Bimodal Plasmonic Devices Reveal Extensive Collagen Deposition in Mesenchymal Stem Cells Cultured on 3D Self‐Assembled Peptide Scaffolds via a Birefringence‐Induced Colorimetric Response

Tissue engineering holds promise for the treatment of osteoarthritis (OA), where protective hydrogel scaffolds have been combined with mesenchymal stem cells (MSCs) to promote chondrogenesis. Quantification of chondrogenesis by MSCs in 3D culture requires the imaging and detection of deposited extracellular matrix (ECM) components like collagen and proteoglycans. ECM protein quantification should be performed in a non-destructive, label-free, and simple manner. Here, we demonstrate a nanoplasmonic colorimetric device for the imaging of collagen requiring only a simple optical microscope. MSCs were encapsulated in the hydrogel-forming peptide Fmoc-diphenylalanine (Fmoc-FF) with arginine glycine aspartic acid (RGD) added. We showed, by colorimetric histology, that increased concentrations of RGD resulted in a significant increase in collagen deposition after 21 days. Traditional techniques such as immunohistological staining were not able to detect any RGD dependent increases in ECM deposition. Through an in-depth biophysical analysis we were able to correlate elevated RGD with enhanced cell-viability, collagen deposition, and reduced hydrogel stability. In summary, plasmon-enhanced colorimetric histology provides a non-destructive, label-free means to image collagen without resorting to destructive sample processing and complex immunohistological staining. This approach holds broad potential for routine quantification of collagen-rich biomaterials, promising widespread applications across research and clinical settings.

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Publication Details

Journal
Macromolecular Bioscience
Published
2025-11-23
DOI
https://doi.org/10.1002/mabi.202500372
Primary Topic
Osteoarthritis Treatment and Mechanisms
Type
article
Field-Weighted Citation Impact
0.00

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article

Bimodal Plasmonic Devices Reveal Extensive Collagen Deposition in Mesenchymal Stem Cells Cultured on 3D Self‐Assembled Peptide Scaffolds via a Birefringence‐Induced Colorimetric Response

Jacqueline M. Orian, Eugeniu Balaur, Nicholas P. Reynolds, Katrina J. Binger et al.
Macromolecular Bioscience
Osteoarthritis Treatment and Mechanisms
article

Bimodal Plasmonic Devices Reveal Extensive Collagen Deposition in Mesenchymal Stem Cells Cultured on 3D Self‐Assembled Peptide Scaffolds via a Birefringence‐Induced Colorimetric Response

Jacqueline M. Orian, Eugeniu Balaur, Nicholas P. Reynolds, Katrina J. Binger, Christopher J.H. Chong, Mirren Charnley, Julian Ratcliffe, Simon Edward Moulton, Brian Abbey, Lilith M. Caballero Aguilar, Emily H. Field, Chad Johnson, Vernise J.T. Lim, Kristian Caracciolo
article en

Abstract

Tissue engineering holds promise for the treatment of osteoarthritis (OA), where protective hydrogel scaffolds have been combined with mesenchymal stem cells (MSCs) to promote chondrogenesis. Quantification of chondrogenesis by MSCs in 3D culture requires the imaging and detection of deposited extracellular matrix (ECM) components like collagen and proteoglycans. ECM protein quantification should be performed in a non-destructive, label-free, and simple manner. Here, we demonstrate a nanoplasmonic colorimetric device for the imaging of collagen requiring only a simple optical microscope. MSCs were encapsulated in the hydrogel-forming peptide Fmoc-diphenylalanine (Fmoc-FF) with arginine glycine aspartic acid (RGD) added. We showed, by colorimetric histology, that increased concentrations of RGD resulted in a significant increase in collagen deposition after 21 days. Traditional techniques such as immunohistological staining were not able to detect any RGD dependent increases in ECM deposition. Through an in-depth biophysical analysis we were able to correlate elevated RGD with enhanced cell-viability, collagen deposition, and reduced hydrogel stability. In summary, plasmon-enhanced colorimetric histology provides a non-destructive, label-free means to image collagen without resorting to destructive sample processing and complex immunohistological staining. This approach holds broad potential for routine quantification of collagen-rich biomaterials, promising widespread applications across research and clinical settings.

Macromolecular BioscienceVol. 26(3)
The University of Melbourne (AU), La Trobe University (AU), Peter MacCallum Cancer Centre (AU), St Vincent's Hospital Melbourne (AU), Monash Alfred Psychiatry Research centre (AU), Monash University (AU), Swinburne University of Technology (AU), St Vincents Institute of Medical Research (AU), RMIT University (AU)
Cancer Research Institute, Australian Nuclear Science and Technology Organisation, Australian Synchrotron, La Trobe University, RMIT University
Openalex Percentile: Top 49%
Osteoarthritis Treatment and Mechanisms
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