Floating drug delivery systems (FDDS) are gastroretentive oral dosage forms designed to remain buoyant in the stomach and prolong gastric residence. They are particularly useful for drugs with a narrow absorption window in the upper gastrointestinal tract, limited intestinal solubility, short biological half-life, or a requirement for local gastric action. However, conventional FDDS are influenced by gastric physiology, fixed dosage designs, limited dose flexibility, and manufacturing challenges Three-dimensional (3D) printing is an additive manufacturing technology that enables precise control over dosage-form geometry, internal architecture, porosity, density, drug loading, and drug-release characteristics. This review discusses the principles and classification of FDDS and explores their integration with 3D printing. Major pharmaceutical printing techniques, including fused deposition modelling (FDM), semi-solid extrusion (SSE), selective laser sintering (SLS), thermal inkjet printing, and binder jetting, are reviewed with emphasis on their applicability to gastroretentive systems. 3D-printed gastroretentive systems have demonstrated rapid buoyancy, prolonged and controlled drug release, customized dosage-form geometry, and the potential for patient-specific dosing. These approaches provide greater flexibility in designing floating systems compared with conventional manufacturing methods. Despite these advantages, challenges related to printable materials, thermal or solvent exposure, drug-loading capacity, dimensional accuracy, scale-up, quality control, reproducibility, and regulatory requirements remain. Advances in pharmaceutical materials, digital design, process monitoring, and predictive modelling may facilitate the translation of 3D-printed FDDS into personalized oral drug delivery.
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Aruna et al. (2026) studied this question.
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