Mueller matrix analysis of a biologically sourced engineered tissue construct as polarimetric phantom.

Mueller matrix polar decomposition method collagen engineered tissue polarimetry second-harmonic generation imaging

Journal

Journal of biomedical optics
ISSN: 1560-2281
Titre abrégé: J Biomed Opt
Pays: United States
ID NLM: 9605853

Informations de publication

Date de publication:
Oct 2024
Historique:
received: 12 08 2024
revised: 07 10 2024
accepted: 10 10 2024
medline: 30 10 2024
pubmed: 30 10 2024
entrez: 30 10 2024
Statut: ppublish

Résumé

The polarimetric properties of biological tissues are often difficult to ascertain independent of their complex structural and organizational features. Conventional polarimetric tissue phantoms have well-characterized optical properties but are overly simplified. We demonstrate that an innovative, biologically sourced, engineered tissue construct better recapitulates the desired structural and polarimetric properties of native collagenous tissues, with the added benefit of potential tunability of the polarimetric response. We bridge the gap between non-biological polarimetric phantoms and native tissues. We aim to evaluate a synthesized tissue construct for its effectiveness as a phantom that mimics the polarimetric properties in typical collagenous tissues. We use a fibroblast-derived, ring-shaped engineered tissue construct as an innovative tissue phantom for polarimetric imaging. We perform polarimetry measurements and subsequent analysis using the Mueller matrix decomposition and Mueller matrix transformation methods. Scalar polarimetric parameters of the engineered tissue are analyzed at different time points for both a control group and for those treated with the transforming growth factor We identify linear retardance and circular depolarization as the parameters that are most sensitive to the tissue culture time and the addition of The engineered tissue construct exhibits changes in polarimetric properties, especially linear retardance and circular depolarization, over culture time and under

Identifiants

pubmed: 39474362
doi: 10.1117/1.JBO.29.10.106002
pii: 240226GR
pmc: PMC11521148
doi:

Substances chimiques

Collagen 9007-34-5
Transforming Growth Factor beta1 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

106002

Informations de copyright

© 2024 The Authors.

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Auteurs

Zixi Lin (Z)

Brown University, School of Engineering, Providence, Rhode Island, United States.

Samantha Madnick (S)

Brown University, Department of Pathology and Laboratory Medicine, Providence, Rhode Island, United States.
Brown University, Center for Alternatives to Animals in Testing, Providence, Rhode Island, United States.

Joshua A Burrow (JA)

Brown University, School of Engineering, Providence, Rhode Island, United States.

Jeffrey R Morgan (JR)

Brown University, Department of Pathology and Laboratory Medicine, Providence, Rhode Island, United States.
Brown University, Center for Alternatives to Animals in Testing, Providence, Rhode Island, United States.

Kimani C Toussaint (KC)

Brown University, School of Engineering, Providence, Rhode Island, United States.
Brown-Lifespan Center for Digital Health, Providence, Rhode Island, United States.

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