Evidence map›Paper›PMID 40584385›Full record

ArticleACS omega2025

Spatial Distribution and Clustering of Glycosaminoglycans in Electrospun Gelatin-Based Scaffolds.

Huiyong Li, Apurva Limaye, Laura Osorno, Omar Alheib, Zhenqin Wang, Anton V Ievlev, Neus Domingo, Treena Arinzeh, Marcus Foston

Abstract read
In one paragraph

Article in ACS omega, 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. 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

9 authors.

Huiyong LiDepartment of Energy, Environmental and Chemical Engineering, Center for Engineering Mechanobiology, Washington University in St. Louis, St. Louis, Missouri 63130, United States.
Apurva LimayeDepartment of Biomedical Engineering, Columbia University, New York, New York 10027, United States.
Laura OsornoDepartment of Biomedical Engineering, Columbia University, New York, New York 10027, United States.
Omar AlheibDepartment of Biomedical Engineering, Columbia University, New York, New York 10027, United States.
Zhenqin WangDepartment of Energy, Environmental and Chemical Engineering, Center for Engineering Mechanobiology, Washington University in St. Louis, St. Louis, Missouri 63130, United States.ORCID https://orcid.org/0000-0002-3630-0502
Anton V IevlevCenter for Nanophase Materials Science, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37831, United States.ORCID https://orcid.org/0000-0003-3645-0508
Neus DomingoCenter for Nanophase Materials Science, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37831, United States.ORCID https://orcid.org/0000-0002-5229-6638
Treena ArinzehDepartment of Biomedical Engineering, Columbia University, New York, New York 10027, United States.
Marcus FostonDepartment of Energy, Environmental and Chemical Engineering, Center for Engineering Mechanobiology, Washington University in St. Louis, St. Louis, Missouri 63130, United States.ORCID https://orcid.org/0000-0002-4227-0362

Funding

A Novel Glycosaminoglycan Mimetic Scaffold for Cartilage Repair - diversity supplementR01AR077056 · NIAMS · NEW JERSEY INSTITUTE OF TECHNOLOGY · PI Treena Lynne Arinzeh · 2021 to 2026
$1.9M
NIAMS NIH HHS R01 AR077056
6 · The paper itself

Abstract

The extracellular matrix (ECM) is comprised of components like collagen, elastin, and glycosaminoglycans (GAGs). Electrospun fibrous scaffolds are designed to replicate the form and composition of the native ECM, often requiring blending of various ECM component mimics to enhance cellular responses. However, the spatial distribution of blended components within these fibers remains unclear. This study investigates the spatial distribution of chondroitin sulfate-C (CSC) in electrospun gelatin-based scaffolds. scanning electron microscopy (SEM), attenuated reflectance-Fourier transform infrared (ATR-FTIR) spectroscopy, X-ray photoelectron spectroscopy (XPS), and Time-of-flight Secondary Ion Mass Spectrometry (ToF-SIMS) were applied for surface and subsurface chemical characterization of the fibrous scaffolds. SEM confirmed a fibrous morphology, while ATR-FTIR and XPS analyses indicated the presence of CSC through the identification of sulfate groups. ToF-SIMS imaging, alongside K-means clustering and Ripley's K function, revealed a nonuniform CSC distribution with higher concentrations at the top layer of the scaffold. This study demonstrates that CSC presentation at the fiber surface varies with depth and differs from bulk incorporation while reveals nanoscale clustering and spatial heterogeneity at both the surface and subsurface of electrospun gelatin fibers. These findings define an underexplored design consideration with potential to influence cell-scaffold interactions.

Identifiers

PMID40584385
PMCPMC12199042

What Socratic holds

Textmetadata
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 Socratic graph.