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透明掺镍 TiO2 薄膜在硼硅酸盐玻璃上的生长、分化和成骨细胞迁移。

Growth, differentiation, and migration of osteoblasts on transparent Ni doped TiO2 thin films deposited on borosilicate glass.

机构信息

CSIR-Centre for Cellular and Molecular Biology, Hyderabad, India.

出版信息

J Biomed Mater Res A. 2012 May;100(5):1168-78. doi: 10.1002/jbm.a.34061. Epub 2012 Feb 15.

Abstract

A simple and cost effective dip coating method was used to deposit thin films of amorphous (AM) or anatase (AN) titanium dioxide (TiO(2)) on borosilicate glass substrates, either with or without prior doping of TiO(2) with nickel (Ni) cations by a specially designed sol gel technique. The objective of the study was to compare the physicochemical and biological properties of these films and assess their use in orthopedic implants or for in vitro cell biological studies. Analytical techniques such as XRD and XPS, in combination with ATR-FTIR and SEM revealed that only AN films, prepared by controlled heating up to 450°C, irrespective of prior doping with Ni, contained significant crystalline structures of variable morphologies. This observation could be linked to the carbon and oxygen contents and the availability of functional groups in the films. Cell biological studies revealed that Ni doping of TiO(2) in both AM and AN films improved the adhesion, spreading, proliferation, differentiation, and migration of MC3T3 cells. Our studies provide a new approach to prepare optically transparent metal surfaces, with tunable physicochemical properties, which could be suitable for eliciting optimal osteoinductive cell responses and permit the detailed in vitro cell biological studies of osteoblasts.

摘要

一种简单且经济有效的浸涂方法被用于在硼硅酸盐玻璃基底上沉积非晶态(AM)或锐钛矿(AN)二氧化钛(TiO2)薄膜,无论是通过专门设计的溶胶凝胶技术预先掺杂 TiO2 用镍(Ni)阳离子还是不掺杂。研究的目的是比较这些薄膜的物理化学和生物学性质,并评估它们在骨科植入物或体外细胞生物学研究中的用途。分析技术,如 XRD 和 XPS,与 ATR-FTIR 和 SEM 结合使用,表明只有通过控制加热至 450°C 制备的 AN 薄膜,无论是否预先掺杂 Ni,都含有具有不同形态的显著结晶结构。这种观察结果可能与薄膜中的碳和氧含量以及官能团的可用性有关。细胞生物学研究表明,在 AM 和 AN 薄膜中掺杂 Ni 可以提高 MC3T3 细胞的粘附、铺展、增殖、分化和迁移。我们的研究提供了一种新的方法来制备具有可调物理化学性质的光学透明金属表面,这些表面可能适合引起最佳的成骨细胞反应,并允许对成骨细胞进行详细的体外细胞生物学研究。

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