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Effect of 3 Preservation Methods (Freezing, Cryopreservation, and Freezing plus Irradiation) on Human Menisci Ultrastructure An Ex Vivo Comparative Study With Fresh Tissue as a Gold Standard

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  • معلومة اضافية
    • Contributors:
      Institut des Sciences du Mouvement Etienne Jules Marey (ISM); Aix Marseille Université (AMU)-Centre National de la Recherche Scientifique (CNRS); Institut du Mouvement et de l’appareil Locomoteur Hôpital Sainte-Marguerite - APHM (IML); Assistance Publique - Hôpitaux de Marseille (APHM)-Hôpital Sainte-Marguerite CHU - APHM (Hôpitaux Sud )-Rhumatologie Sainte- Marguerite - APHM ( Hôpitaux Sud); Assistance Publique - Hôpitaux de Marseille (APHM)-Hôpital Sainte-Marguerite CHU - APHM (Hôpitaux Sud ); Institut de Chimie de Clermont-Ferrand (ICCF); SIGMA Clermont (SIGMA Clermont)-Institut de Chimie - CNRS Chimie (INC-CNRS)-Université Clermont Auvergne 2017-2020 (UCA 2017-2020 )-Centre National de la Recherche Scientifique (CNRS)
    • بيانات النشر:
      HAL CCSD
      SAGE Publications (UK and US)
    • الموضوع:
      2018
    • Collection:
      Aix-Marseille Université: HAL
    • نبذة مختصرة :
      International audience ; Background: Three main meniscus preservation methods have been advocated: freezing (-80 degrees C), freezing with gamma irradiation (-80 degrees C + 25 kGy), and cryopreservation (-140 degrees C). Hypothesis: All preservation methods will result in structural and architectural properties similar to those of fresh meniscus, defined as the gold standard. Study Design: Controlled laboratory study. Methods: Five human intact menisci were collected from 5 patients undergoing total knee arthroplasty. The inclusion criteria were patients <70 years old with primary unilateral (medial) femorotibial knee osteoarthritis and without surgical or traumatic history on the operated knee. Four cubes (9 mm(3)) were cut inside of the white, or avascular, area of each specimen's middle horn and divided into 4 groups: fresh control, frozen (-80 degrees C), cryopreserved (-140 degrees C), and frozen + irradiated (-80 degrees C + 25 kGy). Specimens of the control group were evaluated at day 1, and specimens from the frozen, cryopreserved, and frozen + irradiated groups were evaluated after 1 month of storage. Evaluation was performed with electron microscopy according a validated protocol to analyze (1) mean diameters of the collagen fibers in longitudinal and transverse sections in 5 points per section and (2) validated architectural scores. Results: No significant difference was found between the control and cryopreserved groups regarding mean transverse and longitudinal diameters (transverse: 95.39 15.87 nm vs 99.62 19.23 nm, P = .1; longitudinal: 96.31 +/- 13.96 nm vs 94.57 +/- 16.42 nm, P = .1). Significant differences were found between the control and frozen groups (transverse: 95.39 +/- 15.87 nm vs 70.20 +/- 13.94 nm, P < .001; longitudinal: 96.31 +/- 13.96 nm vs 71.28 +/- 10.64 nm, P < .001) and the control and frozen + irradiated groups (transverse: 95.39 +/- 15.87 nm vs 63.1 +/- 15.57 nm, P < .001; longitudinal: 96.31 +/- 13.96 nm vs 60.9 +/- 14.8 nm, P < .001). Regarding ...
    • Relation:
      hal-01960535; https://hal.science/hal-01960535; https://hal.science/hal-01960535/document; https://hal.science/hal-01960535/file/jacquet2018.pdf
    • الرقم المعرف:
      10.1177/0363546518790504
    • الدخول الالكتروني :
      https://hal.science/hal-01960535
      https://hal.science/hal-01960535/document
      https://hal.science/hal-01960535/file/jacquet2018.pdf
      https://doi.org/10.1177/0363546518790504
    • Rights:
      info:eu-repo/semantics/OpenAccess
    • الرقم المعرف:
      edsbas.F1D4A51A