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[pH对锶离子与去细胞小肠黏膜下层海绵支架螯合作用的影响]

[Effect of pH on the chelation between strontium ions and decellularized small intestinal submucosal sponge scaffolds].

作者信息

Li Y K, Wang M, Tang L, Liu Y H, Chen X Y

机构信息

Department of Prosthodontics, Peking University School and Hospital of Stomatology & National Center of Stomatology & National Clinical Research Center for Oral Diseases & National Engineering Research Center of Oral Biomaterials and Digital Medical Devices & Beijing Key Laboratory of Digital Stomatology, Beijing 100081, China.

Department of Stomatology, Beijing Chao-Yang Hospital, Capital Medical University, Beijing 100020, China.

出版信息

Beijing Da Xue Xue Bao Yi Xue Ban. 2023 Feb 18;55(1):44-51. doi: 10.19723/j.issn.1671-167X.2023.01.007.

Abstract

OBJECTIVE

To investigate the preparation of decellularized small intestinal submucosa (dSIS) sponge scaffolds with chelated strontium (Sr) ions at different pH values, and to select the appropriate pH values for synthesizing Sr/dSIS scaffolds using the physicochemical properties and biocompatibility of the scaffolds as evaluation indexes.

METHODS

(1) Sr/dSIS scaffolds preparation and grouping: After mixing dSIS solution and strontium chloride solution in equal volumes, adjusting pH of the solution to 3, 5, 7, and 9 respectively, porous scaffolds were prepared by freeze-drying method after full reaction at 37℃, which were named Sr/dSIS-3, -5, -7, and -9 respectively, and the dSIS scaffolds were used as the control group. (2) Physicochemical property evaluation: The bulk morphology of the scaffolds was observed in each group, the microscopic morphology analyzed by scanning electron microscopy, and the porosity and pore size determined, the surface elements analyzed by energy spectroscopy, the structure of functional groups analyzed by infrared spectroscopy, the chelation rate determined by atomic spectrophotometry, the water absorption rate detected by using specific gravity method, and the compression strength evaluated by universal mechanical testing machine.(3) Biocompatibility evaluation: The cytotoxicity and proliferative effect to bone mesenchymal stem cells (BMSCs) of each group were evaluated by Calcein-AM/PI double staining method.

RESULTS

Scanning electron microscopy showed that the scaffolds of each group had an interconnected three-dimensional porous structure with no statistical difference in pore size and porosity. Energy spectrum analysis showed that strontium could be detected in Sr/dSIS-5, -7 and -9 groups, and strontium was uniformly distributed in the scaffolds. Functional group analysis further supported the formation of chelates in the Sr/dSIS-5, -7 and -9 groups. Chelation rate analysis showed that the Sr/dSIS-7 group had the highest strontium chelation rate, which was statistically different from the other groups ( < 0.05). The scaffolds in all the groups had good water absorption. The scaffolds in Sr/dSIS-5, -7 and -9 groups showed significantly improved mechanical properties compared with the control group ( < 0.05). The scaffolds in all the groups had good biocompatibility, and the Sr/dSIS-7 group showed the best proliferation of BMSCs.

CONCLUSION

When pH was 7, the Sr/dSIS scaffolds showed the highest strontium chelation rate and the best proliferation effect of BMSCs, which was the ideal pH value for the preparation of the Sr/dSIS scaffolds.

摘要

目的

研究在不同pH值下制备含螯合锶(Sr)离子的去细胞小肠黏膜下层(dSIS)海绵支架,并以支架的理化性质和生物相容性为评价指标,选择合成Sr/dSIS支架的合适pH值。

方法

(1)Sr/dSIS支架制备及分组:将dSIS溶液与氯化锶溶液等体积混合后,分别将溶液pH值调至3、5、7和9,在37℃充分反应后采用冷冻干燥法制备多孔支架,分别命名为Sr/dSIS-3、-5、-7和-9,将dSIS支架作为对照组。(2)理化性质评价:观察各组支架的大体形态,采用扫描电子显微镜分析微观形态,测定孔隙率和孔径,采用能谱分析表面元素,采用红外光谱分析官能团结构,采用原子分光光度法测定螯合率,采用比重法检测吸水率,采用万能材料试验机评估抗压强度。(3)生物相容性评价:采用钙黄绿素-AM/PI双染法评价各组对骨髓间充质干细胞(BMSCs)的细胞毒性和增殖作用。

结果

扫描电子显微镜显示各组支架均具有相互连通的三维多孔结构,孔径和孔隙率无统计学差异。能谱分析显示在Sr/dSIS-5、-7和-9组中可检测到锶,且锶在支架中均匀分布。官能团分析进一步支持了Sr/dSIS-5、-7和-9组中螯合物的形成。螯合率分析显示Sr/dSIS-7组锶螯合率最高,与其他组有统计学差异(<0.05)。所有组的支架均具有良好的吸水性。Sr/dSIS-5、-7和-9组的支架与对照组相比力学性能显著改善(<0.05)。所有组的支架均具有良好的生物相容性,且Sr/dSIS-7组对BMSCs的增殖作用最佳。

结论

pH值为7时,Sr/dSIS支架锶螯合率最高,对BMSCs的增殖作用最佳,是制备Sr/dSIS支架的理想pH值。

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