Skip to content
Open access

Rational design of multicomponent rivaroxaban solid dispersions using thermodynamic and statistical modeling

Aug 2026 · ScienceRise Pharmaceutical Science · 0 citations · 7 references

TL;DR

The phenomenological Jouyban-Acree model combined with statistical simulation minimizes the volume of routine testing and reliably predicts the stability of systems during their industrial scale-up.

Abstract

The aim. The aim of the work is to study the effect of hydrophilic polymers (PVP K-12, PVP K-17, HPC) and excipients (sucrose, mannitol) on rivaroxaban supersaturation, as well as to apply thermodynamic modeling to determine the optimal composition and evaluate the robustness of ternary solid dispersion systems (SDS). Materials and methods. Rivaroxaban, polyvinylpyrrolidone (PVP K-12, K-17), hydroxypropyl cellulose (HPC), sucrose, and mannitol were used to obtain SDS. Fibers were obtained by centrifugal melt spinning at 160 - 200 °C. Equilibrium solubility was determined spectrophotometrically (250 nm) at 25 °C. A log-linear model and Jouyban-Acree polynomials were applied for optimization. The stability of the systems against fluctuations was evaluated using parametric bootstrapping and Monte Carlo simulation. Results. The intrinsic solubility of the drug is 0.017 g/L. The addition of excipients to PVP matrices promoted a nonlinear increase in solubility, with the PVP K-17 and sucrose composition exhibiting the highest effect. In HPC matrices, excipients decreased solubility due to gelation kinetics. According to the Akaike information criterion, the full Jouyban-Acree model was proven to be optimal for describing the systems. Modeling allowed shifting the theoretical optimum of the PVP K-17 + Sucrose composition to a ratio of 5:83:12 with a maximum calculated solubility of 1.470 g/L. Bootstrap analysis confirmed the thermodynamic stability of this system even under 5% technological noise, whereas HPC matrices demonstrated significant variability. Conclusions. The integration of the in silico approach within the Quality by Design framework effectively optimizes the composition of multicomponent rivaroxaban SDS. PVP matrices with sucrose increased the API solubility by more than 86 times. The phenomenological Jouyban-Acree model combined with statistical simulation minimizes the volume of routine testing and reliably predicts the stability of systems during their industrial scale-up

Read PDF

Similar papers

Aug 2026

Mechanistic Insights into Supersaturation Control of Itraconazole Amorphous Solid Dispersions Under Physiological Hydrodynamics: An Experimental and Computational Study

Hydrodynamic shear and medium ionic strength jointly influence ASD supersaturation and precipitation behavior and their simultaneous consideration may improve the biorelevance of ASD dissolution testing.

Dilpreet Singh · 0 citations
Open access Sep 2026

DEVELOPMENT, CHARACTERIZATION AND OPTIMIZATION OF DOLUTEGRAVIR SOLID DISPERSIONS USING PEG 6000 AND PVP K30: COMPARATIVE PROCESSING, FACTORIAL DESIGN AND TABLET DEVELOPMENT

The developed solid-dispersion approach substantially improved dolutegravir solubility and dissolution compared with the pure drug and physical mixtures, confirming the potential of solid dispersion for improving the formulation characteristics of dolutegravir.

Krupaben Pravinbhai Patel, S. Thakral · 0 citations
Open access 2026

Evaluation of release enhancement of efavirenz through poloxamer solid dispersions

Poloxamers are triblock copolymers commonly used in pharmaceutical formulation development to enhance the solubility of poorly water-soluble compounds. The present study investigated the efficiency of the hydrophilic carriers, poloxamer 188 (P188) and poloxamer 407 (P407), in preparing solid dispersions (SDs) of efavir...

E. M. Nazareth, G. D. de Araújo, Felipe Guizze de Souza et al. · 0 citations
Sep 2026

Development and Evaluation of a Prolonged-Release Imeglimin Hydrochloride Matrix Tablet using Hydrophilic-Hydrophobic Polymer Blends

Objective: The present work was aimed at designing and optimizing a prolonged-release matrix tablet of Imeglimin hydrochloride (500 mg) employing binary polymer combinations of hydroxypropyl methylcellulose (HPMC) K100M and Carbopol 940P as rate-controlling polymers for sustained antihyperglycemic action over 12 hours,...

Shailendra Singh Narwariya · 1 citation
Open access Sep 2026

10- Circumventing the Thermal Degradation of Atorvastatin Calcium to Facilitate its Production by Melt Extrusion

Atorvastatin (ATV), a widely used lipid-lowering agent, faces significant formulation challenges due to its poor aqueous solubility and thermal instability. This study aims to develop a melt-extrudable formulation of ATV while mitigating the risk of its thermal degradation. Through the use of hot-melt extrusion (HME) m...

Jehad Nasereddin, Roza Younis, Jameel S. AljaririAlhesan et al. · 0 citations
Oct 2026

Design and optimization of HME-based floating dolutegravir extrudates with enhanced drug release and potent anti-viral activity.

The hot-melt extrusion (HME) technique is quite successful in improving the solubility and bioavailability of poorly water-soluble drugs. Herein, we report the development of optimized dolutegravir floating systems prepared by the HME technique using Design-Expert software. Optimized parameters for floating extrudate i...

Manisha S. Jain, Akash G. R., B. Gowthami et al. · 0 citations

We use cookies to run the site and, with your consent, for analytics and to show ads. See our Cookie Policy.