2016
DOI: 10.1093/icvts/ivw132
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Partial replacement of left hemidiaphragm in dogs by either cryopreserved or decellularized heterograft patch

Abstract: The gross healing process in the decellularized heterograft is similar to the cryopreserved diaphragm but with fewer inflammatory cells and foreign body granulomas on histology. Both of them can be used instead of bioprostheses with regard to the fact that the decellularized patch technique is more complex and expensive. It is recommended to compare them with commercial bioprostheses.

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Cited by 12 publications
(18 citation statements)
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“…According to the literature, the hemidiaphragm of a deceased donor was also considered for tissue engineering purposes. Davari et al, [87] evaluated the effectiveness of cryopreservation versus decellularization before implanting derived hemidiaphragm patches in a canine defect model. Briefly, cryopreservation consisted in freezing the grafts at −80 °C and preserving them for up to 2 months; while decellularization was performed according to a detergent–enzymatic protocol consisting of a dH 2 O soaking-phase followed by 4% sodium deoxycholate and 2000 kU of DNase-I in 1 mol/L NaCl.…”
Section: Skeletal Musclementioning
confidence: 99%
“…According to the literature, the hemidiaphragm of a deceased donor was also considered for tissue engineering purposes. Davari et al, [87] evaluated the effectiveness of cryopreservation versus decellularization before implanting derived hemidiaphragm patches in a canine defect model. Briefly, cryopreservation consisted in freezing the grafts at −80 °C and preserving them for up to 2 months; while decellularization was performed according to a detergent–enzymatic protocol consisting of a dH 2 O soaking-phase followed by 4% sodium deoxycholate and 2000 kU of DNase-I in 1 mol/L NaCl.…”
Section: Skeletal Musclementioning
confidence: 99%
“…The procedure of tissue decellularization is to effectively remove cellular components and residual DNA, but keep the physicochemical structure of the ECM to support seeding cells' survival in a 3D architecture [ 25 , 26 ]. Our protocol includes (1) excision of the rat hemidiaphragm in a sterile environment; (2) put the diaphragm in a tube with 40 mL PBS (50 mL, BD); (3) transfer the diaphragm into a 50 mL tube prefilled with 0.5% SDS; (4) attach tube to rocker (Nutator, number 421105, Beckton Dickinson, MD) and rotate for 0.5/sec for 24 hours; (5) transfer the diaphragm to a fresh tube prefilled with 0.5% sodium dodecyl sulfate (SDS) and rotate for 24 hours; (6) transfer the decellularized tissue into a 50 mL tube with sterile PBS and wash during rotation for 24 hours; and (7) leave the tissue in PBS and store at 4°C.…”
Section: Methodsmentioning
confidence: 99%
“…Decellularized ECM scaffolds have the potential of regenerating the structure and function of their native tissue over commercially available matrices from other tissues. Those decellularized ECM scaffolds have been used in combination with stem cells to construct composite tissues that have been utilized successfully in tissue repair, including diaphragmatic repair [ 23 25 ]. While the current practice of PTFE/Gore-tex® patch repair is reasonably effective with acceptable rates of recurrence and infection, a simple biologic tissue could represent an advantage, especially on the large diaphragmatic defects.…”
Section: Introductionmentioning
confidence: 99%
“…Once deceullularisation has removed cellular material, the remaining ECM retains the native 3D microstructure, molecular composition and growth factors that support skeletal muscle regeneration [25]. Decellularization protocols vary between studies but commonly include the use of detergents and enzymes, such as DNase and Trypsin; the effectiveness of the decellularization protocol is central to minimising scaffold immunogenicity [27][28][29][30][31].…”
Section: Decellularised Scaffoldsmentioning
confidence: 99%