Modernizing Auto-Injector Plungers: Meeting the Challenges of Complex Molecules
As pharmaceutical formulations become more complex, the need for precision and reliability in auto-injector technology has never been greater. Traditional plungers, once considered adequate for simpler drug formulations, are now facing limitations when it comes to delivering modern complex molecules. In this article, we will explore why traditional plungers may not be suitable for these advanced medications and outline key considerations for selecting plungers tailored to the needs of auto-injectors delivering complex molecules.
Challenges with Traditional Plungers:
- Chemical Compatibility:
Traditional plungers are commonly made from materials like rubber or silicone, which may not be compatible with the chemical composition of modern complex molecules. This lack of compatibility can lead to interactions between the plunger material and the drug formulation, potentially causing degradation or alteration of the medication's properties.
- Precision and Dosage Accuracy:
Modern pharmaceuticals often require precise dosing due to their potent nature and narrow therapeutic windows. However, traditional plungers may not offer the level of precision needed to ensure accurate dosing with each injection. Variability in dosing can lead to suboptimal treatment outcomes or adverse effects, impacting patient safety and treatment efficacy.
- Mechanical Performance:
Auto-injectors must deliver medication reliably and consistently, even in challenging conditions. Traditional plungers may exhibit limitations in mechanical performance, such as inconsistent injection forces or difficulty in expelling the medication completely. These issues can undermine patient confidence in the device and compromise treatment adherence.
Overcoming these challenges require consideration of modern, purpose designed components for complex molecules. Some Key Considerations for Choosing Plungers include,
- Material Selection:
Plungers as well as corresponding coating and films should be made from materials that offer superior chemical resistance and stability. These materials should be compatible with a wide range of drug formulations and maintain structural integrity under various conditions.
- Precision Engineering for performance:
Modern plungers should be designed with precision engineering techniques to ensure consistent and reliable performance. Performance, including accuracy of delivered volume, injection (delivery) time, break loose and glide force (BLG) performance, and work of extrusion in different viscosities representative of common biologic drug formulations should be considered. Features such as micro-precision molding and optimized geometries can enhance the functionality of plungers, enabling precise delivery of medication with each injection.
- Compatibility and Integration:
Plungers must integrate seamlessly with the overall design of the auto-injector system to ensure optimal functionality and user experience. Factors such as plunger dimensions, compatibility with needle assemblies, and ease of assembly should be considered to facilitate smooth operation and patient acceptance of the device.
- Regulatory Compliance:
Manufacturers must ensure that the selected plungers meet regulatory standards for safety and efficacy. Compliance with guidelines such as ISO 11608 for auto-injectors and USP <381> for elastomeric closures is essential to ensure product quality and patient safety.
- User Feedback and Usability:
Gathering feedback from end-users, such as patients and healthcare professionals, is crucial in selecting plungers that meet their needs and preferences. Factors such as ease of use, ergonomic design, and patient-friendly features should be taken into account to enhance usability and promote patient adherence to treatment regimens.
Conclusion:
As pharmaceutical formulations continue to advance, the importance of selecting appropriate components for auto-injectors, including plungers, cannot be overstated. By considering factors such as material compatibility, precision engineering, regulatory compliance, user feedback, and usability, manufacturers can ensure that auto-injectors are capable of delivering complex molecules safely and effectively.
By addressing these considerations, manufacturers can develop auto-injectors that meet the evolving needs of patients and healthcare providers, ensuring the safe and effective delivery of modern complex molecules.
To read more details on the Performance of Novapure® Plungers for Syringes in Autoinjector Systems check out our whitepaper.
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References:
Davis, A. M., & Graham, A. D. (2015). Precision Drug Delivery: A Review of Modern Techniques and Emerging Therapeutic Applications. Pharmaceutics, 7(3), 137–143.
Vora, R., Gupta, N., & Mittal, G. (2018). Challenges and Solutions in the Development of High Viscosity Injectable Formulations. Therapeutic Delivery, 9(10), 727–744.
Ratnaparkhi, M. P., Nagarsenker, M. S., & Kulkarni, P. V. (2014). Silicone and Its Applications in Drug Delivery: A Review. Current Drug Delivery, 11(6), 665–684.
Pohl, C., Koch, S., & Berchtold, B. (2017). Cyclic Olefin Copolymers: A Review on Material Design, Synthesis, and Biomedical Applications. ChemistryOpen, 6(4), 456–469.
ISO 11608-1:2014. Needle-based injection systems for medical use – Requirements and test methods – Part 1: Needle-based injection systems. International Organization for Standardization.
NovaPure is a registered trademark of West Pharmaceutical Services, Inc.