S. Otsuki (Osaka, JP)

Osaka Medical and Pharmaceutical University
Degree Year Conferred Field of Study M.D. 1998 Orthopedic Medicine Ph.D. 2008 Orthopedic Medicine Education and Professional Experience 1992 - 1998 Medical School; Osaka Medical College 1998 - 1999 Department of Orthopedic Surgery; Osaka Medical College; Japan 2003 - 2007 Osaka Medical College Graduate School; Japan 2007 - 2008 Research Associate; The Scripps Research Institute; La Jolla; CA 2008 - 2010 Senior Research Associate; The Scripps Research Institute; La Jolla; CA 2011 - present Assistant Professor Department of Orthopedic Surgery; Osaka Medical College Honors and Members 1998 Member; The Japanese Orthopaedic Association 2005 Orthopaedic Specialist of The Japanese Orthopaedic Association 2005 The Certifying Physician of Rheumatoid Arthritis 2007 Member; Orthopaedic Research Society 2008 Member; Osteoarthritis Research Society International Postdoctoral Fellow of Arthritis Foundation ( - 2010) Title: Extracellular sulfatases support cartilage homeostasis by regulating BMP and FGF signaling pathways 2010 Japan Orthopedic and Traumatology Foundation Award 115th The Central Japan Orthopedic Trauma society Award 2011 17th The Japan Society of Cartilage Metabolism Award

Presenter Of 1 Presentation

Cartilage and Meniscus

P-24.1.5 - Novel Meniscal Scaffold Implantation for Irreparable Meniscal Tear Treatment: From Bench to Clinical Trial

Abstract

Purpose

Purpose: The meniscus plays a role in knee load distribution and stabilization. We had shown that polyglycolic acid (PGA) covered with L-lactide-ε-caprolactone copolymer (P(LA/CL)) scaffold was the most effective meniscal defect regeneration in a rabbit model. The purpose of this study was to show the evaluation with meniscal scaffold in a minipig followed for 48 weeks post-implantation and introduce the clinical trial in its first stage.

Methods and Materials

Materials and Methods: The meniscal scaffold was supplied with 50% of strain level and compared with native porcine menisci during biomechanical analysis. Scaffold pieces were incubated in chondrocytes, and the cell viability was evaluated using live/dead assay. Furthermore, 10 mm of meniscus was resected as the defect model in the minipig. PGA scaffold was implanted on the defect and sutured side by side and peripheral rim. Histological analysis was performed till 48 weeks post-scaffold implantation. Finally, arthroscopic implantation has been introduced as the first step of clinical trial.

Results

Results: In vitro, the stress-strain curve of scaffold was comparable with that of native porcine menisci; cells migrated into and were viable in the scaffold. In vivo, the implanted scaffold was covered with the original tissue at 4 weeks and many cells were observed in the implanted scaffold, which was getting absorbed in newly formed tissue. The meniscal shape was preserved after implantation, whereas partial meniscectomy had shrunk at 48 weeks post-implantation (Fig. 1). In the clinical trial, implantation was performed via arthroscopic surgery. The segmented meniscal scaffold was brought to an appropriate position in the knee joint, and rein-type suture was pulled not to push the peripheral side during inside-out suturing (Fig. 2).

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Conclusion

Conclusion: The novel meniscal PGA scaffold improved the initial strength and cell viability in vitro, and triggered meniscal regeneration in vivo. The clinical trial was initiated, and introduced a surgical procedure of scaffold implantation.

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