Evidence map›Paper›PMID 42604840›Full record

ArticleMacromolecular bioscience2026

Hybrid Dynamic-Covalent PEG Hydrogels With Enhanced Stability for Photothermally Triggered Pulsatile Drug Delivery.

Kushal Thapa, Amelia Scott, Mackenzie U Otakpor, Sakib H Bhuiyan, Nathaniel Conrad, Edgar Torres, Dillon Gee, Moriom Afiza, Adrianne M Rosales, Tania Betancourt

Abstract read
In one paragraph

Article in Macromolecular bioscience, 2026. 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

10 authors.

Kushal ThapaMaterials Science, Engineering and Commercialization Program, Texas State University, San Marcos, Texas, USA.ORCID https://orcid.org/0000-0002-8269-9278
Amelia ScottDepartment of Biology, Texas State University, San Marcos, Texas, USA.ORCID https://orcid.org/0009-0009-9386-7642
Mackenzie U OtakporDepartment of Biology, Texas State University, San Marcos, Texas, USA.ORCID https://orcid.org/0000-0002-1585-7782
Sakib H BhuiyanMaterials Science, Engineering and Commercialization Program, Texas State University, San Marcos, Texas, USA.ORCID https://orcid.org/0009-0001-9602-0799
Nathaniel ConradMcKetta Department of Chemical Engineering, The University of Texas at Austin, Austin, Texas, USA.ORCID https://orcid.org/0000-0002-2330-2250
Edgar TorresDepartment of Chemistry and Biochemistry, Texas State University, San Marcos, Texas, USA.ORCID https://orcid.org/0000-0003-2046-7233
Dillon GeeDepartment of Biology, Texas State University, San Marcos, Texas, USA.ORCID https://orcid.org/0009-0005-3332-3820
Moriom AfizaMaterials Science, Engineering and Commercialization Program, Texas State University, San Marcos, Texas, USA.ORCID https://orcid.org/0009-0000-4689-9697
Adrianne M RosalesMcKetta Department of Chemical Engineering, The University of Texas at Austin, Austin, Texas, USA.ORCID https://orcid.org/0000-0003-0207-7661
Tania BetancourtMaterials Science, Engineering and Commercialization Program, Texas State University, San Marcos, Texas, USA.ORCID https://orcid.org/0000-0002-2460-6133

Funding

National Science Foundation Materials Research Science and Engineering Center DMR # 1720595National Science Foundation Materials Research Science and Engineering Center DMR # 2122041National Science Foundation Materials Research Science and Engineering Center DMR # 2308817
6 · The paper itself

Abstract

Hydrogels are three-dimensional elastic networks that have applications in wide array of biomedical fields. Hydrogels can be crosslinked via dynamic covalent bonds (DCB) in order to done them with the ability to be injected, to self-heal, and to respond to stimuli. In our previous work, reversible thiol-conjugate crosslinks were used in the preparation of dynamic poly(ethylene glycol) (PEG) hydrogels. Because the equilibrium state of these reversible thiol-conjugate bonds can be shifted by temperature, both thermal and photothermal stimuli were used to induce the gel-to-sol transition of these materials to develop an on-demand pulsatile cargo release. However, the dynamic nature of the crosslinks resulted in rapid gel dissolution that prevented their use for long-term drug delivery. In this work, the hydrogels were complemented with stable thiol-maleimide crosslinks to decrease their dissolution rate and prolong their functional lifetime. Data shows that even a small addition of thiol-maleimide crosslinks significantly stabilizes the hydrogels, providing improved control of cargo release initiated by photothermal stimuli but does not cause a notable difference in cargo release at physiological temperature when compared to the hydrogels lacking the stable thiol-maleimide crosslinks.

Indexed as

Drug Delivery SystemsHydrogelsPolyethylene GlycolsMaleimidesSulfhydryl CompoundsTemperatureHydrogelsmaleimideMaleimidesPolyethylene GlycolsSulfhydryl Compoundsdrug deliverydynamic covalent bondson‐demand drug deliveryphotothermal activationstimuli‐responsive biomaterialstemperature‐responsive biomaterials

Identifiers

PMID42604840
PMCPMC13477994

What Socratic holds

Textmetadata
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 Socratic graph.