研究目的
To identify nanoscale changes in cell membrane morphology or cell biomechanical properties in disease states or in response to drug treatment for a better understanding of the effects of drugs on disease pathogenesis and recovery.
研究成果
AFM can be used to measure CBPs and to observe cell/CM structure at the nanometer scale. It provides a useful nanotool for the assessment of changes in CM morphology and CBPs that are induced by disease or pharmacological treatment.
研究不足
AFM can only image a maximum scanning area of ~150x150μm, and a maximum depth of 10-20 μm. Each scan typically takes 5–30 min to complete, potentially leading to thermal drift and inaccurate measurement. AFM images can be affected by nonlinearity, hysteresis, and creep of the piezoelectric material, along with cross-talk between the x, y, and z axes. Image artefacts may result from unsuitable or worn tips or from sub-optimal operating environments.