= LhARA radiobiology; meeting: 23Jul26; 14:00 GMT = **ZOOM:** https://imperial-ac-uk.zoom.us/j/98220889714?pwd=SM90vOF7BKSXoU3mD9q7OwBQo4IVB3.1 == Agenda == 1. Long-term LhARA Biology Plan - JMcG&KL: Presentation - General Discussion 2. Overview of Current SCAPA Plan - Solutions to the three main problems: - Move the scatterer further up the beamline (closer to the laser-target). - Use a real-time diagnostic - Investigate how long the cells survive and the cause of death - Additions: - Collect more biology results? - When?: - Robbie mentioned February - Need to be ready to latch onto any downtime of other experiments - More information: https://docs.google.com/document/d/1OTARVtxhLRu02S6CLdRDB2QlGvCqDfZ3aWBifjIFs_Q/edit?tab=t.0 - Steps required: Below and at https://trello.com/invite/b/67587c515b0c69656ee78b48/ATTIe86f94b24e3e5884e4cb87e5ed3b89ab64321B83/poplar 3. Instrumentation Discussion - Options: - Sparse scintillating fibre arrays in the vacuum chamber - Scintillating fibre around the cell dish - Lanex around the cell dish - Integrated Current Transformers (ICTs) - Laser Diagnostics (Backscatter etc) - Replace the scatterer with a scintillating sheet - (RCF around the cell dish (if desperate)) - Testing method: - Calibrate with RCF? - No calibration. Use lots of cell dishes and match the distribution of variation in diagnostic output to the "known" distribution of the shot-to-shot variation - LET Detector 4. BioPrep Discussion - Spatial Variation: Is a CV of 8% acceptable? - Cell Control Survival: - Need to test how long cells can remain vertical - Can reduce the time taken to conduct the irradiations (and therefore the time the cells are vertical for) - Monitor the temperature of the thermostat - Better instrumentation: - Inverted microscope - Multi-chamber haemocytometer - More results (as well as clonogenics): - Comet analyses - X-ray comparison on-site 5. Alternate Beamlines - ELI Rejected - Waiting for feedback 6. Discussion on Ion-Acoustic Plan - Current updates 7. DoNM - 06/08/26 8. AoB === Summary of actions required === In-Beam Diagnostics - **Unassigned**: Acquire a glass sheet - **Unassigned**: Get a new RCF batch and calibrate - **TP**: Testing delaminating EBT3 - **PH**: Obtain transparent fibre or an alternative method for light transport - **PH**: Obtain a lens for hollow fibre tests - **CD**: Simulate energy deposited in transport fibres - **KL, CD, JMcG, PH**: Design a system to make full scifi prototypes - **KL, CD, JMcG, PH**: Make a full scifi prototype - **KL, CD, JMcG, PH**: Discuss visit to Birmingham to test SciFi - **RW, CD**: Study the correlation between laser diagnostics and mean dose - **Unassigned**: Investigate how a phosphor sheet could be incorporated into the design of the cell dish - **CW**: Investigate the feasibility of ICTs for our beamline - **MH**: Investigate LET detector Bio Next Steps - **EM, CD, JMcG**: Write up technical summary of Phase 2 - **EM**: Write up a biology plan for a 2 PMQ setup - **Unassigned**: Obtain an inverted microscope - **Unassigned**: Obtain multi-chamber haemocytometers (Might be able to use Birmingham's) - **Unassigned**: Obtain a thermostat for the incubator - **MB, JP, MB**: Meet up to plan cell survival dry run and a bio plan for a 2 Quad setup - **EM**: Run controls to examine how long the cells can survive vertically Beamline Modelling - **CD**: Examine energy spectra variation - **RW, CD**: Source characterisation Alternate Beamlines - **JMcG**: Simulate BELLA - **JMcG**: Simulate ELI ----