Peter J. H. Scott

Last updated

Peter Scott
Peter J. H. Scott.jpg
BornJuly 27, 1979
CitizenshipBritish and American
Education Loughborough University Durham University
AwardsAcademy for Radiology & Biomedical Imaging Research: 2019 Distinguished Investigator Award
Scientific career
Fields Chemistry
Radiochemistry
Positron emission tomography
Nuclear Medicine
Institutions University of Michigan
Thesis Perfluoroalkanesulfonyl linker units for solid phase organic synthesis
Doctoral advisor Patrick G. Steel
Other academic advisors Huw Davies (chemist)

Peter J. H. Scott FRSC CChem (born July 27, 1979) is a British and American chemist and radiochemist who is a professor of radiology, professor of pharmacology and professor of medicinal chemistry, as well as a core member of the Rogel Cancer Center at the University of Michigan in the United States. [1] [2] He is Chief of Nuclear Medicine and director of the University of Michigan Positron Emission Tomography (PET) Center, [3] and runs a research group developing new radiochemistry methodology and novel PET radiotracers. [4]

Contents

Life

Peter Scott was born and grew up in North East England and attended Whitley Bay High School. He received his undergraduate degree with first class honors in medicinal and pharmaceutical chemistry from Loughborough University in 2001, after conducting research with Raymond Jones. He subsequently obtained his PhD in organic chemistry from Durham University in 2005, where he was a member of Ustinov College, under the mentorship of Patrick G. Steel. Scott then moved to the United States to undertake postdoctoral research in organometallic chemistry at SUNY Buffalo under Huw Davies, and PET radiochemistry at the University of Michigan with Michael Kilbourn.

Research

Scott runs a research group developing new metal-catalyzed methods for incorporating fluorine-18 and carbon-11 into bioactive molecules as well as novel PET radiotracers for imaging neurodegenerative disorders. His methodology work aims to improve the synthesis of PET radiotracers and he has an active collaboration with Prof. Melanie Sanford's group [5] that is funded by NIBIB. [6] Together they have developed methods for the Cu-mediated radiofluorination [7] and radiocyanation of (mesityl)(aryl)iodonium salts, [8] boronic acids [9] [10] and stannanes, [10] [11] as well as new methods for radiofluorination of C-H bonds [12] [13] [14] and aryl halides. [15] Scott has also introduced methods for green radiochemistry, [16] for which he received the Michigan Green Chemistry Governor's Award in 2014. [17] In 2019, Prof. Scott was elected as a Fellow of the Royal Society of Chemistry (FRSC), [18] and received a Distinguished Investigator Award from the Academy for Radiology & Biomedical Imaging Research. [19] In 2021, he was honored as a Fellow of the Society of Nuclear Medicine and Molecular Imaging, [20] and was also recognized by SNMMI in 2023 with the Sam Gambhir Trailblazer Award, [21] created to honor the legacy and memory of the late Sanjiv Sam Gambhir.

Bibliography

1. Linker Strategies in Solid-phase Organic Synthesis (Editor, 2009) [22]
2. Solid-Phase Organic Syntheses, Volume 2: Solid-Phase Palladium Chemistry (Wiley Series on Solid-Phase Organic Syntheses) (Editor, 2012) [23]
3. Radiochemical Syntheses: Radiopharmaceuticals for Positron Emission Tomography, Volume 1 (Editor, 2012) [24]
4. Radiochemical Syntheses: Further Radiopharmaceuticals for Positron Emission Tomography and New Strategies for Their Production, Volume 2 (Editor, 2015) [25]
5. Handbook of Radiopharmaceuticals (2nd Edition): Methodology and Applications (Editor, 2021) [26]
6. Production and Quality Control of Fluorine-18 Labelled Radiopharmaceuticals (co-authored with International Atomic Energy Agency, 2021) [27]

Related Research Articles

<span class="mw-page-title-main">Positron emission tomography</span> Medical imaging technique

Positron emission tomography (PET) is a functional imaging technique that uses radioactive substances known as radiotracers to visualize and measure changes in metabolic processes, and in other physiological activities including blood flow, regional chemical composition, and absorption. Different tracers are used for various imaging purposes, depending on the target process within the body.

<span class="mw-page-title-main">Sodium fluoride</span> Ionic compound (NaF)

Sodium fluoride (NaF) is an inorganic compound with the formula NaF. It is a colorless or white solid that is readily soluble in water. It is used in trace amounts in the fluoridation of drinking water to prevent tooth decay, and in toothpastes and topical pharmaceuticals for the same purpose. In 2020, it was the 265th most commonly prescribed medication in the United States, with more than 1 million prescriptions. It is also used in metallurgy and in medical imaging.

<span class="mw-page-title-main">Bone scintigraphy</span>

A bone scan or bone scintigraphy is a nuclear medicine imaging technique of the bone. It can help diagnose a number of bone conditions, including cancer of the bone or metastasis, location of bone inflammation and fractures, and bone infection (osteomyelitis).

Fluorodeoxyglucose (<sup>18</sup>F) Chemical compound

[18F]Fluorodeoxyglucose (INN), or fluorodeoxyglucose F 18, also commonly called fluorodeoxyglucose and abbreviated [18F]FDG, 2-[18F]FDG or FDG, is a radiopharmaceutical, specifically a radiotracer, used in the medical imaging modality positron emission tomography (PET). Chemically, it is 2-deoxy-2-[18F]fluoro-D-glucose, a glucose analog, with the positron-emitting radionuclide fluorine-18 substituted for the normal hydroxyl group at the C-2 position in the glucose molecule.

<span class="mw-page-title-main">Copper(I) cyanide</span> Chemical compound

Copper(I) cyanide is an inorganic compound with the formula CuCN. This off-white solid occurs in two polymorphs; impure samples can be green due to the presence of Cu(II) impurities. The compound is useful as a catalyst, in electroplating copper, and as a reagent in the preparation of nitriles.

Oxygen-18 is a natural, stable isotope of oxygen and one of the environmental isotopes.

<span class="mw-page-title-main">Fluorine-18</span> Isotope of fluorine emitting a positron

Fluorine-18 (18F) is a fluorine radioisotope which is an important source of positrons. It has a mass of 18.0009380(6) u and its half-life is 109.771(20) minutes. It decays by positron emission 96% of the time and electron capture 4% of the time. Both modes of decay yield stable oxygen-18.

Organofluorine chemistry describes the chemistry of organofluorine compounds, organic compounds that contain a carbon–fluorine bond. Organofluorine compounds find diverse applications ranging from oil and water repellents to pharmaceuticals, refrigerants, and reagents in catalysis. In addition to these applications, some organofluorine compounds are pollutants because of their contributions to ozone depletion, global warming, bioaccumulation, and toxicity. The area of organofluorine chemistry often requires special techniques associated with the handling of fluorinating agents.

<span class="mw-page-title-main">Fluoroiodomethane</span> Chemical compound

Fluoroiodomethane is the halomethane with the formula FCH2I. Also classified as a fluoroiodocarbon (FIC), it is a colorless liquid. It is a reagent for the introduction of the fluoromethyl (FCH2) group.

<span class="mw-page-title-main">Liebeskind–Srogl coupling</span>

The Liebeskind–Srogl coupling reaction is an organic reaction forming a new carbon–carbon bond from a thioester and a boronic acid using a metal catalyst. It is a cross-coupling reaction. This reaction was invented by and named after Jiri Srogl from the Academy of Sciences, Czech Republic, and Lanny S. Liebeskind from Emory University, Atlanta, Georgia, USA. There are three generations of this reaction, with the first generation shown below. The original transformation used catalytic Pd(0), TFP = tris(2-furyl)phosphine as an additional ligand and stoichiometric CuTC = copper(I) thiophene-2-carboxylate as a co-metal catalyst. The overall reaction scheme is shown below.

<span class="mw-page-title-main">2-Fluoroethanol</span> Chemical compound

2-Fluoroethanol is the organic compound with the formula CH2FCH2OH. This colorless liquid is one of the simplest stable fluorinated alcohols. It was once used as a pesticide. The related difluoro- and trifluoroethanols are far less dangerous.

<span class="mw-page-title-main">Brain positron emission tomography</span> Form of positron emission tomography

Brain positron emission tomography is a form of positron emission tomography (PET) that is used to measure brain metabolism and the distribution of exogenous radiolabeled chemical agents throughout the brain. PET measures emissions from radioactively labeled metabolically active chemicals that have been injected into the bloodstream. The emission data from brain PET are computer-processed to produce multi-dimensional images of the distribution of the chemicals throughout the brain.

Melanie Sarah Sanford is an American chemist, currently the Moses Gomberg Distinguished University Professor of Chemistry and Arthur F. Thurnau Professor of Chemistry at the University of Michigan. She is a Fellow for the American Association for the Advancement of Science, and was elected a member of the National Academy of Sciences and the American Academy of Arts and Sciences in 2016. She has served as an executive editor of the Journal of the American Chemical Society since 2021, having been an associate editor of the since 2014.

Radiofluorination is the process by which a radioactive isotope of fluorine is attached to a molecule and is preferably performed by nucleophilic substitution using nitro or halogens as leaving groups. Fluorine-18 is the most common isotope used for this procedure. This is due to its 97% positron emission and relatively long 109.8 min half-life. The half-life allows for a long enough time to be incorporated into the molecule and be used without causing exceedingly harmful effects. This process has many applications especially with the use of positron emission tomography (PET) as the aforementioned low positron energy is able to yield a high resolution in PET imaging.

<span class="mw-page-title-main">Desmethoxyfallypride</span> Chemical compound

Desmethoxyfallypride is a moderate affinity dopamine D2 receptor/D3 receptor antagonist used in medical research, usually in the form of the radiopharmaceuticals desmethoxyfallypride or DMFP(18F) and has been used in human studies as a positron emission tomography (PET) radiotracer.

Fluorodeoxyglycosylamine is a product of fluorodeoxyglucose and biological amines. The Maillard reaction of sugars and amines results in the formation of glycosylamines and Amadori products that are of biological significance, for drug delivery, role in central nervous system, and other potential applications.

<span class="mw-page-title-main">FMISO</span> Chemical compound

18F-FMISO or fluoromisonidazole is a radiopharmaceutical used for PET imaging of hypoxia. It consists of a 2-nitroimidazole molecule labelled with the positron-emitter fluorine-18.

<span class="mw-page-title-main">Dihydrotetrabenazine</span> Chemical compound

Dihydrotetrabenazine or DTBZ is an organic compound with the chemical formula C19H29NO3. It is a close analog of tetrabenazine. DTBZ and its derivatives, when labeled with positron emitting isotopes such as carbon-11 and fluorine-18, are used as PET radioligands for examining VMAT2.

Jason S. Lewis is a British radiochemist whose work relates to oncologic therapy and diagnosis. His research focus is a molecular imaging-based program focused on radiopharmaceutical development as well as the study of multimodality small- and biomolecule-based agents and their clinical translation. He has worked on the development of small molecules as well as radiolabeled peptides and antibodies probing the overexpression of receptors and antigens on tumors.

Neil Vasdev is a Canadian and American radiochemist and expert in nuclear medicine and molecular imaging, particularly in the application of PET. Radiotracers developed by the Vasdev Lab are in preclinical use worldwide, and many have been translated for first-in-human neuroimaging studies. He is the director and chief radiochemist of the Brain Health Imaging Centre and director of the Azrieli Centre for Neuro-Radiochemistry at the Centre for Addiction and Mental Health (CAMH). He is the Tier 1 Canada Research Chair in Radiochemistry and Nuclear Medicine, the endowed Azrieli Chair in Brain and Behaviour and Professor of Psychiatry at the University of Toronto. Vasdev has been featured on Global News, CTV, CNN, New York Times, Toronto Star and the Globe and Mail for his innovative research program.

References

  1. "Radiology | Michigan Medicine | University of Michigan". medicine.umich.edu. January 6, 2014. Retrieved May 1, 2019.
  2. "Medicinal Chemistry | UM College of Pharmacy". pharmacy.umich.edu. Retrieved May 1, 2019.
  3. "PET Center | Radiology | Michigan Medicine | University of Michigan". medicine.umich.edu. January 30, 2014. Retrieved May 1, 2019.
  4. "Peter J. Scott profile". mcommunity.umich.edu.
  5. Haynes, Sarah (October 3, 2018). "UM scientists improve synthesis of PET imaging molecules". lsa.umich.edu.
  6. Scott, Peter; Sanford, Melanie. "Copper-mediated Late-Stage Radiofluorination of Electron-rich Arenes".
  7. Wright, Jay S.; Kaur, Tanpreet; Preshlock, Sean; Tanzey, Sean S.; Winton, Wade P.; Sharninghausen, Liam S.; Wiesner, Nicholas; Brooks, Allen F.; Sanford, Melanie S.; Scott, Peter J. H. (May 26, 2020). "Copper-mediated late-stage radiofluorination: five years of impact on preclinical and clinical PET imaging". Clinical and Translational Imaging. 8 (3): 167–206. doi:10.1007/s40336-020-00368-y. ISSN   2281-5872. PMC   7968072 . PMID   33748018.
  8. Ichiishi, Naoko; Brooks, Allen F.; Topczewski, Joseph J.; Rodnick, Melissa E.; Sanford, Melanie S.; Scott, Peter J. H. (June 20, 2014). "Copper-Catalyzed [ 18 F]Fluorination of (Mesityl)(aryl)iodonium Salts". Organic Letters. 16 (12): 3224–3227. doi:10.1021/ol501243g. ISSN   1523-7060. PMC   4076000 . PMID   24890658.
  9. Mossine, Andrew V.; Brooks, Allen F.; Makaravage, Katarina J.; Miller, Jason M.; Ichiishi, Naoko; Sanford, Melanie S.; Scott, Peter J. H. (December 4, 2015). "Synthesis of [18F]Arenes via the Copper-Mediated [18F]Fluorination of Boronic Acids". Organic Letters. 17 (23): 5780–5783. doi:10.1021/acs.orglett.5b02875. ISSN   1523-7060. PMC   4672358 . PMID   26568457.
  10. 1 2 Makaravage, Katarina J.; Shao, Xia; Brooks, Allen F.; Yang, Lingyun; Sanford, Melanie S.; Scott, Peter J. H. (February 27, 2018). "Copper(II)-Mediated [11C]Cyanation of Arylboronic Acids and Arylstannanes". Organic Letters. 20 (6): 1530–1533. doi:10.1021/acs.orglett.8b00242. ISSN   1523-7060. PMC   5892454 . PMID   29484880.
  11. Makaravage, Katarina J.; Brooks, Allen F.; Mossine, Andrew V.; Sanford, Melanie S.; Scott, Peter J. H. (October 10, 2016). "Copper-Mediated Radiofluorination of Arylstannanes with [18F]KF". Organic Letters. 18 (20): 5440–5443. doi:10.1021/acs.orglett.6b02911. ISSN   1523-7060. PMC   5078836 . PMID   27718581.
  12. McCammant, Matthew S.; Thompson, Stephen; Brooks, Allen F.; Krska, Shane W.; Scott, Peter J. H.; Sanford, Melanie S. (July 21, 2017). "Cu-Mediated C–H 18F-Fluorination of Electron-Rich (Hetero)arenes". Organic Letters. 19 (14): 3939–3942. doi:10.1021/acs.orglett.7b01902. ISSN   1523-7060. PMC   5525103 . PMID   28665619.
  13. Lee, So Jeong; Makaravage, Katarina J.; Brooks, Allen F.; Scott, Peter J. H.; Sanford, Melanie S. (January 18, 2019). "Copper-Mediated Aminoquinoline-Directed Radiofluorination of Aromatic C−H Bonds with K18F". Angewandte Chemie International Edition. 58 (10): 3119–3122. doi:10.1002/anie.201812701. ISSN   1433-7851. PMC   6476334 . PMID   30605563.
  14. Lee, So Jeong; Brooks, Allen F.; Ichiishi, Naoko; Makaravage, Katarina J.; Mossine, Andrew V.; Sanford, Melanie S.; Scott, Peter J. H. (2019). "C–H 18F-fluorination of 8-methylquinolines with Ag[18F]F". Chemical Communications. 55 (20): 2976–2979. doi:10.1039/c9cc00641a. ISSN   1359-7345. PMC   6556205 . PMID   30778496.
  15. Sharninghausen, Liam S.; Brooks, Allen F.; Winton, Wade P.; Makaravage, Katarina J.; Scott, Peter J. H.; Sanford, Melanie S. (2020). "NHC-Copper Mediated Ligand-Directed Radiofluorination of Aryl Halides". Journal of the American Chemical Society. 142 (16): 7362–7367. doi:10.1021/jacs.0c02637. ISSN   0002-7863. PMC   7314054 . PMID   32250612.
  16. Stewart, Megan N.; Hockley, Brian G.; Scott, Peter J. H. (2015). "Green approaches to late-stage fluorination: radiosyntheses of 18F-labelled radiopharmaceuticals in ethanol and water". Chemical Communications. 51 (79): 14805–14808. doi:10.1039/c5cc05919d. ISSN   1359-7345. PMID   26300287.
  17. "Michigan Green Chemistry Governor's Awards Program". michigan.gov.
  18. Fellows. The Times, March 12, 2019, p. 55, col. E&F.
  19. "The Academy for Radiology & Biomedical Imaging Research Announces the Recipients of its Eighth Annual Distinguished Investigator Award" (PDF). acadrad.org.
  20. "SNMMI Fellows". snmmi.org.
  21. "Peter J. H. Scott, PhD, Receives SNMMI Sam Gambhir Trailblazer Award". snmmi.org.
  22. Linker Strategies in Solid-phase Organic Synthesis; https://onlinelibrary.wiley.com/doi/book/10.1002/9780470749043
  23. Solid-Phase Organic Syntheses, Volume 2: Solid-Phase Palladium Chemistry (Wiley Series on Solid-Phase Organic Syntheses); https://onlinelibrary.wiley.com/doi/book/10.1002/9781118336953
  24. Radiochemical Syntheses: Radiopharmaceuticals for Positron Emission Tomography, Volume 1; https://onlinelibrary.wiley.com/doi/book/10.1002/9781118140345
  25. Radiochemical Syntheses: Further Radiopharmaceuticals for Positron Emission Tomography and New Strategies for Their Production, Volume 2; https://onlinelibrary.wiley.com/doi/book/10.1002/9781118834114
  26. Handbook of Radiopharmaceuticals; https://onlinelibrary.wiley.com/doi/book/10.1002/9781119500575
  27. Production and Quality Control of Fluorine-18 Labelled Radiopharmaceuticals; https://www.iaea.org/publications/14925/production-and-quality-control-of-fluorine-18-labelled-radiopharmaceuticals