BIOLOGY AND BIOMEDICAL ENGINEERING |
|
|
|
|
|
In vitro hyperthermia based on a multi-mode detection chip with impedance sensing |
XIE Xinwu1,2, LIU Weiran1, LIU Ran1 |
1. Department of Biomedical Engineering, School of Medicine, Tsinghua University, Beijing 100084, China;
2. Institute of Medical Equipment, China Academy of Military Medical Sciences, Tianjin, 300161, China |
|
|
Abstract Hyperthermia is a useful method for cancer treatment after surgery, chemotherapy and radiotherapy for numerous types of cancers. However, the mechanism is not yet fully understood and some in vitro results cannot be repeated in clinical applications; thus, further research is needed. In this study, a lab-on-a-chip device and a corresponding detection system was constructed to study in vitro hyperthermia. The device incorporated electric cell-substrate impedance sensing (ECIS), morphological imaging, and fluorescence observation during and after cells were thermally treated in situ with automatic on-chip temperature control. The temperature control was tested in an incubator. The cell culture and impedance sensing were also validated. Then, cancer cells were treated and monitored by the system for two hyperthermia conditions. The impedance curve with rectangle hyperthermia control of 41℃ for 2 h shows a "V" shape change during the 41℃ treatment with the cells quickly shrinking and re-adhering without any obvious viability changes in the fluorescent labeling images. However, two hyperthermia pulses at 55℃ for 2 min caused cell impedance "L" shape changes and killed most of the cells. These results demonstrate that this device with un-labeled and labeled methods is a useful tool for in vitro research on thermal therapy.
|
Keywords
electric cell-substrate impedance sensing (ECIS)
hyperthermia
lab on a chip
multi-mode detections
|
|
Issue Date: 15 July 2016
|
|
|
[1] Coffey D S, Getzenberg R H, DeWeese T L. Hyperthermic biology and cancer therapies:A hypothesis for the "Lance Armstrong effect"[J]. JAMA, 2006, 296(4):445-448.
[2] Jones E L, Oleson J R, Prosnitz L R, et al. Randomized trial of hyperthermia and radiation for superficial tumors[J]. Journal of Clinical Oncology, 2005, 23(13):3079-3085.
[3] Roti Roti J L. Cellular responses to hyperthermia (40-46 C):Cell killing and molecular events[J]. International Journal of Hyperthermia, 2008, 24(1):3-15.
[4] Hildebrandt B, Wust P, Ahlers O, et al. The cellular and molecular basis of hyperthermia[J]. Critical reviews in oncology/hematology, 2002, 43(1):33-56.
[5] Zhou J, Wang X, Du L, et al. Effect of hyperthermia on the apoptosis and proliferation of CaSki cells[J]. Molecular medicine reports, 2011, 4(1):187-191.
[6] Lo C M, Keese C R, Giaever I. Impedance analysis of MDCK cells measured by electric cell-substrate impedance sensing[J]. Biophysical journal, 1995, 69(6):2800.
[7] Nguyen T A, Yin T I, Reyes D, et al. Microfluidic chip with integrated electrical cell-impedance sensing for monitoring single cancer cell migration in three-dimensional matrixes[J]. Analytical chemistry, 2013, 85(22):11068-11076.
[8] Xie F, Xu Y, Wang L, et al. Use of cellular electrical impedance sensing to assess in vitro cytotoxicity of anticancer drugs in a human kidney cell nephrotoxicity model[J]. Analyst, 2012, 137(6):1343-1350.
[9] Wang L, Zhu J, Deng C, et al. An automatic and quantitative on-chip cell migration assay using self-assembled monolayers combined with real-time cellular impedance sensing[J]. Lab on a Chip, 2008, 8(6):872-878.
[10] Wang L, Yin H, Xing W, et al. Real-time, label-free monitoring of the cell cycle with a cellular impedance sensing chip[J]. Biosensors and Bioelectronics, 2010, 25(5):990-995.
[11] Giaever I, Keese C R. Monitoring fibroblast behavior in tissue culture with an applied electric field[J]. Proceedings of the National Academy of Sciences, 1984, 81(12):3761-3764.
[12] Wang L, Wang H, Mitchelson K, et al. Analysis of the sensitivity and frequency characteristics of coplanar electrical cell-substrate impedance sensors[J]. Biosensors and Bioelectronics, 2008, 24(1):14-21. |
|
Viewed |
|
|
|
Full text
|
|
|
|
|
Abstract
|
|
|
|
|
Cited |
|
|
|
|
|
Shared |
|
|
|
|
|
Discussed |
|
|
|
|