Feasibility and limitations of the round robin test for assessment of in vitro chondrogenesis evaluation protocol in a tissue-engineered medical product

Author:

Yokoi Masako1,Hattori Koji2,Narikawa Koichi2,Ohgushi Hajime3,Tadokoro Mika3,Hoshi Kazuto4,Takato Tsuyoshi4,Myoui Akira5,Nanno Katsuhiko5,Kato Yukio6,Kanawa Masami6,Sugawara Katsura7,Kobo Tomoko7,Ushida Takashi1

Affiliation:

1. Centre for Disease Biology and Integrative Medicine (CDBIM); Graduate School of Medicine; University of Tokyo; Japan

2. Department of Orthopaedic Surgery; Nara Medical University; Japan

3. Health Research Institute; National Institute of Advanced Industrial Science and Technology; Hyogo; Japan

4. Division of Tissue Engineering; University of Tokyo Hospital; Japan

5. Medical Centre for Translational Research; Osaka University Hospital; Japan

6. Department of Dental and Medical Biochemistry; Graduate School of Biomedical Sciences; Hiroshima University; Japan

7. Japan Tissue Engineering Co. Ltd; Aichi; Japan

Publisher

Wiley

Subject

Biomedical Engineering,Biomaterials,Medicine (miscellaneous)

Reference37 articles.

1. ASTM F 2150-07 Standard guide for characterization and testing of biomaterial scaffolds used in tissue engineered medical products ASTM West Conshohocken, PA, USA

2. ASTM F2312-04 Standard terminology relating to tissue engineered medical products ASTM West Conshohocken, PA, USA

3. ASTM F2027-00 Standard guide for characterization and testing of substrate materials for tissue engineered medical products ASTM West Conshohocken, PA, USA

4. ASTM F2210-02 Standard guide for processing cells, tissues, and organs for use in tissue engineered medical products ASTM West Conshohocken, PA, USA

5. ASTM F2211-04 Standard classification for tissue engineered medical products (TEMPs) ASTM West Conshohocken, PA, USA

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