Characterization of connective tissues using near-infrared spectroscopy and imaging.


Journal

Nature protocols
ISSN: 1750-2799
Titre abrégé: Nat Protoc
Pays: England
ID NLM: 101284307

Informations de publication

Date de publication:
02 2021
Historique:
received: 18 06 2020
accepted: 20 11 2020
pubmed: 20 1 2021
medline: 9 3 2021
entrez: 19 1 2021
Statut: ppublish

Résumé

Near-infrared (NIR) spectroscopy is a powerful analytical method for rapid, non-destructive and label-free assessment of biological materials. Compared to mid-infrared spectroscopy, NIR spectroscopy excels in penetration depth, allowing intact biological tissue assessment, albeit at the cost of reduced molecular specificity. Furthermore, it is relatively safe compared to Raman spectroscopy, with no risk of laser-induced photothermal damage. A typical NIR spectroscopy workflow for biological tissue characterization involves sample preparation, spectral acquisition, pre-processing and analysis. The resulting spectrum embeds intrinsic information on the tissue's biomolecular, structural and functional properties. Here we demonstrate the analytical power of NIR spectroscopy for exploratory and diagnostic applications by providing instructions for acquiring NIR spectra, maps and images in biological tissues. By adapting and extending this protocol from the demonstrated application in connective tissues to other biological tissues, we expect that a typical NIR spectroscopic study can be performed by a non-specialist user to characterize biological tissues in basic research or clinical settings. We also describe how to use this protocol for exploratory study on connective tissues, including differentiating among ligament types, non-destructively monitoring changes in matrix formation during engineered cartilage development, mapping articular cartilage proteoglycan content across bovine patella and spectral imaging across the depth-wise zones of articular cartilage and subchondral bone. Depending on acquisition mode and experiment objectives, a typical exploratory study can be completed within 6 h, including sample preparation and data analysis.

Identifiants

pubmed: 33462441
doi: 10.1038/s41596-020-00468-z
pii: 10.1038/s41596-020-00468-z
doi:

Substances chimiques

Proteoglycans 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1297-1329

Subventions

Organisme : NIAMS NIH HHS
ID : R01 AR056145
Pays : United States

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Auteurs

Isaac O Afara (IO)

Department of Applied Physics, University of Eastern Finland, Kuopio, Finland. isaac.afara@uef.fi.
School of Information Technology and Electrical Engineering, The University of Queensland, Brisbane, Queensland, Australia. isaac.afara@uef.fi.

Rubina Shaikh (R)

Department of Applied Physics, University of Eastern Finland, Kuopio, Finland.
Diagnostic Imaging Centre, Kuopio University Hospital, Kuopio, Finland.

Ervin Nippolainen (E)

Department of Applied Physics, University of Eastern Finland, Kuopio, Finland.

William Querido (W)

Department of Bioengineering, Temple University, Philadelphia, PA, USA.

Jari Torniainen (J)

Department of Applied Physics, University of Eastern Finland, Kuopio, Finland.

Jaakko K Sarin (JK)

Diagnostic Imaging Centre, Kuopio University Hospital, Kuopio, Finland.

Shital Kandel (S)

Department of Bioengineering, Temple University, Philadelphia, PA, USA.

Nancy Pleshko (N)

Department of Bioengineering, Temple University, Philadelphia, PA, USA.

Juha Töyräs (J)

Department of Applied Physics, University of Eastern Finland, Kuopio, Finland.
School of Information Technology and Electrical Engineering, The University of Queensland, Brisbane, Queensland, Australia.
Diagnostic Imaging Centre, Kuopio University Hospital, Kuopio, Finland.

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