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Label-free detection of cellular drug responses by high-throughput bright-field imaging and machine learning.
Kobayashi, Hirofumi; Lei, Cheng; Wu, Yi; Mao, Ailin; Jiang, Yiyue; Guo, Baoshan; Ozeki, Yasuyuki; Goda, Keisuke.
Afiliación
  • Kobayashi H; Department of Chemistry, University of Tokyo, Tokyo, 113-0033, Japan.
  • Lei C; Department of Chemistry, University of Tokyo, Tokyo, 113-0033, Japan. leicheng@chem.s.u-tokyo.ac.jp.
  • Wu Y; Department of Computational Biology, Carnegie Mellon University, Pittsburgh, Pennsylvania, 15213, USA.
  • Mao A; Department of Chemistry, University of Tokyo, Tokyo, 113-0033, Japan.
  • Jiang Y; Department of Chemistry, University of Tokyo, Tokyo, 113-0033, Japan.
  • Guo B; Department of Chemistry, University of Tokyo, Tokyo, 113-0033, Japan.
  • Ozeki Y; Department of Electrical Engineering and Information Systems, University of Tokyo, Tokyo, 113-8656, Japan.
  • Goda K; Department of Chemistry, University of Tokyo, Tokyo, 113-0033, Japan. goda@chem.s.u-tokyo.ac.jp.
Sci Rep ; 7(1): 12454, 2017 09 29.
Article en En | MEDLINE | ID: mdl-28963483
ABSTRACT
In the last decade, high-content screening based on multivariate single-cell imaging has been proven effective in drug discovery to evaluate drug-induced phenotypic variations. Unfortunately, this method inherently requires fluorescent labeling which has several drawbacks. Here we present a label-free method for evaluating cellular drug responses only by high-throughput bright-field imaging with the aid of machine learning algorithms. Specifically, we performed high-throughput bright-field imaging of numerous drug-treated and -untreated cells (N = ~240,000) by optofluidic time-stretch microscopy with high throughput up to 10,000 cells/s and applied machine learning to the cell images to identify their morphological variations which are too subtle for human eyes to detect. Consequently, we achieved a high accuracy of 92% in distinguishing drug-treated and -untreated cells without the need for labeling. Furthermore, we also demonstrated that dose-dependent, drug-induced morphological change from different experiments can be inferred from the classification accuracy of a single classification model. Our work lays the groundwork for label-free drug screening in pharmaceutical science and industry.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Procesamiento de Imagen Asistido por Computador / Paclitaxel / Aprendizaje Automático / Microscopía de Interferencia / Antineoplásicos Fitogénicos Tipo de estudio: Diagnostic_studies Límite: Humans Idioma: En Revista: Sci Rep Año: 2017 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Procesamiento de Imagen Asistido por Computador / Paclitaxel / Aprendizaje Automático / Microscopía de Interferencia / Antineoplásicos Fitogénicos Tipo de estudio: Diagnostic_studies Límite: Humans Idioma: En Revista: Sci Rep Año: 2017 Tipo del documento: Article País de afiliación: Japón