Max Bullock
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Max Bullock has a total of 29 co-authors. Here are the top co-authors by number of shared publications:
- Adam Retter
Centre for Medical Imaging, UCL, London, UK
2 shared publications - Alan Bainbridge
Department of Medical Physics and Biomedical Engineering, University College London Hospital , London, UK
2 shared publications - Christoph Müller
NVision Imaging Technologies GmbH, 89081, Ulm, Germany
2 shared publications - David G. Gadian
Institute of Child Health, University College London, London, UK
2 shared publications - Fiona Gong
UCL, Ctr Med Imaging, Div Med, London, England
2 shared publications - Lorna Smith
UCL, Ctr Med Imaging, Div Med, London, England
2 shared publications
Latest Publications
- Open Access
- 1 January 2023
- Vol. 9 (6) , 20220089
First- in- human in- vivo depiction of paraganglioma metabolism by hyperpolarised 13C-magnetic resonance
Phaeochromocytomas (PCC) and paragangliomas (PGL), cumulatively referred to as PPGLs, are neuroendocrine tumours arising from neural crest- derived cells in the sympathetic and parasympathetic nervous systems. Predicting future tumour behaviour and the likelihood of metastatic disease remains problematic as genotype-phenotype correlations are limited, the disease has variable penetrance and, to date, no reliable molecular, cellular or histological markers have emerged. Tumour metabolism quantification can be considered as a method to delineating tumour aggressiveness by utilising hyperpolarised 13 C- MR (HP- MR). The technique may provide an opportunity to non- invasively characterise disease behaviour. Here, we present the first instance of the analysis of PPGL metabolism via HP- MR in a single case.
- 1 January 2023
- Vol. 9 (6) , 20220089
Open AccessFirst- in- human in- vivo depiction of paraganglioma metabolism by hyperpolarised 13C-magnetic resonance
Phaeochromocytomas (PCC) and paragangliomas (PGL), cumulatively referred to as PPGLs, are neuroendocrine tumours arising from neural crest- derived cells in the sympathetic and parasympathetic nervous systems. Predicting future tumour behaviour and the likelihood of metastatic disease remains problematic as genotype-phenotype correlations are limited, the disease has variable penetrance and, to date, no reliable molecular, cellular or histological markers have emerged. Tumour metabolism quantification can be considered as a method to delineating tumour aggressiveness by utilising hyperpolarised 13 C- MR (HP- MR). The technique may provide an opportunity to non- invasively characterise disease behaviour. Here, we present the first instance of the analysis of PPGL metabolism via HP- MR in a single case.
- Open Access
- 8 March 2022
- Published by Oxford University Press (OUP) in British Journal of Radiology
- Vol. 95 (1134) , 20210770
A reproducible dynamic phantom for sequence testing in hyperpolarised 13C-magnetic resonance
Objective: To develop a phantom system which can be integrated with an automated injection system, eliminating the experimental variability that arises with manual injection; for the purposes of pulse sequence testing and metric derivation in hyperpolarised 13C-MR. Methods: The custom dynamic phantom was machined from Ultem and filled with a nicotinamide adenine dinucleotide and lactate dehydrogenase mixture dissolved in phosphate buffered saline. Hyperpolarised [1-13C]-pyruvate was then injected into the phantom (n = 8) via an automated syringe pump and the conversion of pyruvate to lactate monitored through a 13C imaging sequence. Results: The phantom showed low coefficient of variation for the lactate to pyruvate peak signal heights (11.6%) and dynamic area-under curve ratios (11.0%). The variance for the lactate dehydrogenase enzyme rate constant (kP) was also seen to be low at 15.6%. Conclusion: The dynamic phantom demonstrates high reproducibility for quantification of 13C-hyperpolarised MR-derived metrics. Establishing such a phantom is needed to facilitate development of hyperpolarsed 13C-MR pulse sequenced; and moreover, to enable multisite hyperpolarised 13C-MR clinical trials where assessment of metric variability across sites is critical. Advances in knowledge: The dynamic phantom developed during the course of this study will be a useful tool in testing new pulse sequences and standardisation in future hyperpolarised work.
- 8 March 2022
- Published by Oxford University Press (OUP) in British Journal of Radiology
- Vol. 95 (1134) , 20210770
Open AccessA reproducible dynamic phantom for sequence testing in hyperpolarised 13C-magnetic resonance
Objective: To develop a phantom system which can be integrated with an automated injection system, eliminating the experimental variability that arises with manual injection; for the purposes of pulse sequence testing and metric derivation in hyperpolarised 13C-MR. Methods: The custom dynamic phantom was machined from Ultem and filled with a nicotinamide adenine dinucleotide and lactate dehydrogenase mixture dissolved in phosphate buffered saline. Hyperpolarised [1-13C]-pyruvate was then injected into the phantom (n = 8) via an automated syringe pump and the conversion of pyruvate to lactate monitored through a 13C imaging sequence. Results: The phantom showed low coefficient of variation for the lactate to pyruvate peak signal heights (11.6%) and dynamic area-under curve ratios (11.0%). The variance for the lactate dehydrogenase enzyme rate constant (kP) was also seen to be low at 15.6%. Conclusion: The dynamic phantom demonstrates high reproducibility for quantification of 13C-hyperpolarised MR-derived metrics. Establishing such a phantom is needed to facilitate development of hyperpolarsed 13C-MR pulse sequenced; and moreover, to enable multisite hyperpolarised 13C-MR clinical trials where assessment of metric variability across sites is critical. Advances in knowledge: The dynamic phantom developed during the course of this study will be a useful tool in testing new pulse sequences and standardisation in future hyperpolarised work.