Sudan Black B Pretreatment to Suppress Autofluorescence in Silk Fibroin Scaffolds.

DAPI Sudan Black B autofluorescence phalloidin quenching stain scaffolds silk fibroin

Journal

ACS biomaterials science & engineering
ISSN: 2373-9878
Titre abrégé: ACS Biomater Sci Eng
Pays: United States
ID NLM: 101654670

Informations de publication

Date de publication:
12 06 2023
Historique:
medline: 13 6 2023
pubmed: 12 5 2023
entrez: 12 5 2023
Statut: ppublish

Résumé

Natural polymers are extensively utilized as scaffold materials in tissue engineering and 3D disease modeling due to their general features of cytocompatibility, biodegradability, and ability to mimic the architecture and mechanical properties of the native tissue. A major limitation of many polymeric scaffolds is their autofluorescence under common imaging methods. This autofluorescence, a particular challenge with silk fibroin materials, can interfere with the visualization of fluorescently labeled cells and proteins grown on or in these scaffolds, limiting the assessment of outcomes. Here, Sudan Black B (SBB) was successfully used prefixation prior to cell seeding, in various silk matrices and 3D model systems to quench silk autofluorescence for live cell imaging. SBB was also trialed postfixation in silk hydrogels. We validated that multiple silk scaffolds pretreated with SBB (hexafluoro-2-propanol-silk scaffolds, salt-leached sponges, gel-spun catheters, and sponge-gel composite scaffolds) cultured with fibroblasts, adipose tissue, neural cells, and myoblasts demonstrated improved image resolution when compared to the nonpretreated scaffolds, while also maintaining normal cell behavior (attachment, growth, proliferation, differentiation). SBB pretreatment of silk scaffolds is an option for scaffold systems that require autofluorescence suppression.

Identifiants

pubmed: 37171982
doi: 10.1021/acsbiomaterials.3c00145
doi:

Substances chimiques

Fibroins 9007-76-5
Sudan Black B 9YDL1Q990E
Silk 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

3193-3205

Subventions

Organisme : NIBIB NIH HHS
ID : P41 EB027062
Pays : United States
Organisme : NIBIB NIH HHS
ID : T32 EB016652
Pays : United States
Organisme : NIGMS NIH HHS
ID : K12 GM133314
Pays : United States

Auteurs

Olivia Foster (O)

Department of Biomedical Engineering, Tufts University, 4 Colby St, Medford, Massachusetts 02155, United States.

Sawnaz Shaidani (S)

Department of Biomedical Engineering, Tufts University, 4 Colby St, Medford, Massachusetts 02155, United States.

Sophia K Theodossiou (SK)

Department of Biomedical Engineering, Tufts University, 4 Colby St, Medford, Massachusetts 02155, United States.

Thomas Falcucci (T)

Department of Biomedical Engineering, Tufts University, 4 Colby St, Medford, Massachusetts 02155, United States.

Derek Hiscox (D)

Department of Biomedical Engineering, Tufts University, 4 Colby St, Medford, Massachusetts 02155, United States.

Brooke M Smiley (BM)

Department of Biomedical Engineering, Tufts University, 4 Colby St, Medford, Massachusetts 02155, United States.

Chiara Romano (C)

Department of Biomedical Engineering, Tufts University, 4 Colby St, Medford, Massachusetts 02155, United States.

David L Kaplan (DL)

Department of Biomedical Engineering, Tufts University, 4 Colby St, Medford, Massachusetts 02155, United States.

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Classifications MeSH