Раціональний дизайн багатокомпонентних твердих дисперсій ривароксабану методами термодинамічного та статистичного моделювання

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

Authors

Institutions

Publication Details

Journal
The Scientific Issues of Ternopil Volodymyr Hnatiuk National Pedagogical University Series pedagogy
Published
2026-08-31
Primary Topic
Drug Solubulity and Delivery Systems
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
article

Раціональний дизайн багатокомпонентних твердих дисперсій ривароксабану методами термодинамічного та статистичного моделювання

Володимир Іванович Бессарабов, Олександр Олександрович Чорний, Р. О. Смішко, Вадим Миколайович Лісовий et al.
The Scientific Issues of Ternopil Volodymyr Hnatiuk National Pedagogical University Series pedagogy
Drug Solubulity and Delivery Systems
article

Раціональний дизайн багатокомпонентних твердих дисперсій ривароксабану методами термодинамічного та статистичного моделювання

Володимир Іванович Бессарабов, Олександр Олександрович Чорний, Р. О. Смішко, Вадим Миколайович Лісовий, Вікторія Віталіївна Лижнюк, Володимир Володимирович Федоренко, Володимир Володимирович Яременко, Андрій Михайлович Гой, Анастасія Олександрівна Бегдай, Світлана Миколаївна Гуреєва
article en

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

The Scientific Issues of Ternopil Volodymyr Hnatiuk National Pedagogical University Series pedagogy
Kyiv National University of Technologies and Design (UA), Farmak (Czechia) (CZ), Institute of Physical and Organic Chemistry (BY)
Openalex Percentile: Top 11%
Drug Solubulity and Delivery Systems
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.