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Assessing the effects of intratendinous genipin injections: Mechanical augmentation and spatial distribution in an ex vivo degenerative tendon model

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  • Timo Tondelli
  • Tobias Götschi
  • Roland S Camenzind
  • Jess G Snedeker

Abstract

Background: Tendinopathy is a common musculoskeletal disorder and current treatment options show limited success. Genipin is an effective collagen crosslinker with low cytotoxicity and a promising therapeutic strategy for stabilizing an intratendinous lesion. Purpose: This study examined the mechanical effect and delivery of intratendinous genipin injection in healthy and degenerated tendons. Study design: Controlled laboratory study Methods: Bovine superficial digital flexor tendons were randomized into four groups: Healthy control (N = 25), healthy genipin (N = 25), degenerated control (N = 45) and degenerated genipin (N = 45). Degeneration was induced by Collagenase D injection. After 24h, degenerated tendons were subsequently injected with either 0.2ml of 80mM genipin or buffer only. 24h post-treatment, samples were cyclically loaded for 500 cycles and then ramp loaded to failure. Fluorescence and absorption assays were performed to analyze genipin crosslink distribution and estimate tissue concentration after injection. Results: Compared to controls, genipin treatment increased ultimate force by 19% in degenerated tendons (median control 530 N vs. 633 N; p = 0.0078). No significant differences in mechanical properties were observed in healthy tendons, while degenerated tendons showed a significant difference in ultimate stress (+23%, p = 0.049), stiffness (+27%, p = 0.037), work to failure (+42%, p = 0.009), and relative stress relaxation (-11%, p

Suggested Citation

  • Timo Tondelli & Tobias Götschi & Roland S Camenzind & Jess G Snedeker, 2020. "Assessing the effects of intratendinous genipin injections: Mechanical augmentation and spatial distribution in an ex vivo degenerative tendon model," PLOS ONE, Public Library of Science, vol. 15(4), pages 1-15, April.
  • Handle: RePEc:plo:pone00:0231619
    DOI: 10.1371/journal.pone.0231619
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