Evidence map›Paper›PMID 39788546›Full record

ArticleACS biomaterials science & engineering2025

Controlling Microparticle Aspect Ratio via Photolithography for Injectable Granular Hydrogel Formation and Cell Delivery.

Dean E Stornello, Jun Kim, Zhiyuan Chen, Kyle Heaton, Taimoor H Qazi

Abstract read
In one paragraph

Article in ACS biomaterials science & engineering, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

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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.

Dean E StornelloWeldon School of Biomedical Engineering, Purdue University, West Lafayette 47907-2050, Indiana, United States.
Jun KimWeldon School of Biomedical Engineering, Purdue University, West Lafayette 47907-2050, Indiana, United States.
Zhiyuan ChenWeldon School of Biomedical Engineering, Purdue University, West Lafayette 47907-2050, Indiana, United States.ORCID 0009-0005-5545-520X
Kyle HeatonWeldon School of Biomedical Engineering, Purdue University, West Lafayette 47907-2050, Indiana, United States.
Taimoor H QaziWeldon School of Biomedical Engineering, Purdue University, West Lafayette 47907-2050, Indiana, United States.ORCID 0000-0002-3132-9170

Funding

Leveraging cell-instructive hydrogels to understand microenvironmental impact on wound healing processesR35GM155449 · NIGMS · PURDUE UNIVERSITY · PI Taimoor Hasan Qazi · 2024 to 2026
$1.1M
NIGMS NIH HHS R35 GM155449
6 · The paper itself

Abstract

Granular hydrogels are injectable and inherently porous biomaterials assembled through the packing of microparticles. These particles typically have a symmetric and spherical shape. However, recent studies have shown that asymmetric particles with high aspect ratios, such as fibers and rods, can significantly improve the mechanics, structure, and cell-guidance ability of granular hydrogels. Despite this, it remains unknown how controlled changes in the particle aspect ratio influence the injectability, porosity, and cell-instructive capabilities of granular hydrogels. Part of the challenge lies in obtaining microparticles with precisely tailored dimensions using fabrication methods such as flow-focusing microfluidics or extrusion fragmentation. In this work, we leveraged facile photolithography and photocurable hyaluronic acid to fabricate rod-shaped microparticles with widths and heights of 130 μm and lengths that varied from 260 to 1300 μm to obtain aspect ratios (ARs) of 2, 4, 6, 8, and 10. All AR microparticles formed porous and injectable granular hydrogels after centrifugation jamming. Interestingly, the longest microparticles neither clogged the needle nor fractured after extrusion from a syringe. This was attributed to a relatively low elastic modulus that permitted microparticle pliability and reversible deformation under shear. Cells (NIH/3T3 fibroblasts) mixed with the jammed microparticles and injected into molds remained viable, adhered to the particles' surface, and showed a significant and rapid rate of proliferation over a period of 7 days compared to bulk hydrogels. The proliferation rate and morphology of the cells were significantly influenced by the particle AR, with higher cell numbers observed with intermediate ARs, likely attributable to the surface area available for cell adhesion. These findings showcase the utility of injectable granular hydrogels made with high-aspect-ratio microparticles for biomedical applications.

Indexed as

Biocompatible MaterialsHydrogelsAnimalsHyaluronic AcidInjectionsMiceMicrospheresNIH 3T3 CellsParticle SizePorosityBiocompatible MaterialsHyaluronic AcidHydrogelsanisotropyinjectabilityMAP hydrogelmicrogelsphotomask

Identifiers

PMID39788546
PMCPMC11817678

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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.