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Qu, Jin

Mayo Clinic

Division of Orthopedic Research, Department of Orthopedic Surgery, Biomechanics & Tendon and Soft Tissue Laboratories, Mayo Clinic, 200 First Street SW, Rochester, Minnesota, 55905.

Citations 2

Effects of trypsinization and mineralization on intrasynovial tendon allograft healing to bone
Alphen, Nick A. van, Thoreson, Andrew R. , Chen, Qingshan , An, Kai‐Nan, Amadio, Peter C. , Zhao, Chunfeng , Qu, Jin, Qu, Jin , An, Kai‐Nan , Schmid, Thomas M

Journal of Orthopaedic Research | January 21, 2015 | Volume: 33 | Issue: 4 | Pages: 468-474

10.1002/jor.22779 Get It

ABSTRACTThe purpose of the current study was to develop a novel technology to enhance tendon‐to‐bone interface healing by trypsinizing and mineralizing (TM) an intrasynovial tendon allograft in a rabbit bone tunnel model. Eight rabbit flexor digitorum profundus (FDP) tendons were used to optimize the trypsinization process. An additional 24 FDP tendons were stratified into control and TM groups; in each group, 4 tendons were used for in vitro evaluation of TM and 8 were transplanted into proximal tibial bone tunnels in rabbits. The samples were evaluated histologically and with mechanical testing at postoperative week 8. Maximum failure strength and linear stiffness were not significantly different between the control and TM tendons. A thin fibrous band of scar tissue formed at the graft‐to‐bone interface in the control group. However, only the TM group showed obvious new bone formation inside the tendon graft and a visible fibrocartilage layer at the bone tunnel entrance. This study is the first to explore effects of TM on the intrasynovial allograft healing to a bone tunnel. TM showed beneficial effects on chondrogenesis, osteogenesis, and integration of the intrasynovial tendon graft, but mechanical strength was the same as the control tendons in this short‐term in vivo study. © 2015 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 33:468–474, 2015.
Tendon gradient mineralization for tendon to bone interface integration
Thoreson, Andrew R. , Chen, Qingshan , An, Kai‐Nan, Amadio, Peter C. , Zhao, Chunfeng , Qu, Jin, Qu, Jin , An, Kai‐Nan

Journal of Orthopaedic Research | August 12, 2013 | Volume: 31 | Issue: 11 | Pages: 1713-1719

10.1002/jor.22412 Get It

AbstractTendon‐to‐bone integration is a great challenge for tendon or ligament reconstruction regardless of use of autograft or allograft tendons. We mineralized the tendon, thus transforming the tendon‐to‐bone into a “bone‐to‐bone” interface for healing. Sixty dog flexor digitorum profundus (FDP) tendons were divided randomly into five groups: (1) normal FDP tendon, (2) CaP (non‐extraction and mineralization without fetuin), (3) CaPEXT (Extraction by Na2HPO4 and mineralization without fetuin), (4) CaPFetuin (non‐extraction and mineralization with fetuin), and (5) CaPEXTFetuin (extraction and mineralization with fetuin). The calcium and phosphate content significantly increased in tendons treated with combination of extraction and fetuin compared to the other treatments. Histology also revealed a dense mineral deposition throughout the tendon outer layers and penetrated into the tendon to a depth of 200 µm in a graded manner. Compressive moduli were significantly lower in the four mineralized groups compared with normal control group. No significant differences in maximum failure strength or stiffness were found in the suture pull‐out test among all groups. Mineralization of tendon alters the interface from tendon to bone into mineralized tendon to bone, which may facilitate tendon‐to‐bone junction healing following tendon or ligament reconstruction. © 2013 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 31:1713–1719, 2013