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10.1186/s40001-017-0272-y

http://scihub22266oqcxt.onion/10.1186/s40001-017-0272-y
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C5591503!5591503 !28886732
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suck abstract from ncbi


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pmid28886732
      Eur+J+Med+Res 2017 ; 22 (1 ): 31
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  • Optimized protocol for whole organ decellularization #MMPMID28886732
  • Schmitt A ; Csiki R ; Tron A ; Saldamli B ; Tübel J ; Florian K ; Siebenlist S ; Balmayor E ; Burgkart R
  • Eur J Med Res 2017[Sep]; 22 (1 ): 31 PMID28886732 show ga
  • BACKGROUND: The idea of tissue decellularization to gain matrices for tissue engineering is promising. The aim of the present study is to establish a safe and reproducible protocol for solid tissue decellularization that prevents the architecture of the matrix with the inherent vascular network. METHODS: The study was performed in rat kidneys which were decellularized by a SDS-based perfusion protocol. Perfusion time and SDS concentration were systematically changed to obtain the shortest and most gentle protocol that leads to complete decellularization. RESULTS: We investigated kinetics of protein elution, decellularization success, and remaining cell toxicity. This resulted in a reproducible protocol, leading to safe decellularization with prevention of the inherent vascular network, without remaining detectable cell toxicity. The established protocol leads to solid tissue decellularization in only 7 h, which is by far shorter than the previously published methods. CONCLUSION: The established technique has the potential to become a relevant platform technology for tissue engineering of solid tissues. It provides a solution for the yet-unsolved problem of vascularization.
  • |*Tissue Scaffolds [MESH]
  • |Animals [MESH]
  • |Histological Techniques/*methods [MESH]
  • |Kidney/*cytology [MESH]
  • |Rats [MESH]
  • |Rats, Sprague-Dawley [MESH]


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