海藻酸钠/富血小板血浆sr 2+多孔微载体的体外降解行为和生物相容性

Jinxing Chen, Zhihua Zhou, Wei Wu, Wenjuan Liu, Zemei Fang, Yan Gan, Jianjun Fang
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引用次数: 0

摘要

摘要多孔微载体作为细胞载体在组织工程领域引起了广泛的研究兴趣。采用乳化法结合冷冻干燥法制备了海藻酸钠(SA)和海藻酸钠/富血小板血浆(SA/PRP)多孔微载体(SA- sr2 +和SA/PRP- sr2 +)。研究了SA- sr2 +和SA/PRP-Sr2+多孔微载体在磷酸盐缓冲盐水(PBS)中的体外降解行为。通过培养大鼠骨髓间充质干细胞(rBMSCs),研究了SA- sr2 +和SA/PRP-Sr2+多孔微载体的细胞增殖能力和成骨活性。在降解过程中,SA- sr2 +和SA/PRP-Sr2+多孔微载体的降解行为表现出相似的变化,包括PBS的pH、失重和形貌的变化。降解6周后,SA- sr2 +和SA/PRP-Sr2+多孔微载体部分塌陷。在培养14 d时,SA/PRP-Sr2+多孔微载体的细胞增殖能力和骨诱导能力均高于SA- sr2 +多孔微载体。关键词:海藻酸钠富血小板血浆微载体体外降解生物相容性免责声明作为对作者和研究人员的服务,我们提供此版本的已接受稿件(AM)。在最终出版版本记录(VoR)之前,将对该手稿进行编辑、排版和审查。在制作和印前,可能会发现可能影响内容的错误,所有适用于期刊的法律免责声明也与这些版本有关。本工作得到湖南省教育厅科研基金(No. 21A0323)和国家化学工程与材料实验教学示范中心的资助。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
In-Vitro Degradation Behaviors and Biocompatibility of Sodium Alginate/Platelet-Rich Plasma-Sr 2+ Porous Microcarriers
AbstractPorous microcarriers as cell carriers have attracted extensive research interest in tissue engineering. In this work sodium alginate (SA) and sodium alginate/platelet-rich plasma (SA/PRP) porous microcarriers cross-linked by SrCl2 (SA-Sr2+ and SA/PRP-Sr2+) were prepared using an emulsion method combined with a freeze-drying method. The in-vitro degradation behaviors of the SA-Sr2+ and SA/PRP-Sr2+ porous microcarriers in phosphate-buffered saline (PBS) were investigated. The cell proliferation ability and osteogenic activity of the SA-Sr2+ and SA/PRP-Sr2+ porous microcarriers were investigated by culturing rat bone marrow mesenchymal stem cells (rBMSCs). During the degradation process, the degradation behaviors, including changes of the pH of the PBS and the weight loss and morphology, of both the SA-Sr2+ and SA/PRP-Sr2+ porous microcarriers showed a similar change. After 6 weeks of degradation, parts of both the SA-Sr2+ and SA/PRP-Sr2+ porous microcarriers collapsed. The SA/PRP-Sr2+ porous microcarriers showed higher cell proliferation ability and osteoinductive ability than the SA-Sr2+ porous microcarriers during a culture time of 14 days.Keywords: sodium alginateplatelet-rich plasmaporous microcarriersin-vitro degradationbiocmpatibilityDisclaimerAs a service to authors and researchers we are providing this version of an accepted manuscript (AM). Copyediting, typesetting, and review of the resulting proofs will be undertaken on this manuscript before final publication of the Version of Record (VoR). During production and pre-press, errors may be discovered which could affect the content, and all legal disclaimers that apply to the journal relate to these versions also. AcknowledgementsThis work was financially supported by the Scientific Research Fund of the Hunan Provincial Education Department (No. 21A0323) and the National Experimental Teaching Demonstration Center of Chemical Engineering and Materials.
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