Regulatory Forum Opinion Piece*: Imaging Applications in Toxicologic Pathology—Recommendations for Use in Regulated Nonclinical Toxicity Studies

Author:

Maronpot Robert R.1,Nyska Abraham2,Troth Sean P.3,Gabrielson Kathleen4,Sysa-Shah Polina4,Kalchenko Vyacheslav5,Kuznetsov Yuri5,Harmelin Alon5,Schiffenbauer Yael S.6,Bonnel David7,Stauber Jonathan7,Ramot Yuval8

Affiliation:

1. Maronpot Consulting LLC, Raleigh, North Carolina, USA

2. Toxicologic Pathology, Sackler School of Medicine, Tel Aviv University, Timrat, Israel

3. Merck & Co., Inc., West Point, Pennsylvania, USA

4. Department of Molecular and Comparative Pathobiology, School of Medicine, Johns Hopkins University, Baltimore, Maryland, USA

5. Department of Veterinary Resources, Weizmann Institute of Science, Rehovot, Israel

6. Aspect Imaging, Shoham, Israel

7. ImaBiotech, Lille, Parc Eurasanté, France

8. Hadassah–Hebrew University Medical Center, Jerusalem, Israel

Abstract

Available imaging systems for use in preclinical toxicology studies increasingly show utility as important tools in the toxicologic pathologist’s armamentarium, permit longitudinal evaluation of functional and morphological changes in tissues, and provide important information such as organ and lesion volume not obtained by conventional toxicology study parameters. Representative examples of practical imaging applications in toxicology research and preclinical studies are presented for ultrasound, positron emission tomography/single-photon emission computed tomography, optical, magnetic resonance imaging, and matrix-assisted laser desorption ionization—imaging mass spectrometry imaging. Some of the challenges for making imaging systems good laboratory practice–compliant for regulatory submission are presented. Use of imaging data on a case-by-case basis as part of safety evaluation in regulatory submissions is encouraged.

Publisher

SAGE Publications

Subject

Cell Biology,Toxicology,Molecular Biology,Pathology and Forensic Medicine

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