Glycerol monostearate-based solid oleogels for dosage form individualization by molding designed using Design of
Asta Kabels1, Helena Sundgaard Trabjerg1, Felix Paulus1
1Drug Transport and Delivery Group, Department of Physics, Chemistry and Pharmacy, University of Southern Denmark, 5230 Odense, Denmark.
None:
Solidification of lipid-based formulations and dosage form individualization are two trends seen in oral drug delivery. This study proposes an approach for obtaining individualized solid lipid-based formulations, namely, glycerol monostearate-based solid oleogels individualized by molding. Oleogels consist of oil immobilized by a gelling agent. We investigated if it is possible to obtain glycerol monostearate-based oleogels that possess textural properties enabling them to be handled as solid dosage forms. Using DoE, the design space for preparing solid oleogels was established. Here, hardness and stiffness, derived from texture analysis, were used as responses in addition to moldability. The DoE study showed that glycerol monostearate-based solid oleogels can be obtained within a certain design space dependent on the gelling agent concentration, sorbitan monooleate concentration and gel setting temperature. Addition of sorbitan monooleate influenced the textural properties in a non-linear manner. The moldability evaluation yielded limits for hardness and stiffness where molding was possible. To assess the predictability of the DoE models, oleogels with new compositions within the design space were prepared and tested. As a proof-of-concept, ibuprofen-loaded oleogels were prepared and characterized in terms of textural properties, correctness of dosing, and drug release. The textural properties of ibuprofen-loaded oleogels were similar to those without ibuprofen when avoiding low gel setting temperatures. Correct dosing is possible as indicated by tests for uniformity of mass and content uniformity. Before testing ibuprofen release, disintegration was evaluated, indicating very slow disintegration. Disintegration was significantly improved by croscarmellose sodium and sodium starch glycolate. Similarly, during dissolution testing 70 and 25 % ibuprofen was released from glycerol monostearate-based solid oleogels with and without disintegrant, respectively. This study has established a first platform for moldable solid oleogels.
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