» Articles » PMID: 36406717

In-process Monitoring of a Tissue-engineered Oral Mucosa Fabricated on a Micropatterned Collagen Scaffold: Use of Optical Coherence Tomography for Quality Control

Overview
Journal Heliyon
Specialty Social Sciences
Date 2022 Nov 21
PMID 36406717
Authors
Affiliations
Soon will be listed here.
Abstract

Background: We previously reported a novel technique for fabricating dermo-epidermal junction (DEJ)-like micropatterned collagen scaffolds to manufacture an produced oral mucosa equivalent (EVPOME) for clinical translation; however, more biomimetic micropatterns are required to promote oral keratinocyte-based tissue engineering/regenerative medicine. In addition, in-process monitoring for quality control of tissue-engineered products is key to successful clinical outcomes. However, evaluating three-dimensional tissue-engineered constructs such as EVPOME is challenging. This study aimed to update our technique to fabricate a more biomimetic DEJ structure of oral mucosa and to investigate the efficacy of optical coherence tomography (OCT) in combination with deep learning for non-invasive EVPOME monitoring.

Methods: A picosecond laser-textured microstructure mimicking DEJ on stainless steel was used as a negative mould to fabricate the micropatterned collagen scaffold. During EVPOME manufacturing, OCT was applied twice to monitor the EVPOME and evaluate its epithelial thickness.

Findings: Our moulding system resulted in successful micropattern replication on the curved collagen scaffold. OCT imaging visualised the epithelial layer and the underlying micropatterned scaffold in EVPOME, enabling to non-invasively detect specific defects not found before the histological examination. Additionally, a gradual increase in epithelial thickness was observed over time.

Conclusion: These findings demonstrate the feasibility of using a stainless-steel negative mould to create a more biomimetic micropattern on collagen scaffolds and the potential of OCT imaging for quality control in oral keratinocyte-based tissue engineering/regenerative medicine.

Citing Articles

Recent trends and perspectives in reconstruction and regeneration of intra/extra-oral wounds using tissue-engineered oral mucosa equivalents.

Izumi K, Yortchan W, Aizawa Y, Kobayashi R, Hoshikawa E, Ling Y Jpn Dent Sci Rev. 2023; 59:365-374.

PMID: 37954029 PMC: 10632115. DOI: 10.1016/j.jdsr.2023.10.002.

References
1.
Toma A, Fuller J, Willett N, Goudy S . Oral wound healing models and emerging regenerative therapies. Transl Res. 2021; 236:17-34. PMC: 8380729. DOI: 10.1016/j.trsl.2021.06.003. View

2.
Spoler F, Forst M, Marquardt Y, Hoeller D, Kurz H, Merk H . High-resolution optical coherence tomography as a non-destructive monitoring tool for the engineering of skin equivalents. Skin Res Technol. 2006; 12(4):261-7. DOI: 10.1111/j.0909-752X.2006.00163.x. View

3.
Nakajima T, Sasaki K, Yamamori A, Sakurai K, Miyata K, Watanabe T . A simple three-dimensional gut model constructed in a restricted ductal microspace induces intestinal epithelial cell integrity and facilitates absorption assays. Biomater Sci. 2020; 8(20):5615-5627. DOI: 10.1039/d0bm00763c. View

4.
Upadhyay A, Pillai S, Khayambashi P, Sabri H, Lee K, Tarar M . Biomimetic Aspects of Oral and Dentofacial Regeneration. Biomimetics (Basel). 2020; 5(4). PMC: 7709662. DOI: 10.3390/biomimetics5040051. View

5.
Magin C, Neale D, Drinker M, Willenberg B, Reddy S, La Perle K . Evaluation of a bilayered, micropatterned hydrogel dressing for full-thickness wound healing. Exp Biol Med (Maywood). 2016; 241(9):986-95. PMC: 4950347. DOI: 10.1177/1535370216640943. View