Optical Coherence Tomography (OCT) to Evaluate Cartilage Tissue Engineering

被引:1
|
作者
Gavenis, K. [1 ]
Schmitt, R. [2 ]
Eder, K. [2 ]
Mumme, T. [1 ]
Andereya, S. [1 ]
Schneider, U. [3 ]
Mueller-Rath, R. [1 ]
机构
[1] Rhein Westfal TH Aachen, Klin Orthopadie & Unfallchirurg, D-52074 Aachen, Germany
[2] Fraunhofer Inst Prod Technol IPT, Aachen, Germany
[3] Arthro Nova Clin, Tegernsee, Germany
来源
关键词
optical coherence tomography (OCT); contained defect model; cartilage tissue engineering; nude mouse model;
D O I
10.1055/s-2008-1038948
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
Aim: The aim of this study was to investigate hyaline cartilage defects treated with cell-seeded artificial matrix systems (two different collagen type I gels) with the method of optical coherence tomography (OCT) and to correlate the results with conventional histological and immunocytochemical staining. Method: Osteochondral blocks were harvested from 20 patients undergoing total knee replacement and trimmed to 2 x 2 cm. Under sterile conditions, chondral defects of 8 mm diameter were either filled with a collagen type I gel plug seeded with autologous chondrocytes (2 x 10(5)/mL gel), or with a corresponding gel plug which was stabilised by a 20-fold compression. Of each group, 5 specimens were cultivated for 6 weeks under standardised in vitro conditions (37 degrees C, 5% CO2, humidified atmosphere), while the remaining 5 specimens were implanted subcutaneously in nude mice (BALBc -/-). Immediately after recovery, the repair tissue and bonding zones were investigated by OCT. Subsequently, specimens were decalcified and investigated by H&E staining and collagen type II immunostaining. The results of OCT and conventional staining were correlated. Results: By OCT, repair tissue could be investigated up to 1.6 mm in depth, physically limited by the utilised OCT system. In the denser hyaline cartilage regions, OCT resolution was reduced. Regardless of cultivation (in vitro or nude mouse), ultrastructural features of the repair tissue could be demonstrated. In particular, ultrastructural differences between the two investigated collagen gels could be detected. Moreover, the bonding region between repair tissue and hyaline cartilage could be evaluated by OCT investigation. The results of the OCT measurements were confirmed by H&E and collagen type II immunostaining. Conclusion: By OCT, repair tissue generated by the treatment of cartilage defects with tissue-engineered matrix systems could be evaluated in vitro. Future studies may show if repair tissue quality may be monitored in situ by OCT.
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收藏
页码:788 / 792
页数:5
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