Evidence map›Paper›PMID 33376325›Full record

ReviewInternational journal of nanomedicine2020

Self-Assembling Peptides as an Emerging Platform for the Treatment of Metabolic Syndrome.

Luis Alberto Castillo-Díaz, Juan Alberto Ruiz-Pacheco, Mohamed Ahmed Elsawy, Juana Elizabeth Reyes-Martínez, Andrea Isabel Enríquez-Rodríguez

Open access · goldAbstract readReview
In one paragraph

Review in International journal of nanomedicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.0field-weighted citation impact, top 27% of its field
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

8 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. RGD-functionalised self-assembling peptide hydrogel induces a proliferative profile in human osteoblasts in vitro.Journal of peptide science : an official publication of the European Peptide Society · 2025
    Article
  3. Article
  4. Review
  5. Review
  6. Effects of Microalgae on Metabolic Syndrome.Antioxidants (Basel, Switzerland) · 2023
    Review
  7. Article
  8. Review
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

5 authors at 4 institutions in 2 countries.

Luis Alberto Castillo-DíazDepartment of Medicine and Health Sciences, University of Sonora, Hermosillo, Sonora, Mexico.ORCID 0000-0001-9944-9040
Juan Alberto Ruiz-PachecoWest Biomedical Research Center, National Council of Science and Technology, Guadalajara, Jalisco, Mexico.ORCID 0000-0001-6762-3358
Mohamed Ahmed ElsawyLeicester Institute for Pharmaceutical Innovation, Leicester School of Pharmacy, De Montfort University, Leicester, Leicestershire, UK.ORCID 0000-0003-3964-2150
Juana Elizabeth Reyes-MartínezDepartment of Biology, University of Guanajuato, Guanajuato, Guanajuato, Mexico.ORCID 0000-0001-8569-7799
Andrea Isabel Enríquez-RodríguezDepartment of Medicine and Health Sciences, University of Sonora, Hermosillo, Sonora, Mexico.
Universidad de Sonora · MXDe Montfort University · GBSecretaría de Ciencia, Humanidades, Tecnología e Innovación · MXUniversidad de Guanajuato · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Metabolic syndrome comprises a cluster of comorbidities that represent a major risk of developing chronic diseases, such as type II diabetes, cardiovascular diseases, and stroke. Alarmingly, metabolic syndrome reaches epidemic proportions worldwide. Today, lifestyle changes and multiple drug-based therapies represent the gold standard to address metabolic syndrome. However, such approaches face two major limitations: complicated drug therapeutic regimes, which in most cases could lead to patient incompliance, and limited drug efficacy. This has encouraged scientists to search for novel routes to deal with metabolic syndrome and related diseases. Within such approaches, self-assembled peptide formulations have emerged as a promising alternative for treating metabolic syndrome. In particular, self-assembled peptide hydrogels, either as acellular or cell-load three-dimensional scaffoldings have reached significant relevance in the biomedical field to prevent and restore euglycemia, as well as for controlling cardiovascular diseases and obesity. This has been possible thanks to the physicochemical tunability of peptides, which are developed from a chemical toolbox of versatile amino acids enabling flexibility of designing a wide range of self-assembled/co-assembled nanostructures forming biocompatible viscoelastic hydrogels. Peptide hydrogels can be combined with several biological entities, such as extracellular matrix proteins, drugs or cells, forming functional biologics with therapeutic ability for treatment of metabolic syndrome-comorbidities. Additionally, self-assembly peptides combine safety, tolerability, and effectivity attributes; by this presenting a promising platform for the development of novel pharmaceuticals capable of addressing unmet therapeutic needs for diabetes, cardiovascular disorders and obesity. In this review, recent advances in developing self-assembly peptide nanostructures tailored for improving treatment of metabolic syndrome and related diseases will be discussed from basic research to preclinical research studies. Challenges facing the development of approved medicinal products based on self-assembling peptide nanomaterials will be discussed in light of regulatory requirement for clinical authorization.

Indexed as

AnimalsHumansHydrogelsMetabolic SyndromeNanostructuresPeptidesHydrogelsPeptidescardiovascular diseasediabeteshydrogelmetabolic syndromenanomaterialsobesitypeptide

Identifiers

PMID33376325
PMCPMC7762440
OpenAlexW3113384562

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.