Evidence map›Paper›PMID 41486856›Full record

ArticleJournal of biomedical materials research. Part A2026

Nonionic Surfactant as a Tool to Modify Electrospun Fiber Properties for In Vitro Fibrous Connective Tissue Models.

Katherine L Meinhold, Jennifer L Robinson

Abstract read
In one paragraph

Article in Journal of biomedical materials research. Part A, 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

2 authors.

Katherine L MeinholdDepartment of Bioengineering, University of Washington, Seattle, Washington, USA.ORCID 0009-0009-9142-6827
Jennifer L RobinsonDepartment of Bioengineering, University of Washington, Seattle, Washington, USA.ORCID 0000-0003-0052-3517

Funding

Biomaterial technologies for interrogating sex differences in tissue repair and homeostasisR35GM143081 · NIGMS · UNIVERSITY OF WASHINGTON · PI ROBINSON, JENNIFER LINDSEY · 2021 to 2025
$2.0M
NIGMS NIH HHS R35 GM143081NIH NIGMS Maximizing Investigators Research Award R35GM143081University of Kansas Self Graduate ProgramUniversity of Washington Startup and Endowment
6 · The paper itself

Abstract

Injuries to dense connective tissues, including the knee menisci, contribute to altered joint biomechanics and degeneration. Though meniscal tears are the most common intra-articular knee injury, potential drivers of regenerative treatments remain unknown. Tissue culture scaffolds which effectively recapitulate the fibrous, anisotropic structure and mechanics of meniscus tissue are essential components for in vitro models to investigate meniscus regeneration. Electrospinning poly-ε-caprolactone (PCL) is commonly employed to create meniscus-mimetic scaffolds. However, PCL fiber hydrophobicity often requires post-fabrication treatment to establish adequate hydrophilicity for processing and efficacy in vitro. Nonionic surfactants, like Span80, are common additives in the electrospinning process that are leveraged to increase hydrophilicity in a single step. This study investigates the effects of increasing Span80 concentration, in both unaligned and aligned electrospun fibers, on sample morphology (fiber diameter, alignment), tensile mechanical properties, surface properties (wettability via water contact angle, serum protein adsorption), and meniscal cell adhesion and matrix protein production. A low concentration of Span80 (10%) had a minimal impact on fiber diameter, fiber alignment, and tensile properties, while significantly increasing sample wettability and meniscal cell adhesion and fibronectin production. On the other hand, a higher Span80 concentration (30%) significantly decreased fiber diameter, tensile properties, and cell numbers, especially in aligned scaffolds. Overall, these results illustrate the utility of Span80, in a concentration dependent manner, for modulating surface wettability, protein adsorption, and tensile properties of meniscus-mimetic fibrous scaffolds while maintaining the material-cell compatibility, representing an adaptable in vitro model designed to interrogate cell behavior in a biologically relevant environment.

Indexed as

Connective TissueMeniscusNanofibersPolyestersSurface-Active AgentsTissue ScaffoldsAnimalsCell AdhesionTensile StrengthTissue EngineeringpolycaprolactonePolyestersSurface-Active Agentselectrospinningextracellular matrix modelin vitro modelnonionic surfactantprimary meniscus cells

Identifiers

PMID41486856
PMCPMC13215567

What OpenQuestion holds

Textmetadata
LicenceTDM
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.