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磷酸二钙陶瓷的体外离子吸附及细胞相容性

In vitro ion adsorption and cytocompatibility of dicalcium phosphate ceramics.

作者信息

Schamel Martha, Barralet Jake E, Groll Jürgen, Gbureck Uwe

机构信息

Department of Functional Materials in Medicine and Dentistry, University of Würzburg, 97070 Würzburg, Germany.

Department of Surgery, Faculty of Medicine, Faculty of Dentistry, McGill University, Montreal, Quebec H3A 2B2 Canada.

出版信息

Biomater Res. 2017 Jun 8;21:10. doi: 10.1186/s40824-017-0096-4. eCollection 2017.

Abstract

BACKGROUND

cell testing of degradable bioceramics such as brushite or monetite is often challenging due to the ion release into or adsorption from the culture medium. These ionic changes are then mostly responsible for cell proliferation and activity, which prohibits the investigation of effects originating from surface topography or further material modifications.

METHODS

Here, we aimed to solve this problem by developing a pre-conditioning regime following the repeated immersion of brushite and monetite samples in various Ca, Mg and PO containing electrolytes, followed by studying ion adsorption / release as well as changes in phase composition and in vitro cytocompatibility with MG63 cells.

RESULTS

The results demonstrated that by using DMEM cell culture medium in a ratio of 10 ml/sample was sufficient to minimize changes of ionic composition after 7 d with a daily change of the medium. This leads to changes of the surface composition with dissolution of the brushite phase. In turn, this also positively influences the cytocompatibility with a 2-3 fold higher cell number and cell activity on the DMEM pretreated surfaces.

CONCLUSIONS

Controlled sample washing prior to cell testing using DMEM medium seems to be a valuable procedure not only to stabilize the pH during cell culture but also to maintain ion concentrations within a cell friendly range.

摘要

背景

由于离子释放到培养基中或从培养基中吸附,对诸如透钙磷石或磷酸氢钙二水合物等可降解生物陶瓷进行细胞测试往往具有挑战性。这些离子变化大多是细胞增殖和活性的原因,这阻碍了对源自表面形貌或进一步材料改性的影响的研究。

方法

在此,我们旨在通过开发一种预处理方案来解决这个问题,该方案包括将透钙磷石和磷酸氢钙二水合物样品反复浸入各种含钙、镁和磷的电解质中,然后研究离子吸附/释放以及相组成变化和与MG63细胞的体外细胞相容性。

结果

结果表明,以10 ml/样品的比例使用DMEM细胞培养基足以在每天更换培养基的情况下,在7天后将离子组成的变化降至最低。这导致透钙磷石相溶解,从而使表面组成发生变化。反过来,这也对细胞相容性产生积极影响,在DMEM预处理的表面上,细胞数量和细胞活性提高了2至3倍。

结论

在细胞测试前使用DMEM培养基对样品进行受控洗涤似乎是一种有价值的方法,不仅可以在细胞培养过程中稳定pH值,还可以将离子浓度维持在细胞友好的范围内。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a16c/5465584/d2a10712e70c/40824_2017_96_Fig1_HTML.jpg

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