResearchT32CA080416 · NCI · UNIVERSITY OF WASHINGTON · PI STODDARD, BARRY L. · 1998 to 2023
$9.7M
Mechanisms of T Cell Quiescence and ExhaustionR01AI132819 · NIAID · SEATTLE CHILDREN'S HOSPITAL · PI Surojit Sarkar · 2019 to 2026
$5.0M
Testing a cancer patient-specific SARS-CoV-2 vaccine in chemotherapy- and radiation-treated pediatric brain tumor mouse modelsR01CA114567 · NCI · SEATTLE CHILDREN'S HOSPITAL · PI OLSON, JAMES M · 2006 to 2023
$4.9M
Immunoregulatory Mechanisms of BiTE Efficacy in the Cold Neuroblastoma TMEU01CA281848 · NCI · SEATTLE CHILDREN'S HOSPITAL · PI Vandana Kalia, JAMES M OLSON · 2023 to 2026
$3.5M
Combinations of Synergistic Bispecific Human Antibodies: A Novel Strategy for the Treatment of NeuroblastomaU01CA232490 · NCI · SEATTLE CHILDREN'S HOSPITAL · PI OLSON, JAMES M · 2018 to 2020
$2.4M
Mimicking, Exploiting, and Understanding Biology's Heterogeneity in 4DR35GM138036 · NIGMS · UNIVERSITY OF WASHINGTON · PI Cole A DeForest · 2020 to 2026
$2.3M
Molecular Medicine Training ProgramT32GM095421 · NIGMS · UNIVERSITY OF WASHINGTON · PI HAWN, THOMAS R, LILES, W. CONRAD · 2011 to 2020
$1.6M
A Comprehensive analysis and the impact of promemory gene incorporation on CAR T cell memory differentiation in the context of solid tumorsF32CA265056 · NCI · SEATTLE CHILDREN'S HOSPITAL · PI REED, STEVEN JAMES · 2021 to 2022
$139k
NCI NIH HHS F32 CA265056NCI NIH HHS R01 CA114567NCI NIH HHS T32 CA080416NCI NIH HHS U01 CA232490NCI NIH HHS U01 CA281848NIAID NIH HHS R01 AI132819NIGMS NIH HHS R35 GM138036NIGMS NIH HHS T32 GM095421
6 · The paper itself

Abstract

Hydrogels generally have broad utilization in healthcare due to their tunable structures, high water content, and inherent biocompatibility. FDA-approved applications of hydrogels include spinal cord regeneration, skin fillers, and local therapeutic delivery. Drawbacks exist in the clinical hydrogel space, largely pertaining to inconsistent therapeutic exposure, short-lived release windows, and difficulties inserting the polymer into tissue. In this study, we engineered injectable, biocompatible hydrogels that function as a local protein therapeutic depot with a high degree of user-customizability. We showcase a PEG-based hydrogel functionalized with bioorthogonal strain-promoted azide-alkyne cycloaddition (SPAAC) handles for its polymerization and functionalization with a variety of payloads. Small-molecule and protein cargos, including chemokines and antibodies, were site-specifically modified with hydrolysable "azidoesters" of varying hydrophobicity via direct chemical conjugation or sortase-mediated transpeptidation. These hydrolysable esters afforded extended release of payloads linked to our hydrogels beyond diffusion; with timescales spanning days to months dependent on ester hydrophobicity. Injected hydrogels polymerize

Indexed as

ChemokinesControlled ReleaseDrug DeliveryHydrogelMelanomaSortaseSPAACTherapeutic

Identifiers

PMID37693598
PMCPMC10491173

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.