Evidence map›Paper›PMID 39451320›Full record

ArticleGels (Basel, Switzerland)2024

Development of Polyvinyl Alcohol Hydrogels for Controlled Glucose Release in Biomedical Applications.

Rosa M Quispe-Siccha, Osvaldo I Medina-Sandoval, Abraham Estrada-Tinoco, Jorge A Pedroza-Pérez, Adolfo Martínez-Tovar, Irma Olarte-Carrillo, Rafael Cerón-Maldonado, Arturo Reding-Bernal, Juan C López-Alvarenga

Abstract read
In one paragraph

Article in Gels (Basel, Switzerland), 2024. 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
–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

8 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. 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

9 authors.

Rosa M Quispe-SicchaResearch and Technological Development Unit, Research Department, General Hospital of Mexico, "Dr. Eduardo Liceaga", Mexico City 06726, Mexico.
Osvaldo I Medina-SandovalInterdisciplinary Biotechnology Professional Unit, National Polytechnic Institute, Mexico City 07340, Mexico.
Abraham Estrada-TinocoInterdisciplinary Biotechnology Professional Unit, National Polytechnic Institute, Mexico City 07340, Mexico.
Jorge A Pedroza-PérezInterdisciplinary Biotechnology Professional Unit, National Polytechnic Institute, Mexico City 07340, Mexico.
Adolfo Martínez-TovarHematology Laboratory, General Hospital of Mexico "Dr. Eduardo Liceaga", Mexico City 06726, Mexico.
Irma Olarte-CarrilloHematology Laboratory, General Hospital of Mexico "Dr. Eduardo Liceaga", Mexico City 06726, Mexico.
Rafael Cerón-MaldonadoHematology Laboratory, General Hospital of Mexico "Dr. Eduardo Liceaga", Mexico City 06726, Mexico.ORCID 0000-0003-0935-4107
Arturo Reding-BernalResearch Department, General Hospital of Mexico "Dr. Eduardo Liceaga", Mexico City 06726, Mexico.
Juan C López-AlvarengaPopulation Health & Biostatistics, School of Medicine, University of Texas Rio Grande Valley, Edinburgh, TX 78539, USA.ORCID 0000-0002-0966-8766

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Polyvinyl alcohol (PVA) hydrogels have a wide range of applications in the pharmaceutical and biomedicine fields due to their exceptional biophysical properties. The study focuses on preparing and characterizing capsule-shaped PVA hydrogels to enhance their biocompatibility and porosity for controlled glucose release and cell proliferation. The hydrogels were prepared using different concentrations (Cs) and molecular weights (MWs) of PVA, with two different lengths, A (10 mm) and B (20 mm), to control glucose release over 60 min. The preparation process involved PVA gel preparation and PVA hydrogel formation. A total of 500 µL of glucose was injected into all dehydrated hydrogels in groups A and B. Glucose release was studied by immersing the hydrogels in saline at 37 °C with stirring at 500 rpm. The SUP-B15 cell line was grown in six A1 hydrogels for biocompatibility testing. The results indicate that all hydrogels remained stable at 37 °C without degrading. Those with a higher C and MW exhibited a denser and less porous structure, lower glucose storage capacity, and higher elongation at break. Significant differences in glucose release, diffusion speed, and flux were observed, which were more evident in A1 > A4, B1 > B4, and B1 > A1 over 60 min. A1 and B1 had higher values because their higher porosity distribution allowed glucose to diffuse more easily. B1, being larger, has more glucose due to its increased length. The cell growth response and viability at 48 h in contact with the hydrogels was similar to that of the control (4.5 × 10

Indexed as

cell growthdehydrationdiffusion speedflowglucose releasepermeabilitypolyvinyl alcohol hydrogelstorage capacitythermal resistance

Identifiers

PMID39451320
PMCPMC11507832

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.