Representative training data sets are critical for accurate machine-learning classification of microscopy images of particles formed by lipase-catalyzed polysorbate hydrolysis.
David N Greenblott, Christopher P Calderon, Theodore W Randolph
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引用次数: 0
Abstract
Polysorbate 20 (PS20) is commonly used as an excipient in therapeutic protein formulations. However, over the course of a therapeutic protein product's shelf life, minute amounts of co-purified host-cell lipases may cause slow hydrolysis of PS20, releasing fatty acids (FAs). These FAs may precipitate to form subvisible particles that can be detected and imaged by various techniques, e.g., flow imaging microscopy (FIM). Images of particles can then be classified using supervised convolutional neural networks (CNNs). However, CNNs should be trained on representative images of particles which, as we demonstrate in this work, may be challenging to obtain. Here, we tested several rapid techniques to create FA particles and examined whether CNNs trained on microscopy images of these rapidly formed particles could accurately classify images of particles that had been produced by kinetically slower lipase-catalyzed hydrolysis of PS20. CNNs trained on images of rapidly produced particles were less accurate in classifying images of FA particles that had been produced by enzymatic hydrolysis of PS20 than CNNs trained with images of particles generated by the same slow hydrolysis, highlighting the importance of using representative image data sets for training CNN classifiers.
期刊介绍:
The Journal of Pharmaceutical Sciences will publish original research papers, original research notes, invited topical reviews (including Minireviews), and editorial commentary and news. The area of focus shall be concepts in basic pharmaceutical science and such topics as chemical processing of pharmaceuticals, including crystallization, lyophilization, chemical stability of drugs, pharmacokinetics, biopharmaceutics, pharmacodynamics, pro-drug developments, metabolic disposition of bioactive agents, dosage form design, protein-peptide chemistry and biotechnology specifically as these relate to pharmaceutical technology, and targeted drug delivery.