Characterizing the pore structure of cryo-polymers

Cryogels are porous, sponge-like materials comprising an interconnected network of macropores, which are of great importance for applications such as 3D scaffolds for tissue culture, filters, or membranes. The application of cryogels is dependent on the size of their interconnected pores. In this project, various cryogels were prepared and pores were analyzed with automated methods.

A comprehensive image analysis process utilizing both classical thresholding and deep learning (DL) with Cellpose was developed.

Image preprocessing and Cellpose model training. Images with manually annotated pores were read into memory and separated into images and regions of interest (ROIs), with enhancements improving the visibility of the ridges around the pores. The ROIs were expanded to include the area around the pores and these enhanced images were used to train the Cellpose model. The trained model was then saved and used in the next compartment for pore segmentation.
Trained Cellpose. Cellpose model trained in the left figure to segment cryogel pores in electron micrographs and to measure their morphological properties. The image reading and annotations process was the same as described in the left caption. Because the Cellpose training node used ridge-enhanced images, the analyzable micrographs also went through the same procedure. The Cellpose node received the trained model from the Cellpose training compartment. The identified pores were filtered for size and shape. The provided ROIs were used to measure the area and shape parameters of the pores. The calculated values were saved for further analysis.

The analysis of electron micrographs was conducted using JIPipe, a software that automates the measurement of pore morphology. This was achieved by integrating classical global and local thresholding methods with a deep learning approach that employed the Cellpose algorithm with transfer learning, thereby enhancing the recognition of pores. The manual annotation and the training of two Cellpose models enabled the precise segmentation and quantification of pore characteristics. This demonstrated that the DL method is more accurate than manual and mercury intrusion porosimetry measurements in providing detailed morphological parameters.

The cryogel gels displayed robust reliability, with a high proportion of values obtained from manual and automated measurements showing minimal discrepancy. Additionally, cryogels prepared by the conventional method exhibited notable reproducibility.

Pore segmentation process using a trained Cellpose model. Electron micrograph (A) before and (B) after the ridge enhancement, respectively. The gradient flows (C) and the probability map (D). Segmented pore outlines (E, yellow lines), shown also in an overlay with the raw image (F).

The deep learning-based algorithms developed in this project offer a significant advantage over classical and manual segmentation techniques for characterising objects with diverse shapes, sizes, and grey values. As evidenced by our transfer learning approach for identifying smaller pores, these algorithms demonstrate the capacity to adapt readily to new object types. The pipeline was effective in segmenting individual pores, thereby facilitating a detailed morphological analysis of objects and entire samples. In comparison to manual techniques, our automated methodology yields objective outcomes that are consistent with expert analysis in a considerably shorter time frame. Our algorithmic approach demonstrated that the syringe-based method reliably produces cryogels with consistent pore sizes.

Experimenal Collaborators

Laboratory of Organic Chemistry and Macromolecular Chemistry (IOMC) at the Friedrich Schiller University in Jena

Jena Center for Soft Matter (JCSM) at the Friedrich Schiller University in Jena

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