Evidence map›Paper›PMID 40366348›Full record

ArticleMacromolecular bioscience2025

Self-Assembly Pathway Influence on Dehydropeptide-Based Gel Properties and Drug Release.

Sérgio R S Veloso, Thangavel Vijayakanth, Sudha Shankar, Natalia Fridman, Sigal Rencus-Lazar, Loic Hilliou, Pedro V Rodrigues, Cacilda Moura, Paula M T Ferreira, Miguel A Correa-Duarte and 2 more

Abstract read
In one paragraph

Article in Macromolecular bioscience, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Coarse-Graining Self-Assembly by the Stochastic Landscape Method.Journal of chemical theory and computation · 2025
    Article
  3. Article
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

12 authors.

Sérgio R S VelosoPhysics Centre of Minho and Porto Universities (CF-UM-UP) and LaPMET Associate Laboratory, University of Minho, Campus de Gualtar, Braga, 4710-057, Portugal.
Thangavel VijayakanthShmunis School of Biomedicine and Cancer Research, George S. Wise Faculty of Life Sciences, Tel Aviv University, Tel Aviv, 6997801, Israel.ORCID 0000-0003-4456-5655
Sudha ShankarShmunis School of Biomedicine and Cancer Research, George S. Wise Faculty of Life Sciences, Tel Aviv University, Tel Aviv, 6997801, Israel.
Natalia FridmanSchulich Faculty of Chemistry, Technion-Israel Institute of Technology, Haifa, 32000, Israel.
Sigal Rencus-LazarShmunis School of Biomedicine and Cancer Research, George S. Wise Faculty of Life Sciences, Tel Aviv University, Tel Aviv, 6997801, Israel.
Loic HilliouDepartment of Polymer Engineering, Institute for Polymers and Composites (IPC), University of Minho, Guimarães, 4804-533, Portugal.
Pedro V RodriguesDepartment of Polymer Engineering, Institute for Polymers and Composites (IPC), University of Minho, Guimarães, 4804-533, Portugal.
Cacilda MouraPhysics Centre of Minho and Porto Universities (CF-UM-UP) and LaPMET Associate Laboratory, University of Minho, Campus de Gualtar, Braga, 4710-057, Portugal.
Paula M T FerreiraChemistry Centre of the University of Minho, Campus de Gualtar, Braga, 4710-057, Portugal.
Miguel A Correa-DuarteCINBIO, Universidad de Vigo, Vigo, 36310, Spain.
Elisabete M S CastanheiraPhysics Centre of Minho and Porto Universities (CF-UM-UP) and LaPMET Associate Laboratory, University of Minho, Campus de Gualtar, Braga, 4710-057, Portugal.
Ehud GazitShmunis School of Biomedicine and Cancer Research, George S. Wise Faculty of Life Sciences, Tel Aviv University, Tel Aviv, 6997801, Israel.ORCID 0000-0001-5764-1720

Funding

Ministerio de Ciencia e Innovación de España PID2020-113704RB-I00/AEI/10.13039/501100011033Ministerio de Ciencia e Innovación de España TED2021-132101B-I00/AEI/ 10.13039/501100011033Portuguese Foundation for Science and Technology (FCT) CEECINST/00156/2018/CP1642/CT0012Portuguese Foundation for Science and Technology (FCT) UID/00686(CQUM)Portuguese Foundation for Science and Technology (FCT) UID/04650(CF-UM-UP)Xunta de Galicia
6 · The paper itself

Abstract

Low-molecular-weight peptide-based hydrogels formed through self-assembly have emerged as promising candidates for biomedical applications. While the self-assembly process is known to affect the network morphology, its impact on mechanical properties and drug delivery remains poorly understood. In this work, it is explored how different gelation conditions influence the morphology, properties, and drug release profiles of dehydropeptide-based gels. Additionally, it is presented and analyzed, for the first time, the crystal structure of a naphthalene N-capped dehydropeptide (2-Naph-L-Phe-Z-ΔPhe-OH), which reveals a maximum pore diameter of ≈4.08 Å. By changing the preparation conditions, it is found that the stiffness of the hydrogels can vary by nearly three orders of magnitude. Employing spectroscopic and imaging techniques, the relationship between the gelation methods and the resulting mechanical properties is investigated. These findings suggest that the assembly structure, morphology, and non-covalent interactions significantly influence the release profile of model drugs such as doxorubicin, methotrexate, and curcumin. These results provide valuable insights into how preparation conditions can impact the properties of peptide-based hydrogels and their drug release profiles.

Indexed as

Drug LiberationHydrogelsPeptidesCurcuminDoxorubicinDrug Delivery SystemsMethotrexateCurcuminDoxorubicinHydrogelsMethotrexatePeptidescrystallographydehydropeptidesdrug releaseself‐assemblysupramolecular gels

Identifiers

PMID40366348
PMCPMC12434655

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.