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Raman needle arthroscopy for in vivo molecular assessment of cartilage

Authors :
Kimberly R. Kroupa
Man I Wu
Juncheng Zhang
Magnus Jensen
Wei Wong
Julie B. Engiles
Thomas P. Schaer
Mark W. Grinstaff
Brian D. Snyder
Mads S. Bergholt
Michael B. Albro
Source :
Journal of Orthopaedic Research

Abstract

The development of treatments for osteoarthritis (OA) is burdened by the lack of standardized biomarkers of cartilage health that can be applied in clinical trials. We present a novel arthroscopic Raman probe that can “optically biopsy” cartilage and quantify key ECM biomarkers for determining cartilage composition, structure, and material properties in health and disease. Technological and analytical innovations to optimize Raman analysis include: 1) multivariate decomposition of cartilage Raman spectra into ECM-constituent-specific biomarkers (glycosaminoglycan [GAG], collagen [COL], water [H2O] scores), and 2) multiplexed polarized Raman spectroscopy to quantify superficial zone collagen anisotropy via a PLS-DA-derived Raman collagen alignment factor (RCAF). Raman measurements were performed on a series of ex vivo cartilage models: 1) chemically GAG-depleted bovine cartilage explants (n=40), 2) mechanically abraded bovine cartilage explants (n=30), 3) aging human cartilage explants (n=14), and 4) anatomical-site-varied ovine osteochondral explants (n=6). Derived Raman GAG score biomarkers predicted 95%, 66%, and 96% of the variation in GAG content of GAG-depleted bovine explants, human explants, and ovine explants, respectively (p2O scores) predicted 94% of the variation in elastic modulus of ovine explants (pin vivo Raman arthroscopy assessment of an ovine femoral condyle through intraarticular entry into the synovial capsule. This work advances Raman arthroscopy towards a transformative low cost, minimally invasive diagnostic platform for objective monitoring of treatment outcomes from emerging OA therapies.

Details

Language :
English
ISSN :
1554527X and 07360266
Database :
OpenAIRE
Journal :
Journal of Orthopaedic Research
Accession number :
edsair.doi.dedup.....2d6bf1edb1e15b907a4cff5db2ed5358
Full Text :
https://doi.org/10.1002/jor.25155