Dynamic Interaction between an AFM Oscillating Cantilever and Human Liver Epithelial Cells: Analysis of Cellular Mechanical Properties

Document Type : Original Article

Authors

1 Department of Mechanical Engineering, Damavand branch, Islamic Azad University, Damavand, Tehran, Iran

2 Associate Professor , Department of Biomedical Engineering, CT.C., Islamic Azad University, Tehran, Iran

3 Assistant Professor, Department of Physics, Dam.c., Islamic Azad University, Damavand, Iran

4 Department of Biomedical Engineering, CT.C., Islamic Azad University, Tehran, Iran

10.66224/masm.2026.2105527.1206
Abstract
In this study, the nanomechanical properties and dynamic response of healthy and cancerous human liver cells before and after treatments were investigated using atomic force microscopy (AFM). The Young’s modulus of healthy and untreated cancerous cells was measured at 2.940±1.069kPa and 0.785±0.282kPa, respectively. Treatment with cisplatin, atmospheric cold plasma (DBD), and their combined therapy increased the Young’s modulus of cancer cells to 2.218، 2.780 and 3.660±1.811, respectively. Furthermore, the enhanced cellular stiffness induced a shift in the AFM cantilever resonance frequency toward higher values, increasing the first-mode frequency from 3.98 kHz to 4.35 kHz. An analytical model based on Timoshenko beam theory and the DMT contact model showed excellent agreement with experimental and finite element method (FEM) results, with a relative error below 7.205%. These findings demonstrate that coupling nanomechanical characterization with AFM dynamic analysis provides a precise and non-destructive tool for evaluating cancer cell mechanical properties and monitoring therapeutic efficacy.

Keywords


[1] Ashkin A. Acceleration and trapping of particles by radiation pressure. Phys Rev Lett. 1970;24(4):156–9.
[2] Neuman KC, Block SM. Optical trapping. Rev Sci Instrum. 2004;75(9):2787–809.
[3] Fazal FM, Block SM. Optical tweezers study life at the single-molecule level. Nat Photonics. 2011;5(6):318–21.
[4] Svoboda K, Block SM. Biological applications of optical forces. Annu Rev Biophys Biomol Struct. 1994;23(1):247–85.
[5] Bustamante C, Macosko JC, Wuite GJ. Measurement of mechanical properties of single DNA molecules by optical tweezers. Science. 1996;271(5250):792–4.
[6] Mehta AD, et al. Single-molecule biomechanics with optical methods. Science. 1999;283(5408):1689–95.
[7] Hochmuth RM. Micropipette aspiration of living cells. J Biomech. 2000;33(1):15–22.
[8] Theret DP, et al. The application of a homogeneous half-space model in the analysis of endothelial cell leukocyte adherence. J Biomech Eng. 1988;110(3):190–9.
[9] Müller DJ, Dufrêne YF. Atomic force microscopy as a multifunctional molecular toolbox in nanobiotechnology. Nat Nanotechnol. 2008;3(5):261–9.
[10] Butt HJ, Cappella B, Kappl M. Force measurements with the atomic force microscope: Technique, interpretation and applications. Surf Sci Rep. 2005;59(1–6):1–152.
[11] Binnig G, Quate CF, Gerber C. Atomic force microscope. Phys Rev Lett. 1986;56(9):930–3.
[12] Dufrêne YF, et al. Imaging modes of atomic force microscopy for application in molecular and cell biology. Nat Nanotechnol. 2017;12(4):295–307.
[13] Radmacher M. Measuring the elastic properties of living cells by the atomic force microscope. Methods Cell Biol. 2002;68:67–90.
[14] Keidar M. Plasma for cancer treatment. Plasma Sources Sci Technol. 2015;24(3):033001.
[15] Laroussi M. Low temperature plasma-based sterilization: Overview and state-of-the-art. IEEE Trans Plasma Sci. 2002;30(4):1409–15.
[16] Fridman A. Plasma chemistry. Cambridge: Cambridge University Press; 2008.
[17] Kogelschatz U. Dielectric-barrier discharges: Their history, discharge physics, and industrial applications. Plasma Chem Plasma Process. 2003;23(1):1–46.
[18] Lu X, et al. Guided ionization waves: Theory and experiments. Phys Rep. 2014;540(3):123–67.
[19] Graves DB. The emerging role of reactive oxygen and nitrogen species in redox biology and some implications for plasma applications to medicine and biology. J Phys D Appl Phys. 2012;45(26):263001.
[20] Bruggeman PJ, et al. Plasma–liquid interactions: A review and roadmap. Plasma Sources Sci Technol. 2016;25(5):053002.
[21] Trachootham D, et al. Targeting cancer cells by ROS-mediated mechanisms: A radical way to kill cancer. Nat Rev Drug Discov. 2009;8(7):579–91.
[22] Liou GY, Storz P. Reactive oxygen species in cancer. Free Radic Res. 2010;44(5):479–96.
[23] Vandamme M, et al. ROS implication in a new antitumor strategy based on non-thermal plasma. Int J Cancer. 2012;130(9):2185–94.
[24] Barekzi N, Laroussi M. Effects of low temperature plasmas on cancer cells. Plasma Process Polym. 2013;10(12):1039–50.
[25] Kim SJ, et al. Atmospheric pressure plasma jet induced cell death in human cervical cancer cells. J Appl Phys. 2011;109(8):083301.
[26] Kim JY, et al. Cold atmospheric plasma for selective cancer treatment. Biotechnol Bioeng. 2012;109(1):288–96.
[27] Yan D, et al. Principles of cold atmospheric plasma-induced cancer cell death: Reactive oxygen and nitrogen species-induced cellular damage. Sci Signal. 2021;14(680).
[28] Lin A, et al. Non-thermal plasma as a unique delivery system of short-lived reactive oxygen and nitrogen species for immunogenic cell death in melanoma. Adv Sci. 2019;6(6):1802062.
[29] von Woedtke T, et al. Plasma medicine: A brief introduction. Clin Plasma Med. 2013;1(1):2–8.
[30] Laroussi M. From killing bacteria to destroying cancer cells: 20 years of plasma medicine. Plasma Process Polym. 2014;11(12):1138–41.
[31] Metelmann HR, et al. Comprehensive clinical plasma medicine. Cham: Springer; 2018.
[32] Lin Y, et al. Determination of in-plane elasticity of cell layers using microfluidic systems. Lab Chip. 2015;15:450–8.
[33] Omidvar R, et al. Evaluation of the elasticity and viscoelasticity of breast cancer cells using atomic force microscopy. J Mech Behav Biomed Mater. 2014;38:216–27.
[34] Zhu Y, et al. Biomechanical characterization of anti-cancer drug effects on cells using AFM. Micron. 2012;43(12):1321–8.
[35] Efremov YM, et al. Mechanical properties of fibroblasts depending on cancer transformation level. BioNanoScience. 2014;4(3):238–47.
Volume 5, Issue 4
Winter 2026
Pages 568-589

  • Receive Date 10 September 2026
  • Revise Date 25 September 2026
  • Accept Date 11 October 2026