Assessment of Cavitation Intensity in Accelerating Syringes of Spring-Driven Autoinjectors
Javad Eshraghi1, Jean-Christophe Veilleux2, Galen Shi2
1Department of Mechanical Engineering, Purdue University, West Lafayette, IN, 47907, USA. jeshragh@purdue.edu.
Pharmaceutical Research
|July 19, 2022
Summary
Cavitation in autoinjectors (AIs) causes shock waves damaging drugs. Design parameters like spring force and air gap size significantly impact AI cavitation severity.
Area of Science:
- Biomedical Engineering
- Fluid Dynamics
- Pharmaceutical Technology
Background:
- Cavitation, a phenomenon of vapor-filled bubble formation and collapse due to pressure changes, can occur in autoinjectors (AIs).
- This collapse generates shock waves, potentially damaging sensitive protein drug molecules and the device itself.
- Understanding and mitigating cavitation is crucial for ensuring AI functionality and drug integrity.
Purpose of the Study:
- To investigate the influence of key design parameters on the risk and severity of cavitation in autoinjectors.
- To analyze the effects of air gap size, syringe filling volume, fluid viscosity, and drive spring force on cavitation dynamics.
- To quantify cavitation intensity using the extension rate as a key metric.
Main Methods:
- Development of a model autoinjector platform to record syringe and cavitation dynamics.
- Estimation of cavitation intensity through the measurement of the extension rate.
- Systematic variation of design parameters to study their impact on cavitation severity.
Main Results:
- Cavitation collapse generates intense shock waves and high extension rates.
- Higher syringe acceleration and filling volume increase the extension rate.
- Increased fluid viscosity and larger air gap size decrease the extension rate.
Conclusions:
- The most severe cavitation is observed with higher drive spring force and smaller air gap size.
- Less viscous fluids and larger filling volumes exacerbate cavitation severity.
- Optimizing AI design parameters is essential to minimize cavitation and protect drug products.


