A surface-independent bioglue using photo-crosslinkable benzophenone moiety.


Journal

RSC advances
ISSN: 2046-2069
Titre abrégé: RSC Adv
Pays: England
ID NLM: 101581657

Informations de publication

Date de publication:
22 Apr 2024
Historique:
received: 11 03 2024
accepted: 09 04 2024
medline: 24 4 2024
pubmed: 24 4 2024
entrez: 24 4 2024
Statut: epublish

Résumé

Surface coating technology is broadly demanded across various fields, including marine and biomedical materials; therefore, a facile and versatile approach is desired. This study proposed an attractive surface coating strategy using photo-crosslinkable benzophenone (BP) moiety for biomaterials application. BP-containing "bioglue" polymer can effectively crosslink with all kinds of surfaces and biomolecules. Upon exposure to ultraviolet (UV) light, free radical reaction from the BP glue facilitates the immobilization of diverse molecules onto different substrates in a straightforward and user-friendly manner. Through either one-step, mixing the bioglue with targeted biomolecules, or two-step methods, pre-coating the bioglue and then adding targeted biomolecules, polyacrylic acid (PAA), cyclic RGD-containing peptides, and proteins (gelatin, collagen, and fibronectin) were successfully immobilized on substrates. After drying the bioglue, targeted biomolecules can still be immobilized on the surfaces preserving their bioactivity. Cell culture on biomolecule-immobilized surfaces using NIH 3T3 fibroblasts and human bone marrow stem cells (hBMSCs) showed significant improvement of cell adhesion and activity compared to the unmodified control in serum-free media after 24 hours. Furthermore, hBMSCs on the fibronectin-immobilized surface showed an increased calcium deposition after 21 days of osteogenic differentiation, suggesting that the immobilized fibronectin is highly bioactive. Given the straightforward protocol and substrate-independent bioglue, the proposed coating strategy is promising in broad-range fields.

Identifiants

pubmed: 38655476
doi: 10.1039/d4ra01866d
pii: d4ra01866d
pmc: PMC11036370
doi:

Types de publication

Journal Article

Langues

eng

Pagination

12966-12976

Informations de copyright

This journal is © The Royal Society of Chemistry.

Déclaration de conflit d'intérêts

The authors declare no competing interests.

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Auteurs

Yue Shi (Y)

Oujiang Laboratory, Key Laboratory of Alzheimer's Disease of Zhejiang Province, Institute of Aging, Wenzhou Medical University Wenzhou Zhejiang 325000 China py.wang@ojlab.ac.cn.

Xuelian Tao (X)

Shenzhen Key Laboratory of Biomimetic Materials and Cellular Immunomodulation, Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences Shenzhen Guangdong 518055 China.

Ping Du (P)

Shenzhen Key Laboratory of Biomimetic Materials and Cellular Immunomodulation, Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences Shenzhen Guangdong 518055 China.

Paul Pasic (P)

CSIRO Manufacturing Research Way Clayton Victoria 3168 Australia.

Lars Esser (L)

CSIRO Manufacturing Research Way Clayton Victoria 3168 Australia.

Hsien-Yeh Chen (HY)

Department of Chemical Engineering, National Taiwan University Taipei Taiwan.

Helmut Thissen (H)

CSIRO Manufacturing Research Way Clayton Victoria 3168 Australia.

Peng-Yuan Wang (PY)

Oujiang Laboratory, Key Laboratory of Alzheimer's Disease of Zhejiang Province, Institute of Aging, Wenzhou Medical University Wenzhou Zhejiang 325000 China py.wang@ojlab.ac.cn.

Classifications MeSH