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Lipid Nanoparticle Technologies after the mRNA Platform Era: Manufacturing Fragility, Platform Logic, and System Design
The clinical success of mRNA–lipid nanoparticle vaccines transformed lipid nanoparticle technology from a specialised drug delivery field into a central modality for modern biopharmaceutical development. That success demonstrated that nucleic acid therapeutics can be manufactured, distributed, and deployed at unprecedented speed when formulation science, process engineering, and regulatory urgency align. Yet the same success also exposed how dependent LNP products remain on tightly constrained composition, process history, and cold-chain stability. The central problem is that processes optimised rapidly under pandemic conditions do not automatically constitute robust manufacturing platforms. Many LNP processes remain product-specific, empirically tuned, and sensitive to changes in lipid composition, aqueous phase conditions, mixing geometry, and downstream handling. The language of “platform” is therefore often stronger than the underlying evidence for generalisable process robustness. The review maps the structural and functional logic of LNP platforms, evaluates how mRNA delivery requirements shaped formulation choices, and assesses preclinical and manufacturing evidence across laboratory, preclinical, and scalable production contexts. It identifies recurrent fragility points including mixing sensitivity, particle heterogeneity, aggregation, mRNA degradation, storage instability, and incomplete comparability evidence after process change. Five tables summarise platform design, mRNA delivery requirements, manufacturing evidence, fragility points, and a system design strategy for robust LNP production. The post-mRNA era requires a shift from emergency product development to platform-centred system design. LNP manufacturing must become modular, measurable, scalable, and quality-resilient rather than merely reproducible under narrowly defined conditions. Achieving this transition is essential if LNP technologies are to move beyond COVID-19 vaccines into broader therapeutic applications and more equitable global health deployment.
Journal of Applied Pharmaceutical Technologies and Systems
Review | Open access | 10 January 2026 | Article: 187
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Advanced Characterization of Bio-Nano Systems Advanced Drug Delivery Technologies Automation, Robotics and Digitalization in Pharmaceutical Manufacturing Bio-Nano Environmental Monitoring and Remediation Bio-Nano Interfaces and Interactions Bio-Nano Reproducibility, Standardization, Quality and Regulation Bio-Nano Systems Bio-Nano Technologies for Food, Agriculture and Industrial Biotechnology Bio-Nano Translation, Scale-up and Manufacturing Bio-enabled and Bio-inspired Nanoscale Materials Bioactive Scaffolds and Biomimetic Materials Biocompatibility, Biodistribution and Degradation Bioelectronics and Nano-Bioelectronics Biological Information Transfer and Bio-inspired Communication Systems Biologics Manufacturing Technologies Biomaterials Biopharmaceutical Processing and Manufacturing Biosensors, Nanosensors and Bioanalytical Platforms Clinical and Biomedical Technologies Computational Modeling and Simulation of Bio-Nano Systems Controlled, Targeted and Responsive Delivery Platforms Data and Reporting Standards Diagnostic and Therapeutic Applications Drug Delivery Systems Drug Formulation and Dosage-form Development Environmental Fate and Risk Evaluation of Bio-Nano Materials Good Manufacturing Practice (GMP) and Manufacturing Compliance Green Pharmaceutical Engineering and Resource Efficiency Green and Sustainable Synthesis of Nanomaterials Interdisciplinary Health Sciences Lab-on-chip and Micro/Nanofluidic Systems Lyophilization Machine Learning and Data-driven Methods for Bio-Nano Systems Medical and Dental Applications Modeling, Simulation and Computational Methods for Pharmaceutical Processes Molecular and Nanoscale Communication Nano-Bio Imaging and Contrast Agents Nano-enabled Biomedical Technologies Nano-enabled Drug Delivery Nanobiotechnology and Bionanotechnology Nanomaterials for Biomedical and Biological Applications Nanomedicine and Nano-enabled Therapeutic Systems Nanopharmaceuticals Nanotechnology Nanotechnology in Dentistry and Oral Health Nanotoxicology and Bio-Nano Safety Assessment Open Science Optical and Photonic Bio-Nano Systems Pharmaceutical Contamination Control Pharmaceutical Engineering Pharmaceutical Manufacturing Sustainability Pharmaceutical Manufacturing Systems Pharmaceutical Manufacturing Technologies Pharmaceutical Materials and Excipients Pharmaceutical Nanotechnology Pharmaceutical Packaging and Container-closure Systems Pharmaceutical Particle Engineering and Processing Pharmaceutical Process Development Pharmaceutical Process Monitoring and Real-time Quality Assurance Pharmaceutical Process Optimization Pharmaceutical Process Validation Pharmaceutical Production Systems Pharmaceutical Production Technologies Pharmaceutical Quality Control and Quality Assurance Pharmaceutical Regulatory Science and Validation Studies Pharmaceutical Scale-up and Technology Transfer Pharmaceutical Stability, Storage and Cold Chain Pharmaceutical Supply, Distribution, Traceability and Serialization Pharmaceutical Technology Point-of-care Technologies Process Analytical Technology (PAT) Publication Ethics Quality and Production Technologies Quality by Design (QbD) and Design of Experiments Research Integrity Smart Materials with Nanoscale Structure or Function Sterile Manufacturing and Aseptic Processing Theranostics Tissue Engineering and Regenerative Medicine Translational Research Translational and Industrial Pharmaceutical Studies Wearable and Implantable Biointerfaces




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