Rachel E Nuttall

School of Bioengineering and Imaging Sciences, King's College London 4th Floor Lambeth Wing, St Thomas' Hospital London SE1 7EH UK.

3 publications 2023 – 2025 ORCID

What does Rachel E Nuttall research?

Rachel E Nuttall studies how to create effective medical tracers that utilize radioactive materials to both diagnose diseases and treat them, specifically in the context of cancer. She has developed a method for attaching glucose molecules to radioactive atoms like technetium and rhenium. This allows for a versatile platform that can be used in medical applications to detect tumors through imaging scans while also delivering radiation therapy to destroy cancer cells, all using a single type of molecule. This research aims to improve the efficiency and safety of cancer treatments.

Key findings

  • Successfully achieved over 95% success rate in attaching radioactive atoms to glucose-based compounds.
  • Tested in mice showed that the resulting molecules traveled quickly through the bloodstream.
  • Demonstrated that these molecules can be safely cleared through the kidneys while remaining stable in the body.

Frequently asked questions

Does Dr. Nuttall study cancer treatment?
Yes, her work focuses on developing methods to use radioactive molecules for both diagnosing and treating cancer.
What techniques does Dr. Nuttall use in her research?
She uses a method called hydrophosphination to attach glucose molecules to radioactive atoms, enhancing their use in medical applications.
Is Dr. Nuttall's work relevant to patients undergoing cancer treatment?
Absolutely! Her research aims to create medical tracers that can improve the effectiveness of cancer diagnostics and therapies.

Publications in plain English

Maleic anhydride derived diphosphines: adaptable chelators for receptor-targetedTc,Cu andRe radiotracers.

2025

Chemical science

Nuttall RE, Hungnes IN, Pham TT, Carter OWL, Rigby A +11 more

Plain English
This study focused on developing two new chemical compounds, called DP and DP, that help attach radioactive materials to cancer-targeting molecules for better imaging of tumors using a technique called SPECT. The researchers found that these new compounds led to improved results, with a high success rate in radiolabelling, such as 90% yields, and showed promising imaging properties in mouse models of prostate cancer. This is important because it could lead to more effective and efficient ways to detect and treat cancer in the future. Who this helps: Patients with cancer, particularly those with prostate cancer.

PubMed

Versatile Diphosphine Chelators for Radiolabeling Peptides withTc andCu.

2023

Inorganic chemistry

Hungnes IN, Pham TT, Rivas C, Jarvis JA, Nuttall RE +5 more

Plain English
Researchers created a new method using diphosphine chelators to attach radioactive materials to peptides for better imaging in medical scans called SPECT and PET. They tested this method on certain cancer-targeting peptides and achieved successful results: two of the new radiotracers had high yields of 81% and 88% in just 5 minutes at 100°C, and over 95% yield with copper, meaning they worked very efficiently. This is important because it could lead to improved imaging techniques for diagnosing diseases like cancer, allowing doctors to see and target specific areas in the body more effectively. Who this helps: This helps patients who need accurate imaging for cancer diagnosis and treatment.

PubMed

Diphosphine Bioconjugates via Pt(0)-Catalyzed Hydrophosphination. A Versatile Chelator Platform for Technetium-99m and Rhenium-188 Radiolabeling of Biomolecules.

2023

Inorganic chemistry

Nuttall RE, Pham TT, Chadwick AC, Hungnes IN, Firth G +5 more

Plain English
Researchers developed a new chemical method to attach glucose molecules to special compounds that can grab onto radioactive atoms (technetium and rhenium), making it possible to create medical tracers that both diagnose diseases and treat them simultaneously. They successfully attached these radioactive atoms to glucose-based compounds with very high efficiency (over 95% success rate), and tests in mice showed the resulting molecules traveled quickly through the bloodstream and were safely cleared through the kidneys while remaining stable in the body. This breakthrough could allow doctors to use a single type of molecule for both detecting tumors with imaging scans and destroying cancer cells with radiation therapy.

PubMed

Publication data sourced from PubMed . Plain-English summaries generated by AI. Not medical advice.