Image-analysis based readout method for biochip: Automated quantification of immunomagnetic beads, micropads and patient leukemia cell. (June 2020)

• Record Type: Journal Article
• Authors: Uslu, Fatma; Icoz, Kutay; Tasdemir, Kasim; Doğan, Refika S.; Yilmaz, Bulent
• Is Part Of: Micron. Volume 133(2020)
• Publication Date: 2020-06
• Subjects: Biochip -- Image processing -- Leukemia cells -- Micropads -- Immunomagnetic beads -- Bright-field optical microscope; Microscopy -- Periodicals; Electron Probe Microanalysis -- Periodicals; Microscopy -- Periodicals; Microscopie -- Périodiques; Microscopy; Periodicals; 502.82
• DOI: 10.1016/j.micron.2020.102863
• Languages: English
• ISSNs: 0968-4328

Abstract

Highlights: Bright field optical microscope images processed to detect immunomagnetic beads, patient leukemia cells and micropads. No cell staining and no fluorescent labeling. Simple but time-efficient color, shape and size-based object detection methods incorporated. Patient response to chemotherapy was monitored. 95 % precision and 97 % recall for detecting patient leukemia cells were reported. Abstract: For diagnosing and monitoring the progress of cancer, detection and quantification of tumor cells is utmost important. Beside standard bench top instruments, several biochip-based methods have been developed for this purpose. Our biochip design incorporates micron size immunomagnetic beads together with micropad arrays, thus requires automated detection and quantification of not only cells but also the micropads and the immunomagnetic beads. The main purpose of the biochip is to capture target cells having different antigens simultaneously. In this proposed study, a digital image processing-based method to quantify the leukemia cells, immunomagnetic beads and micropads was developed as a readout method for the biochip. Color, size-based object detection and object segmentation methods were implemented to detect structures in the images acquired from the biochip by a bright field optical microscope. It has been shown that manual counting and flow cytometry results are in good agreement with the developed automated counting. Average precision is 85 % and average error rate is 13 % for all images of patient samples, average precision is 99 % and average error rate is 1% for cell culture images. With the optimized micropad size, proposed method can reach up to 95 % precision rate for patient samples with an execution time of 90 s per image.