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Development of a Cost-Effective and Simple Protocol for Decellularization and Preservation of Human Amniotic Membrane As a Soft Tissue Replacement and Delivery System for Bone Marrow Stromal Cells Publisher Pubmed



Gholipourmalekabadi M1, 2 ; Mozafari M1, 3 ; Salehi M2 ; Seifalian A1 ; Bandehpour M2, 4 ; Ghanbarian H2, 4 ; Urbanska AM5 ; Sameni M2 ; Samadikuchaksaraei A6, 7 ; Seifalian AM1, 8
Authors

Source: Advanced Healthcare Materials Published:2015


Abstract

The aim of this study is to develop a simple andcost-effective method for decellularization and preservation of human amniotic membrane (HAM) as a soft tissue replacement and a delivery system for stem cells. The HAM is decellularized (D) using new chemical and mechanical techniques. The decellularization scaffold is evaluated histologically and fully characterized. The cell adhesion and proliferation on the scaffold are also investigated and the biocompatibility of D tissues is evaluated in vivo. The histological studies reveal that the cells are successfully removed from the D tissue. The DNA extraction shows more than 95% cell removal (p = 0.001). The in vitro results indicate that the decellularisation process does not deteriorate the mechanical properties of the tissue, whereas it increases the in vitro biodegradation value (p < 0.05). In the D samples, there is no significant cytotoxicity, and no changes are found in the rate of cell proliferation (p > 0.05). Immunohistochemistry staining indicates that all the tested components remain unchanged within the D tissues. The count of inflammatory cells show that the decellularization process slightly increases the biocompatibility of the tissue after 7 days post-surgery. The results indicate that scaffold proves to be reproducible, rapid, and cost-effective, with a potential role for clinical application. Human amniotic membrane (HAM) is successfully decellularized by non-enzymatic agents as a cost-effective and simple protocol. The samples are stained with immunohistochemistry (IHC), hematoxylin and eosin, and DAPI (4′,6-diamidino-2-phenylindole) to evaluate histologically the removal of cells from tissue. The results show the fully removal of cells from the tissue, while the extracellular matrix of the HAM remains unchanged. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
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