No abstract

Although preclinical experiments are ultimately required to evaluate new therapeutic ultrasound exposures and devices prior to clinical trials, in vitro experiments can play an important role in the developmental process. A variety of in vitro methods have been developed, where each of these has demonstrated their utility for various test purposes. These include inert tissue-mimicking phantoms, which can incorporate thermocouples or cells and ex vivo tissue. Cell-based methods have also been used, both in monolayer and suspension. More biologically relevant platforms have also shown utility, such as blood clots and collagen gels. Each of these methods possesses characteristics that are well suited for various well-defined investigative goals. None, however, incorporate all the properties of real tissues, which include a 3D environment and live cells that may be maintained long-term post-treatment. This review is intended to provide an overview of the existing application-specific in vitro methods available to therapeutic ultrasound investigators, highlighting their advantages and limitations. Additional reporting is presented on the exciting and emerging field of 3D biological scaffolds, employing methods and materials adapted from tissue engineering. This type of platform holds much promise for achieving more representative conditions of those found in vivo, especially important for the newest sphere of therapeutic applications, based on molecular changes that may be generated in response to non-destructive exposures.

Artificial intelligence (AI) is one of the most promising approaches to health innovation. The use of AI in image recognition considerably extends findings beyond the constraints of human sight. The application of AI in medical imaging, which relies on picture interpretation, is beneficial for automatic diagnosis. Diagnostic radiology is evolving from a subjective perceptual talent to a more objective science thanks to AI. Automatic object detection in medical images is an essential AI technology in medicine. The problem of detecting brain tumors at an early stage is well advanced with convolutional neural network (CNN) and deep learning algorithms (DLA). The problem is that those algorithms require a training phase with a big database of more than 500 images and time-consuming with a complex computational and expensive infrastructure. This study proposes a classical automatic segmentation method for detecting brain tumors in the early stage using MRI images. It is based on a multilevel thresholding technique on a harmony search algorithm (HSO); the algorithm was developed to suit MRI brain segmentation, and parameters selection was optimized for the purpose. Multiple thresholds, based on the variance and entropy functions, break the histogram into multiple portions, and different colors are associated with each portion. To eliminate the tiny arias supposed as noise and detect brain tumors, morphological operations followed by a connected component analysis are utilized after segmentation. The brain tumor detection performance is judged using performance parameters such as Accuracy, Dice Coefficient, and Jaccard index. The results are compared to those acquired manually by experts in the field. The results were further compared with different CNN and DLA approaches using Brain Images dataset called the “BraTS 2017 challenge”. The average Dice Index was used as a performance measure for the comparison. The results of the proposed approach were found to be competitive in accuracy to those obtained by CNN and DLA methods and much better in terms of execution time, computational complexity, and data management.

Breast cancer ranks among the leading causes of death for women globally, making it imperative to swiftly and precisely detect the condition to ensure timely treatment and enhanced chances of recovery. This study focuses on transfer learning with 3D U-Net models to classify ductal carcinoma, the most frequent subtype of breast cancer, in histopathology imaging. In this research work, a dataset of 162 microscopic images of breast cancer specimens is utilized for breast histopathology analysis. Preprocessing the original image data includes shrinking the images, standardizing the intensities, and extracting patches of size 50 × 50 pixels. The retrieved patches were employed to construct a basic 3D U-Net model and a refined 3D U-Net model that had been previously trained on an extensive medical image segmentation dataset. The findings revealed that the fine-tuned 3D U-Net model (97%) outperformed the simple 3D U-Net model (87%) in identifying ductal cancer in breast histopathology imaging. The fine-tuned model exhibited a smaller loss (0.003) on the testing data (0.041) in comparison to the simple model. The disparity in the training and testing accuracy reveals that the fine-tuned model may have overfitted to the training data indicating that there is room for improvement. To progress in computer-aided diagnosis, the research study also adopted various data augmentation methodologies. The experimental approach that was put forward achieved state-of-the-art performance, surpassing the benchmark techniques used in previous studies in the same field, and exhibiting greater accuracy. The presented scheme has promising potential for better cancer detection and diagnosis in practical applications of mammography.