In this study a planar-surface photonic crystal (PC) biosensor for quantitative kinetic label-free imaging of cell-surface interactions is demonstrated. the monitoring of Rhein-8-O-beta-D-glucopyranoside live cell-substrate interactions with spatial resolution sufficient for observing intracellular attachment strength gradients and the extensions of filopodia from the cell body. The evolution of cell morphology during the attachment and spreading process of 3T3 fibroblast cells is usually compared between planar and grating-structured PC biosensors. The planar surface effectively eliminates the directionally biased cellular attachment behaviors that are observed around the grating-structured surface. This work represents an important step forward in the development of label-free techniques for observing cellular processes without unintended external environmental modulation. 1 Introduction The critical role of the interactions between cells and their microenvironment upon directing and controlling cell behavior within the context of a diverse set of cellular processes has been extensively studied due to promising applications in tissue engineering regenerative medicine and preclinical pharmaceutical analysis.[1-3] Importantly the spatial and temporal dynamics of cell-surface interactions are a fundamental aspect of the biology of how cells communicate with Rhein-8-O-beta-D-glucopyranoside their environment. Total internal reflectance fluorescence microscopy and confocal fluorescence microscopy have been the most widely used tools for visualization of cell-surface interactions through the use of fluorescent dyes that can be specifically targeted to bind with membrane components.[4 5 Although detailed information about cell adhesion activity can be provided by these methods the rapid rate of fluorophore photo-bleaching poses a severe practical restriction upon the period during Rhein-8-O-beta-D-glucopyranoside which the cells can be observed and is not capable of quantification of the engagement between the cell and the surface it is attached to. Therefore fluorescence imaging is not suitable for long-term monitoring of cells especially for extremely important activities that occur over extended time scales such as cell differentiation metastasis and chemotaxis. Label-free biosensors have been developed that are able to overcome the inherent challenges in the label-based cell detection methods to provide noninvasive and nondestructive measurements of cell behavior.[7-9] Instead of relying upon fluorescent tags label-free biosensors are designed to measure an intrinsic property of cells such as dielectric permittivity mass or electrical impedance. For example biosensor technologies using prism coupler-based and grating coupler-based surface plasmon resonance (SPR) are capable of detecting cell attachment between a metal surface and the membrane proteins in living cells.[10 11 Electrical sensing approaches have also been reported to supply label-free detection of cells by tracking the electrical conductivity distribution within cells upon a microelectrode-covered substrate. Biosensor-based recognition of cell-surface interactions is particularly Rhein-8-O-beta-D-glucopyranoside desirable when the transducer surface area just responds to cell attachment events that happen in the transducer-cell interface (and therefore gauge the strength of engagement from the cell membrane with the top) instead of sensing the majority properties from the cell. Just a few from the label-free biosensing techniques are capable of imaging cell-surface relationships. Specifically SPR imaging and photonic crystal improved microscopy (PCEM) possess demonstrated the capability to generate pictures from the magnitude of cell-surface connection Rhein-8-O-beta-D-glucopyranoside with subcell spatial quality [13-15] and PCEM may be the only method of show submicron spatial Adipoq quality utilizing a low-magnification (10×) objective.[16 17 Photonic crystal (PC) biosensors have already been demonstrated like a versatile system for an array of label-free biological assays including DNA microarrays disease sensing cell attachment characterization and high throughput medication testing.[16 18 The structure found in this function is a 1D Personal computer slab with alternating high and low refractive index levels having a grating period.