Excipient effects on supersaturation, particle size dynamics, and thermodynamic activity of multidrug amorphous formulations

• Published in: International journal of pharmaceutics Vol. 666; p. 124738
• Main Authors: El Sayed, Mira, Alhalaweh, Amjad, Kovac, Lucia, Bergström, Christel A.S.
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 05-12-2024
• Subjects: Amorphous solubility; Dissolution; Excipients; Farmaceutisk vetenskap; Flux; Multidrug formulations; Particle size dynamics; Pharmaceutical Science; Supersaturation; FDA; ATV; DLS; PVP; Amorphous solubility; TPGS; ASD; Multidrug formulations; DSC; RTV; HPLC; PXRD; LLPS; Excipients; SDS; Flux; Supersaturation; Dissolution; BCS; CAS; HPMCAS; PVPVA; Particle size dynamics; GRAS; HPMC
• ISSN: 0378-5173; 1873-3476; 1873-3476
• DOI: 10.1016/j.ijpharm.2024.124738

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Multidrug formulations enhance patient compliance and extend the life cycle of pharmaceutical products. To overcome solubility challenges for multidrug combinations, amorphous formulations are commonly used. However, the excipients for creating amorphous formulations are often selected without an understanding of their effects on the bioavailability of the drugs. In this context, we investigated the impact of three types of excipients (polymers, surfactants and amino acids) on the supersaturation and thermodynamic activity of multidrug amorphous formulations. Additionally, we studied the particle size dynamics of the colloidal phase formed as a result of liquid–liquid phase separation. The amorphous solubility of two drugs, atazanavir and ritonavir, was determined in solutions containing predissolved excipients and the particle size dynamics of the colloidal particles was measured by dynamic light scattering. Dissolution experiments of atazanavir and ritonavir were conducted in predissolved sodium dodecyl sulfate (SDS), an anionic surfactant, and alanine solutions under non-sink conditions. Membrane transport of the drugs was evaluated using a MicroFLUX setup. The polymers had only minor effects on the amorphous solubility, but SDS significantly increased the solubilities of both drugs. In contrast, the other non-ionic surfactants and amino acids reduced the solubility of atazanavir but had no negative effect on ritonavir. Polymers were effective in maintaining supersaturation and preventing the coarsening of the colloidal particles. Conversely, alanine was neither able to inhibit the solution crystallization nor increase the flux of either drug. Despite the increase in the amorphous solubility of both drugs in SDS, flux was reduced. These results highlight the importance of properly selecting excipients for supersaturating amorphous formulations. The choice of excipient impacts the thermodynamic activity, the phase behaviour of the drugs and hence, the resulting absorption after oral intake.