RESUMEN
Gold nanoparticles (AuNPs) are extensively used in cellular imaging, single-particle tracking, disease diagnosis, studying membrane protein interaction, and drug delivery. Understanding the dynamics of AuNP uptake in live cells is crucial for optimizing their efficacy and safety. Traditional manual methods for quantifying AuNP uptake are time-consuming and subjective, limiting their scalability and accuracy. The available fluorescence-based techniques are limited to photobleaching and photoblinking. Optical microscopy techniques are limited by diffraction limits. Electron microscopy-based imaging techniques are destructive and unsuitable for live cell imaging. Furthermore, the resulting images may contain hundreds of particles with varied intensities, blurring, and substantial occlusion, making it difficult to manually quantify AuNP uptake. To overcome this issue and measure AuNP uptake by live cells, we annotated a dataset of dark-field images of 50 nanometer-radius AuNPs at different incubation durations. Then, to count the number of particles present in a cell, we created a customized multi-column convolutional neural network (MC-CNN). The customized MC-CNN outperformed typical particle counting architectures when compared to spectroscopy-based counting. This will allow researchers to gain a better understanding of AuNP behavior and interactions with cells, paving the way for advancements in nanomedicine, drug delivery, and biomedical research. The code for this paper is available at the following link: https://github.com/Namerlight/LabelFree_AuNP_Quantification.