Cell responses on a H2Ti3O7 nanowire film

被引:4
|
作者
Wang, Liming [1 ]
Zhou, Beibei [1 ]
Huang, Xiaoxiao [1 ]
Dong, Lingqing [1 ]
Cheng, Kui [1 ]
Weng, Wenjian [1 ]
机构
[1] Zhejiang Univ, Sch Mat Sci & Engn, State Key Lab Silicon Mat, Hangzhou 310027, Zhejiang, Peoples R China
来源
RSC ADVANCES | 2017年 / 7卷 / 53期
基金
中国国家自然科学基金;
关键词
TIO2-DERIVED TITANATE NANOTUBES; TITANIUM IMPLANTS; STEM-CELLS; DIFFERENTIATION; PHOSPHATE; CALCIUM; ACID; NANOFIBERS; MECHANISM; SURFACES;
D O I
10.1039/c7ra06029g
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Alkali treatment has been widely used for the surface modification of Ti and Ti alloys for clinical applications. However, the mechanism underlying the effects of the alkali-treated Ti surface on the cell response still needs to be explored. In this study, we demonstrated that the cell responses on a H2Ti3O7 nanowire film, normally titanate generated on a Ti surface via alkali treatment and ion exchange, were sensitive to the surface hydroxyl groups of the H2Ti3O7 nanowire films, i.e. the total amount as well as comparative ratio of the distinct type of surface hydroxyl groups (bridging-OH and terminal-OH). The surface hydroxyl groups of H2Ti3O7 nanowires were further controlled via heat treatment to produce anatase TiO2 nanowire films. Although there was no difference in both topographies, cells on a H2Ti3O7 nanowire film showed more elongated shape than those on an anatase nanowire film. Moreover, the expression of ALP of cells on H2Ti3O7 upregulated as compared to that on the anatase nanowire film at day 4, suggesting enhanced osteogenic capacity at an early stage. These results could be attributed to the difference in the distinct ratio of the terminal hydroxyl groups to the bridging hydroxyl groups, which was 0.42 for the H2Ti3O7 nanowire film and 0.75 for the anatase nanowire film. It appeared that the bridging hydroxyl groups on H2Ti3O7 were efficient in attracting Ca2+, which influenced the cell morphology and further upregulated the early differentiation.
引用
收藏
页码:33606 / 33613
页数:8
相关论文
共 50 条
  • [1] Formation Mechanism of H2Ti3O7 Nanotubes
    Peng, L.-M. (plm@ele.pku.edu.cn), 1600, American Physical Society (91):
  • [2] Structural and Electronic Properties of Na2Ti3O7 and H2Ti3O7
    Abass, Sara A. H.
    Seriani, Nicola
    PHYSICA STATUS SOLIDI B-BASIC SOLID STATE PHYSICS, 2018, 255 (08):
  • [3] Activity and selectivity of V2O5/H2Ti3O7, V2O5-WO3/H2Ti3O7 and Al2O3/H2Ti3O7 model catalysts during the SCR-NO with NH3
    Mejia-Centeno, Isidro
    Castillo, Salvador
    Camposeco, Roberto
    Marin, Jesus
    Garcia, Luz A.
    Fuentes, Gustavo A.
    CHEMICAL ENGINEERING JOURNAL, 2015, 264 : 873 - 885
  • [4] Preparation and characterizations of Na2Ti3O7, H2Ti3O7 and TiO2 Nanobelts
    Wang, Yanmin
    Liu, Hong
    EMERGING FOCUS ON ADVANCED MATERIALS, PTS 1 AND 2, 2011, 306-307 : 1233 - +
  • [5] LITHIUM ION TITRATION OF LAYERED TITANIC ACID, H2TI3O7
    IZAWA, H
    YASUDA, F
    KIKKAWA, S
    KOIZUMI, M
    CHEMISTRY LETTERS, 1985, (11) : 1775 - 1778
  • [6] CATION-EXCHANGE SELECTIVITY OF LAYERED TITANATES, H2TI3O7
    IZAWA, H
    KIKKAWA, S
    KOIZUMI, M
    JOURNAL OF SOLID STATE CHEMISTRY, 1985, 60 (02) : 264 - 267
  • [7] EFFECT OF INTERCALATED ALKYLAMMONIUM ON CATION-EXCHANGE PROPERTIES OF H2TI3O7
    IZAWA, H
    KIKKAWA, S
    KOIZUMI, M
    JOURNAL OF SOLID STATE CHEMISTRY, 1987, 69 (02) : 336 - 342
  • [8] H2Ti3O7 Nanotubes Decorated with Silver Nanoparticles for Photocatalytic Degradation of Atenolol
    Hinojosa-Reyes, Mariana
    Camposeco-Solis, Roberto
    Ruiz, Facundo
    Nino Martinez, Nereyda
    Rodriguez Gonzalez, Vicente
    Compean-Jasso, M. E.
    JOURNAL OF NANOMATERIALS, 2017, 2017
  • [9] Formation mechanism of H2Ti3O7 nanotubes -: art. no. 256103
    Zhang, S
    Peng, LM
    Chen, Q
    Du, GH
    Dawson, G
    Zhou, WZ
    PHYSICAL REVIEW LETTERS, 2003, 91 (25)
  • [10] Controllable Synthesis and Photocatalytic Properties Study of Na2Ti3O7 and H2Ti3O7 Nanotubes with High Exposed Facet (010)
    Du, Quanchao
    Lu, Gongxuan
    JOURNAL OF NANOSCIENCE AND NANOTECHNOLOGY, 2015, 15 (06) : 4385 - 4391