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Preparation and Characterization of a Brain Decellularized Scaffold |
Zheng Fangping1*, Mao Kaili1, Zhao Yingzheng2 |
1Department of Pharmacy, People's Hospital of Quzhou, Quzhou 324000, Zhejiang, China 2School of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou 325025, Zhejiang, China |
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Abstract The aim of this work is to prepare a brain decellularized scaffold by chemical extraction combined with oscillation, and to perform preliminary characterization. Twenty SD rats were divided into decellularization and control group. In the decellularization group, the brain extracellular matrix (dBECM) was prepared by chemical extraction combined with oscillation, successively with 3% TritionX-100, 1%SDS,4% deoxycholic acid sodium and deionized water in 37℃. The microscopic morphology of dBECM was observed by scanning electron microscopy. The decellularization was analyzed by HE staining and DAPI staining. The components were identified by Masson staining and immunofluorescence staining. A lot of collagen fibers could be seen with HE and immunohistochemistry stain but no visible cell nuclei remained after decellularization. The degree of decellularization was about 99%. Masson staining and immunofluorescence staining revealed that dBECM retained elastin (4±1.1%), laminin (19±1.6%), fibronectin (9±2.1%) and collagen IV (16±1.9%). In conclusion, the method of chemical extraction combined with oscillation can effectively remove all cellular components while retain the extracellular matrix and three-dimensional structure. It is a convenient and ideal preparation method on decellularized brain scaffold for tissue engineering.
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Received: 11 April 2017
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