Metformin is a relatively old drug mainly used to treat type 2 and gestational diabetes, which needs to be administered two or three times a day in high doses. It has a high aqueous solubility and is poorly absorbed following oral intake. Aiming to achieve a gastroretentive formulation for prolonged release of this drug, an expandable device based on an osmotically driven mechanism (ORODS, Organ-Retentive Osmotically Driven System) was developed. The system consists of an osmotic unit obtained from tubular dialysis membranes filled with an osmotic agent, and one or more drug release units containing metformin. Osmotic units were fabricated using dialysis membranes with different cutoffs (3.5–5 and 12–14 kD) and different osmotic agents, namely sodium chloride or mannitol. Drug release units were obtained by tableting metformin in admixture with high-viscosity hypromellose (Methocel® K15M) to give prolonged-release hydrophilic matrix systems. Multi-layered matrices having drug-free external layers were also designed, which led to a range of different release rates. The assembled ORODS devices were loaded into hard-gelatin capsules suitable for oral administration and, when in contact with pH 1.2 fluid, rapidly expanded thanks to osmotic water inflow, thus potentially preventing transit through the open pylorus in an in vivo setting. Metformin-containing units ultimately dissolved and/or eroded, while the osmotic units shrank and disassembled thereby ideally allowing for physiological emptying of the device from the stomach and intestinal elimination.

Gastroretentive systems for prolonged release of metformin based on osmotically driven expansion / M. Cirilli, S. Moutaharrik, L. Palugan, M.E. Coldani, A. Buscarini, G. Bruni, A. Gazzaniga, A. Maroni, A. Foppoli, M. Cerea. - In: INTERNATIONAL JOURNAL OF PHARMACEUTICS. - ISSN 0378-5173. - 681:(2025 Aug), pp. 125856.1-125856.26. [10.1016/j.ijpharm.2025.125856]

Gastroretentive systems for prolonged release of metformin based on osmotically driven expansion

M. Cirilli
Primo
;
S. Moutaharrik
Secondo
;
L. Palugan;M.E. Coldani;A. Buscarini;A. Gazzaniga;A. Maroni;A. Foppoli
Penultimo
;
M. Cerea
Ultimo
2025

Abstract

Metformin is a relatively old drug mainly used to treat type 2 and gestational diabetes, which needs to be administered two or three times a day in high doses. It has a high aqueous solubility and is poorly absorbed following oral intake. Aiming to achieve a gastroretentive formulation for prolonged release of this drug, an expandable device based on an osmotically driven mechanism (ORODS, Organ-Retentive Osmotically Driven System) was developed. The system consists of an osmotic unit obtained from tubular dialysis membranes filled with an osmotic agent, and one or more drug release units containing metformin. Osmotic units were fabricated using dialysis membranes with different cutoffs (3.5–5 and 12–14 kD) and different osmotic agents, namely sodium chloride or mannitol. Drug release units were obtained by tableting metformin in admixture with high-viscosity hypromellose (Methocel® K15M) to give prolonged-release hydrophilic matrix systems. Multi-layered matrices having drug-free external layers were also designed, which led to a range of different release rates. The assembled ORODS devices were loaded into hard-gelatin capsules suitable for oral administration and, when in contact with pH 1.2 fluid, rapidly expanded thanks to osmotic water inflow, thus potentially preventing transit through the open pylorus in an in vivo setting. Metformin-containing units ultimately dissolved and/or eroded, while the osmotic units shrank and disassembled thereby ideally allowing for physiological emptying of the device from the stomach and intestinal elimination.
Gastroretentive; Expandable; GREDDS; Metformin; Diabetes; Hydrophilic matrices; Dialysis membrane; ORODS; Osmotic expansion;
Settore CHEM-08/A - Tecnologia, socioeconomia e normativa dei medicinali e dei prodotti per il benessere e per la salute
ago-2025
19-giu-2025
https://www.sciencedirect.com/science/article/pii/S0378517325006933?via=ihub
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/1172877
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