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Charge injection based electrical stimulation on polypyrrole planar electrodes to regulate cellular osteogenic differentiation.
Liu, Zongguang; Dong, Lingqing; Cheng, Kui; Luo, Zhongkuan; Weng, Wenjian.
Afiliação
  • Liu Z; School of Materials Science and Engineering, State Key Laboratory of Silicon Materials, Zhejiang University Hangzhou 310027 China wengwj@zju.edu.cn.
  • Dong L; School of Materials Science and Engineering, State Key Laboratory of Silicon Materials, Zhejiang University Hangzhou 310027 China wengwj@zju.edu.cn.
  • Cheng K; The Affiliated Stomatologic Hospital, School of Medicine, Zhejiang University Hangzhou 310003 China.
  • Luo Z; School of Materials Science and Engineering, State Key Laboratory of Silicon Materials, Zhejiang University Hangzhou 310027 China wengwj@zju.edu.cn.
  • Weng W; Zhejiang-California International NanoSystems Institute Hangzhou 310058 China.
RSC Adv ; 8(33): 18470-18479, 2018 May 17.
Article em En | MEDLINE | ID: mdl-35541122
In this study, polypyrrole (Ppy) electrodes were prepared to support an electrical stimulation to MC3T3-E1 cells for regulating their osteogenic differentiation. The charge injection capacity (C Q) of the Ppy electrodes could be adjusted by the Ppy thickness, and a higher C Q could make the electrode able to produce a higher charge injection quantity (Q inj) at applied voltage. The Q inj onto electrode could be considered as the intensity of the stimulation pulse to cells, and the pulse frequency means the number of electric stimulation with Q inj at one second. Hence, we conducted the present work in the view of Q inj. When the cells were electrically stimulated for 1 hour per day, the electrodes with Q inj ranged in 0.08-0.15 µQ had an obvious role in enhancing cellular osteogenic differentiation whereas Q inj of lower than 0.03 µQ or more than 0.30 µQ gave the stimulations with no or negative effects. And the stimulation with 1 or 25 Hz showed to enhance the differentiation, whereas the stimulation with 50 Hz gave an inhibiting effect. We further found the osteogenic differentiation potential triggered by electrical simulation was related to cell growth stage, and the stimulation carried out at early stage (day 2-5) during 8 days cell culture showed more contribution to enhancing osteogenic differentiation than that at later stage (day 6-8). It is proposed that the desired stimulation effects require that an appropriate voltage-gated calcium ion channel and efficient intracellular calcium ion oscillation are well activated. This work therefore reveals Q inj as an important electrode parameter to decide effective simulations and provides an insight into understanding of the role of electrode material characters in regulating cellular osteogenic differentiation during stimulation.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: RSC Adv Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: RSC Adv Ano de publicação: 2018 Tipo de documento: Article